Stress proteins may provide a link between the immune response to infection and autoimmunity |
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Authors: | Lamb, J. R. Bal, V. Mendez-Samperio, P. Mehiert, A. So, A. Rothbard, J. Jindal, S. Young, R. A. Young, D. B. |
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Affiliation: | 1 MRC Tuberculosis and Related Infections Unit London W12 OHS, UK 2 Dept of Rheumatology, Royal Postgraduate Medical School, Hammersmith Hospital London W12 OHS, UK 3 Imperial Cancer Research Fund, Lincons Inn Fields London, UK 4 Whitehead Institute for Biomedical Research Cambridge, Mass, USA |
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Abstract: | Stress proteins are frequently the target of humoral and cell-mediatedimmune responses to infection. These proteins belong to highlyconserved gene families and there is substantial sequence homologybetween antigens produced by pathogenic organisms and the correspondingproteins from mammalian cells. Human T cells from sites of infectiousand autoimmune lesions proliferate in response to stress proteins,and mapping of antigenic determinants on a mycobacterial stressprotein shows that both species specific and highly conserved,self-like, regions of the molecule can take partin immune recognition. It is proposed that the lymphocyte populationinduced in response to stress proteins of pathogens during infectionincludes cells capable of autolmmune recognition of the correspondingself protein. Local accumulation of self stress proteins—inresponse to viral infection, for example—may subsequentlyprovide a stimulus for proliferation of such autoreactive lymphocytes,thereby triggering a cycle of events which may contribute tothe pathological damage associated with autoimmune disease. |
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Keywords: | heat-shock proteins mycobacterial antigens T cells epitope mapping |
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