Lymphocytes influence Leishmania major pathogenesis in a strain-dependent manner

被引:8
|
作者
Abu Musa, Md. [1 ,2 ,3 ]
Nakamura, Risa [1 ,2 ,3 ]
Hena, Asma [2 ,3 ]
Varikuti, Sanjay [4 ]
Nakhasi, Hira L. [5 ]
Goto, Yasuyuki [6 ]
Satoskar, Abhay R. [4 ]
Hamano, Shinjiro [1 ,2 ,3 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Doctoral Leadership Program, Nagasaki, Japan
[2] Nagasaki Univ, Inst Trop Med NEKKEN, Dept Parasitol, Nagasaki, Japan
[3] Nagasaki Univ, Inst Trop Med NEKKEN, Joint Usage Res Ctr Trop Dis, Nagasaki, Japan
[4] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[5] US FDA, Div Emerging & Transfus Transmitted Dis, CBER, Silver Spring, MD USA
[6] Univ Tokyo, Grad Sch Agr & Life Sci, Lab Mol Immunol, Bunkyo Ku, Tokyo, Japan
来源
PLOS NEGLECTED TROPICAL DISEASES | 2019年 / 13卷 / 11期
关键词
SCID MICE; T-CELLS; INFECTION; BALB/C; SUSCEPTIBILITY; AMAZONENSIS; EXPRESSION; HOST; SKIN;
D O I
10.1371/journal.pntd.0007865
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Cutaneous leishmaniasis (CL) is the most common form of leishmaniasis and is caused by several species of Leishmania parasite. Clinical presentation of CL varies from a self-healing infection to a chronic form of the disease determined by the virulence of infecting Leishmania species and host immune responses to the parasite. Mouse models of CL show contradictory roles of lymphocytes in pathogenesis, while acquired immune responses are responsible for host protection from diseases. To reconcile the inconclusive roles of acquired immune responses in pathogenesis, we infected mice from various genetic backgrounds with two pathogenic strains of Leishmania major, Friedlin or 5ASKH, and assessed the outcome of the infections. Our findings showed that the genetic backgrounds of L. major determine the impact of lymphocytes for pathogenesis. In the absence of lymphocytes, L. major Friedlin induced the lowest inflammatory reaction and pathology at the site of infection, while 5ASKH infection induced a strong inflammatory reaction and severe pathology. Lymphocytes ameliorated 5ASKH mediated pathology, while it exacerbated pathology during Friedlin infection. Excess inflammatory reactions, like the recruitment of macrophages, neutrophils, eosinophils and production of pro-inflammatory cytokines, together with uncontrolled parasite growth in the absence of lymphocytes during 5ASKH infection may induce severe pathology development. Taken together our study provides insight into the impact of differences in the genetic background of Leishmania on CL pathogenesis. Author summary Cutaneous leishmaniasis is caused by different species and sub-species of the intracellular parasite Leishmania. It is prevalent mainly in tropical and sub-tropical parts of the world. Disease manifestations range from self-healing cutaneous lesions to chronic form of the disease, depending on the infecting species of Leishmania and host immune protection. The mechanisms of pathogenesis are largely unknown. Lymphocytes play a central role in the protection against Leishmania infection; however, their role in pathogenesis is poorly defined. Experimental infection studies showed the inconsistent role of lymphocytes in pathogenesis. Here, we compared disease outcomes in mice infected with different strains of Leishmania major, either Friedlin or 5ASKH. The pathogenesis caused by L. major 5ASKH infection was suppressed by the lymphocytes, while it was augmented by the lymphocytes during L. major Friedlin infection. Thus we found that the influence of lymphocytes in pathogenesis was determined by the genetic background of the parasites.
引用
收藏
页数:15
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