| Literature DB >> 27717503 |
Wan-Dang Wang1, Yu-Chi Gao2, Yuan-Bin Lu2, Jun-Ai Zhang2, Gan-Bin Liu3, Bin Kong2, Wen-Yu Xiang2, You-Chao Dai2, Shi-Yan Yu2, Yan Jia2, Xiao-Xia Fu4, Lai-Long Yi3, Bin-Ying Zheng4, Zheng W Chen5, Jixin Zhong6, Jun-Fa Xu7.
Abstract
Despite past extensive studies on B and T lymphocyte attenuator (BTLA)-mediated negative regulation of T cell activation, the role of BTLA in antigen presenting cells (APCs) in patients with active pulmonary tuberculosis (ATB) remains poorly understood. Here, we demonstrate that BTLA expression on CD11c APCs increased in patients with ATB. Particularly, BTLA expression in CD11c APCs was likely associated with the attenuated stimulatory capacity on T cells (especially CD8+ T cell) proliferation. BTLA-expressing CD11c APCs showed lower antigen uptake capacity, lower CD86 expression, higher HLA-DR expression, and enhanced IL-6 secretion, compared to counterpart BTLA negative CD11c APCs in healthy controls (HC). Interestingly, BTLA-expressing CD11c APCs from ATB patients displayed lower expression of HLA-DR and less IL-6 secretion, but higher expression of CD86 than those from HC volunteers. Mixed lymphocyte reaction suggests that BTLA expression is likely associated with positive rather than conventional negative regulation of CD11c APCs stimulatory capacity. This role is impaired in ATB patients manifested by low expression of HLA-DR and low production of IL-6. This previous unappreciated role for BTLA may have implications in the prevention and treatment of patients with ATB.Entities:
Keywords: Antigen uptake; B and T lymphocyte attenuator; CD11c APCs; CD86; HLA-DR; HLA-I(A,B,C); IL-6; Stimulatory capacity
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Year: 2016 PMID: 27717503 DOI: 10.1016/j.cellimm.2016.09.015
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868