Kostense Stefan, Vandenberghe Kristin, Joling Jeanine, Van Baarle Debbie, Nanlohy Nening, Manting Erik, Miedema Frank
Department of Clinical Viro-Immunology, CLB/Sanquin Blood Supply Foundation, University of Amsterdam, Plesmanlaan 125, 1066 CX Amsterdam, The Netherlands.
Blood. 2002 Apr 1;99(7):2505-11. doi: 10.1182/blood.v99.7.2505.
Although CD8(+) T cells initially suppress human immunodeficiency virus (HIV) replication, cytotoxic T-cell precursor frequencies eventually decline and fail to prevent disease progression. In a longitudinal study including 16 individuals infected with HIV-1, we studied both the number and function of HIV-specific CD8(+) T cells by comparing HLA-peptide tetramer staining and peptide-induced interferon-gamma (IFN-gamma) production. Numbers of IFN-gamma-producing T cells declined during progression to acquired immunodeficiency syndrome (AIDS), whereas the number of tetramer+ T cells in many individuals persisted at high frequencies. Loss of IFN-gamma-producing T cells correlated with declining CD4(+) T-cell counts, consistent with the need of CD4(+) T-cell help in maintaining adequate CD8(+) T-cell function. These data indicate that the loss of HIV-specific CD8(+) T-cell activity is not due to physical depletion, but is mainly due to progressively impaired function of HIV-specific CD8(+) T cells.
虽然CD8(+) T细胞最初可抑制人类免疫缺陷病毒(HIV)复制,但细胞毒性T细胞前体频率最终会下降,无法阻止疾病进展。在一项纳入16名HIV-1感染者的纵向研究中,我们通过比较HLA-肽四聚体染色和肽诱导的干扰素-γ(IFN-γ)产生,研究了HIV特异性CD8(+) T细胞的数量和功能。在进展为获得性免疫缺陷综合征(AIDS)的过程中,产生IFN-γ的T细胞数量下降,而许多个体中四聚体+ T细胞的数量则持续保持在高频水平。产生IFN-γ的T细胞数量减少与CD4(+) T细胞计数下降相关,这与维持适当CD8(+) T细胞功能需要CD4(+) T细胞辅助一致。这些数据表明,HIV特异性CD8(+) T细胞活性的丧失并非由于细胞数量的耗尽,而是主要由于HIV特异性CD8(+) T细胞功能逐渐受损。