Goonetilleke Nilu, Moore Stephen, Dally Len, Winstone Nicola, Cebere Inese, Mahmoud Abdul, Pinheiro Susana, Gillespie Geraldine, Brown Denise, Loach Vanessa, Roberts Joanna, Guimaraes-Walker Ana, Hayes Peter, Loughran Kelley, Smith Carole, De Bont Jan, Verlinde Carl, Vooijs Danii, Schmidt Claudia, Boaz Mark, Gilmour Jill, Fast Pat, Dorrell Lucy, Hanke Tomas, McMichael Andrew J
Centre for Clinical Vaccinology and Tropical Medicine and MRC Human Immunology Unit, University of Oxford, Oxford OX3 7LJ, United Kingdom.
J Virol. 2006 May;80(10):4717-28. doi: 10.1128/JVI.80.10.4717-4728.2006.
A double-blind randomized phase I trial was conducted in human immunodeficiency virus type 1 (HIV-1)-negative subjects receiving vaccines vectored by plasmid DNA and modified vaccinia virus Ankara (MVA) expressing HIV-1 p24/p17 gag linked to a string of CD8(+) T-cell epitopes. The trial had two groups. One group received either two doses of MVA.HIVA (2x MVA.HIVA) (n=8) or two doses of placebo (2x placebo) (n=4). The second group received 2x pTHr.HIVA followed by one dose of MVA.HIVA (n=8) or 3x placebo (n=4). In the pTHr.HIVA-MVA.HIVA group, HIV-1-specific T-cell responses peaked 1 week after MVA.HIVA vaccination in both ex vivo gamma interferon (IFN-gamma) ELISPOT (group mean, 210 spot-forming cells/10(6) cells) and proliferation (group mean stimulation index, 37), with assays detecting positive responses in four out of eight and five out of eight subjects, respectively. No HIV-1-specific T-cell responses were detected in either assay in the 2x MVA.HIVA group or subjects receiving placebo. Using a highly sensitive and reproducible cultured IFN-gamma ELISPOT assay, positive responses mainly mediated by CD4(+) T cells were detected in eight out of eight vaccinees in the pTHr.HIVA-MVA.HIVA group and four out of eight vaccinees in the 2x MVA.HIVA group. Importantly, no false-positive responses were detected in the eight subjects receiving placebo. Of the 12 responders, 11 developed responses to previously identified immunodominant CD4(+) T-cell epitopes, with 6 volunteers having responses to more than one epitope. Five out of 12 responders also developed CD8(+) T-cell responses to the epitope string. Induced T cells produced a variety of anti-viral cytokines, including tumor necrosis factor alpha and macrophage inflammatory protein 1 beta. These data demonstrate that prime-boost vaccination with recombinant DNA and MVA vectors can induce multifunctional HIV-1-specific T cells in the majority of vaccinees.
在接受由质粒 DNA 和表达与一串 CD8(+) T 细胞表位相连的 HIV-1 p24/p17 gag 的改良安卡拉痘苗病毒(MVA)作为载体的疫苗的 1 型人类免疫缺陷病毒(HIV-1)阴性受试者中进行了一项双盲随机 1 期试验。该试验有两组。一组接受两剂 MVA.HIVA(2x MVA.HIVA)(n = 8)或两剂安慰剂(2x 安慰剂)(n = 4)。第二组接受 2x pTHr.HIVA 后再接种一剂 MVA.HIVA(n = 8)或 3x 安慰剂(n = 4)。在 pTHr.HIVA-MVA.HIVA 组中,在 MVA.HIVA 接种后 1 周,HIV-1 特异性 T 细胞反应在体外γ干扰素(IFN-γ)ELISPOT(组均值,210 个斑点形成细胞/10(6) 个细胞)和增殖试验(组均值刺激指数,37)中均达到峰值,检测到分别有八分之四和八分之五的受试者出现阳性反应。在 2x MVA.HIVA 组或接受安慰剂的受试者的任何一项试验中均未检测到 HIV-1 特异性 T 细胞反应。使用高度灵敏且可重复的培养 IFN-γ ELISPOT 试验,在 pTHr.HIVA-MVA.HIVA 组的八名受试者中有八名检测到主要由 CD4(+) T 细胞介导的阳性反应,在 2x MVA.HIVA 组的八名受试者中有四名检测到阳性反应。重要的是,在接受安慰剂的八名受试者中未检测到假阳性反应。在 12 名有反应者中,11 人对先前确定的免疫优势 CD4(+) T 细胞表位产生反应,6 名志愿者对不止一个表位有反应。12 名有反应者中有 5 人也对表位串产生了 CD8(+) T 细胞反应。诱导的 T 细胞产生了多种抗病毒细胞因子,包括肿瘤坏死因子α和巨噬细胞炎性蛋白 1β。这些数据表明,用重组 DNA 和 MVA 载体进行初免-加强免疫接种可在大多数接种者中诱导多功能 HIV-1 特异性 T 细胞。