Yasutomi Y, McAdam S N, Boyson J E, Piekarczyk M S, Watkins D I, Letvin N L
Harvard Medical School, Beth Israel Hospital, Boston, MA 02215.
J Immunol. 1995 Mar 1;154(5):2516-22.
In light of the importance of virus-specific CTL in the control of the spread of the AIDS virus, it will be important to assess the generation of these effector cell responses in trials of novel vaccine strategies for the prevention of AIDS virus infections. To facilitate such studies in the simian immunodeficiency virus (SIV)/macaque model for AIDS, we have defined a rhesus monkey SIVmac CTL epitope carboxy terminus to both the CD4-binding and V4 regions of the envelope glycoprotein. We also used one-dimensional isoelectric focusing to characterize the MHC class I molecule of the rhesus monkey that binds this 9-amino-acid SIVmac envelope fragment. Cloning and sequencing of the cDNA encoding this rhesus monkey MHC class I molecule demonstrated that it is a newly described HLA-B homologue, Mamu-B*01. The definition of this viral CTL epitope and its restricting MHC class I molecule will facilitate the use of the SIVmac/rhesus monkey model for studies of envelope-based vaccine strategies for the prevention of AIDS.
鉴于病毒特异性CTL在控制艾滋病病毒传播中的重要性,在预防艾滋病病毒感染的新型疫苗策略试验中评估这些效应细胞反应的产生将非常重要。为了在艾滋病的猿猴免疫缺陷病毒(SIV)/猕猴模型中促进此类研究,我们确定了一个恒河猴SIVmac CTL表位,该表位位于包膜糖蛋白的CD4结合区和V4区的羧基末端。我们还使用一维等电聚焦来表征结合这个9氨基酸SIVmac包膜片段的恒河猴MHC I类分子。编码该恒河猴MHC I类分子的cDNA的克隆和测序表明,它是一个新描述的HLA - B同源物,Mamu - B*01。这种病毒CTL表位及其限制性MHC I类分子的确定将有助于利用SIVmac/恒河猴模型研究基于包膜的预防艾滋病疫苗策略。