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Defining the T cell antigen proteome of wasp venom
被引:5
作者:
Aslam, A.
Kessler, B.
Batycka, M.
O'Callaghan, C. A.
Misbah, S. A.
Warrell, D. A.
Ogg, G.
[1
]
机构:
[1] Univ Oxford, Weatherall Inst Mol Med, MRC, Human Immunol Unit, Oxford OX3 9DS, England
[2] Univ Oxford, Weatherall Inst Mol Med, Nuffield Dept Clin Med, Oxford OX3 9DS, England
[3] Oxford Radcliffe Hosp NHS Trust, Oxford, England
[4] Churchill Hosp, Dept Dermatol, Oxford OX3 7LJ, England
基金:
英国医学研究理事会;
关键词:
elispot;
gel-filtration/ion exchange chromatography;
proteome;
wasp allergy;
D O I:
10.1111/j.1365-2222.2006.02569.x
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 [免疫学];
摘要:
Background While modulation of T cell function is believed to be important in the successful acquisition of clinical tolerance during venom immunotherapy, little is known of the role of wasp venom specific T cell antigens. Objective We sought comprehensively to characterize the T cell proteome for wasp venom to facilitate the future development of T cell-based immunotherapeutic approaches. Methods Using peripheral blood mononuclear cells from wasp venom-allergic individuals and IL-4 ELISPOT analysis, we characterized T cell responses to whole venom and gel filtration/ion exchange-fractionated venom. Reactive fractions were purified and identified using highly sensitive electrospray ion-trap mass spectrometry. Results Wasp venom-allergic individuals have detectable whole wasp venom-specific T cells directly ex vivo, which show rapid IL-4 effector function. T cell responses to gel filtration/ion exchange fractionated venom were dominated by responses to phospholipase A(1), hyaluronidase and antigen 5. Conclusion Although it is likely that there are many T cell antigens within wasp venom, the main responses are to proteins coincident with the known IgE-binding proteins.
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页码:1274 / 1280
页数:7
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