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Impaired regulatory function of granzyme B-producing B cells against T cell inflammatory responses in lupus mice
by
Zhao, Zhen
, Su, Yin
, Xue, Jimeng
, Hu, Fanlei
, Zhong, Hua
, Wang, Ziye
, Li, Hongchao
, Zhu, Huaqun
, Bai, Mingxin
, Li, Xin
, Yao, Ranran
, Xu, Liling
in
Animals
/ Antibodies
/ Apoptosis
/ Autoimmune diseases
/ autoimmunity
/ B cells
/ B-lymphocytes
/ B-Lymphocytes, Regulatory - metabolism
/ Cell growth
/ Cytokines
/ Cytotoxicity
/ Flow cytometry
/ Granzymes - metabolism
/ Humans
/ Immunology and Inflammation
/ Lupus
/ Lupus Erythematosus, Systemic
/ Lymphocytes
/ Mice
/ Mice, Inbred C57BL
/ Pathogenesis
/ T cell receptors
/ T cells
/ T-Lymphocytes, Regulatory
/ Transplants & implants
2023
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Impaired regulatory function of granzyme B-producing B cells against T cell inflammatory responses in lupus mice
by
Zhao, Zhen
, Su, Yin
, Xue, Jimeng
, Hu, Fanlei
, Zhong, Hua
, Wang, Ziye
, Li, Hongchao
, Zhu, Huaqun
, Bai, Mingxin
, Li, Xin
, Yao, Ranran
, Xu, Liling
in
Animals
/ Antibodies
/ Apoptosis
/ Autoimmune diseases
/ autoimmunity
/ B cells
/ B-lymphocytes
/ B-Lymphocytes, Regulatory - metabolism
/ Cell growth
/ Cytokines
/ Cytotoxicity
/ Flow cytometry
/ Granzymes - metabolism
/ Humans
/ Immunology and Inflammation
/ Lupus
/ Lupus Erythematosus, Systemic
/ Lymphocytes
/ Mice
/ Mice, Inbred C57BL
/ Pathogenesis
/ T cell receptors
/ T cells
/ T-Lymphocytes, Regulatory
/ Transplants & implants
2023
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Impaired regulatory function of granzyme B-producing B cells against T cell inflammatory responses in lupus mice
by
Zhao, Zhen
, Su, Yin
, Xue, Jimeng
, Hu, Fanlei
, Zhong, Hua
, Wang, Ziye
, Li, Hongchao
, Zhu, Huaqun
, Bai, Mingxin
, Li, Xin
, Yao, Ranran
, Xu, Liling
in
Animals
/ Antibodies
/ Apoptosis
/ Autoimmune diseases
/ autoimmunity
/ B cells
/ B-lymphocytes
/ B-Lymphocytes, Regulatory - metabolism
/ Cell growth
/ Cytokines
/ Cytotoxicity
/ Flow cytometry
/ Granzymes - metabolism
/ Humans
/ Immunology and Inflammation
/ Lupus
/ Lupus Erythematosus, Systemic
/ Lymphocytes
/ Mice
/ Mice, Inbred C57BL
/ Pathogenesis
/ T cell receptors
/ T cells
/ T-Lymphocytes, Regulatory
/ Transplants & implants
2023
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Impaired regulatory function of granzyme B-producing B cells against T cell inflammatory responses in lupus mice
Journal Article
Impaired regulatory function of granzyme B-producing B cells against T cell inflammatory responses in lupus mice
2023
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Overview
ObjectiveRecently, a new subtype of granzyme B (GrB)-producing Breg cells has been identified, which was proven to be involved in autoimmune disease. Our recent report demonstrated that GrB-producing Breg cells were correlated with clinical and immunological features of SLE. However, the effect of GrB-producing Breg cells in lupus mice is unclear.MethodsGrB expression in naïve and lupus mouse B cells was analysed using flow cytometry, PCR, ELISA and ELISpot assays. To study the role of GrB-producing B cells in a lupus model, GrB knockout (KO) and wild-type (WT) mice were intraperitoneally injected with monoclonal cells from the mutant mouse strain B6.C-H-2bm12 (bm12) for 2 weeks. In addition, the function of GrB-producing Breg cells in naïve and lupus mice was further explored using in vitro B cells-CD4+CD25− T cell co-culture assays with GrB blockade/KO of B cells.ResultsB cells from the spleens of WT C57BL/6 (B6) mice could express and secret GrB (p<0.001). GrB-producing Breg cells from WT mice showed their regulatory functions on CD4+CD25− T cell. While the frequency of GrB-producing Breg cells was significantly decreased (p=0.001) in lupus mice (p<0.001). Moreover, GrB-producing Breg cells in lupus mice failed to suppress T cell-mediated proinflammatory responses, partially due to the impaired capacity of downregulating the T cell receptor-zeta chain and inducing CD4+CD25− T cell apoptosis.ConclusionThis study further revealed the function and mechanism of GrB-producing Breg cells in regulating T cell homeostasis in lupus mice and highlighted GrB-producing Breg cells as a therapeutic target in SLE.
Publisher
Lupus Foundation of America,BMJ Publishing Group LTD,BMJ Publishing Group
Subject
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