DNA Priming Increases Frequency of T-Cell Responses to a Vesicular Stomatitis Virus HIV Vaccine with Specific Enhancement of CD8+ T-Cell Responses by Interleukin-12 Plasmid DNA.

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-11-06 Print Date: 2017-11-01 DOI:10.1128/CVI.00263-17
Shuying S Li, Nidhi K Kochar, Marnie Elizaga, Christine M Hay, Gregory J Wilson, Kristen W Cohen, Stephen C De Rosa, Rong Xu, Ayuko Ota-Setlik, Daryl Morris, Greg Finak, Mary Allen, Hong-Van Tieu, Ian Frank, Magdalena E Sobieszczyk, Drew Hannaman, Raphael Gottardo, Peter B Gilbert, Georgia D Tomaras, Lawrence Corey, David K Clarke, Michael A Egan, John H Eldridge, M Juliana McElrath, Nicole Frahm
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引用次数: 29

Abstract

The HIV Vaccine Trials Network (HVTN) 087 vaccine trial assessed the effect of increasing doses of pIL-12 (interleukin-12 delivered as plasmid DNA) adjuvant on the immunogenicity of an HIV-1 multiantigen (MAG) DNA vaccine delivered by electroporation and boosted with a vaccine comprising an attenuated vesicular stomatitis virus expressing HIV-1 Gag (VSV-Gag). We randomized 100 healthy adults to receive placebo or 3 mg HIV-MAG DNA vaccine (ProfectusVax HIV-1 gag/pol or ProfectusVax nef/tat/vif, env) coadministered with pIL-12 at 0, 250, 1,000, or 1,500 μg intramuscularly by electroporation at 0, 1, and 3 months followed by intramuscular inoculation with 3.4 × 107 PFU VSV-Gag vaccine at 6 months. Immune responses were assessed after the prime and boost and 6 months after the last vaccination. High-dose pIL-12 increased the magnitude of CD8+ T-cell responses postboost compared to no pIL-12 (P = 0.02), while CD4+ T-cell responses after the prime were higher in the absence of pIL-12 than with low- and medium-dose pIL-12 (P ≤ 0.05). The VSV boost increased Gag-specific CD4+ and CD8+ T-cell responses in all groups (P < 0.001 for CD4+ T cells), inducing a median of four Gag epitopes in responders. Six to 9 months after the boost, responses decreased in magnitude, but CD8+ T-cell response rates were maintained. The addition of a DNA prime dramatically improved responses to the VSV vaccine tested previously in the HVTN 090 trial, leading to broad epitope targeting and maintained CD8+ T-cell response rates at early memory. The addition of high-dose pIL-12 given with a DNA prime by electroporation and boosted with VSV-Gag increased the CD8+ T-cell responses but decreased the CD4+ responses. This approach may be advantageous in reshaping the T-cell responses to a variety of chronic infections or tumors. (This study has been registered at ClinicalTrials.gov under registration no. NCT01578889.).

Abstract Image

Abstract Image

白细胞介素-12质粒DNA特异性增强t细胞对水疱性口炎病毒HIV疫苗的CD8+ t细胞应答,从而提高t细胞应答频率
HIV疫苗试验网络(HVTN) 087疫苗试验评估了增加剂量的il -12(作为质粒DNA递送的白细胞介素-12)佐剂对HIV-1多抗原(MAG) DNA疫苗的免疫原性的影响,该疫苗由电穿孔递送,并由含有表达HIV-1 Gag的减毒水疱性口炎病毒(VSV-Gag)的疫苗增强。我们将100名健康成人随机分组,分别接受安慰剂或3mg HIV-MAG DNA疫苗(ProfectusVax HIV-1 gag/pol或ProfectusVax nef/tat/vif, env)与il -12在0,250,1,000或1,500 μg的情况下在0,1和3个月通过电穿孔肌肉注射,然后在6个月肌肉注射3.4 × 107 PFU VSV-Gag疫苗。免疫应答在初次接种和加强接种后以及最后一次接种后6个月进行评估。高剂量的il -12增强后CD8+ t细胞的应答量比未添加il -12时增加(P = 0.02),而未添加il -12时,CD4+ t细胞的应答量比低、中剂量的il -12高(P≤0.05)。VSV增强了所有组中Gag特异性CD4+和CD8+ T细胞的应答(CD4+ T细胞的P < 0.001),在应答者中诱导了4个Gag表位。增强后6至9个月,反应幅度下降,但CD8+ t细胞反应率保持不变。添加DNA引物显著改善了先前在HVTN 090试验中测试的VSV疫苗的应答,导致广泛的表位靶向,并在早期记忆中维持CD8+ t细胞应答率。通过电穿孔给药和VSV-Gag增强的高剂量pIL-12增加了CD8+ t细胞应答,但降低了CD4+应答。这种方法可能有利于重塑t细胞对各种慢性感染或肿瘤的反应。(本研究已在ClinicalTrials.gov注册,注册号为:NCT01578889)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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