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使用亚型一致Env 的 DNA 初免-蛋白加强免疫在诱导针对中国流行的 HIV-1 亚型 BC 病毒的中和抗体反应方面是有效的。

DNA prime-protein boost using subtype consensus Env was effective in eliciting neutralizing antibody responses against subtype BC HIV-1 viruses circulating in China.

机构信息

Jiangsu Province Key Laboratory in Infectious Diseases, The First Affiliated Hospital of Nanjing Medical University; Nanjing, China.

出版信息

Hum Vaccin Immunother. 2012 Nov 1;8(11):1630-7. doi: 10.4161/hv.21648. Epub 2012 Oct 30.

Abstract

Previously, we have shown that DNA prime-protein boost is effective in eliciting neutralizing antibodies (NAb) against randomly selected HIV-1 isolates. Given the genetic diversity of HIV-1 viruses and the unique predominant subtypes in different geographic regions, it is critical to test the DNA prime-protein boost approach against circulating viral isolates in key HIV endemic areas. In the current study, the same DNA prime-protein boost vaccine was used as in previous studies to investigate the induction of NAb responses against HIV-1 clade BC, a major subtype circulating in China. A codon optimized gp120-BC DNA vaccine, based on the consensus envelope (Env) antigen sequence of clade BC, was constructed and a stable CHO cell line expressing the same consensus BC gp120 protein was produced. The immunogenicity of this consensus gp120-BC was examined in New Zealand White rabbits by either DNA prime-protein boost or protein alone vaccination approaches. High levels of Env-specific antibody responses were elicited by both approaches. However, DNA prime-protein boost but not the protein alone immune sera contained significant levels of NAb against pseudotyped viruses expressing HIV-1 BC Env antigens. Furthermore, high frequencies of CD4 binding site-targeted antibodies were found in the DNA prime- protein boost rabbit sera indicating that the positive NAb may be the result of antibodies against conformationally sensitive epitopes on HIV-1 Env. The findings support that DNA prime-protein boost was effective in eliciting NAb against a key HIV-1 virus subtype in China. This result may lead to the development of regional HIV vaccines through this approach.

摘要

先前,我们已经证明 DNA 疫苗-蛋白疫苗加强免疫方案能够有效地诱导针对随机选择的 HIV-1 分离株的中和抗体(NAb)。鉴于 HIV-1 病毒的遗传多样性以及不同地理区域中独特的主要亚型,对关键 HIV 流行地区的循环病毒分离株进行 DNA 疫苗-蛋白疫苗加强免疫方案的测试至关重要。在本研究中,我们使用了与先前研究相同的 DNA 疫苗-蛋白疫苗加强免疫方案,以研究针对中国主要流行的 HIV-1 亚型 clade BC 的 NAb 反应的诱导。构建了一种基于 clade BC 共识包膜(Env)抗原序列的优化密码子 gp120-BC DNA 疫苗,并生产了一种稳定表达相同共识 BC gp120 蛋白的 CHO 细胞系。通过 DNA 疫苗-蛋白疫苗加强免疫或单独蛋白疫苗接种方案,在新西兰白兔中检查了这种共识 gp120-BC 的免疫原性。两种方法都能引起高水平的 Env 特异性抗体反应。然而,只有 DNA 疫苗-蛋白疫苗加强免疫免疫血清而不是单独蛋白免疫血清含有针对表达 HIV-1 BC Env 抗原的假型病毒的显著水平的 NAb。此外,在 DNA 疫苗-蛋白疫苗加强免疫兔血清中发现了高频率的 CD4 结合位点靶向抗体,表明阳性 NAb 可能是针对 HIV-1 Env 上构象敏感表位的抗体的结果。这些发现支持 DNA 疫苗-蛋白疫苗加强免疫方案能够有效地诱导针对中国主要 HIV-1 病毒亚型的 NAb。该结果可能通过该方法导致区域性 HIV 疫苗的开发。

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