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Distinct IgG recognition patterns during progression of subclinical and clinical infection with lymphadenopathy associated virus/human T lymphotropic virus.

机译:在亚临床和临床感染与淋巴结病相关病毒/人T淋巴细胞病毒的亚临床和临床感染过程中存在明显的IgG识别模式。

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摘要

Longitudinal IgG recognition patterns of viral proteins were studied in 15 men who had seroconverted for lymphadenopathy associated virus/human T lymphotropic virus (LAV/HTLV-III). Antibodies to the major viral core protein p24, which is a cleavage product of the gag gene encoded precursor protein pr55, appeared first. These were soon followed by antibodies to pr55 and more gradually by antibodies to the other gag gene encoded cleavage product p18, the env gene encoded transmembrane glycoprotein gp41, the env gene encoded glycoproteins gp65 and gp110, and the putative pol gene product p33. In 13 subjects who remained healthy the reactivity to the different proteins increased or stabilised with time, while in two men who developed acquired immune deficiency syndrome (AIDS) the reactivity, most noticeably to gag encoded proteins, diminished before or at the onset of symptoms.
机译:在15名因淋巴结病相关病毒/人T淋巴病毒(LAV / HTLV-III)血清转化的男性中研究了病毒蛋白的纵向IgG识别模式。首先出现了针对主要病毒核心蛋白p24的抗体,该抗体是gag基因编码的前体蛋白pr55的裂解产物。紧随其后的是针对pr55的抗体,随后逐渐是针对其他gag基因编码的切割产物p18,env基因编码的跨膜糖蛋白gp41,env基因编码的糖蛋白gp65和gp110和推定pol基因产物p33的抗体。在13位保持健康的受试者中,对不同蛋白质的反应性随时间增加或稳定,而在两名患有后天免疫机能丧失综合症(AIDS)的男性中,其反应性(最明显的是gag编码的蛋白质)在症状发作之前或症状发作时减弱。

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