Cellular immune responses of schistosomiasis patients are altered by human immunodeficiency virus type 1 coinfection

被引:54
作者
Mwinzi, PNM
Karanja, DMS
Colley, DG
Orago, ASS
Secor, WE
机构
[1] CDCP, Immunol Branch, Div Parasit Dis, Natl Ctr Infect Dis, Atlanta, GA 30341 USA
[2] Kenya Govt Med Res Ctr, Ctr Vector Biol & Control Res, Kisumu, Kenya
[3] Kenyatta Univ, Dept Zool, Nairobi, Kenya
关键词
D O I
10.1086/322783
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 vitro studies suggest that CD4(+) cells with a T helper 2 (Th2) phenotype better support human immunodeficiency virus type 1 (HIV-1) replication than do cells of the Th1 phenotype. As a result, Th2-type immune responses may be substantially affected by HIV-1 coinfection. To test this hypothesis, a comparison was done of proliferation and cytokine production by peripheral blood mononuclear cells from patients with schistosomiasis who were positive or negative for HIV-1. Patients with schistosomiasis with HIV-1 coinfections had significantly lower interleukin (IL)-4 and IL-10 production than did HIV-1-negative individuals. In contrast, interferon-gamma production levels were similar between the 2 groups. Furthermore, in patients with HIV-1, a decrease in CD4(+) T cells was correlated with an increased Th1: Th2 cytokine production ratio. The effect of praziquantel treatment on proliferation and cytokine responses also differed between HIV-1 infection groups. Thus, HIV-1 infection affects immune response patterns of patients with schistosomiasis.
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收藏
页码:488 / 496
页数:9
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