[血清学方法检测HIV感染]。

Zeitschrift fur Hautkrankheiten Pub Date : 1990-07-01
B L Schmidt
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引用次数: 0

摘要

我们简要地描述了抗原检测的主要技术,并讨论了常规筛选和构象分析的利弊。对于HIV 1和HIV 2感染的分化,合成gp36 (HIV 2)和gp41 (HIV 1)抗原表位对应的肽段效果最好。市售抗原检测相对不敏感。新技术,如聚合酶链反应,可以在100,000个未感染细胞中检测出一个感染细胞中的病毒DNA。然而,由于这些方法是基于核酸探针,它们是相当费力的,不能取代抗体测试;但它们可能用于早期识别感染艾滋病毒的婴儿或用于确认感染的急性期。关于早期预后,即。在出现临床症状前2年,以下标记物被发现是有用的:新蝶呤、β -2微球蛋白、淋巴细胞亚群CD4、CD8、Leu2+7+、活化的t细胞,以及抗p31、p24和p17抗体的减少。
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[Detection of HIV infection by serologic procedures].

We briefly describe the principal techniques of antigen detection and discuss the pros and cons of routine screening and conformation assays. Regarding the differentiation of HIV 1 and HIV 2 infection, synthetic peptides corresponding to the antigenic epitopes of gp36 (HIV 2) and gp41 (HIV 1) yielded the best results. Commercially available antigen tests are relatively insensitive. New techniques, such as the polymerase chain reaction, allow the dedection of viral DNA in one infected cell out of 100,000 non-infected cells. However, since these methods are based on nucleic acid probes, they are rather laborious and cannot replace antibody tests; but they may be of use for early identification of HIV-infected infants or for the confirmation of the acute phase of the infection (CDCI). With regard to early prognosis--i.e. up to 2 years before the development of clinical symptoms__the following markers have been found useful: neopterine, beta-2-microglobulin, the lymphocyte subsets CD4, CD8, Leu2+7+, activated T-cells, as well as the decrease of antibodies against p31, p24 and p17.

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