Hartmann P, Plum G
Department of Internal Medicine I, University of Cologne, Germany.
Diagn Microbiol Infect Dis. 1999 Jun;34(2):147-52. doi: 10.1016/s0732-8893(99)00005-x.
Protective immunity to mycobacterial infections develops in immunocompetent hosts after activation of alpha beta- and gamma delta-T cells in association with the generation of a protection-specific cytokine profile that stimulates the bactericidal potential of the macrophages. The maintenance of a delicate balance between Th1 and Th2 response is decisive for infection control and prevention of exacerbation of disease. Mycobacterial infection in the immunocompromised host is mainly due to the diminished cellular immune function. In addition, nontuberculous mycobacteria isolated from AIDS patients have special virulence factors that promote development of disease by further compromising the function of an already damaged cytokine network.
在免疫功能正常的宿主中,对分枝杆菌感染的保护性免疫在αβ和γδ T细胞激活后产生,同时伴随着产生一种保护特异性细胞因子谱,该谱刺激巨噬细胞的杀菌潜力。Th1和Th2反应之间微妙平衡的维持对于感染控制和疾病恶化的预防至关重要。免疫功能低下宿主中的分枝杆菌感染主要是由于细胞免疫功能减弱。此外,从艾滋病患者中分离出的非结核分枝杆菌具有特殊的毒力因子,可通过进一步损害已经受损的细胞因子网络的功能来促进疾病发展。