作者: S L Reiner , R M Locksley
DOI: 10.1146/ANNUREV.IY.13.040195.001055
关键词: Disease 、 Biology 、 Infectious disease (medical specialty) 、 Immunology 、 Immunity 、 Interleukin 12 、 Virology 、 Priming (immunology) 、 Leishmania major 、 Effector 、 Phenotype
摘要: Experimental infection with the intracellular protozoan Leishmania major con stitutes a particularly versatile model for assessing role of CD4+ subset de velopment in host response to infectious disease. The association Thl development control infection, and Th2 cell pro gressive disease, has been well established. capacity manipulate out come, using distinct immunologic interventions, both genetically resistant susceptible mice identified key effector cytokines that must be present during time initial priming T cells order affect CD4 switch phenotype. Roles interferon-y (IFN-y), interleukin 12 (IL-12), IL-4 maturation have demonstrated, although additional undefined signals are required. Study BALB/c mouse shown fail ure downmodulate production is critically associated failure develop appropriate responses. Use murine L. continues elucidate new methods vaccine suggests promising system identification genes determine susceptibil ity i nfectio n.