Burwitz Benjamin J, Greene Justin M, O'Connor David H
Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Curr HIV Res. 2009 Jan;7(1):51-6. doi: 10.2174/157016209787048492.
An HIV vaccine remains elusive despite the concerted efforts of investigators and clinicians over the past two decades. Animal models are regularly used to obtain new insights on disease pathogenesis and have become invaluable tools in the translation of treatments from basic research laboratories to the clinic. Vaccination of macaques with live, attenuated simian immunodeficiency virus is currently the most effective method of garnering protection against subsequent pathogenic SIV challenge. However, immunization of humans with live, attenuated HIV is not feasible due to safety concerns. Therefore, clues to an effective and safe vaccine against HIV may be found by studying immune correlates of protection in the live, attenuated, vaccinated macaque model. Previous studies have identified the immune correlates of protection against Friend retrovirus in live, attenuated vaccinated mice using allogeneic adoptive transfers. Similar experiments in macaques have thus far been hindered due to the vast genetic diversity found within outbred populations. Here we review the current state of SIV adoptive transfer research and present a novel macaque model that allows for allogeneic adoptive transfers.
尽管在过去二十年里研究人员和临床医生共同努力,但HIV疫苗仍然难以研制成功。动物模型经常被用于获取有关疾病发病机制的新见解,并且已成为从基础研究实验室到临床治疗转化过程中非常宝贵的工具。用减毒活猿猴免疫缺陷病毒对猕猴进行疫苗接种是目前获得针对后续致病性SIV攻击的保护的最有效方法。然而,出于安全考虑,用减毒活HIV对人类进行免疫接种是不可行的。因此,通过研究减毒活疫苗接种猕猴模型中保护的免疫相关因素,可能会找到有效且安全的HIV疫苗的线索。先前的研究已经使用同种异体过继转移确定了减毒活疫苗接种小鼠中抗Friend逆转录病毒保护的免疫相关因素。由于远交群体中存在巨大的遗传多样性,迄今为止,猕猴中的类似实验受到了阻碍。在这里,我们综述了SIV过继转移研究的现状,并提出了一种允许同种异体过继转移的新型猕猴模型。