CD4+ T cell response to Leishmania spp. in non-infected individuals

被引:6
|
作者
Gabaglia, CR
Valle, MT
Fenoglio, D
Barcinski, MA
Manca, F
机构
[1] LIAI, Div Immune Regulat, San Diego, CA 92121 USA
[2] Univ Genoa, Immunol Lab, I-16126 Genoa, Italy
[3] Osped San Martino Genova, Genoa, Italy
[4] Univ Sao Paulo, Dept Parasitol, Sao Paulo, Brazil
[5] Natl Canc Inst, Div Expt Med, Rio De Janeiro, Brazil
关键词
CD4(+) T cell lines; non-infected individuals; Leishmania sp; memory T cells; cytokines;
D O I
10.1016/S0198-8859(00)00119-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell mediated immunity is known to play a central role ill the host response to control intracellular pathogens. This work demonstrates the presence of specific CD4(+) T cells to Leishmania spp, antigens in peripheral mononuclear cells of naive individuals (normal volunteers from non-endemic regions). The responder population was expanded by generation of antigen-specific T cell lines, which were produced by repeated stimulation with fixed promastigotes and autologous irradiated PBMC as antigen presenting cells. The leishmania-T cell lines were shown to proliferate in response to different species of the parasite (L. amazonensis, L, braziliensis, and L, donovani), but nut to other recall antigens such as Candida albicans or tetanus toxoid. A preferential expansion of IFN gamma and IL-2 producing Th1-like T cells was observed. The leishmania-reactive cells were distributed between CD4(+) CD45RA(+) ("naive") and CD4(+) CD45R0(+) ("memory") populations. Although limiting dilution analysis showed a precursor frequency 3 times lower within the naive compartment, similar numbers of T cell lines were derived from both purified subpopulations. This study using leishmania-specific CD4(+) T cell lines produced from normal individuals should provide information on cellular immune responses that are triggered bi the parasite and how infection impacts the naive T cell repertoire. (C) American Society for Histocompatibility and Immunogenetics, 2000. Published by Elsevier Science Inc.
引用
收藏
页码:531 / 537
页数:7
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