Handman E
Infection and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, The Royal Melbourne Hospital, Parkville 3050, Australia.
Clin Microbiol Rev. 2001 Apr;14(2):229-43. doi: 10.1128/CMR.14.2.229-243.2001.
Leishmaniae are obligatory intracellular protozoa in mononuclear phagocytes. They cause a spectrum of diseases, ranging in severity from spontaneously healing skin lesions to fatal visceral disease. Worldwide, there are 2 million new cases each year and 1/10 of the world's population is at risk of infection. To date, there are no vaccines against leishmaniasis and control measures rely on chemotherapy to alleviate disease and on vector control to reduce transmission. However, a major vaccine development program aimed initially at cutaneous leishmaniasis is under way. Studies in animal models and humans are evaluating the potential of genetically modified live attenuated vaccines, as well as a variety of recombinant antigens or the DNA encoding them. The program also focuses on new adjuvants, including cytokines, and delivery systems to target the T helper type 1 immune responses required for the elimination of this intracellular organism. The availability, in the near future, of the DNA sequences of the human and Leishmania genomes will extend the vaccine program. New vaccine candidates such as parasite virulence factors will be identified. Host susceptibility genes will be mapped to allow the vaccine to be targeted to the population most in need of protection.
利什曼原虫是单核吞噬细胞内的专性细胞内原生动物。它们可引发一系列疾病,严重程度从可自行愈合的皮肤损伤到致命的内脏疾病不等。在全球范围内,每年有200万新病例,世界上十分之一的人口有感染风险。迄今为止,尚无针对利什曼病的疫苗,控制措施依靠化疗来缓解病情以及依靠病媒控制来减少传播。然而,一项主要针对皮肤利什曼病的疫苗研发计划正在进行中。在动物模型和人体中的研究正在评估基因改造的减毒活疫苗以及多种重组抗原或编码它们的DNA的潜力。该计划还侧重于新型佐剂,包括细胞因子,以及针对消除这种细胞内生物体所需的1型辅助性T细胞免疫反应的递送系统。在不久的将来,人类和利什曼原虫基因组DNA序列的可得性将扩展疫苗计划。诸如寄生虫毒力因子等新的候选疫苗将被识别出来。宿主易感性基因将被定位,以便使疫苗能够针对最需要保护的人群。