Author:
Zou Shi,Xiang Yanni,Guo Wei,Zhu Qi,Wu Songjie,Tan Yuting,Yan Yajun,Shen Ling,Feng Yong,Liang Ke
Abstract
BackgroundAlthough γδ T cells play an essential role in immunity againstHuman Immunodeficiency Virus(HIV) orMycobacterium tuberculosis(MTB), they are poorly described in HIV infection with tuberculosis (TB).MethodsThe phenotypic and functional properties of peripheral blood γδ T cells in patients with HIV/TB co-infection were analyzed compared to healthy controls and patients with HIV mono-infection or TB by direct intracellular cytokine staining (ICS).ResultsThe percentage of Vδ1subset in HIV/TB group was significantly higher than that in TB group, while the decreased frequency of the Vδ2and Vγ2Vδ2subsets were observed in HIV/TB group than in TB group. The percentage of CD4+CD8-Vδ2subset in HIV/TB group was markedly lower than in TB group. However, the percentage of CD4+CD8+Vδ2subset in HIV/TB group was markedly higher than HIV group or TB group. A lower percentage TNF-α and a higher percentage of IL-17A of Vδ2subset were observed in HIV/TB group than that in HIV mono-infection. The percentage of perforin-producing Vδ2subset was significantly lower in HIV/TB group than that in HIV group and TB group.ConclusionsOur data suggested that HIV/TB co-infection altered the balance of γδ T cell subsets. The influence of HIV/TB co-infection on the function of γδ T cells to produce cytokines was complicated, which will shed light on further investigations on the mechanisms of the immune response against HIV and/or MTB infection.
Subject
Infectious Diseases,Microbiology (medical),Immunology,Microbiology
Cited by
1 articles.
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