Suppr超能文献

美拉尼西亚人对I型人类嗜T淋巴细胞病毒免疫显性gag和env表位的体液免疫反应。

Humoral responses to the immunodominant gag and env epitopes of human T-lymphotropic virus type I among Melanesians.

作者信息

Lal R B, Rudolph D L, Nerurkar V R, Yanagihara R

机构信息

Retrovirus Diseases Branch, Centers for Disease Control, Atlanta, Georgia.

出版信息

Viral Immunol. 1992 Winter;5(4):265-72. doi: 10.1089/vim.1992.5.265.

Abstract

The immune responsiveness to the immunodominant B-cell epitopes of human T-lymphotropic virus type I (HTLV-I), derived from the external envelope glycoprotein (recombinant MTA-1(162-209), synthetic Env-1(194-214), and Env-5(242-257)) and the gag-encoded matrix protein (Gag-1a(102-117)), was analyzed in 19 HTLV-I-seropositive and 51 HTLV I-seroindeterminate Melanesians from Papua New Guinea and the Solomon Islands. The reactivities of seropositive Melanesian specimens to MTA-1 (100%), Env-5 (89%), and Gag-1a (79%) were similar to that seen with U.S. specimens, while reactivity to Env-1 was lower in Melanesian specimens (68%). Minimal reactivity was found to the env epitopes among the 51 HTLV-I-seroindeterminate Melanesians, but 29 (57%) reacted to Gag-1a. The failure to detect HTLV-I gag, pol, env, and tax gene sequences by polymerase chain reaction among the seroindeterminate Melanesians suggests that such reactivities to the Gag-1a epitope represent cross-reacting antibodies with closely related microbial or cellular proteins.

摘要

对来自巴布亚新几内亚和所罗门群岛的19名人类嗜T淋巴细胞病毒I型(HTLV-I)血清阳性和51名HTLV-I血清学不确定的美拉尼西亚人,分析了其对HTLV-I免疫显性B细胞表位的免疫反应性。这些表位来源于外膜糖蛋白(重组MTA-1(162 - 209)、合成Env-1(194 - 214)和Env-5(242 - 257))以及gag编码的基质蛋白(Gag-1a(102 - 117))。血清阳性美拉尼西亚标本对MTA-1(100%)、Env-5(89%)和Gag-1a(79%)的反应性与美国标本相似,而美拉尼西亚标本对Env-1的反应性较低(68%)。在51名HTLV-I血清学不确定的美拉尼西亚人中,对env表位的反应性极低,但有29人(57%)对Gag-1a有反应。在血清学不确定的美拉尼西亚人中,通过聚合酶链反应未能检测到HTLV-I的gag、pol、env和tax基因序列,这表明对Gag-1a表位的这种反应性代表了与密切相关的微生物或细胞蛋白发生交叉反应的抗体。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验