Walker B D, Flexner C, Paradis T J, Fuller T C, Hirsch M S, Schooley R T, Moss B
Infectious Disease Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114.
Science. 1988 Apr 1;240(4848):64-6. doi: 10.1126/science.2451288.
Characterization of the host immune response to human immunodeficiency virus type 1 (HIV-1) is critical to the rational design of an effective AIDS vaccine. In this study, cytotoxic T lymphocytes (CTL) specific for HIV-1 reverse transcriptase (RNA-dependent DNA polymerase) were found in blood samples from HIV-1-infected individuals. CTL targets were prepared by immortalizing B cells from ten seropositive and six seronegative individuals, and then infecting these cells with recombinant vaccinia viruses containing HIV-1 genes. CTL directed against autologous B lymphoblasts expressing HIV-1 reverse transcriptase were detected in fresh blood samples from eight HIV-1 seropositive subjects, but in no seronegative controls. The effector cells were identified as major histocompatibility complex-restricted CD3+CD8+ lymphocytes. Because the HIV-1 pol gene is highly conserved among different isolates and generates both humoral and cellular immune responses, it bears consideration for inclusion in a candidate AIDS vaccine.
了解宿主对1型人类免疫缺陷病毒(HIV-1)的免疫反应对于合理设计有效的艾滋病疫苗至关重要。在本研究中,在HIV-1感染个体的血液样本中发现了对HIV-1逆转录酶(依赖RNA的DNA聚合酶)具有特异性的细胞毒性T淋巴细胞(CTL)。通过将来自10名血清阳性和6名血清阴性个体的B细胞永生化,然后用含有HIV-1基因的重组痘苗病毒感染这些细胞来制备CTL靶标。在8名HIV-1血清阳性受试者的新鲜血液样本中检测到针对表达HIV-1逆转录酶的自体B淋巴母细胞的CTL,但在血清阴性对照中未检测到。效应细胞被鉴定为主要组织相容性复合体限制的CD3 + CD8 +淋巴细胞。由于HIV-1 pol基因在不同分离株中高度保守,并产生体液免疫和细胞免疫反应,因此在候选艾滋病疫苗中考虑纳入该基因。