Currier Jeffrey R, deSouza Mark, Chanbancherd Penprapa, Bernstein Wendy, Birx Deborah L, Cox Josephine H
U.S. Military HIV Research Program, Rockville, Maryland 20850, USA.
J Virol. 2002 May;76(10):4971-86. doi: 10.1128/jvi.76.10.4971-4986.2002.
For this report, the rapid identification and characterization of human immunodeficiency virus type 1 (HIV-1)-derived broadly cross-subtype-reactive CD8 cytotoxic T lymphocyte (CTL) epitopes were performed. Using a gamma interferon (IFN-gamma) Elispot assay-based approach and a panel of recombinant vaccinia viruses expressing gag, env, pol, and nef genes representing the seven most predominant subtypes and one circulating recombinant form of HIV-1, the subtype specificity and cross-subtype reactivity of a CD8 response were directly measured from circulating peripheral blood mononuclear cells (PBMC). Enhanced sensitivity of detection of CD8 responses from cryopreserved PBMC was achieved using autologous vaccinia virus-infected B-lymphoblastoid cell lines as supplemental antigen-presenting cells. Of eleven subjects studied, six exhibited broadly cross-subtype-reactive CD8-mediated IFN-gamma production (at least seven of eight subtypes recognized) to at least one major gene product from HIV-1. Screening of subjects showing broadly cross-subtype-specific responses in the vaccinia virus-based enzyme-linked immunospot (Elispot) assay using a panel of overlapping peptides resulted in the identification of cross-subtype responses down to the 20-mer peptide level in less than 3 days. Three subjects showed broad cross-subtype reactivity in both the IFN-gamma Elispot assay and the standard chromium release cytotoxicity assay. Fine mapping and HLA restriction analysis of the response from three subjects demonstrated that this technique can be used to define epitopes restricted by HLA-A, -B, and -C alleles. In addition, the ability of all three epitopes to be processed from multiple subtypes of their parent proteins and presented in the context of HLA class I molecules following de novo synthesis is shown. While all three minimal epitopes mapped here had previously been defined as HIV-1 epitopes, two are shown to have novel HLA restriction alleles and therefore exhibit degenerate HLA binding capacity. These findings provide biological validation of HLA supertypes in HIV-1 CTL recognition and support earlier studies of cross-subtype CTL responses during HIV-1 infection.
在本报告中,我们对1型人类免疫缺陷病毒(HIV-1)衍生的广泛交叉亚型反应性CD8细胞毒性T淋巴细胞(CTL)表位进行了快速鉴定和表征。采用基于γ干扰素(IFN-γ)酶联免疫斑点分析的方法以及一组表达gag、env、pol和nef基因的重组痘苗病毒,这些基因代表了HIV-1的七种最主要亚型和一种循环重组形式,直接从循环外周血单核细胞(PBMC)中测量CD8反应的亚型特异性和交叉亚型反应性。使用自体痘苗病毒感染的B淋巴母细胞系作为补充抗原呈递细胞,提高了从冷冻保存的PBMC中检测CD8反应的灵敏度。在研究的11名受试者中,6名对HIV-1的至少一种主要基因产物表现出广泛的交叉亚型反应性CD8介导的IFN-γ产生(至少识别8种亚型中的7种)。使用一组重叠肽对在基于痘苗病毒的酶联免疫斑点(Elispot)分析中显示出广泛交叉亚型特异性反应的受试者进行筛选,结果在不到3天的时间内鉴定出低至20聚体肽水平的交叉亚型反应。三名受试者在IFN-γ Elispot分析和标准铬释放细胞毒性分析中均表现出广泛的交叉亚型反应性。对三名受试者反应的精细定位和HLA限制性分析表明,该技术可用于定义受HLA-A、-B和-C等位基因限制的表位。此外,还显示了所有三个表位能够从其亲本蛋白的多个亚型中加工出来,并在从头合成后在HLA I类分子的背景下呈递。虽然这里定位的所有三个最小表位以前都被定义为HIV-1表位,但其中两个显示具有新的HLA限制性等位基因,因此表现出简并的HLA结合能力。这些发现为HIV-1 CTL识别中的HLA超型提供了生物学验证,并支持了HIV-1感染期间交叉亚型CTL反应的早期研究。