Literature DB >> 27717503

BTLA-expressing CD11c antigen presenting cells in patients with active tuberculosis exhibit low capacity to stimulate T cell proliferation.

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.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Antigen uptake; B and T lymphocyte attenuator; CD11c APCs; CD86; HLA-DR; HLA-I(A,B,C); IL-6; Stimulatory capacity

Mesh:

Substances:

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


  7 in total

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2.  Characterization of multiple soluble immune checkpoints in individuals with different Mycobacterium tuberculosis infection status and dynamic changes during anti-tuberculosis treatment.

Authors:  Huaxin Chen; Jingyu Zhou; Xinguo Zhao; Qianqian Liu; Lingyun Shao; Yehan Zhu; Qinfang Ou
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3.  Investigation of BTLA tagging variants with risk of esophagogastric junction adenocarcinoma.

Authors:  Weifeng Tang; Shuchen Chen; Mingqiang Kang; Jun Liu; Chao Liu
Journal:  Biosci Rep       Date:  2019-12-20       Impact factor: 3.840

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Journal:  Clin Transl Immunology       Date:  2021-02-18

Review 5.  Pathological and protective roles of dendritic cells in Mycobacterium tuberculosis infection: Interaction between host immune responses and pathogen evasion.

Authors:  Hongmin Kim; Sung Jae Shin
Journal:  Front Cell Infect Microbiol       Date:  2022-07-28       Impact factor: 6.073

6.  Elevation in the counts of IL-35-producing B cells infiltrating into lung tissue in mycobacterial infection is associated with the downregulation of Th1/Th17 and upregulation of Foxp3+Treg.

Authors:  Chen Chen; Huan Xu; Ying Peng; Hong Luo; Gui-Xian Huang; Xian-Jin Wu; You-Chao Dai; Hou-Long Luo; Jun-Ai Zhang; Bi-Ying Zheng; Xiang-Ning Zhang; Zheng W Chen; Jun-Fa Xu
Journal:  Sci Rep       Date:  2020-08-06       Impact factor: 4.379

7.  BTLA-Expressing Dendritic Cells in Patients With Tuberculosis Exhibit Reduced Production of IL-12/IFN-α and Increased Production of IL-4 and TGF-β, Favoring Th2 and Foxp3+ Treg Polarization.

Authors:  Jun-Ai Zhang; Yuan-Bin Lu; Wan-Dang Wang; Gan-Bin Liu; Chen Chen; Ling Shen; Hou-Long Luo; Huan Xu; Ying Peng; Hong Luo; Gui-Xian Huang; Du-Du Wu; Bi-Ying Zheng; Lai-Long Yi; Zheng W Chen; Jun-Fa Xu
Journal:  Front Immunol       Date:  2020-03-31       Impact factor: 7.561

  7 in total

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