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HIV特异性CD8(+) T细胞的频率与功能

Frequency and function of HIV-specific CD8(+) T cells.

作者信息

Migueles S A, Connors M

机构信息

Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Building 10, Room 11B-09, 10 Center Dr MSC 1876, Bethesda, MD 20892-1876, USA.

出版信息

Immunol Lett. 2001 Nov 1;79(1-2):141-50. doi: 10.1016/s0165-2478(01)00276-0.

Abstract

The virus-specific CD8(+) T cell responses of 27 HIV-infected patients were studied, including a unique cohort of long term nonprogressors (LTNP) with normal CD4(+) T cell counts, low levels of plasma viral RNA, strong proliferative responses to HIV antigens and an over-representation of the HLA B*5701 class I allele. The frequencies of CD8(+) T cells specific to the majority of HIV gene products were measured by flow cytometric detection of intracellular interferon-gamma (IFN-gamma) in response to HIV-vaccinia recombinant infected autologous B cells. Very high frequencies (1.4-22%) of circulating CD8(+) T cells were found to be HIV-specific and were not only found in LTNP with reduced plasma virus. No correlation was evident between the frequency of HIV-specific CD8(+) T cells and levels of plasma viremia. In each case, the vast majority of cells (up to 17.2%) responded to Gag-Pol gene products. Although similar frequencies of Gag peptide-specific CD8(+) T cells were found in LTNP and progressors by either intracellular IFN-gamma or MHC class I tetramer staining, the breadth of these responses was greater in patients with progressive HIV infection compared with the LTNP group. The frequency of CD8(+) T cells specific for a single peptide was not representative of an individual patient's total HIV-specific CD8(+) T cell response. These data demonstrate that high numbers of HIV-specific CD8(+) T cells exist even in patients with high level viremia and progressive disease. Further, they suggest that other qualitative parameters of the CD8(+) T cell response may differentiate some patients with very low levels of plasma virus and nonprogressive infection.

摘要

对27名HIV感染患者的病毒特异性CD8(+) T细胞反应进行了研究,其中包括一组独特的长期不进展者(LTNP),他们的CD4(+) T细胞计数正常,血浆病毒RNA水平低,对HIV抗原的增殖反应强烈,且HLA B*5701 I类等位基因的比例过高。通过流式细胞术检测细胞内干扰素-γ(IFN-γ)对HIV-痘苗重组体感染的自体B细胞的反应,来测量大多数HIV基因产物特异性CD8(+) T细胞的频率。发现循环CD8(+) T细胞的频率非常高(1.4-22%)是HIV特异性的,不仅在血浆病毒减少的LTNP中发现。HIV特异性CD8(+) T细胞的频率与血浆病毒血症水平之间没有明显的相关性。在每种情况下,绝大多数细胞(高达17.2%)对Gag-Pol基因产物有反应。尽管通过细胞内IFN-γ或MHC I类四聚体染色在LTNP和疾病进展者中发现了相似频率的Gag肽特异性CD8(+) T细胞,但与LTNP组相比,进行性HIV感染患者的这些反应的广度更大。单一肽特异性CD8(+) T细胞的频率并不代表个体患者总的HIV特异性CD8(+) T细胞反应。这些数据表明,即使在病毒血症水平高且疾病进展的患者中也存在大量的HIV特异性CD8(+) T细胞。此外,它们表明CD8(+) T细胞反应的其他定性参数可能区分一些血浆病毒水平非常低且感染不进展的患者。

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