摘要
为了建立敏感、特异的人类免疫缺陷病毒(HIV)抗体检测方法,采用固相法合成了HIV-1和HIV-2的9条多肽,多肽分别位于HIVgp41、p24和gp36区域,长度为10~27个氨基酸。以合成肽为抗原分别包被酶标板,采用间接ELISA法,比较检测了10份抗-HIV-1型和4份抗-HIV-2型阳性血清,结果表明gp41的10肽(SP1)、21肽(SP5)、26肽(SP6)、27肽(SP7)均能检出100%的抗-HIV-1阳性血清,以SP7抗原性最强。gp36的26肽(SP8)、27肽(SP9)能检出全部的抗-HIV-2阳性血清,两者对抗-HIV-2血清的亲和性相似,但对抗-HIV-1型血清的反应性以SP8强。以SP7和SP8混合包板,能同时检出全部抗-HIV-1和抗-HIV-2阳性血清;与UBI试剂比较,检测了60份抗-HIV阳性血清标本及96份阴性血清标本,其阳性符合率为98.33%(59/60),阴性符合率为100%,总符合率为99.36%(155/156)。表明SP7和SP8混合包板可用于HIV感染的诊断。
To establish a ELISA method to detect the infection of human immunodificiency virus (HIV), we synthesized nine peptides ranging in length between 10~27 amino acid (aa) of HIV located in the regions of gp41, p24 of HIV 1 and gp36 of HIV 2, according to the published amino acid sequence and the position of antigenic determinants of viruses, by a solid phase method. We detected 10 positive sera of HIV 1 and 4 positive sera of HIV 2 by a indirect ELISA using these synthetic peptides as the coating antigen. The results indicated that all of 10 serum specimens of HIV 1 were positive using SP1, 5, 6, and 7 derived from gp41, and SP7 was the best in antigenicity. The 4 serum specimens of HIV 2 were positive using SP8 and SP9 in the region of gp36 and their antigenicity to HIV 2 were similar, but the antigenicity of SP8 to HIV 1 was higher than that of SP9. All sera of HIV 1 and HIV 2 were positive using SP7 and SP8 as the mixed coating antigen. A comparison of our reagent with UBI reagent in detection of 60 positive and 96 negative control sera for HIV showed that the coincident rate for positive ness was 98.33% (59/60), for negative ness was 100%, and the general coincident rate was 99.36% (155/156). It is concluded that SP7 and SP8 as the mixed coating antigen are applicable in the diagnosis of HIV infection.
出处
《中华内科杂志》
CAS
CSCD
北大核心
1997年第2期105-107,共3页
Chinese Journal of Internal Medicine