Transient T cell receptor β-chain variable region-specific expansions of CD4+ and CD8+ T cells during the early phase of pediatric human immunodeficiency virus infection:: Characterization of expanded cell populations by T cell receptor phenotyping

被引:25
|
作者
Soudeyns, H
Champagne, P
Holloway, CL
Silvestri, GU
Ringuette, N
Samson, J
Lapointe, N
Sékaly, RP
机构
[1] McGill Univ, Inst Rech Clin Montreal, Immunol Lab, Montreal, PQ, Canada
[2] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[3] McGill Univ, Dept Med, Div Expt Med, Montreal, PQ, Canada
[4] Hop St Justine, Ctr Maternel & Infantile SIDA, Montreal, PQ H3T 1C5, Canada
[5] Univ Montreal, Dept Microbiol & Immunol, Montreal, PQ, Canada
[6] Univ Ancona, Osped Regionale Torrette, Ancona, Italy
关键词
D O I
10.1086/315181
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 receptor (TCR) repertoire perturbations ape commonly detected in CD8(+) T cells during adult primary human immunodeficiency virus (HIV) infection and have been associated with HN-specific cytotoxic T cell responses, By use of flow cytometry, transient high-level TCR beta-chain variable region-specific expansions of CD4(+) and CD8(+) T cells were observed more frequently in HIV-infected children than in children exposed to HIV who remained uninfected. TCR beta-chain diversity analysis and diversity-specific polymerase chain reaction were used to study the clonality of expanded CD4(+) and CD8(+) subsets. In CD8(+) T cells, structural features of the complement-determining regions 3 were altered during the course of the expansion, and persistent TCR clonotypes were observed, consistent with antigen-driven selection. In contrast, TCR beta-chain variable region-specific expansions without clonotypic overrepresentation or persistence were observed in CD4(+) T cells, possibly related to HIV-specific helper T cell responses or to the progressive destruction of the CD4(+) cell compartment.
引用
收藏
页码:107 / 120
页数:14
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