Li Shuying S, Kochar Nidhi K, Elizaga Marnie, Hay Christine M, Wilson Gregory J, Cohen Kristen W, De Rosa Stephen C, Xu Rong, Ota-Setlik Ayuko, Morris Daryl, Finak Greg, Allen Mary, Tieu Hong-Van, Frank Ian, Sobieszczyk Magdalena E, Hannaman Drew, Gottardo Raphael, Gilbert Peter B, Tomaras Georgia D, Corey Lawrence, Clarke David K, Egan Michael A, Eldridge John H, McElrath M Juliana, Frahm Nicole
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Infectious Diseases Division, University of Rochester Medical Center, Rochester, New York, USA.
Clin Vaccine Immunol. 2017 Nov 6;24(11). doi: 10.1128/CVI.00263-17. Print 2017 Nov.
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 / or ProfectusVax //, ) 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 × 10 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 ( = 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 ( ≤ 0.05). The VSV boost increased Gag-specific CD4 and CD8 T-cell responses in all groups ( < 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.).
艾滋病疫苗试验网络(HVTN)087疫苗试验评估了增加剂量的pIL-12(以质粒DNA形式递送的白细胞介素-12)佐剂对通过电穿孔递送的HIV-1多抗原(MAG)DNA疫苗免疫原性的影响,该疫苗随后用包含表达HIV-1 Gag的减毒水疱性口炎病毒(VSV-Gag)的疫苗加强免疫。我们将100名健康成年人随机分为接受安慰剂组或3毫克HIV-MAG DNA疫苗(ProfectusVax HIV-1 / 或ProfectusVax // )组,在第0、1和3个月通过电穿孔分别与0、250、1000或1500微克pIL-12肌肉注射联合给药,然后在第6个月肌肉接种3.4×10 PFU VSV-Gag疫苗。在初次免疫和加强免疫后以及最后一次接种后6个月评估免疫反应。与未使用pIL-12相比,高剂量pIL-12增加了加强免疫后CD8 T细胞反应的强度(P = 0.02),而在初次免疫后,未使用pIL-12时的CD4 T细胞反应高于低剂量和中剂量pIL-12组(P≤0.05)。VSV加强免疫在所有组中均增加了Gag特异性CD4和CD8 T细胞反应(CD4 T细胞P < 0.001),在反应者中诱导出中位数为四个Gag表位。加强免疫后6至9个月,反应强度下降,但CD8 T细胞反应率得以维持。DNA初次免疫的加入显著改善了对先前在HVTN 090试验中测试的VSV疫苗的反应,导致广泛的表位靶向并在早期记忆中维持CD8 T细胞反应率。通过电穿孔与DNA初次免疫联合使用高剂量pIL-12并以VSV-Gag加强免疫增加了CD8 T细胞反应,但降低了CD4反应。这种方法在重塑对各种慢性感染或肿瘤的T细胞反应方面可能具有优势。(本研究已在ClinicalTrials.gov注册,注册号为NCT01578889。)