Torres J V, Anderson D E, Malley A, Banapour B, Axthelm M K, Benjamini E, Gardner M B
Department of Microbiology and Immunology, School of Medicine, University of California, Davis 95616.
J Med Primatol. 1993 Feb-May;22(2-3):129-37.
We analyzed SIV-specific monkey sera to localize B-cell epitopes of the envelope glycoprotein of SIV (gp130), using overlapping synthetic peptides representing the entire SIV gp130 protein and sera from experimentally infected monkeys and monkeys immunized with whole, inactivated SIV. A B-cell epitope which induces neutralizing antibody production and T-cell responses was characterized as well as a new B-cell epitope and a previously described neutralizing epitopes. Vaccinated monkey sera recognize the three epitopes differentially relative to unimmunized controls, and a correlation appears to exist between degree of cross-neutralization by infected monkey sera and degree of binding to these three regions.
我们使用代表整个SIV gp130蛋白的重叠合成肽以及来自实验感染猴和用完整灭活SIV免疫的猴的血清,分析了SIV特异性猴血清,以定位SIV包膜糖蛋白(gp130)的B细胞表位。鉴定出了一个可诱导中和抗体产生和T细胞应答的B细胞表位、一个新的B细胞表位以及一个先前描述的中和表位。接种疫苗的猴血清相对于未免疫对照对这三个表位的识别存在差异,并且感染猴血清的交叉中和程度与对这三个区域的结合程度之间似乎存在相关性。