Characterization of the T-Cell receptor Vβ repertoire in the human immune response against Leishmania parasites

被引:22
作者
Clarencio, Jorge
de Oliveira, Camila I.
Bomfim, Gloria
Pompeu, Margarida M.
Teixeira, Maria Jania
Barbosa, Theolis C.
Souza-Neto, Sebastiao
Carvalho, Edgar M.
Brodskyn, Claudia
Barral, Aldina
Barral-Netto, Manoel
机构
[1] Fiocruz MS, Ctr Pesquisas Goncalo Moniz, BR-40296710 Salvador, BA, Brazil
[2] UFBA, Fac Med, BR-40025010 Salvador, BA, Brazil
[3] UFC, BR-60430160 Fortaleza, Ceara, Brazil
[4] UFBA, ICS, Dept Biointeracao, BR-40110160 Salvador, BA, Brazil
[5] Inst Invest Imunol, Sao Paulo, Brazil
关键词
D O I
10.1128/IAI.00265-06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
In order to explore a possible presence of hyperreactive T-cell clones in human cutaneous leishmaniasis (CL), we have investigated, by How cytometry, the expression of V beta chains of T-cell receptors (TCRs) in the following types of cells: (i) peripheral blood mononuclear cells (PBMCs) from CL patients, which were then compared to those from normal volunteers; (ii) unstimulated and soluble Leishmania antigen-stimulated draining lymph node cells from CL patients; (iii) PBMCs from volunteers before versus after Leishmania immunization; and (iv) PBMCs from healthy volunteers that were primed in vitro with live Leishmania parasites. Our results show a modulation in the TCR V beta repertoire during CL and after antigen stimulation of patients' cells. Vaccination, however, leads to a broad expansion of different V beta TCRs. We also observed an association between TCR V beta 12 expression, T-cell activation, and gamma interferon production upon in vitro priming with Leishmania. Collectively, these results both indicate that infection with live parasites or exposure to parasite antigen can modulate the TCR V beta repertoire and suggest that TCR V beta 12 may be implicated in the response to Leishmania.
引用
收藏
页码:4757 / 4765
页数:9
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