Na Chen , Leidan Zhang , Xinyue Wang , Zhijiao He , Di Wang , Juan Du , Meiju Deng , Mengyuan Zhang , Meiqing Jiang , Yuqing Wei , Meng Zhao , Ying Liu , Xiaolei Wang , Hongxin Zhao , Yaxian Kong
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引用次数: 0
Abstract
Persistent immune activation is a key factor contributing to AIDS progression and non-AIDS-associated complications. NKT-like cells were found to exert immunosuppressive roles under some pathological situations by Foxp3 upregulation. Here, we found that Foxp3 was mainly expressed on CD4+NKT-like cells in untreated people living with HIV (PLWH) and the frequencies of Foxp3+CD4+NKT-like cells were correlated with HIV disease progression. Furthermore, the percentage of Foxp3+CD4+NKT-like cells was positively associated with immune activation and systematic inflammation. Foxp3+CD4+NKT-like cells might exert immunomodulatory effects by elevating the expression of TGF-β, IL-10, CD39, CD25, GITR, Ki67 and TIGIT. However, our analyses further identified Foxp3+CD4+NKT-like cells as a distinct subset that differed from conventional regulatory T cells. Notably, patients with higher baseline levels of Foxp3+CD4+NKT-like cells had a greater risk of poor immune reconstitution. These findings emphasized the importance of Foxp3+CD4+NKT-like cells during HIV infection and revealed its predictive role in immune reconstitution.
期刊介绍:
Clinical Immunology publishes original research delving into the molecular and cellular foundations of immunological diseases. Additionally, the journal includes reviews covering timely subjects in basic immunology, along with case reports and letters to the editor.