Oftung F, Lundin K E, Meloen R, Mustafa A S
Department of Vaccinology, National Institute of Public Health, Oslo, Norway.
FEMS Immunol Med Microbiol. 1999 Jun;24(2):151-9. doi: 10.1111/j.1574-695X.1999.tb01276.x.
We have in this work mapped epitopes and HLA molecules used in human T cell recognition of the Mycobacterium leprae LSR protein antigen. HLA typed healthy subjects immunized with heat killed M. leprae were used as donors to establish antigen reactive CD4+ T cell lines which were screened for proliferative responses against overlapping synthetic peptides covering the C-terminal part of the antigen sequence. By using this approach we were able to identify two epitope regions represented by peptide 2 (aa 29-40) and peptide 6 (aa 49-60), of which the former was mapped in detail by defining the N- and C-terminal amino acid positions necessary for T cell recognition of the core epitope. MHC restriction analysis showed that peptide 2 was presented to T cells by allogeneic cells coexpressing HLA-DR4 and DRw53 or DR7 and DRw53. In contrast, peptide 6 was presented to T cells only in the context of HLA-DR5 molecules. In conclusion, the M. leprae LSR protein antigen can be recognized by human T cells in the context of multiple HLA-DR molecules, of which none are reported to be associated with the susceptibility to develop leprosy. The results obtained are in support of using the LSR antigen in subunit vaccine design.
在这项研究中,我们绘制了麻风分枝杆菌LSR蛋白抗原在人类T细胞识别中所涉及的表位和HLA分子。以经热灭活麻风分枝杆菌免疫的HLA分型健康受试者作为供体,建立抗原反应性CD4+ T细胞系,并用覆盖抗原序列C端部分的重叠合成肽对其进行增殖反应筛选。通过这种方法,我们能够鉴定出由肽2(氨基酸29 - 40)和肽6(氨基酸49 - 60)代表的两个表位区域,其中通过确定T细胞识别核心表位所需的N端和C端氨基酸位置,对前者进行了详细定位。MHC限制性分析表明,肽2由共表达HLA - DR4和DRw53或DR7和DRw53的同种异体细胞呈递给T细胞。相比之下,肽6仅在HLA - DR5分子的背景下呈递给T细胞。总之,麻风分枝杆菌LSR蛋白抗原可在多种HLA - DR分子的背景下被人类T细胞识别,其中没有一种被报道与麻风易感性相关。所获得的结果支持在亚单位疫苗设计中使用LSR抗原。