Warren A P, Thomas D B
National Institute for Medical Research, Mill Hill, London, England.
AIDS Res Hum Retroviruses. 1992 May;8(5):559-64. doi: 10.1089/aid.1992.8.559.
A CD4+ and gp120-specific T-cell line, and subclone, were established from BALB/c mice following immunization with recombinant gp120, using an adjuvant formulation (alum) acceptable for use in the human. The recognition specificity was determined against a panel of synthetic peptides corresponding to the primary sequence of the HXB2 strain of human immunodeficiency virus (HIV). An epitope was identified, corresponding to amino acid residues 322-341, and a further series of truncated peptides established the minimum determinant to be 327-341. Possible reasons for the immunodominance of the V3 loop, and adjacent regions, for both antibody and T-cell recognition are discussed.
用一种可用于人类的佐剂配方(明矾)对BALB/c小鼠进行重组gp120免疫后,建立了一个CD4+和gp120特异性T细胞系及其亚克隆。针对一组与人类免疫缺陷病毒(HIV)HXB2株一级序列相对应的合成肽,确定了其识别特异性。鉴定出一个对应于氨基酸残基322 - 341的表位,进一步的一系列截短肽确定最小决定簇为327 - 341。讨论了V3环及相邻区域在抗体和T细胞识别中免疫显性的可能原因。