Menon Veena, Ayala Victor I, Rangaswamy Sneha P, Kalisz Irene, Whitney Stephen, Galmin Lindsey, Ashraf Asma, LaBranche Celia, Montefiori David, Petrovsky Nikolai, Kalyanaraman Vaniambadi S, Pal Ranajit
Advanced BioScience Laboratories, Inc., Rockville, MD, USA.
Indian Institute of Technology Madras, Chennai 600036, India.
J Gen Virol. 2017 Aug;98(8):2143-2155. doi: 10.1099/jgv.0.000863. Epub 2017 Jul 31.
The partial success of the RV144 trial underscores the importance of envelope-specific antibody responses for an effective HIV-1 vaccine. Oligomeric HIV-1 envelope proteins delivered with a potent adjuvant are expected to elicit strong antibody responses with broad neutralization specificity. To test this hypothesis, two SIV envelope proteins were formulated with delta inulin-based adjuvant (Advax) and used to immunize nonhuman primates. Oligomeric gp140-gp145 from SIVmac251 and SIVsmE660 was purified to homogeneity. Oligomers showed high-affinity interaction with CD4 and were highly immunogenic in rabbits, inducing Tier 2 SIV-neutralizing antibodies. The immunogenicity of an oligomeric Env DNA prime and protein boost together with Advax was evaluated in Chinese rhesus macaques. DNA administration elicited antibodies to both envelopes, and titres were markedly enhanced following homologous protein boosts via intranasal and intramuscular routes. Strong antibody responses were detected against the V1 and V2 domains of gp120. During peak immune responses, a low to moderate level of neutralizing activity was detected against Tier 1A/1B SIV isolates, with a moderate level noted against a Tier 2 isolate. Increased serum antibody affinity to SIVmac251 gp140 and generation of Env-specific memory B cells were observed in the immunized macaques. Animals were subjected to low-dose intravaginal challenge with SIVmac251 one week after the last protein boost. One out of three immunized animals was protected from infection. Although performed with a small number of macaques, this study demonstrates the utility of oligomeric envelopes formulated with Advax in eliciting broad antibody responses with the potential to provide protection against SIV transmission.
RV144试验的部分成功凸显了包膜特异性抗体反应对于有效的HIV-1疫苗的重要性。与强效佐剂一起递送的寡聚HIV-1包膜蛋白有望引发具有广泛中和特异性的强烈抗体反应。为了验证这一假设,将两种SIV包膜蛋白与基于菊粉的佐剂(Advax)一起配制,并用于免疫非人灵长类动物。从SIVmac251和SIVsmE660中纯化出寡聚gp140-gp145至同质。寡聚体显示出与CD4的高亲和力相互作用,并且在兔中具有高度免疫原性,可诱导2级SIV中和抗体。在中国恒河猴中评估了寡聚Env DNA初免和蛋白加强免疫联合Advax的免疫原性。DNA给药引发了针对两种包膜的抗体,并且在通过鼻内和肌肉内途径进行同源蛋白加强免疫后,滴度显著提高。检测到针对gp120的V1和V2结构域的强烈抗体反应。在免疫反应高峰期,检测到针对1A/1B级SIV分离株的低至中等水平的中和活性,针对2级分离株的中和活性为中等水平。在免疫的猕猴中观察到血清抗体对SIVmac251 gp140的亲和力增加以及Env特异性记忆B细胞的产生。在最后一次蛋白加强免疫后一周,对动物进行低剂量的SIVmac251阴道内攻击。三只免疫动物中有一只受到感染保护。尽管该研究是用少量猕猴进行的,但它证明了用Advax配制的寡聚包膜在引发广泛抗体反应方面的效用,有可能提供针对SIV传播的保护。