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Brazilian Journal of Medical and Biological Research
On-line version ISSN 1414-431X
BACELLAR, O.; RUSSO, C. and CARVALHO, E.M.. Regulation of T cell response to leishmania antigens by determinants of histocompatibility leukocyte class I and II molecules. Braz J Med Biol Res [online]. 1998, vol.31, n.12, pp.1575-1581. ISSN 1414-431X. http://dx.doi.org/10.1590/S0100-879X1998001200010.
It has been shown that HLA class I molecules play a significant role in the regulation of the proliferation of T cells activated by mitogens and antigens. We evaluated the ability of mAb to a framework determinant of HLA class I molecules to regulate T cell proliferation and interferon gamma (IFN-g) production against leishmania, PPD, C. albicans and tetanus toxoid antigens in patients with tegumentary leishmaniasis and healthy subjects. The anti-major histocompatibility complex (MHC) mAb (W6/32) suppressed lymphocyte proliferation by 90% in cultures stimulated with aCD3, but the suppression was variable in cultures stimulated with leishmania antigen. This suppression ranged from 30-67% and was observed only in 5 of 11 patients. IFN-g production against leishmania antigen was also suppressed by anti-HLA class I mAb. In 3 patients IFN-g levels were suppressed by more than 60%, while in the other 2 cultures IFN-g levels were 36 and 10% lower than controls. The suppression by HLA class I mAb to the proliferative response in leishmaniasis patients and in healthy controls varied with the antigens and the patients or donors tested. To determine whether the suppression is directed at antigen presenting cells (APCs) or at the responding T cells, experiments with antigen-primed non-adherent cells, separately incubated with W6/32, were performed. Suppression of proliferation was only observed when the W6/32 mAb was added in the presence of T cells. These data provide evidence that a mAb directed at HLA class I framework determinants can suppress proliferation and cytokine secretion in response to several antigens.
Keywords : HLA class I; tegumentary leishmaniasis; modulation of T cell response by HLA class I; interferon-g and HLA class I; soluble antigen and HLA class I.