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中国HIV-1 C/B'重组毒株和B'毒株感染者Nef特异性T细胞免疫应答的研究
引用本文:刘宏伟,洪坤学,马军,袁霖,刘沙,陈健平,张远志,阮玉华,王哲,邵一鸣.中国HIV-1 C/B'重组毒株和B'毒株感染者Nef特异性T细胞免疫应答的研究[J].中华微生物学和免疫学杂志,2008,28(11).
作者姓名:刘宏伟  洪坤学  马军  袁霖  刘沙  陈健平  张远志  阮玉华  王哲  邵一鸣
作者单位:1. 河南疾病预防控制中心性病艾滋病研究所,郑州,450016
2. 中国疾病预防控制中心艾滋病中心病毒免疫室,北京,100050
3. 新疆疾病预防控制中心
摘    要:目的 研究中国主要流行的HIV-1 C/B'重组毒株和B'亚型毒株感染者Nef特异性T细胞反应特征,确定两种亚型感染者共同识别的免疫优势区.方法 本研究以59名HIV-1 C/B'重组毒株、27名B'亚型毒株感染者为研究对象,用ELISPOT检测针对HIV-1型C/B'Nef重叠多肽产生IFN-γ的特异性T细胞反应.结果 44例(74.58%)HIV-1 C/B'重组毒株感染者产生Nef特异性T细胞反应,主要识别EVA7081.1、5、6、7、43、44、45、47、48、49这10条多肽,氨基酸序列为Nef63~115和117~139的区域.20例(74.07%)的HIV-1 B'毒株感染者产生Nef特异性T细胞反应,主要识别EVA7081.1、2、43、49这4条多肽,氨基酸序列为Nef 63~77和87~119的区域.两种亚型感染者特异性T细胞反应的强度和广度与病毒载量和CIM细胞数不相关.结论 中国HIV-1 C/B'重组毒株和B'亚型毒株感染者共同识别氨基酸序列为Nef63~77和87~115的免疫优势区,提示此区域可用于疫苗的设计.

关 键 词:人免疫缺陷病毒  特异性T细胞反应  酶联免疫斑点试验(ELISPOT)  γ-干扰素

Nef-specific T lymphocyte responses in Chinese HIV-1 recombinant subtype C/B' and subtype B' in-fectors
LIU Hong-wei,HONG Kun-xue,MA Jun,YUAN Lin,LIU Sha,CHEN Jian-ping,ZHANG Yuan-zhi,RUAN Yu-hua,WANG Zhe,SHAO Yi-ming.Nef-specific T lymphocyte responses in Chinese HIV-1 recombinant subtype C/B' and subtype B' in-fectors[J].Chinese Journal of Microbiology and Immunology,2008,28(11).
Authors:LIU Hong-wei  HONG Kun-xue  MA Jun  YUAN Lin  LIU Sha  CHEN Jian-ping  ZHANG Yuan-zhi  RUAN Yu-hua  WANG Zhe  SHAO Yi-ming
Abstract:Objective To analyze character of Nef-specific T lymphocyte responses in Chinese HIV-1 recombinant subtype C/B' and subtype B' infectors and to identify the common immunodominant re-gions recognized by these infectors. Methods Fifty-nine HIV-1 recombinant subtype C/B' infectors and 27 subtype B' infectors were tested by IFN-γ enzyme linked immunospot (ELISPOT) assay using HIV-1 C/B' Nef overlapping peptides. Results Nef-specific T-cell responses of IFN-γ secretion were identified in 44 (74.58%) out of 59 HIV-1 recombinant subtype C/B' infectors. Ten peptides, EVA7081.1,5, 6, 7,43, 44, 45, 47, 48, 49 were mainly recognized. Amino acid position was from Nef63 to 115 and 117 to 139. Twenty of 27 (74.07%) HIV-1 subtype B' infectors recognized peptides. EVA7081.1,2, 43 and 49 were mainly recognized. Amino acid position was from Nef 63 to 77 and 87 to 119. There was no correlation be-tween the Nef-specific IFN-production of HIV-1-specific T cells responses and viral load or CD4 T cell count in both subtype infectors. Conclusion The immunodominant regions, from Nef63 to 77 and 87 to 115 were recognized by both Chinese HIV-1 recombinant subtype C/B' infectors and subtype B' infectors. These re-gions could be used in design of vaccine.
Keywords:Nef
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