Kaur A, Alexander L, Staprans S I, Denekamp L, Hale C L, McClure H M, Feinberg M B, Desrosiers R C, Johnson R P
Division of Immunology, New England Regional Primate Research Center, Harvard Medical School, Southborough, MA 01772, USA.
Eur J Immunol. 2001 Nov;31(11):3207-17. doi: 10.1002/1521-4141(200111)31:11<3207::aid-immu3207>3.0.co;2-h.
Although CTL escape has been well documented in pathogenic simian immunodeficiency virus (SIV) infection, there is no information on CTL escape in nonpathogenic SIV infection in nonhuman primate hosts like the sooty mangabeys. CTL responses and sequence variation in the SIV nef gene were evaluated in one sooty mangabey and one rhesus macaque inoculated together with the same stock of cloned SIVmac239. Each animal developed an immunodominant response to a distinct CTL epitope in Nef, aa 157-167 in the macaque and aa 20-28 in the mangabey. Nonsynonymous mutations in their respective epitopes were observed in both animals and resulted in loss of CTL recognition. These mutations were present in the majority of proviral DNA sequences at 16 weeks post infection in the macaque and >2 years post infection in the mangabey. These results document the occurrence of CTL escape in a host that does not develop AIDS, and adds to the growing body of evidence that CTL exert significant selective pressure in SIV infection.
尽管在致病性猿猴免疫缺陷病毒(SIV)感染中,CTL逃逸现象已有充分记载,但在诸如乌黑白眉猴等非人灵长类宿主的非致病性SIV感染中,尚无关于CTL逃逸的信息。对一只乌黑白眉猴和一只恒河猴接种同一批克隆的SIVmac239毒株后,评估了它们的CTL反应以及SIV nef基因的序列变异情况。每只动物都对Nef中一个独特的CTL表位产生了免疫显性反应,猕猴中的表位为aa 157 - 167,白眉猴中的表位为aa 20 - 28。在两只动物中均观察到其各自表位的非同义突变,导致CTL识别丧失。这些突变存在于猕猴感染后16周以及白眉猴感染后2年以上的大多数前病毒DNA序列中。这些结果证明了在未发展为艾滋病的宿主体内发生了CTL逃逸,并且进一步增加了越来越多的证据,表明CTL在SIV感染中施加了显著的选择压力。