Harris D P, Vordermeier H M, Friscia G, Román E, Surcel H M, Pasvol G, Moreno C, Ivanyi J
MRC Tuberculosis and Related Infections Unit, Royal Postgraduate Medical School, London, United Kingdom.
J Immunol. 1993 Jun 1;150(11):5041-50.
The specificity of the T cell-immune repertoire at the level of individual antigenic determinants could play a fundamental role in the immunopathogenesis of tuberculous infections. Therefore, we analyzed the immunogenicity, genetic restriction, and epitope core structure of two adjacent, yet distinct, immunodominant T cell determinants from the 19-kDa Ag of Mycobacterium tuberculosis. After immunization with two peptides comprising residues 45 to 64 and 61 to 80, vigorous in vitro proliferative responses to the homologous peptide were elicited in five different strains of C57BL/10 mice (H-2b,k,d,s,f), indicating that both epitopes were recognized in a genetically permissive manner. When immunized with intact 19-kDa protein, lymph node cells from the same mouse strains responded to both peptides, with the exception of H-2b mice, which did not respond to p45-64. Delayed-type hypersensitivity responses in C57BL/10 (H-2b) mice were elicited by p61-80 only, whereas in H-2d mice both peptides were delayed-type hypersensitivity negative, despite eliciting pronounced proliferative responses. Analysis of the proliferative responses of human PBMC in purified protein derivative-positive healthy subjects and tuberculosis patients revealed significant differences in the antigenicity to the two peptides. All purified protein derivative-positive healthy and diseased individuals manifested strong responses to p45-64, indicating HLA permissive recognition. In contrast, pronounced responses to p61-80 were detected only in patients with lymphatic tuberculosis. Epitope core structures, composed of 6 or 7 residues within each peptide, have been mapped with peptides of overlapping sequence. Significantly, for both epitopes, the core sequences recognized by both human and murine T cells were almost identical. We conclude that despite many similarities between murine and human T cell epitope recognition, distinct differences in the responsiveness of the infected host could play a role in pathogenesis. Furthermore, the genetically permissive nature of the identified epitopes is a potentially important attribute for the development of peptide-based diagnostic reagents and vaccines.
在个体抗原决定簇水平上,T细胞免疫库的特异性可能在结核感染的免疫发病机制中发挥重要作用。因此,我们分析了来自结核分枝杆菌19-kDa抗原的两个相邻但不同的免疫显性T细胞决定簇的免疫原性、遗传限制性和表位核心结构。用包含第45至64位和第61至80位残基的两种肽免疫后,在五种不同品系的C57BL/10小鼠(H-2b、k、d、s、f)中引发了对同源肽的强烈体外增殖反应,表明这两个表位均以遗传允许的方式被识别。用完整的19-kDa蛋白免疫时,同一小鼠品系的淋巴结细胞对两种肽均有反应,但H-2b小鼠除外,其对p45-64无反应。C57BL/10(H-2b)小鼠仅由p61-80引发迟发型超敏反应,而在H-2d小鼠中,尽管引发了明显的增殖反应,但两种肽均为迟发型超敏反应阴性。对纯化蛋白衍生物阳性的健康受试者和结核病患者的人外周血单核细胞增殖反应的分析显示,对这两种肽的抗原性存在显著差异。所有纯化蛋白衍生物阳性的健康和患病个体对p45-64均表现出强烈反应,表明HLA允许识别。相比之下,仅在淋巴结核患者中检测到对p61-80的明显反应。由每个肽内6或7个残基组成的表位核心结构已用重叠序列的肽进行了定位。值得注意的是,对于这两个表位,人和鼠T细胞识别的核心序列几乎相同。我们得出结论,尽管人和鼠T细胞表位识别之间有许多相似之处,但感染宿主反应性的明显差异可能在发病机制中起作用。此外,所鉴定表位的遗传允许性质对于基于肽的诊断试剂和疫苗的开发是一个潜在的重要属性。