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Элементы биологической целесообразности стресc–реакции






Изменения, возникающие при интенсивной стрессовой реакции, трудно отнести к адаптационным. Поэтому их характеризуют как патологический стресс или, иначе, дистресс. Вместе с тем, трудно себе представить, чтобы стандартная адаптационная реакция на необычные ситуации, потенциально угрожающие организму, была бы столь биологически нецелесообразной. Рассмотрим её элементы.

Стресс высокой интенсивности приводит к апоптотической гибели большей части тимоцитов. К действию глюкокортикоидов, как отмечалось выше, наиболее чувствительны кортикальные тимоциты фенотипа CD4CD8, не экспрессирующие протоонкоген Вс1–2. Это определило их первоначальное название как чувствительные к кортизону клетки. Именно среди этой популяции тимических клеток и содержатся потенциально аутоагрессивные, не прошедшие отбор T–лимфоциты. При повреждении зоны тимуса они могут выйти в кровь или окружающие ткани и нанести существенный вред организму (а встреча с инфекцией может и не состояться). Высокая концентрация ГКС предотвращает такой вариант развития событий.

К действию ГКС, индуцирующих апоптоз, высоко чувствительны T–киллеры и NK, то есть клетки-эффекторы противовирусного иммунитета. Стратегия иммунной защиты от внутриклеточных паразитов заключается не в нейтрализации патогена, а в разрушении инфицированной клетки вместе с инфекционным агентом. Повреждение, вызванное клетками–киллерами, является обязательной платой за выздоровление при болезнях вирусной этиологии [59]. Одновременное разрушение большого массива поражённых вирусом клеток может нанести существенный вред организму [72]. Яркий пример вреда, который может нанести противовирусный иммунный ответ, проиллюстрирован следующими данными. Мышей заражали внутричерепным введением вируса лимфоцитарного хориоменингита. У нормальных инфицированных животных после этого возникает острое воспаление сосудистого сплетения, эпендимы, мягкой и паутинной оболочек мозга. Мыши погибали через 6–8 дней от полного разрушения ткани мозговых оболочек. Иммуносупрессированные мыши, заражённые этим вирусом, по продолжительности жизни не отличались от незаражённых, хотя в течение всей жизни в их мозговых оболочках обнаруживали персистенцию вируса. При введении таким животным нормальных T–клеток они быстро погибали от изменений, характерных для лимфоцитарного хориоменингита. Очевидно, что цитотоксические лимфоциты, специфичные к использованному вирусу, вызывают разрушение клеток, содержащих этот вирус, что приводит к разрушению мозговых оболочек. Вероятно, интенсивный синтез АКТГ, индуцируемый вирусной инфекцией, является одним из механизмов регуляции, сдерживающим развитие противовирусного иммунитета и уменьшающим тем самым интенсивность повреждения.

Биологически целесообразной является, по-видимому и конечная стадия стресса — стадия истощения. Как отмечалось выше, в основе стресc–реакции лежит гиперпродукция ГКС. Чем продолжительнее стресс и выше уровень гормонов, тем более выражено не только угнетение функций лимфоцитов, но и повреждение других тканей. Повышенное содержание в крови ГКС сопровождается подавлением воспалительной реакции, задержкой заживления ран, развитием некроза. Вызываемое ГКС повышенное выделение с мочой азотсодержащих соединений свидетельствует о распаде тканевых белков, что может привести к атрофии скелетных мышц, истончению эпидермиса, распаду эпителиальных клеток соединительной ткани. Длительный интенсивный стресс заканчивается стадией истощения. Надпочечники уменьшаются в размерах, значительно снижается содержание ГКС в крови. Эта стадия, вероятно, является необходимым условием для восстановления повреждений, полученных организмом как в результате действия факторов, вызвавших стресс, так и самого стресса. Снижение уровня ГКС в стадии истощения сопровождается нормализацией синтеза белков, восстановлением барьерной функции, уменьшением уровня апоптотической гибели клеток. Усиливается миграция стволовых клеток из костного мозга (глава 3 «Миграция стволовых клеток, T– и B–лимфоцитов», раздел «Контроль рециркуляции стволовых клеток»). Их поступление с кровотоком в повреждённую ткань способствует её восстановлению. Иначе говоря, несмотря на высокую чувствительность организма в стадии истощения к действию повреждающих факторов, в благоприятных условиях эта стадия стресса способствует восстановлению повреждённых органов и систем.

Таким образом, при интенсивной стресc–реакции организм, для того чтобы все силы направить на преодоление опасности, угрожающей жизни в данный момент, приостанавливает действие клеток-эффекторов, развитие противовирусного иммунитета, способного нанести вред организму. Одновременно с этим, в стадии истощения, возникают условия для нормализации нарушенных функций. Эти рассуждения подводят нас к мысли о том, что деление на физиологический и патологический стрессы, стресс и дистресс в значительной мере условно. Стресc–реакция — это один из механизмов физиологической реакции организма на чрезвычайные обстоятельства [84]. Цель реакции — избежать опасности, угрожающей жизни в данный момент. Стресс — это один из механизмов, с помощью которых все системы жизнеобеспечения направляются на достижение этой цели.

ЛИТЕРАТУРА

1. Marsh, D.G., and L.R. Freidhoff. 1992. ALBE, an allergen database. IUIS, Baltimore, MD, Edition 1.0.

2. Marsh, D. G., L. Goodfriend, T. P. King, H. Lowenstein, and T. A. E. Platts-Mills. 1986. Allergen nomenclature. Bull WHO 64: 767-770.

3. King, T.P., P.S. Norman, and J.T. Cornell. 1964. Isolation and characterization of allergen from ragweed pollen. II. Biochemistry 3: 458-468.

4. Lowenstein, H. 1980. Timothy pollen allergens. Allergy 35: 188-191.

5. Aukrust, L. 1980. Purification of allergens in Cladosporium herbarum. Allergy 35: 206-207.

6. Demerec, M., E. A. Adelberg, A. J. Clark, and P. E. Hartman. 1966. A proposal for a uniform nomenclature in bacterial genetics. Genetics 54: 61-75.

7. Bodmer, J. G., E. D. Albert, W. F. Bodmer, B. Dupont, H. A. Erlich, B. Mach, S. G. E. Marsh, W. R. Mayr, P. Parham, T. Sasuki, G. M. Th. Schreuder, J. L. Strominger, A. Svejgaard, and P. I. Terasaki. 1991. Nomenclature for factors of the HLA system, 1990. Immunogenetics 33: 301-309.

8. Griffith, I.J., J. Pollock, D.G. Klapper, B.L. Rogers, and A.K. Nault. 1991. Sequence polymorphism of Amb a I and Amb a II, the major allergens in Ambrosia artemisiifolia (short ragweed). Int. Arch. Allergy Appl. Immunol. 96: 296-304.

9. Roebber, M., D. G. Klapper, L. Goodfriend, W. B. Bias, S. H. Hsu, and D. G. Marsh. 1985. Immunochemical and genetic studies of Amb t V (Ra5G), an Ra5 homologue from giant ragweed pollen. J. Immunol. 134: 3062-3069.

10. Metzler, W. J., K. Valentine, M. Roebber, M. Friedrichs, D. G. Marsh, and L. Mueller. 1992. Solution structures of ragweed allergen Amb t V. Biochemistry 31: 5117-5127.

11. Metzler, W. J., K. Valentine, M. Roebber, D. G. Marsh, and L. Mueller. 1992. Proton resonance assignments and three-dimensional solution structure of the ragweed allergen Amb a V by nuclear magnetic resonance spectroscopy. Biochemistry 31: 8697-8705.

12. Goodfriend, L., A.M. Choudhury, J. Del Carpio, and T.P. King. 1979. Cytochromes C: New ragweed pollen allergens. Fed. Proc. 38: 1415.

13. Ekramoddoullah, A. K. M., F. T. Kisil, and A. H. Sehon. 1982. Allergenic cross reactivity of cytochrome c from Kentucky bluegrass and perennial ryegrass pollens. Mol. Immunol. 19: 1527-1534.

14. Ansari, A. A., E. A. Killoran, and D. G. Marsh. 1987. An investigation of human response to perennial ryegrass (Lolium perenne) pollen cytochrome c (Lol p X). J. Allergy Clin. Immunol. 80: 229-235.

15. Morgenstern, J.P., I.J. Griffith, A.W. Brauer, B.L. Rogers, J.F. Bond, M.D. Chapman, and M. Kuo. 1991. Amino acid sequence of Fel d I, the major allergen of the domestic cat: protein sequence analysis and cDNA cloning. Proc. Natl. Acad. Sci. USA 88: 9690-9694.

16. Griffith, I.J., S. Craig, J. Pollock, X. Yu, J.P. Morgenstern, and B.L.Rogers. 1992. Expression and genomic structure of the genes encoding FdI, the major allergen from the domestic cat. Gene 113: 263-268.

17. Weber, A., L. Marz, and F. Altmann. 1986. Characteristics of the asparagine-linked oligosaccharide from honey-bee venom phospholipase A2. Comp. Biochem. Physiol. 83B: 321-324.

18. Weber, A., H. Schroder, K. Thalberg, and L. Marz. 1987. Specific interaction of IgE antibodies with a carbohydrate epitope of honey bee venom phospholipase A2. Allergy 42: 464-470.

19. Stanworth, D. R., K. J. Dorrington, T. E. Hugli, K. Reid, and M. W. Turner. 1990. Nomenclature for synthetic peptides representative of immunoglobulin chain sequences. Bulletin WHO 68: 109-111.

20. Rafnar, T., I. J. Griffith, M. C. Kuo, J. F. Bond, B. L. Rogers, and D.G. Klapper. 1991. Cloning of Amb a I (Antigen E), the major allergen family of short ragweed pollen. J. Biol. Chem. 266: 1229-1236.

21. Rogers, B.L., J.P. Morgenstern, I.J. Griffith, X.B. Yu, C.M. Counsell, A.W. Brauer, T.P. King, R.D. Garman, and M.C. Kuo. 1991. Complete sequence of the allergen Amb a II: recombinant expression and reactivity with T cells from ragweed allergic patients. J. Immunol. 147: 2547-2552.

22. Klapper, D.G., L. Goodfriend, and J.D. Capra. 1980. Amino acid sequence of ragweed allergen Ra3. Biochemistry 19: 5729-5734.

23. Ghosh, B., M.P. Perry, T. Rafnar, and D.G. Marsh. 1993. Cloning and expression of immunologically active recombinant Amb a V allergen of short ragweed (Ambrosia artemisiifolia) pollen. J. Immunol. 150: 5391-5399.

24. Roebber, M., R. Hussain, D. G. Klapper, and D. G. Marsh. 1983. Isolation and properties of a new short ragweed pollen allergen, Ra6. J. Immunol. 131: 706-711.

25. Lubahn, B., and D.G. Klapper. 1993. Cloning and characterization of ragweed allergen Amb a VI (abst). J. Allergy Clin. Immunol. 91: 338.

26. Roebber, M., and D.G. Marsh. 1991. Isolation and characterization of allergen Amb a VII from short ragweed pollen. J. Allergy Clin. Immunol. 87: 324.

27 Goodfriend L, Choudhury AM, Klapper DG, Coulter KM, Dorval G, DelCarpio J, Osterland CK. Ra5G, a homologue of Ra5 in giant ragweed pollen: isolation, HLA-DR-associated activity and amino acid sequence. Mol Immunol 22: 899-906, 1985.

28 Himly M, Jahn-Schmid B, Dedic A, Kelemen P, Wopfner N, Altmann F, van Ree R, Briza P, Richter K, Ebner C, Ferreira F. Art v 1, the major allergen of mugwort pollen, is a modular glycoprotein with a defensin-like and a hydroxyproline-rich domain. FASEB J 17: 106-108, 2003.

28A Nilsen, B. M., K. Sletten, M. O'Neill, B. Smestead Paulsen, and H. van Halbeek. 1991. Structural analysis of the glycoprotein allergen Art v II from pollen of mugwort (Artemesia vulgaris). J. Biol. Chem. 266: 2660-2668.

29 Wopfner N, Willeroidee M, Hebenstreit D, van Ree R, Aalbers M, Briza P, Thalhamer J, Ebner C, Richter K, Ferreira F. Molecular and immunological characterization of profilin from mugwort pollen. Biol Chem 383: 1779-1789, 2002.

29A Jimenez A, Moreno C, Martinez J, Martinez A, Bartolome B, Guerra F, Palacios R 1994. Sensitization to sunflower pollen: only an occupational allergy? Int Arch Allergy Immunol 105: 297-307.

29B Barderas R, Villalba M, Lombardero M, Rodriguez R. Identification and characterization of Che a 1 allergen from Chenopodium album pollen. Int Arch Allergy Immunol 127: 47-54, 2002.

29C Carnes J, Fernandez-Caldas E, Casanovas M, Lahoz C, Colas C. Immunochemical characterization of Salsola kali pollen extracts. Allergy 56, Supplement 68: 274, 2001.

29D Giuliani A, Pini C, Bonini S, Mucci N, Ferroni L, Vicari G: Isolation and purification of a major allergen from Parietaria officinalis pollen. Allergy 42: 434-440, 1987.

30 Smith, P.M., Suphioglu, C., Griffith, I.J., Theriault, K., Knox, R.B. and Singh, M.B. 1996. Cloning and expression in yeast Pichia pastoris of a biologically active form of Cyn d 1, the major allergen of Bermuda grass pollen. J. Allergy Clin. Immunol. 98: 331-343.

31 Suphioglu, C., Ferreira, F. and Knox, R.B. 1997. Molecular cloning and immunological characterisation of Cyn d 7, a novel calcium-binding allergen from Bermuda grass pollen. FEBS Lett. 402: 167-172.

31a. Asturias JA, Arilla MC, Gomez-Bayon N, Martinez J, Martinez A, and Palacios R. 1997. Cloning and high level expression of Cynodon dactylon (Bermuda grass) pollen profilin (Cyn d 12) in Escherichia coli: purification and characterization of the allergen. Clin Exp Allergy 27: 1307-1313.

32. Mecheri, S., G. Peltre, and B. David. 1985. Purification and characterization of a major allergen from Dactylis glomerata pollen: The Ag Dg 1. Int. Arch. Allergy Appl. Immunol. 78: 283-289.

33. Roberts, A.M., L.J. Bevan, P.S. Flora, I. Jepson, and M.R. Walker. 1993. Nucleotide sequence of cDNA encoding the Group II allergen of Cocksfoot/Orchard grass (Dactylis glomerata), Dac g II. Allergy 48: 615-623.

33a. Guerin-Marchand, C., Senechal, H., Bouin, A.P., Leduc-Brodard, V., Taudou, G., Weyer, A., Peltre, G. and David, B. 1996. Cloning, sequencing and immunological characterization of Dac g 3, a major allergen from Dactylis glomerata pollen. Mol. Immunol. 33: 797-806.

34. Klysner, S., K. Welinder, H. Lowenstein, and F. Matthiesen. 1992. Group V allergens in grass pollen IV. Similarities in amino acid compositions and amino terminal sequences of the group V allergens from Lolium perenne, Poa pratensis and Dactylis glomerata. Clin. Exp. Allergy 22: 491-497.

35. Perez, M., G. Y. Ishioka, L. E. Walker, and R. W. Chesnut. 1990. cDNA cloning and immunological characterization of the rye grass allergen Lol p I. J. Biol. Chem. 265: 16210-16215.

36. Griffith, I. J., P. M. Smith, J. Pollock, P. Theerakulpisut, A. Avjioglu, S. Davies, T. Hough, M. B. Singh, R. J. Simpson, L. D. Ward, and R. B. Knox. 1991. Cloning and sequencing of Lol p I, the major allergenic protein of rye-grass pollen. FEBS Letters 279: 210-215.

37. Ansari, A. A., P. Shenbagamurthi, and D.G. Marsh. 1989. Complete amino acid sequence of a Lolium perenne (perennial rye grass) pollen allergen, Lol p II. J. Biol. Chem. 264: 11181-11185.

37a. Sidoli, A., Tamborini, E., Giuntini, I., Levi, S., Volonte, G., Paini, C., De Lalla, C., Siccardi, A.G., Baralle, F.E., Galliani, S. and Arosio, P. 1993. Cloning, expression, and immunological characterization of recombinant Lolium perenne allergen Lol p II. J. Biol. Chem. 268: 21819-21825.

38. Ansari, A. A., P. Shenbagamurthi, and D. G. Marsh. 1989. Complete primary structure of a Lolium perenne (perennial rye grass) pollen allergen, Lol p III: Comparison with known Lol p I and II sequences. Biochemistry 28: 8665-8670.

39. Singh, M. B., T. Hough, P. Theerakulpisut, A. Avjioglu, S. Davies, P. M. Smith, P. Taylor, R. J. Simpson, L. D. Ward, J. McCluskey, R. Puy, and R.B. Knox. 1991. Isolation of cDNA encoding a newly identified major allergenic protein of rye-grass pollen: Intracellular targeting to the amyloplost. Proc. Natl. Acad. Sci. 88: 1384-1388.

39a. van Ree R, Hoffman DR, van Dijk W, Brodard V, Mahieu K, Koeleman CA, Grande M, van Leeuwen WA, Aalberse RC. 1995. Lol p XI, a new major grass pollen allergen, is a member of a family of soybean trypsin inhibitor-related proteins. J Allergy Clin Immunol 95: 970-978.

40. Suphioglu, C. and Singh, M.B. 1995. Cloning, sequencing and expression in Escherichia coli of Pha a 1 and four isoforms of Pha a 5, the major allergens of canary grass pollen. Clin. Exp. Allergy 25: 853-865.

41 Dolecek, C., Vrtala, S., Laffer, S., Steinberger, P., Kraft, D., Scheiner, O. and Valenta, R. 1993. Molecular characterization of Phl p II, a major timothy grass (Phleum pratense) pollen allergen. FEBS Lett. 335: 299-304.

41A Fischer S, Grote M, Fahlbusch B, Muller WD, Kraft D, Valenta R. 1996. Characterization of Phl p 4, a major timothy grass (Phleum pratense) pollen allergen. J Allergy Clin Immunol 98: 189-198.

42 Matthiesen, F., and H. Lowenstein. 1991. Group V allergens in grass pollens. I. Purification and characterization of the group V allergen from Phleum pratense pollen, Phl p V. Clin. Exp. Allergy 21: 297-307.

43 Petersen, A., Bufe, A., Schramm, G., Schlaak, M. and Becker, W.M. 1995. Characterization of the allergen group VI in timothy grass pollen (Phl p 6). II. cDNA cloning of Phl p 6 and structural comparison to grass group V. Int. Arch. Allergy Immunol. 108: 55-59.

43A Marknell DeWitt A, Niederberger V, Lehtonen P, Spitzauer S, Sperr WR, Valent P, Valenta R, Lidholm J. Molecular and immunological characterization of a novel timothy grass (Phleum pratense) pollen allergen, Phl p 11. Clin Exp Allergy 32: 1329-1340, 2002.

44 Valenta, R., Ball, T., Vrtala, S., Duchene, M., Kraft, D. and Scheiner, O. 1994. cDNA cloning and expression of timothy grass (Phleum pratense) pollen profilin in Escherichia coli: comparison with birch pollen profilin. Biochem. Biophys. Res. Commun. 199: 106-118.

46 Esch, R. E., and D. G. Klapper. 1989. Isolation and characterization of a major cross-reactive grass group I allergenic determinant. Mol. Immunol. 26: 557-561.

47. Olsen, E., L. Zhang, R. D. Hill, F. T. Kisil, A. H. Sehon, and S. Mohapatra. 1991. Identification and characterization of the Poa p IX group of basic allergens of Kentucky bluegrass pollen. J. Immunol. 147: 205-211.

48. Avjioglu, A., M. Singh, and R.B. Knox. 1993. Sequence analysis of Sor h I, the group I allergen of Johnson grass pollen and it comparison to rye-grass Lol p I (abst). J. Allergy Clin. Immunol. 91: 340.

52. Kos T, Hoffmann-Sommergruber K, Ferreira F, Hirschwehr R, Ahorn H, Horak F, Jager S, Sperr W, Kraft D, Scheiner O. 1993. Purification, characterization and N-terminal amino acid sequence of a new major allergen from European chestnut pollen--Cas s 1. Biochem Biophys Res Commun 196: 1086-92.

53. Diaz-Perales A, Lombardero M, Sanchez-Monge R, Garcia-Selles FJ, Pernas M, Fernandez-Rivas M, Barber D, Salcedo G. 2000. Lipid-transfer proteins as potential plant panallergens: cross-reactivity among proteins of Artemisia pollen, Castaneae nut and Rosaceae fruits, with different IgE-binding capacities. Clin Exp Allergy 30: 1403-1410.

54. Ipsen, H., and O.C. Hansen. 1991. The NH2-terminal amino acid sequence of the immunochemically partial identical major allergens of alder (Alnus glutinosa) Aln g I, birch (Betula verrucosa) Bet v I, hornbeam (Carpinus betulus) Car b I and oak (Quercus alba) Que a I pollens. Mol. Immunol. 28: 1279-1288.

55. Taniai, M., S. Ando, M. Usui, M. Kurimoto, M. Sakaguchi, S. Inouye, and T. Matuhasi. 1988. N-terminal amino acid sequence of a major allergen of Japanese cedar pollen (Cry j I). FEBS Lett. 239: 329-332.

56. Griffith, I.J., A. Lussier, R. Garman, R. Koury, H. Yeung, and J. Pollock. 1993. The cDNA cloning of Cry j I, the major allergen of Cryptomeria japonica (Japanese cedar) (abst). J. Allergy Clin.Immunol. 91: 339.

57. Sakaguchi, M., S. Inouye, M. Taniai, S. Ando, M. Usui, and T. Matuhasi. Identification of the second major allergen of Japanese cedar pollen. Allergy 45: 309-312, 1990.

57A Yokoyama M, Miyahara M, Shimizu K, Kino K, Tsunoo H. Purification, identification, and cDNA cloning of Jun a 2, the second major allergen of mountain cedar pollen. Biochem Biophys Res Commun 275: 195-202, 2000.

57B Midoro-Horiuti T, Goldblum RM, Kurosky A, Wood TG, Brooks EG. Variable Expression of Pathogenesis-Related Protein Allergen in Mountain Cedar (Juniperus ashei) Pollen. J Immunol 164: 2188-2192, 2000.

57C Tinghino R., Barletta B., Palumbo S., Afferni C., Iacovacci P., Mari A., Di Felice G., Pini, C. Molecular characterization of a cross-reactive Juniperus oxycedrus pollen allergen, Jun o 2: a novel calcium-binding allergen J. Allergy Clin. Immunol. 101: 772-777, 1998.

58 Gross GN, Zimburean JM, Capra JD. Isolation and partial characterization of the allergen in mountain cedar pollen. Scand J Immunol 8: 437-441, 1978.

58A Obispo TM, Melero JA, Carpizo JA, Carreira J, Lombardero M. The main allergen of Olea europaea (Ole e I) is also present in other species of the oleaceae family. Clin Exp Allergy 23: 311-316, 1993.

58B Midoro-Horiuti T, Goldblum RM, Brooks EG. Identification of mutations in the genes for the pollen allergens of eastern red cedar (Juniperus virginiana). Clin Exp Allergy 31: 771-778, 2001.

59 Lombardero M., Barbas J.A., Moscoso del Prado J., Carreira J. cDNA sequence analysis of the main olive allergen, Ole e I. Clin. Exp. Allergy 24: 765-770, 1994.

60 Villalba, M., E. Batanero, C. Lopez-Otin, L.M. Sanchez, R.I. Monsalve, M.A. Gonzalez de la Pena, C. Lahoz, and R. Rodriguez. Amino acid sequence of Ole e I, the major allergen from olive tree pollen (Olea europaea). Eur. J. Biochem. 216: 863-869, 1993.

60A Asturias JA, Arilla MC, Gomez-Bayon N, Martinez J, Martinez A, Palacios R. Cloning and expression of the panallergen profilin and the major allergen (Ole e 1) from olive tree pollen. J Allergy Clin Immunol 100: 365-372, 1997.

60B Batanero E, Villalba M, Ledesma A Puente XS, Rodriguez R. Ole e 3, an olive-tree allergen, belongs to a widespread family of pollen proteins. Eur J Biochem 241: 772-778, 1996.

60C Batanero E, Ledesma A, Villalba M, Rodriguez R. Purification, amino acid sequence and immunological characterization of Ole e 6, a cysteine-enriched allergen from olive tree pollen. FEBS Lett. 410: 293-296, 1997.

60D Tejera ML, Villalba M, Batanero E, Rodriguez R. Identification, isolation, and characterization of Ole e 7, a new allergen of olive tree pollen. J Allergy Clin Immunol 104: 797-802, 1999.

60E Ledesma A, Villalba M, Rodriguez R. Cloning, expression and characterization of a novel four EF-hand Ca(2+)-binding protein from olive pollen with allergenic activity. FEBS Lett 466: 192-196, 2000.

60F Barral P, Batanero E, Palomares O, Quiralte J, Villalba M, Rodriguez R. A major allergen from pollen defines a novel family of plant proteins and shows intra- and interspecies [correction of interspecie] cross-reactivity. J Immunol 172: 3644-3651, 2004.

61 Yi FC, Cheong N, Shek PC, Wang DY, Chua KY, Lee BW. Identification of shared and unique immunoglobulin E epitopes of the highly conserved tropomyosins in Blomia tropicalis and Dermatophagoides pteronyssinus. Clin Exp Allergy 32: 1203-1210, 2002.

61A Ramos JD, Cheong N, Lee BW, Chua KY. cDNA cloning and expression of Blo t 11, the Blomia tropicalis allergen homologous to paramyosin. Int Arch Allergy Immunol 126: 286-293, 2001.

62 Chua, K. Y., G. A. Stewart, and W. R. Thomas. Sequence analysisof cDNA encoding for a major house dust mite allergen, Der p I. J. Exp. Med. 167: 175-182, 1988.

62A Chua, K. Y., C. R. Doyle, R. J. Simpson, K. J. Turner, G. A. Stewart, and W. R. Thomas. Isolation of cDNA coding for the major mite allergen Der p II by IgE plaque immunoassay. Int. Arch. Allergy Appl. Immunol. 91: 118-123, 1990.

62B Smith AM, Benjamin DC, Derewenda U, Smith WA, Thomas WR, Chapman MD. Sequence polymorphisms and antibody binding to the group 2 dust mite allergens. Int Arch Allergy Immunol 124: 61-63, 2001.

62C Smith AM, Benjamin DC, Hozic N, Derewenda U, Smith WA, Thomas WR, Gafvelin G, van Hage-Hamsten M, Chapman MD. The molecular basis of antigenic cross-reactivity between the group 2 mite allergens. J Allergy Clin Immunol 107: 977-984, 2001.

63 Smith WA, Thomas WR. Comparative analysis of the genes encoding group 3 allergens from Dermatophagoides pteronyssinus and Dermatophagoides farinae. Int Arch Allergy Immunol 109: 133-140, 1996.

64 Lake, F.R., L.D. Ward, R.J. Simpson, P.J. Thompson, and G.A. Stewart. House dust mite-derived amylase: Allergenicity and physicochemical characterisation. J. Allergy Clin. Immunol. 87: 1035-1042, 1991.

65 Tovey, E. R., M. C. Johnson, A. L. Roche, G. S. Cobon, and B. A. Baldo. Cloning and sequencing of a cDNA expressing a recombinant house dust mite protein that binds human IgE and corresponds to an important low molecular weight allergen. J. Exp. Med. 170: 1457-1462, 1989.

66 Yasueda, H., T. Shida, T. Ando, S. Sugiyama, and H. Yamakawa. 1991. Allergenic and proteolytic properties of fourth allergens from Dermatophagoides mites. In: «Dust Mite Allergens and Asthma. Report of the 2nd international workshop» A. Todt, Ed., UCB Institute of Allergy, Brussels, Belgium, pp. 63-64.

67 Shen, H.-D., K.-Y. Chua, K.-.L. Lin, K.-H. Hsieh, and W.R. Thomas. Molecular cloning of a house dust mite allergen with common antibody binding specificities with multiple components in mite extracts. Clin. Exp. Allergy 23: 934-940, 1993.

67A O’Neil GM, Donovan GR, Baldo BA. Cloning and charaterisation of a major allergen of the house dust mite Dermatophagoides pteronyssinus, homologous with glutathione S-transferase. Biochim Biophys Acta, 1219: 521-528, 1994.

67B King C, Simpson RJ, Moritz RL, Reed GE, Thompson PJ, Stewart GA. The isolation and characterization of a novel collagenolytic serine protease allergen (Der p 9) from the dust mite Dermatophagoides pteronyssinus. J Allergy Clin Immunol 98: 739-747, 1996.

67C Lee CS, Tsai LC, Chao PL, Lin CY, Hung MW, Chien AI, Chiang YT, Han SH. Protein sequence analysis of a novel 103-kDa Dermatophagoides pteronyssinus mite allergen and prevalence of serum immunoglobulin E reactivity to rDer p 11 in allergic adult patients. Clin Exp Allergy 34: 354-362, 2004.

68 Lind P, Hansen OC, Horn N. The binding of mouse hybridoma and human IgE antibodies to the major fecal allergen, Der p I of D. pteronyssinus. J. Immunol. 140: 4256-4262, 1988.

69 Dilworth, R. J., K. Y. Chua, and W. R. Thomas. Sequence analysis of cDNA coding for a mojor house dust allergn Der f I. Clin. Exp. Allergy 21: 25-32, 1991.

70 Nishiyama, C., T. Yunki, T. Takai, Y. Okumura, and H. Okudaira. Determination of three disulfide bonds in a major house dust mite allergen, Der f II. Int. Arch. Allergy Immunol. 101: 159-166, 1993.

70A Trudinger, M., K. Y. Chua, and W. R. Thomas. cDNA encoding the major dust mite allergen Der f II. Clin. Exp. Allergy 21: 33-38, 1991.

71 Shen HD, Chua KY, Lin WL, Hsieh KH, Thomas WR. Molecular cloning and immunological characterization of the house dust mite allergen Der f 7. Clin Exp Allergy 25: 1000-1006, 1995.

71A Tategaki A, Kawamoto S, Aki T, Jyo T, Suzuki O, Shigeta S, Ono K. Newly described house dust mite allergens. ACI International suppl. 1: 74-76, 2000.

72 Aki T, Kodama T, Fujikawa A, Miura K, Shigeta S, Wada T, Jyo T, Murooka Y, Oka S, Ono K. Immunochemical characteristion of recombinant and native tropomyosins as a new allergen from the house dust mite Dermatophagoides farinae. J Allergy Clin Immunol 96: 74-83, 1995.

72A Tsai L, Sun Y, Chao P, Ng H, Hung M, Hsieh K, Liaw S, Chua K. Sequence analysis and expression of a cDNA clone encoding a 98-kDa allergen in Dermatophagoides farinae. Clin Exp Allergy 29: 1606-1613, 1999.

72B Gafvelin G, Johansson E, Lundin A, Smith AM, Chapman MD, Benjamin DC, Derewenda U, Van Hage-Hamsten M. Cross-reactivity studies of a new group 2 allergen from the dust mite Glycyphagus domesticus, Gly d 2, and group 2 allergens from Dermatophagoides pteronyssinus, Lepidoglyphus destructor, and Tyrophagus putrescentiae with recombinant allergens. J Allergy Clin Immunol 107: 511-518, 2001.

73 van Hage-Hamsten, M., T. Bergman, E. Johansson, B. Persson, H. Jornvall, B. Harfast, and S.G.O. Johansson. N-terminal amino acid sequence of major allergen of the mite lepidoglyphus destructor (abst). J. Allergy Clin. Immunol. 91: 353, 1993.

74 Varela J, Ventas P, Carreira J, Barbas JA, Gimenez-Gallego G, Polo F. Primary structure of Lep d I, the main Lepidoglyphus destructor allergen. Eur J Biochem 225: 93-98, 1994.

74A Schmidt M, van der Ploeg I, Olsson S, van Hage Hamsten M. The complete cDNA encoding the Lepidoglyphus destructor major allergen Lep d 1. FEBS Lett 370: 11-14, 1995.

75 Eriksson TLJ, Rasool O, Huecas S, Whitley P, Crameri R, Appenzeller U, Gafvelin G, van Hage-Hamsten M. Cloning of three new allergens from the dust mite Lepidoglyphus destructor using phage surface display technology. Eur. J. Biochem. 268: 287-294, 2001.

75A Saarne T, Kaiser L, Rasool O, Huecas S, van Hage-Hamsten M, Gafvelin G: Cloning and characterisation of two IgE-binding proteins, homologous to tropomyosin and a-tubulin, from the mite Lepidoglyphus destructor. Int Arch Allergy Immunol 130: 258-265, 2003.

75B Eriksson TL, Johansson E, Whitley P, Schmidt M, Elsayed S, van Hage-Hamsten M. Cloning and characterisation of a group II allergen from the dust mite Tyrophagus putrescentiae. Eur. J. Biochem. 251 (1-2), 443-447, 1998.

76. Rautiainen J, Rytkonen M, Pelkonen J, Pentikainen J, Perola O, Virtanen T, Zeiler T, Mantyjarvi R. BDA20, a major bovine dander allergen characterized at the sequence level is Bos d 2. Submitted.

77. Gjesing B, Lowenstein H. Immunochemistry of food antigens. Ann Allergy 53: 602, 1984.

78. de Groot, H., K.G.H. Goei, P. van Swieten, and R.C. Aalberse. Affinity purification of a major and a minor allergen from dog extract: Serologic activity of affiity-purified Can f I and Can f I-depleted extract. J. Allergy Clin. Immunol. 87: 1056-1065, 1991.

79. Konieczny, A. Personal communication; Immunologic Pharmaceutical Corp.

79A. Bulone, V. Separation of horse dander allergen proteins by two-dimensional electrophoresis. Molecular characterisation and identification of Equ c 2.0101 and Equ c 2.0102 as lipocalin proteins. Eur J Biochem 253: 202-211, 1998.

79B. Swiss-Prot acc. P81216, P81217.

79C. Dandeu J. P., Rabillon J., Divanovic A., Carmi-Leroy A., David B. (1993). Hydrophobic interaction chromatography for isolation and purification of Equ c 1, the horse major allergen. J. Chromatogr. 621: 23-31.

79D. Goubran Botros H., Rabillon J., Gregoire C., David B., Dandeu J.P. 1998. Thiophilic absorption chromatography: purification of Equ c 2 and Equ c 3, two horse allergens from horse sweat. J. Chromatogr. B 710: 57-65.

79E. Hilger C, Kohnen M, Grigioni F, Lehners C, Hentges F. Allergic cross-reactions between cat and pig serum albumin. Allergy 52: 179-187, 1997; and Hilger C, Grigioni F, Hentges F. Sequence of the gene encoding cat (Felis domesticus) serum albumin. Gene 169: 295-296, 1996.

79F. Ichikawa K, Vailes LD, Pomes A, Chapman MD. Molecular cloning, expression and modeling of cat allergen, cystatin (Fel d 3), a cysteine protease inhibitor. Clin Exp Allergy, In Press 2001.

80 Fahlbusch B, Rudeschko O, Szilagyi U, Schlott B, Henzgen M, Schlenvoigt G, Schubert H. Purification and partial characterization of the major allergen, Cav p 1, from guinea pig Cavia porcellus. Allergy 57: 417-422, 2002.

81 McDonald, B., M. C. Kuo, J. L. Ohman, and L. J. Rosenwasser. 1988. A 29 amino acid peptide derived from rat alpha 2 euglobulin triggers murine allergen specific human T cells (abst). J. Allergy Clin. Immunol. 83: 251.

81A Clarke, A. J., P. M. Cissold, R. A. Shawi, P. Beattie, and J. Bishop. 1984. Structure of mouse urinary protein genes: differential splicing configurations in the 3'-non-coding region. EMBO J 3: 1045-1052.

82. Longbottom, J. L. 1983. Chracterization of allergens from the urines of experimental animals. McMillan Press, London, pp. 525-529.

83. Laperche, Y., K. R. Lynch, K. P. Dolans, and P. Feigelsen. 1983. Tissue-specific control of alpha 2u globulin gene expression: constitutive synthesis in submaxillary gland. Cell 32: 453-460.

83A. Bush RK, Sanchez H, Geisler D. 1999. Molecular cloning of a major Alternaria alternata allergen, rAlt a 2. J Allergy Clin Immunol 104: 665-671.

83B. Aukrust L, Borch SM. 1979. Partial purification and characterization of two Cladosporium herbarum allergens. Int Arch Allergy Appl Immunol 60: 68-79.

83C. Sward-Nordmo M, Paulsen BS, Wold JK. 1988. The glycoprotein allergen Ag-54 (Cla h II) from Cladosporium herbarum. Structural studies of the carbohydrate moiety. Int Arch Allergy Appl Immunol 85: 288-294.

84 Shen, et al. J. Allergy Clin. Immunol. 103: S157, 1999.

84A Crameri R. Epidemiology and molecular basis of the involvement of Aspergillus fumigatus in allergic diseases. Contrib. Microbiol. Vol. 2, Karger, Basel (in press).

84B Shen, et al. (manuscript submitted), 1999

84C Shen HD, Ling WL, Tan MF, Wang SR, Chou H, Han SIH. Vacuolar serine proteinase: A major allergen of Aspergillus fumigatus. 10th International Congress of Immunology, Abstract, 1998.

85 Kumar A, Reddy LV, Sochanik A, Kurup VP. 1993. Isolation and characterization of a recombinant heat shock protein of Aspergillus fumigatus. J. Allergy Clin. Immunol. 91: 1024-1030.

85A Saxena S, Madan T, Muralidhar K, Sarma PU. 2003. cDNA cloning, expression and characterization of an allergenic L3 ribosomal protein of Aspergillus fumigatus. Clin Exp Immunol 134: 86-91.

85B Baur X, Melching-Kollmuss S, Koops F, Strassburger K, Zober A. IgE-mediated allergy to phytase -- a new animal feed additive. Allergy 57: 943-945, 2002.

86A Shen HD, Lin WL, Tsai JJ, Liaw SF, Han SH. 1996. Allergenic components in three different species of Penicillium: crossreactivity among major allergens. Clin Exp Allergy 26: 444-451.

86B. Shen, et al. Abstract; The XVIII Congress of the European Academy of Allergology and Clinical Immunology, Brussels, Belgium, 3-7 July 1999.

87 Shen HD, Lin WL, Tam MF, Wang SR, Tzean SS, Huang MH, Han SH. Characterization of allergens from Penicillium oxalicum and P. notatum by immunoblotting and N-terminal amino acid sequence analysis. Clin Exp Allergy 29: 642-651, 1999.

87A Shen HD, Liaw SF, Lin WL, Ro LH, Yang HL, Han SH. Molecular cloning of cDNA coding for the 68 kDa allergen of Penicillium notatum using MoAbs. Clin Exp Allergy 25: 350-356, 1995.

87B Shen HD, Wang CW, Lin WL, Lai HY, Tam MF, Chou H, Wang SR, Han SH. cDNA cloning and immunologic characterization of Pen o 18, the vacuolar serine protease major allergen of Penicillium oxalicum. J Lab Clin Med 137: 115-124, 2001.

88 Woodfolk JA, Wheatley LM, Piyasena RV, Benjamin DC, Platts-Mills TA.1998. Trichophyton antigens associated with IgE antibodies and delayed type hypersensitivity. Sequence homology to two families of serine proteinases. J Biol Chem 273: 29489-96.

88A Deuell, B., L.K. Arruda, M.L. Hayden, M.D. Chapman and T.A.E. Platts-Mills. 1991. Trichophyton tonsurans Allergen I. J. Immunol. 147: 96-101.

89 Shen, H.D., K.B. Choo, H.H. Lee, J.C. Hsieh, and S.H. Han. 1991. The 40 kd allergen of Candida albicans is an alcohol dehydrogenease: molecular cloning and immunological analysis using monoclonal antibodies. Clin. Exp. Allergy 21: 675-681.

89A Horner WE, Reese G, Lehrer SB. 1995. Identification of the allergen Psi c 2 from the basidiomycete Psilocybe cubensis as a fungal cyclophilin. Int Arch Allergy Immunol 107: 298-300.

89B Chang CY, Chou H, Tam MF, Tang RB, Lai HY, Shen HD. Characterization of Enolase Allergen from Rhodotorula mucilaginosa. J Biomed Sci 9: 645-655, 2002.

90 Yasueda H, Hashida-Okado T, Saito A, Uchida K, Kuroda M, Onishi Y, Takahashi K, Yamaguchi H, Takesako K, Akiyama K. Identification and cloning of two novel allergens from the lipophilic yeast, Malassezia furfur. Biochem Biophys Res Commun 248: 240-244, 1998. NB: strain TIMM2782 (Teikyo University Institute for Medical Mycology) equal to strain CBS1878 (Central Bureau von Schimmelkulturen).

90A Onishi Y, Kuroda M, Yasueda H, Saito A, Sono-Koyama E, Tunasawa S, Hashida-Okado T, Yagihara T, Uchida K, Yamaguchi H, Akiyama K, Kato I, Takesako K. Two-dimensional electrophoresis of Malassezia allergens for atopic dermatitis and isolation of Mal f 4 homologs with mitochondrial malate dehydrogenase. Eur J Biochem 261: 148-154, 1999. NB: strain TIMM2782 (Teikyo University Institute for Medical Mycology) equal to strain CBS1878 (Central Bureau von Schimmelkulturen).

91 Schmidt M, Zargari A, Holt P, Lindbom L, Hellman U, Whitley P, van der Ploeg I, Harfast B, Scheynius A. The complete cDNA sequence and expression of the first major allergenic protein of Malassezia furfur, Mal f 1. Eur J Biochem 246: 181-185, 1997. NB: strain ATCC no. 42132 (American Type Culture Collection).

91A Rasool O, Zargari A, Almqvist J, Eshaghi H, Whitley P, Scheynius A. Cloning, characterization and expression of complete coding sequences of three IgE binding Malassezia furfur allergens, Mal f 7, Mal f 8 and Mal f 9. Eur J Biochem 267: 4355-4361, 2000. NB: strain ATCC no. 42132 (American Type Culture Collection).

91B NB:; strain 4625 (Indian Agricultural Research Institute, PUSA; New Delhi, India).

92 Kuchler, K., M. Gmachl, M. J. Sippl, and G. Kreil. 1989. Analysis of the cDNA for phospholipase A2 from honey bee venom glands: The deduced amino acid sequence reveals homology to the corresponding vertebrate enzymes. Eur. J. Biochem. 184: 249-254.

93 Gmachl, M., and G. Kreil. 1993. Bee venom hyaluronidase is homologous to a membrane protein of mammalian sperm. Proc. Natl. Acad. Sci. USA 90: 3569-3573.

93A Hoffman DR. 1977. Allergens in bee venom III. Identification of allergen B as an acid phosphatase. J Allergy Clin. Immunol. 59: 364-366.

94 Habermann, E. 1972. Bee and wasp venoms. Science 177: 314-322.

95 Hoffman DR, Jacobson RS. 1996. Allergens in Hymenoptera venom XXVII: Bumblebee venom allergy and allergens. J. Allergy Clin. Immunol. 97: 812-821.

95A Hoffman DR, El-Choufani AE, Smith MM, de Groot H. 2001. Occupational allergy to bumblebee venom: Allergens of Bombus terrestris. J Allergy Clin Immunol In press.

95B Helm R, Cockrell G, Stanley JS, Brenner RJ, Burks W, Bannon GA. 1996. Isolation and characterization of a clone encoding a majore allergen (Bla g Bd90K) involved in IgE mediated cockroach hypersensitivity. J Allerg Clin Immunol 98: 172-180.

95C Pomes A, Melen E, Vailes LD, Retief JD, Arruda LK, Chapman MD. 1998. Novel allergen structures with tandem amino acid repeats derived from German and American cockroach. J Biol Chem 273: 30801-30807.

96 Arruda LK, Vailes LD, Mann BJ, Shannon J, Fox JW, Vedvick TS, Hayden ML, Chapman MD. Molecular cloning of a major cockroach (Blattella germanica) allergen, Bla g 2. Sequence homology to the aspartic proteases. J Biol Chem 270: 19563-19568, 1995.

97 Arruda LK, Vailes LD, Hayden ML, Benjamin DC, Chapman MD. Cloning of cockroach allergen, Bla g 4, identifies ligand binding proteins (or calycins) as a cause of IgE antibody responses. J Biol Chem 270: 31196-31201, 1995.

98 Arruda LK, Vailes LD, Benjamin DC, Chapman MD. Molecular cloning of German Cockroach (Blattella germanica) allergens. Int Arch Allergy Immunol 107: 295-297, 1995.

98A Wu CH, Wang NM, Lee MF, Kao CYY, Luo SF. 1998. Cloning of the American cockroach Cr-PII allergens: Evidence for the existence of cross-reactive allergens between species. J Allergy Clin Immunol 101: 832-840.

98B Melen E, Pomes A, Vailes LD, Arruda LK, Chapman MD. 1999. Molecular cloning of Per a 1 and definition of the cross-reactive Group 1 cockroach allergens. J Allergy Clin Immunol 103: 859-64.

98C Wu CH, Lee MF, Liao SC, Luo SF. Sequencing analysis of cDNA clones encoding the American cockroach Cr-PI allergens. J Biol Chem 271: 17937-17943, 1996.

98D Wu CH, Lee MF, Wang NM, Luo SF. Sequencing and immunochemical characterization of the American cockroach Per a 3 (Cr-PI) isoallergenic variants. Molecular Immunol 34: 1-8, 1997.

98E Santos ABR, Chapman MD, Aalberse RC, Vailes LD, Ferriani VPL, Oliver C, Rizzo MC, Naspitz CK, Arruda LK. 1999. Cockroach allergens and asthma in Brazil: Identification of tropomyosin as a major allergen with potential cross-reactivity with mite and shrimp allergens. J Allergy Clin Immunol 104: 329-337.

98F Asturias JA, Gomez-Bayon N, Arilla MC, Martinez A, Palacios R, Sanchez-Gascon, Martinez J. 1999. Molecular characterization of American cockroach tropomyosin (Periplaneta americana allergen 7), a cross-reactive allergen. J Immunol 162: 4342-4348.

99 Mazur, G., X. Baur, and V. Liebers. 1990. Hypersensitivity to hemoglobins of the Diptera family Chironomidae: Structural and functional studies of their immunogenic/allergenic sites. Monog. Allergy 28: 121-137.

99A Moneo I, Vega JM, Caballero ML, Vega J, Alday E. Isolation and characterization of Tha p 1, a major allergen from the pine processionary caterpillar Thaumetopoea pityocampa. Allergy 58: 34-37, 2003.

100 Soldatova, L., L. Kochoumian, and T.P. King. 1993. Sequence similarity of a hornet (D. maculata) venom allergen phospholipase A1 with mammalian lipases. FEBS Letters 320: 145-149.

101 Lu, G., L. Kochoumian and T.P. King. Whiteface hornet venom allergen hyaluronidase: cloning and its sequence similarity with other proteins (abst.). 1994. J. Allergy Clin. Immunol. 93: 224.

102 Fang, K. S. F., M. Vitale, P. Fehlner, and T. P. King. 1988. cDNA cloning and primary structure of a white-faced hornet venom allergen, à í ò è ã å í 5. Proc. Natl. Acad. Sci., USA 85: 895-899.

103 King, T. P., D. C. Moran, D. F. Wang, L. Kochoumian, and B.T. Chait. 1990. Structural studies of a hornet venom allergen à í ò è ã å í 5, Dol m V and its sequence similarity with other proteins. Prot. Seq. Data Anal. 3: 263-266.

104. Lu, G., M. Villalba, M.R. Coscia, D.R. Hoffman, and T.P. King. 1993. Sequence analysis and à í ò è ã å í cross reactivity of a venom allergen à í ò è ã å í 5 from hornets, wasps and yellowjackets. J. Immunol. 150: 2823-2830.

105. King, T. P. and Lu, G. 1997. Unpublished data.

105A. King TP, Lu G, Gonzalez M, Qian N and Soldatova L. 1996. Yellow jacket venom allergens, hyaluronidase and phospholipase: sequence similarity and antigenic cross-reactivity with their hornet and wasp homologs and possible implications for clinical allergy. J. Allergy Clin. Immunol. 98: 588-600.

106. Hoffman, D.R. 1993. Allergens in hymenoptera venom XXV: The amino acid sequences of à í ò è ã å í 5 molecules and the structural basis of antigenic cross-reactivity. J. Allergy Clin. Immunol. 92: 707-716.

107. Hoffman DR. 1992. Unpublished data.

108. Hoffman DR. The complete amino acid sequence of a yellowjacket venom phospholipase (abst). J. Allergy Clin. Immunol. 91: 187, 1993.

109. Jacobson RS, Hoffman DR, Kemeny DM. The cross-reactivity between bee and vespid hyaluronidases has a structural basis (abst). J. Allergy Clin. Immunol. 89: 292, 1992.

110. Hoffman DR. Allergens in Hymenoptera venom XXIV: The amino acid sequences of imported fire ant venom allergens Sol i II, Sol i III, and Sol i IV. J. Allergy Clin. Immunol 91: 71-78, 1993.

111. Schmidt M, Walker RB, Hoffman DR, McConnell TJ. Nucleotide sequence of cDNA encoding the fire ant venom protein Sol i II. FEBS Letters 319: 138-140, 1993.

111A. Paddock CD, McKerrow JH, Hansell E, Foreman KW, Hsieh I, Marshall N. Identification, cloning, and recombinant expression of procalin, a major triatomine allergen. J Immunol 167: 2694-2699, 2001.

112. Elsayed S, Bennich H. The primary structure of Allergen M from cod. Scand J Immunol 3: 683-686, 1974.

113. Elsayed S, Aas K, Sletten K, Johansson SGO. Tryptic cleavage of a homogeneous cod fish allergen and isolation of two active polypeptide fragments. Immunochemistry 9: 647-661, 1972.

114. Hoffman, D. R. 1983. Immunochemical identification of the allergens in egg white. J. Allergy Clin. Immunol. 71: 481-486.

115. Langeland, T. 1983. A clinical and immunological study of allergy to hen's egg white. IV. specific IgE antibodies to individual allergens in hen's egg white related to clinical and immunolgical parameters in egg-allergic patients. Allergy 38: 493-500.

116 Daul CB, Slattery M, Morgan JE, Lehrer SB. 1993. Common crustacea allergens: identification of B cell epitopes with the shrimp specific monoclonal antibodies. In: «Molecular Biology and Immunology of Allergens» (D. Kraft and A. Sehon, eds.). CRC Press, Boca Raton. pp. 291-293.

116A Shanti KN, Martin BM, Nagpal S, Metcalfe DD, Subba Rao PV. Identification of tropomyosin as the major shrimp allergen and characterization of its IgE-binding epitopes. J. Immunol. 151: 5354-5363, 1993.

117 Yu CJ, Lin YF, Chiang BL, Chow LP. Proteomics and Immunological Analysis of a Novel Shrimp Allergen, Pen m 2. J Immunol 170: 445-453, 2003.

117A Miyazawa M, Fukamachi H, Inagaki Y, Reese G, Daul CB, Lehrer SB, Inouye S, Sakaguchi M. Identification of the first major allergen of a squid (Todarodes pacificus). J. Allergy Clin. Immunol. 98: 948-953, 1996.

117B Asturias JA, Eraso E, Arilla MC, Gomez-Bayon N, Inacio F, Martinez A. Cloning, isolation, and IgE-binding properties of Helix aspersa (brown garden snail) tropomyosin. Int Arch Allergy Immunol 128: 90-96, 2002.

117C Lopata AL, Zinn C, Potter PC. Characteristics of hypersensitivity reactions and identification of a unique 49 kd IgE-binding protein (Hal-m-1) in abalone (Haliotis midae). J. Allergy Clin. Immunol. 100: 642-648, 1997.

117D Hoffmann-Sommergruber K, O'Riordain G, Ahorn H, Ebner C, Laimer Da Camara Machado M, Puhringer H, Scheiner O, Breiteneder H. Molecular characterization of Dau c 1, the Bet v 1 homologous protein from carrot and its cross-reactivity with Bet v 1 and Api g 1. Clin. Exp. Allergy 29: 840-847, 1999.

118 Monsalve RI, Gonzalez de la Pena MA, Menendez-Arias L, Lopez-Otin C, Villalba M, Rodriguez R. Characterization of a new mustard allergen, Bra j IE. Detection of an allergenic epitope. Biochem. J. 293: 625-632 1993.

118A. Monsalve RI, Gonzalez de la Pena MA, Lopez-Otin C, Fiandor A, Fernandez C, Villalba M, Rodriguez R. 1997. Detection, isolation and complete amino acid sequence of an aeroallergenic protein from rapeseed flour. Clin Exp Allergy 27: 833-841.

119. Mena, M., R. Sanchez-Monge, L. Gomez, G. Salcedo, and P. Carbonero. A major barley allergen associated with baker's asthma disease is a glycosylated monomeric inhibitor of insect alpha-amylase: cDNA cloning and chromosomal location of the gene. Plant Molec. Biol. 20: 451-458, 1992.

119A. Palosuo K, Varjonen E, Kekki OM, Klemola T, Kalkkinen N, Alenius H, Reunala T. Wheat omega-5 gliadin is a major allergen in children with immediate allergy to ingested wheat. J. Allergy Clin. Immunol. 108: 634-638, 2001.

119B. Xu H, Theerakulpisut P, Goulding N, Suphioglu C, Singh M. B. Bhalla P. L. Cloning expression and immunological characterization of Ory s 1, the major allergen of rice pollen. Gene 164: 255-259, 1995.

119C. Pastorello EA, Ortolani C, Farioli L, Pravettoni V, Ispano M, Borga A, Bengtsson A, Incorvaia C, Berti C, Zanussi C. Allergenic cross-reactivity among peach, apricot, plum, and cherry in patients with oral allergy syndrome: an in vivo and in vitro study. J. Allergy Clin. Immunol. 94: 699-707, 1994.

119D. Diaz-Perales A, Tabar AI, Sanchez-Monge R, Garcia BE, Gomez B, Barber D, Salcedo G. Characterization of asparagus allergens: a relevant role of ò ð à í ñ ï î ð ò ¸ ð ë è ï è ä î â s. J Allergy Clin Immunol 110: 790-796, 2002.

119E Galleguillos F, Rodriguez JC. Asthma caused by bromelin inhalation. Clin Allergy 8: 21-24, 1978.

119F Baur X. Studies on the specificity of human IgE-antibodies to the plant proteases papain and bromelain. Clin Allergy 9: 451-457, 1979.

119G Gailhofer G, Wilders-Truschnig M, Smolle J, Ludvan M. Asthma caused by bromelain: an occupational allergy. Clin Allergy 18: 445-450, 1988.

120. Menendez-Arias, L., I. Moneo, J. Dominguez, and R. Rodriguez. 1988. Primary structure of the major allergen of yellow mustard (Sinapis alba L.) seed, Sin a I. Eur. J. Biochem. 177: 159-166.

120A Gonzalez R, Varela J, Carreira J, Polo F. Soybean hydrophobic protein and soybean hull allergy. Lancet 346: 48-49, 1995.

120B Kleine-Tebbe J, Vogel L, Crowell DN, Haustein UF, Vieths S. Severe oral allergy syndrome and anaphylactic reactions caused by a Bet v 1- related PR-10 protein in soybean, SAM22. J Allergy Clin Immun ol 110: 797-804, 2002.

120C Sanchez-Monge R, Pascual CY, Diaz-Perales A, Fernandez-Crespo J, Martin-Esteban M, Salcedo G. Isolation and characterization of relevant allergens from boiled lentils. J. Allergy Clin. Immunol. 106: 955-961, 2000.

121 Gavrovic-Jankulovic M, cIrkovic T, Vuckovic O, Atanaskovic-Markovic M, Petersen A, Gojgic G, Burazer L, Jankov RM. Isolation and biochemical characterization of a thaumatin-like kiwi allergen. J Allergy Clin Immun ol 110: 805-810, 2002.

121A Pastorello EA, Varin E, Farioli L, Pravettoni V, Ortolani C, Trambaioli C, Fortunato D, Giuffrida MG, Rivolta F, Robino A, Calamari AM, Lacava L, Conti A. The major allergen of sesame seeds (Sesamum indicum) is a 2S albumin. J. Chromatogr. B Biomed. Sci. Appl. 756: 85-93, 2001.

121B Moneo I, Caballero ML, Gomez F, Ortega E, Alonso MJ. Isolation and characterization of a major allergen from the fish parasite Anisakis simplex. J. Allergy Clin. Immunol. 106: 177-182, 2000.

121C Asturias JA, Eraso E, Martinez A. 2000. Is tropomysoin an allergen in Anisakis? Allergy 55: 898-890.

122 Christie, J. F., B. Dunbar, I. Davidson, and M. W. Kennedy. 1990. N-terminal amino acid sequence identity between a major allergen of Ascaris lumbricoides and Ascaris suum and MHC-restricted IgE responses to it. Immunology 69: 596-602.

122A Baur X, Konig G, Bencze K, Fruhmann G. Clinical symptoms and results of skin test, Ð À Ñ Ò and bronchial provocation test in thirty-three papain workers: evidence for strong immunogenic potency and clinically relevant 'proteolytic effects of airborne papain'. Clin Allergy 12: 9-17, 1982.

122B Onizuka R, Kamiya H, Muramoto K, Goto R, Inoue K, Kumamoto K, Nakajima Y, Iida S, Ishigami F. Purification of the major allergen of red soft coral (Dendronephthya nipponica). Int Arch Allergy Immunol 125: 135-143, 2001.

123. Czuppon AB, Chen Z, Rennert S, Engelke T, Meyer HE, Heber M, Baur X. The rubber elongation factor of rubber trees (Hevea brasiliensis) is the major allergen in latex. J Allergy Clin Immunol 92: 690-697, 1993.

124. Attanayaka DPSTG, Kekwick RGO, Franklin FCH. 1991. Molecular cloning and nucleotide sequencing of the rubber elongation factor gene from hevea brasiliensis. Plant Mol Biol 16: 1079-1081.

125. Chye ML, Cheung KY. 1995. J 1, 3-glucanase is highly expressed in Laticifers of Hevea brasiliensis. Plant Mol Biol 26: 397-402.

126. Alenius H, Palosuo T, Kelly K, Kurup V, Reunala T, Makinen-Kiljunen S, Turjanmaa K Fink J. 1993. IgE reactivity to 14-kD and 27-kD natural rubber proteins in Latex-allergic children with Spina bifida and other congenital anomalies. Int Arch Allergy Immunol 102: 61-66.

127. Yeang HY, Cheong KF, Sunderasan E, Hamzah S, Chew NP, Hamid S, Hamilton RG, Cardosa MJ. 1996. The 14.6 kD (REF, Hev b 1) and 24 kD (Hev b 3) rubber particle proteins are recognized by IgE from Spina Bifida patients with Latex allergy. J Allerg Clin Immunol in press.

128. Sunderasan E, Hamzah S, Hamid S, Ward MA, Yeang HY, Cardosa MJ. 1995. Latex B-serum J-1, 3-glucanase (Hev b 2) and a component of the microhelix (Hev b 4) are major Latex allergens. J nat Rubb Res 10: 82-99.

129 Ahrazem O, Lopez-Torrejon G, Ibanez MD, Lombardero M, Sanchez-Monge R, Sastre J, Barber D, Salcedo G. Purification, characterization and molecular cloning of Lipid Transfer Proteins from citrus fruits. Unpublished 2004.

130 Asturias JA, Arilla MC, Gomez-Bayon N, Martinez J, Martinez A, Palacios R. Cloning and expression of the panallergen profilin and the major allergen (Ole e 1) from olive tree pollen. J. Allergy Clin. Immunol. 100: 365-372, 1997a.

131 Asturias JA, Arilla MC, Gomez-Bayon N, Martinez A, Martinez J, Palacios R. Analysis of recombinant allergen Par j 3 (profilin) from Parietaria judaica. Unpublished, 1997b.

132 Asturias JA, Arilla MC, Gomez-Bayon N, Martinez J, Martinez A, Palacios R. New allergen from the american cockroach (Periplaneta americana). Unpublished 1997c.

133 Asturias JA, Arilla MC, Gomez-Bayon N, Martinez J, Martinez A, Palacios R. Cloning and expression of profilin allergen from Hevea brasiliensis. Unpublished 1997d.

134 Atkinson RG, Perry J, Matsui T, Ross GS, MacRae EA. A stress-, pathogenesis-, and allergen-related cDNA in apple fruit is also ripening-related. New Zealand J Crop Horticul Sci 24: 103-107, 1996.

135 Au L-C, Lin S-T, Peng H-J, Chang Z-N. Cloning of new isoallergens of Cyn d 1. Unpublished 1999.

136 Batanero E, Villalba M, Lopez-Otin C, Rodriguez R. Isolation and characterization of an olive allergen-like protein from lilac pollen. Sequence analysis of three cDNA encoding protein isoforms. Eur. J. Biochem. 221: 187-193, 1994.

137 Batanero E, Gonzalez De La Pena MA, Villalba M, Monsalve RI, Martin-Esteban M, Rodriguez R. Isolation, cDNA cloning and expression of Lig v 1, the major allergen from privet pollen. Clin. Exp. Allergy 26: 1401-1410, 1996.

138 Beezhold D.H., Hickey V.L., Kostyal D.A., Sussman G.L. Characterization of new isoforms of the latex allergen, Hev b 8. Unpublished 1999.

139 Breiteneder H, Pettenburger K, Bito A, Valenta R, Kraft D, Rumpold H, Scheiner O, Breitenbach M. The gene coding for the major birch pollen allergen BetvI, is highly homologus to a pea disease resistance response gene. EMBO J. 8: 1935-1938, 1989.

140 Breiteneder H, Ferreira F, Hoffmann-Sommergruber K, Ebner C, Breitenbach M, Rumpold H, Kraft D, Scheiner O. Four recombinant isoforms of Cor a I, the major allergen of hazel pollen, show different IgE-binding properties. Eur. J. Biochem. 212: 355-362, 1993.

141 Breiteneder H, Hoffmann-Sommergruber K, O'Riordain G, Susani M, Ahorn H, Ebner C, Kraft D, Scheiner O. Molecular characterization of Api g 1, the major allergen of celery (Apium graveolens), and its immunological and structural relationships to a group of 17-kDa tree pollen allergens. Eur. J. Biochem. 233: 484-489, 1995.

142 Bufe A, Becker WM, Schramm G, Petersen A, Mamat U, Schlaak M. Major allergen Phl p Va (timothy grass) bears at least two different IgE-reactive epitopes. J. Allergy Clin. Immunol. 94: 173-181 1994.

143 Bufe A, Schramm G, Keown MB, Schlaak M, Becker WM. Major allergen Phl p Vb in timothy grass is a novel pollen RNase. FEBS Lett. 363: 6-12, 1995.

144 Bulone V, Krogstad-Johnsen T, Smestad-Paulsen B. Separation of horse dander allergen proteins by two-dimensional electrophoresis--molecular characterisation and identification of Equ c 2.0101 and Equ c 2.0102 as lipocalin proteins. Eur. J. Biochem. 253: 202-211, 1998.

145 Caballero JL. Unpublished 2001.

146 Chua KY, Kehal PK, Thomas WR. Sequence polymorphisms of cDNA clones encoding the mite allergen Der p I. Int. Arch. Allergy Immunol. 101: 364-368, 1993.

147 Chua KY, Huang CH, Shen HD, Thomas WR. Analysis of sequence polymorphism of a major mite allergen, Der p 2. Clin. Exp. Allergy. 26: 829-837, 1996

148 Chang ZN, Peng HJ, Lee WC, Chen TS, Chua KY, Tsai LC, Chi CW, Han SH. Sequence polymorphism of the group 1 allergen of Bermuda grass pollen. Clin. Exp. Allergy 29: 488-496, 1999.

149 Costa MA, Colombo P, Izzo V, Kennedy H, Venturella S, Cocchiera R, Mistrello G, Falagiani P, Geraci D. cDNA cloning, expression and primary structure of Par j I, a major allergen of Parietaria judaica pollen. FEBS Lett. 341: 182-186, 1994.

150 De Vouge MW, Thaker AJ, Curran IH, Zhang L, Muradia G, Rode H, Vijay HM. Isolation and expression of a cDNA clone encoding an Alternaria alternata Alt a 1 subunit. Int. Arch. Allergy Immunol. 111: 385-395, 1996.

151 Duro G, Colombo P, Costa MA, Izzo V, Porcasi R, Di Fiore R, Locorotondo G, Mirisola MG, Cocchiera R, Geraci D. cDNA cloning, sequence analysis and allergological characterization of Par j 2.0101, a new major allergen of the Parietaria judaica pollen. FEBS Lett. 399: 295-298, 1996.

152 Ferreira F, unpublished 2005.

153 Gafvelin G, Johansson E, Lundin A, van Hage-Hamsten M. Cloning of Gly d 2 from Glycyphagus domesticus. Crossreactivity to Group 2 mite allergens. Unpublished 1999.

154 Gafvelin G, Johansson E, Lundin A, Smith AM, Chapman MD, Benjamin DC, Derewenda U, Van Hage-Hamsten M. Cross-reactivity studies of a new group 2 allergen from the dust mite Glycyphagus domesticus, Gly d 2, and group 2 allergens from Dermatophagoides pteronyssinus, Lepidoglyphus destructor, and Tyrophagus putrescentiae with recombinant allergens. J. Allergy Clin. Immunol. 107: 511-518, 2001.

155 Ganglberger E, Scheiner O, Breiteneder H. Molecular and immunological characterisation of profilin from Hevea brasiliensis. Unpublished 1999.

156 Gao ZS et al. Unpublished 2004.

157 Gehlhar K, Schramm G, Petersen A, Becker W, Schlaak M, Bufe A. Structurally different allergenic isovariants in grass pollen (group V) show identical IgE reactivity but variable allergenicity: implication for immunotherapy. Unpublished 1996.

158 Geraci D. Unpublished 1995.

159 Gonzalez R, Varela J, Carreira J, Polo F. Soybean hydrophobic protein and soybean hull allergy. Lancet 346: 48-49, 1995.

160 Griffith IJ, Smith PM, Pollock J, Theerakulpisut P, Avjioglu A, Davies S, Hough T, Singh MB, Simpson RJ, Ward LD, Knox RB. Cloning and sequencing of Lol pI, the major allergenic protein of rye-grass pollen. FEBS Lett. 279: 210-215, 1991.

161 Helm R, Cockrell G, Stanley JS, Brenner RJ, Burks W, Bannon GA. Isolation and characterization of a clone encoding a major allergen (Bla g Bd90K) involved in IgE-mediated cockroach hypersensitivity. J. Allergy Clin. Immunol. 98: 172-180, 1996.

162 Hoffmann-Sommergruber K, Vanek-Krebitz M, Radauer C, Wen J, Ferreira F, Scheiner O, Breiteneder H. Genomic characterization of members of the Bet v 1 family: genes coding for allergens and pathogenesis-related proteins share intron positions. Gene 197: 91-100, 1997.

163 Hoffmann-Sommergruber K, O'Riordain G, Ahorn H, Ebner C, Laimer Da Camara Machado M, Puhringer H, Scheiner O, Breiteneder H. Molecular characterization of Dau c 1, the Bet v 1 homologous protein from carrot and its cross-reactivity with Bet v 1 and Api g 1. Clin. Exp. Allergy 29: 840-847, 1999.

164 Hoffmann-Sommergruber K, Ferris R, Pec M, O'Riordain G, Kraft D, Scheiner O, Breiteneder H. Molecular cloning and expression of a new major celery allergen, Api g 2, a distant relative of the Bet v 1 PRP-family. Unpublished 2000.

165 Holm J, Baerentzen G, Gajhede M, Ipsen H, Larsen JN, Lowenstein H, Wissenbach M, Spangfort MD. Molecular basis of allergic cross-reactivity between group 1 major allergens from birch and apple. J Chromatogr B Biomed Sci Appl 756: 307-313, 2001.

166 Jin HS, Oh SH, Hong C-S. cDNA sequence encoding major Der f 2 isoform in Korea. Unpublished 2001.

167 Kaiser L, Gafvelin G, Johansson E, Van Hage-Hamsten M, Rasool O. Lep d 2 polymorphisms in wild and cultured Lepidoglyphus destructor mites. Eur J Biochem 270: 646-653, 2003.

168 Kao CYY, Wu JD, Wu CH. Sequencing analysis and characterization of cDNA encoding Cr-PII allergens of American cockroach. Unpublished 1997.

169 Karamloo F, Schmitz N, Scheurer S, Foetisch K, Hoffmann A, Haustein D, Vieths S. Molecular cloning and characterization of a birch pollen minor allergen, Bet v 5, belonging to a family of isoflavone reductase-related proteins. J. Allergy Clin. Immunol. 104: 991-999, 1999.

170 Karamloo F, Wangorsch A, Haustein D, Vieths S. Characterization Bet v 6.0102, a high-IgE binding variant of the birch pollen minor allergen, Bet v 6. Unpublished 2000.

171 Komiyama N, Sone T, Shimizu K, Morikubo K, Kino K. cDNA cloning and expression of Cry j II the second major allergen of Japanese cedar pollen. Biochem. Biophys. Res. Commun. 201: 1021-1028, 1994.

172 Laffer S, Valenta R, Vrtala S, Susani M, van Ree R, Kraft D, Scheiner O, Duchene M. Complementary DNA cloning of the major allergen Phl p I from timothy grass (Phleum pratense); recombinant Phl p I inhibits IgE binding to group I allergens from eight different grass species. J. Allergy Clin. Immunol. 94: 689-698, 1994.

173 Larsen JN, Stroman P, Ipsen H. PCR based cloning and sequencing of isogenes encoding the tree pollen major allergen Car b I from Carpinus betulus, hornbeam. Mol. Immunol. 29: 703-711, 1992.

174 Larsen JN. PCR based cloning and sequencing of isogenes encoding the tree pollen major allergen Bet v 1 from Betula verrucosa, white birch. Unpublished 1996a.

175 Larsen JN. PCR based cloning and sequencing of isogenes encoding the tree pollen major allergen Car b 1 from Carpinus betulus, Hornbeam. Unpublished 1996b.

176 Lin X, Hwang G-J, Zimmerman JL. Isolation and characterization of a diverse set of genes from carrot somatic embryos. Unpublished 1996.

177 Lombardero M, Barbas JA, Moscoso del Prado J, Carreira J. cDNA sequence analysis of the main olive allergen, Ole e I. Clin. Exp. Allergy 24: 765-770, 1994.

178 Lopez-Torrejon G, Sanchez-Monge R, Martin-Esteban M, Diaz-Perales A, Pascual CY, Salcedo G. Mature 48 kDa vicilin is a major allergen from lentil. Unpublished 2003.

179 Luettkopf D, Scheurer S, Haustein D, Vieths S. Cloning and immunological characterization of the major hazelnut allergen, Cor a 1.0401. Unpublished 1999.

180 Luettkopf D, Scheurer S, Haustein D, Vieths S. Characterization of Cor a 1.0402-1.0404, variants of the major hazelnut allergen. Unpublished 2000.

181 Ma Y, Breiteneder H, Hoffmann-Sommergruber K. Molecular characterization of apple profilin (Mal d 4) as a relevant food allergen. Unpublished 2002.

182 Mantyjarvi RA, Parkkinen S, Rytkonen M, Pentikainen J, Pelkonen J, Rautiainen J, Virtanen T. cDNA cloning of the predominant allergen of bovine dander; a new member in the lipocalin family. Unpublished 1996.

183 Melen E, Pomes A, Vailes LD, Arruda LK, Chapman MD. Molecular cloning of Per a 1 and definition of the cross-reactive Group 1 cockroach allergens. J. Allergy Clin. Immunol. 103: 859-864, 1999.

184 Miao Z, Gaynor JJ. Molecular cloning, characterization and expression of Mn-superoxide dismutase from the rubber tree (Hevea brasiliensis). Plant Mol. Biol. 23: 267-277, 1993.

185 Monsalve RI, Villalba M, Rodriguez R. Cloning and expression of Cup s 1, the major allergen of the pollen of Cupressus sempervirens. Unpublished 2000.

186 Namba M, Kurose M, Torigoe K, Hino K, Taniguchi Y, Fukuda S, Usui M, Kurimoto M. Molecular cloning of the second major allergen, Cry j II, from Japanese cedar pollen. FEBS Lett. 353: 124-128, 1994.

187 Nandy A, Kniest FM, Cromwell O, Fiebig H. Variants of the house dust mite allergen der f2. Patent: WO 2004007542-A, 2004.

188 Ong EK, Griffith IJ, Knox RB, Singh MB. Cloning of a cDNA encoding a group-V (group-IX) allergen isoform from rye-grass pollen that demonstrates specific antigenic immunoreactivity. Gene






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