Department of Immunology, Tuberculosis Research Centre (ICMR), Chennai, India.
Med Microbiol Immunol. 2010 Feb;199(1):11-25. doi: 10.1007/s00430-009-0129-2. Epub 2009 Nov 10.
The Mycobacterium tuberculosis (M. tuberculosis)-specific culture filtrate protein-10 (CFP-10) is highly recognized by M. tuberculosis infected subjects. In the present study, the proliferative response and IFN-gamma secretion was found for C-terminal peptides of the protein (Cfp6(51-70), Cfp7(61-80), Cfp8(71-90), and Cfp9(81-100)). The alleles HLA DRB1 *04 and HLA DRB1 *10 recognized the C-terminal peptides Cfp7, Cfp8, and Cfp9 in HHC. Cfp6 was predominantly recognized by the alleles HLA DRB1 *03 and HLA DRB1 *15 by PTB. The minimal nonameric epitopes from the C-terminal region were CFP-10(56-64) and CFP-10(76-84). These two peptides deserve attention for inclusion in a vaccine against tuberculosis in this region.
结核分枝杆菌(M. tuberculosis)特异性培养滤液蛋白 10(CFP-10)在结核分枝杆菌感染的患者中受到高度认可。在本研究中,发现了该蛋白的 C 末端肽(Cfp6(51-70)、Cfp7(61-80)、Cfp8(71-90)和 Cfp9(81-100))的增殖反应和 IFN-γ分泌。等位基因 HLA DRB1 * 04 和 HLA DRB1 * 10 识别 HHC 中的 C 末端肽 Cfp7、Cfp8 和 Cfp9。Cfp6 主要被等位基因 HLA DRB1 * 03 和 HLA DRB1 * 15 识别。来自 C 末端区域的最小非九肽表位是 CFP-10(56-64)和 CFP-10(76-84)。这两个肽值得关注,因为它们可能包含在针对该区域的结核病疫苗中。