Excler Jean-Louis, Robb Merlin L, Kim Jerome H
U.S. Military HIV Research Program; Division of Retrovirology; Walter Reed Army Institute of Research; Bethesda, MD USA; Henry M. Jackson Foundation for the Advancement of Military Medicine; Bethesda, MD USA.
U.S. Military HIV Research Program; Division of Retrovirology; Walter Reed Army Institute of Research; Bethesda, MD USA.
Hum Vaccin Immunother. 2014;10(6):1734-46. doi: 10.4161/hv.28462. Epub 2014 Mar 17.
The development of a safe and effective preventive HIV-1 vaccine remains a public health priority. Despite scientific difficulties and disappointing results, HIV-1 vaccine clinical development has, for the first time, established proof-of-concept efficacy against HIV-1 acquisition and identified vaccine-associated immune correlates of risk. The correlate of risk analysis showed that IgG antibodies against the gp120 V2 loop correlated with decreased risk of HIV infection, while Env-specific IgA directly correlated with increased risk. The development of vaccine strategies such as improved envelope proteins formulated with potent adjuvants and DNA and vectors expressing mosaics, or conserved sequences, capable of eliciting greater breadth and depth of potentially relevant immune responses including neutralizing and non-neutralizing antibodies, CD4+ and CD8+ cell-mediated immune responses, mucosal immune responses, and immunological memory, is now proceeding quickly. Additional human efficacy trials combined with other prevention modalities along with sustained funding and international collaboration remain key to bring an HIV-1 vaccine to licensure.
开发一种安全有效的预防性HIV-1疫苗仍然是公共卫生领域的优先事项。尽管存在科学难题且结果令人失望,但HIV-1疫苗的临床开发首次确立了针对HIV-1感染的概念验证疗效,并确定了与疫苗相关的风险免疫相关因素。风险相关因素分析表明,针对gp120 V2环的IgG抗体与HIV感染风险降低相关,而Env特异性IgA则与风险增加直接相关。目前,疫苗策略的开发正在迅速推进,例如使用强效佐剂配制的改良包膜蛋白、表达嵌合体或保守序列的DNA和载体,这些能够引发更广泛、更深入的潜在相关免疫反应,包括中和抗体和非中和抗体、CD4+和CD8+细胞介导的免疫反应、粘膜免疫反应以及免疫记忆。开展更多人体疗效试验并结合其他预防方式,以及持续的资金投入和国际合作,仍然是使HIV-1疫苗获得许可的关键。