Papagno L, Appay V, Sutton J, Rostron T, Gillespie G M A, Ogg G S, King A, Makadzanhge A T, Waters A, Balotta C, Vyakarnam A, Easterbrook P J, Rowland-Jones S L
MRC Human Immunology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Oxford, UK.
Clin Exp Immunol. 2002 Dec;130(3):509-17. doi: 10.1046/j.1365-2249.2002.02005.x.
The mechanisms underlying non-progression in HIV-1 infection are not well understood; however, this state has been associated previously with strong HIV-1-specific CD8+ T cell responses and the preservation of proliferative CD4+ T cell responses to HIV-1 antigens. Using a combination of interferon-gamma (IFN-gamma) ELISpot assays and tetramer staining, the HIV-1-specific CD8+ T cell populations were quantified and characterized in untreated long-term HIV-1-infected non-progressors and individuals with slowly progressive disease, both in relation to CD4+ T cell responses, and in comparison with responses to cytomegalovirus (CMV) antigens. High levels of CD8+ T cell responses specific for HIV-1 or CMV were observed, but neither their frequency nor their phenotype seemed to differ between the two patient groups. Moreover, while CMV-specific CD4+ T cell responses were preserved in these donors, IFN-gamma release by HIV-1-specific CD4+ T cells was generally low. These data raise questions with regard to the role played by CD8+ T cells in the establishment and maintenance of long-term non-progression.
HIV-1感染不进展的潜在机制尚未完全明确;然而,此前这种状态与强烈的HIV-1特异性CD8+ T细胞反应以及对HIV-1抗原的增殖性CD4+ T细胞反应的维持有关。通过结合干扰素-γ(IFN-γ)酶联免疫斑点分析和四聚体染色,对未经治疗的长期HIV-1感染非进展者和疾病进展缓慢者体内的HIV-1特异性CD8+ T细胞群体进行了定量和特征分析,分析内容既涉及CD4+ T细胞反应,也与对巨细胞病毒(CMV)抗原的反应进行了比较。观察到针对HIV-1或CMV的高水平CD8+ T细胞反应,但两个患者组之间它们的频率和表型似乎均无差异。此外,虽然这些供体中CMV特异性CD4+ T细胞反应得以保留,但HIV-1特异性CD4+ T细胞释放的IFN-γ通常较低。这些数据引发了关于CD8+ T细胞在长期不进展的建立和维持中所起作用的疑问。