Koenig S, Fuerst T R, Wood L V, Woods R M, Suzich J A, Jones G M, de la Cruz V F, Davey R T, Venkatesan S, Moss B
Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
J Immunol. 1990 Jul 1;145(1):127-35.
Epitope mapping of a MHC class I-restricted cytotoxic T cell response to nef, a regulatory protein of HIV, was performed with fresh PBMC from HIV-seropositive donors and target cells pulsed with a panel of overlapping peptides of the nef protein. These nef-specific CTL recognized a synthetic peptide of 10 residues derived from a nonamphipathic, highly conserved region of the nef protein in association with the HLA A3.1 molecule. Using human cell transfectants expressing mutations of the A3 molecule, we demonstrated that the amino acid at position 152 of the A3.1 molecule appears to be critical for detection of this response. Thus, rapid analysis of the epitopes of HIV proteins stimulating CTL responses can be achieved using a combination of fresh donor PBMC and target cells pulsed with synthesized peptides.
利用来自HIV血清阳性供体的新鲜外周血单核细胞(PBMC)和用一组重叠的nef蛋白肽脉冲处理的靶细胞,对HIV调节蛋白nef的MHC I类限制性细胞毒性T细胞反应进行了表位作图。这些nef特异性CTL识别来自nef蛋白非两亲性、高度保守区域的10个残基的合成肽,并与HLA A3.1分子相关联。使用表达A3分子突变的人细胞转染体,我们证明A3.1分子第152位的氨基酸对于检测这种反应似乎至关重要。因此,结合新鲜供体PBMC和用合成肽脉冲处理的靶细胞,可以快速分析刺激CTL反应的HIV蛋白表位。