Nathanson N, Mathieson B J
Office of AIDS Research, National Institutes of Health, Bethesda, MD 20892-2340, USA.
J Infect Dis. 2000 Aug;182(2):579-89. doi: 10.1086/315707. Epub 2000 Jul 28.
Over the last 12 years, many human immunodeficiency virus (HIV) vaccine candidates have been tried in humans, with disappointing results. In particular, recombinant envelope proteins have failed to elicit strong cellular immune responses or neutralizing antibody against many wild-type isolates of HIV-1. Attenuated strains of simian immunodeficiency virus (SIV), although capable of protecting against virulent strains of SIV, often retain residual pathogenicity. These difficulties suggest that it will be necessary to address a number of biological questions that underpin the rational development of an AIDS vaccine: (1) Will natural infection with HIV protect against superinfection? (2) Is partial protection induced by an HIV vaccine adequate to prevent AIDS? (3) What are the immune correlates of protection for an AIDS vaccine? (4) Will a monotypic HIV-1 vaccine confer cross-clade immunity? (5) Is mucosal immunity important for an effective AIDS vaccine? (6) Is there a rationale for therapeutic immunization? Ongoing research that is addressing these questions should lead to the formulation of a safe and effective AIDS vaccine.
在过去12年里,许多人类免疫缺陷病毒(HIV)疫苗候选物已在人体中进行试验,但结果令人失望。特别是,重组包膜蛋白未能引发针对许多HIV-1野生型分离株的强烈细胞免疫反应或中和抗体。猿猴免疫缺陷病毒(SIV)减毒株虽然能够预防毒性较强的SIV毒株,但往往仍具有残余致病性。这些困难表明,有必要解决一些支撑艾滋病疫苗合理研发的生物学问题:(1)HIV自然感染能否预防再次感染?(2)HIV疫苗诱导的部分保护是否足以预防艾滋病?(3)艾滋病疫苗保护的免疫相关因素有哪些?(4)单一型HIV-1疫苗能否提供跨亚型免疫?(5)黏膜免疫对有效的艾滋病疫苗是否重要?(6)治疗性免疫接种是否有理论依据?针对这些问题的正在进行的研究应能促成安全有效的艾滋病疫苗的研制。