Leishmania vaccine development: exploiting the host-vector-parasite interface

被引:46
作者
Reed, S. G. [1 ,2 ]
Coler, R. N. [1 ,2 ]
Mondal, D. [3 ]
Kamhawi, S. [4 ]
Valenzuela, J. G. [4 ]
机构
[1] Infect Dis Res Inst, Seattle, WA 98102 USA
[2] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[3] Int Ctr Diarrhoeal Dis Res, Ctr Nutr & Food Secur, Parasitol Lab, Dhaka 1000, Bangladesh
[4] NIAID, Vector Mol Biol Sect, LMVR, NIH, Rockville, MD USA
基金
美国国家卫生研究院; 比尔及梅琳达.盖茨基金会;
关键词
Leishmania; vaccine; sand fly; saliva; adjuvant; DELAYED-TYPE HYPERSENSITIVITY; LUTZOMYIA-LONGIPALPIS SALIVA; CELL-MEDIATED-IMMUNITY; GROWTH-FACTOR-BETA; SAND FLY SALIVA; VISCERAL LEISHMANIASIS; CUTANEOUS LEISHMANIASIS; RECOMBINANT K-39; CLONED ANTIGEN; KALA-AZAR;
D O I
10.1586/14760584.2016.1105135
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Visceral leishmaniasis (VL) is a disease transmitted by phlebotomine sand flies, fatal if untreated, and with no available human vaccine. In rodents, cellular immunity to Leishmania parasite proteins as well as salivary proteins of the sand fly is associated with protection, making them worthy targets for further exploration as vaccines. This review discusses the notion that a combination vaccine including Leishmania and vector salivary antigens may improve vaccine efficacy by targeting the parasite at its most vulnerable stage just after transmission. Furthermore, we put forward the notion that better modeling of natural transmission is needed to test efficacy of vaccines. For example, the fact that individuals living in endemic areas are exposed to sand fly bites and will mount an immune response to salivary proteins should be considered in pre-clinical and clinical evaluation of leishmaniasis vaccines. Nevertheless, despite remaining obstacles there is good reason to be optimistic that safe and effective vaccines against leishmaniasis can be developed.
引用
收藏
页码:81 / 90
页数:10
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