Biomarkers for Zoonotic Visceral Leishmaniasis in Latin America

被引:11
作者
Brodskyn, Claudia I. [1 ]
Kamhawi, Shaden [2 ]
机构
[1] Fiocruz Bahia, Inst Goncalo Moniz, Salvador, BA, Brazil
[2] NIAID, NIH, Bethesda, MD 20892 USA
关键词
zoonotic visceral leishmaniasis; Leishmania infantum; biomarkers; cytokines/chemokines; canine visceral leishmaniasis; human visceral leishmaniasis; HUMAN IMMUNE-RESPONSE; LUTZOMYIA-LONGIPALPIS; ANTIBODY-RESPONSE; INTERFERON-GAMMA; SALIVARY-GLAND; EXPOSURE; DOGS; MARKERS; VECTOR; PATHOGENESIS;
D O I
10.3389/fcimb.2018.00245
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In Latin America, zoonotic visceral leishmaniasis (ZVL) arising from infection by L. infantum is primarily transmitted by Lutzomyia longipalpis sand flies. Dogs, which are chronic reservoirs of L. infantum, are considered a significant risk factor for acquisition of ZVL due to their close proximity to humans. In addition, as a vector-borne disease the intensity of exposure to vector sand flies can also enhance the risk of developing ZVL. Traditionally, IFN-gamma and IL-10 are considered as the two main cytokines which determine the outcome of visceral leishmaniasis. However, more recently, the literature has demonstrated that different mediators, such as lipid mediators (PGE-2, PGF-2 alfa, LTB-4, resolvins) and other important inflammatory and anti-inflammatory cytokines are also involved in the pathogenicity of ZVL. Analysis of a greater number of mediators allows for a more complete view of disease immunopathogenesis. Additionally, our knowledge has expanded to encompass different biomarkers associated to disease severity and healing after specific treatments. These parameters can also be used to better define new potential targets for vaccines and chemotherapy for ZVL. Here, we will provide an overview of ZVL biomarkers identified for both humans and dogs and discuss their merits and shortcomings. We will also discuss biomarkers of vector exposure as an additional tool in our arsenal to combat ZVL.
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页数:10
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