Wang Q L, Wang H T, Blalock E, Müller S, Köhler H
Markey Cancer Center, University of Kentucky Medical Center, Lexington 40536-0096, USA.
J Clin Invest. 1995 Aug;96(2):775-80. doi: 10.1172/JCI118122.
Antibodies against HIV-1 proteins in HIV-1-infected individuals share a cross-reactive idiotype defined by the monoclonal antiidiotypic antibody 1F7 (5). Using a computer algorithm based on the molecular recognition theory, regions of inverse hydropathy between the variable sequence of 1F7 and human monoclonal anti-HIV-1 antibodies were identified, which are assumed to be involved in idiotype-antiidiotype contacts. A peptide was designed from the proposed contact in the variable heavy chain framework 3-complementarity determining region 3 (FR3-CDR3) of human antibodies and was synthesized. This peptide is recognized by the antiidiotype 1F7 and inhibits the binding of 1F7 to human anti-HIV-1 antibodies which express the 1F7 idiotype. A survey of normal and HIV-1-infected sera revealed the presence of antibodies in infected sera which bind to the FR3-CDR3 peptide. The biological relevance of autoantibodies against a self idiotope associated with HIV-1 infection is discussed in the context of the regulation of the antibody response to HIV-1.
HIV-1感染个体中针对HIV-1蛋白的抗体具有一种由单克隆抗独特型抗体1F7定义的交叉反应独特型(5)。利用基于分子识别理论的计算机算法,确定了1F7可变序列与人单克隆抗HIV-1抗体之间的反向亲水性区域,这些区域被认为参与独特型-抗独特型接触。根据人抗体可变重链框架3-互补决定区3(FR3-CDR3)中提议的接触设计了一种肽并进行了合成。该肽可被抗独特型抗体1F7识别,并抑制1F7与表达1F7独特型的人抗HIV-1抗体的结合。对正常血清和HIV-1感染血清的调查显示,感染血清中存在与FR3-CDR3肽结合的抗体。在针对HIV-1的抗体反应调节背景下,讨论了针对与HIV-1感染相关的自身独特位的自身抗体的生物学相关性。