Skeiky Yasir A W, Alderson Mark R, Ovendale Pamela J, Lobet Yves, Dalemans Wilfried, Orme Ian M, Reed Steven G, Campos-Neto Antonio
Corixa Corporation, Seattle, WA, USA.
Vaccine. 2005 Jun 10;23(30):3937-45. doi: 10.1016/j.vaccine.2005.03.003. Epub 2005 Mar 30.
MTB41 is a Mycobacterium antigen that is recognized by CD4+ T cells early after experimental infection of mice with Mycobacterium tuberculosis and by PBMC from healthy PPD positive individuals. Immunization of mice with plasmid DNA encoding the MTB41 gene sequence results in the development of antigen-specific CD4+ and CD8+ T cells, and protection against challenge with virulent M. tuberculosis. In the present studies, in contrast to DNA immunization, we show, that a strong MTB41-specific CD4+ T cell response, but no MHC class I restricted cytotoxic T lymphocyte (CTL) activity is detected in the spleen cells of infected mice. Therefore, this data suggests that the induction of CD8+ T cell response to MTB41 epitopes by DNA immunization may not be relevant to protection because these epitopes are not recognized during the infectious process. We also compared the repertoire of rMTB41 epitope recognition by CD4+ T cells of M. tuberculosis-infected mice with the recognition repertoire of mice immunized with the recombinant rMTB41 protein. Both regimens of sensitization lead to the recognition of the same molecular epitope. Coincidentally, immunization with the soluble recombinant protein plus adjuvant, a regimen known to generate primarily CD4+ T cells, resulted in induction of protection comparable to BCG in two well-established animal models of tuberculosis (mice and guinea pigs).
MTB41是一种结核分枝杆菌抗原,在小鼠经结核分枝杆菌实验性感染后早期可被CD4+ T细胞识别,也可被健康的PPD阳性个体的外周血单核细胞(PBMC)识别。用编码MTB41基因序列的质粒DNA免疫小鼠,可导致抗原特异性CD4+和CD8+ T细胞的产生,并对强毒力结核分枝杆菌的攻击产生保护作用。在本研究中,与DNA免疫不同,我们发现,在感染小鼠的脾细胞中检测到强烈的MTB41特异性CD4+ T细胞反应,但未检测到MHC I类限制性细胞毒性T淋巴细胞(CTL)活性。因此,该数据表明,DNA免疫诱导的针对MTB41表位的CD8+ T细胞反应可能与保护作用无关,因为在感染过程中这些表位未被识别。我们还比较了结核分枝杆菌感染小鼠的CD4+ T细胞对重组MTB41表位的识别谱与用重组rMTB41蛋白免疫的小鼠的识别谱。两种致敏方案均导致对相同分子表位的识别。巧合的是,在两种成熟的结核病动物模型(小鼠和豚鼠)中,用可溶性重组蛋白加佐剂免疫(一种已知主要产生CD4+ T细胞的方案)所诱导的保护作用与卡介苗相当。