Endsley Janice J, Hogg Alison, Shell Lis J, McAulay Martin, Coffey Tracey, Howard Chris, Capinos Scherer Charles F, Waters W Ray, Nonnecke Brian, Estes D Mark, Villarreal-Ramos Bernardo
Department of Pediatrics and Sealy Center for Vaccine Development, University of Texas Medical Branch, Galveston, TX 77555, United States.
Vaccine. 2007 Dec 5;25(50):8384-94. doi: 10.1016/j.vaccine.2007.10.011. Epub 2007 Oct 23.
The effector mechanisms used by CD4+ T cells to control mycobacteria differ between humans and rodent models of TB and should be investigated in additional animal models. In these studies, the bovine model was used to characterize the mycobactericidal CD4+ T cell response induced by vaccination with the attenuated Mycobacterium bovis bacillus Calmette-Guérin (BCG). Antigenic stimulation of peripheral blood CD4+ T cells from BCG-vaccinated cattle enhanced expression of perforin and IFNgamma in cells expressing a CD45RA-CD45RO+CD62L+ cell surface phenotype, enhanced transcription of granulysin, IFNgamma, perforin, IL-4, IL-13, and IL-21, and enhanced anti-mycobacterial activity of CD4+ T cells against BCG-infected macrophages.
CD4+ T细胞用于控制分枝杆菌的效应机制在人类和结核病啮齿动物模型之间存在差异,应在其他动物模型中进行研究。在这些研究中,使用牛模型来表征用减毒牛分枝杆菌卡介苗(BCG)接种诱导的杀分枝杆菌CD4+ T细胞反应。对来自接种BCG的牛的外周血CD4+ T细胞进行抗原刺激,可增强表达CD45RA-CD45RO+CD62L+细胞表面表型的细胞中穿孔素和IFNγ的表达,增强颗粒溶素、IFNγ、穿孔素、IL-4、IL-13和IL-21的转录,并增强CD4+ T细胞对BCG感染巨噬细胞的抗分枝杆菌活性。