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典型文献
An IgD-Fc-Ig fusion protein restrains the activation of T and B cells by inhibiting IgD-IgDR-Lck signaling in rheumatoid arthritis
文献摘要:
Rheumatoid arthritis(RA)is a chronic systemic autoimmune disease characterized by synovitis and the destruction of small joints.Emerging evidence shows that immunoglobulin D(IgD)stimulation induces T-cell activation,which may contribute to diseases pathogenesis in RA.In this study,we investigated the downstream signaling pathways by which IgD activated T cells as well as the possible role of IgD in the T-B interaction.Peripheral blood mononuclear cells were isolated from peripheral blood of healthy controls and RA patients.We demonstrated that IgD activated T cells through IgD receptor(IgDR)-lymphocyte-specific protein tyrosine kinase(Lck)-zeta-associated protein 70(ZAP70)/phosphatidylinositol 3-kinase(PI3K)/nuclear factor kappa-B(NF-κB)signaling pathways;IgD-induced CD4+T cells promoted the proliferation of CD19+B cells in RA patients.A novel fusion protein IgD-Fc-Ig(composed of human IgD-Fc domain and IgG1 Fc domain,which specifically blocked the IgD-IgDR binding)inhibited the coexpression of IgDR and phosphorylated Lck(p-Lck)and the expression levels of p-Lck,p-ZAP70,p-PI3K on CD4+T cells,and decreased NF-κB nuclear translocation in Jurkat cells.Meanwhile,IgD-Fc-Ig downregulated the expression levels of CD40L on CD4+T cells as well as CD40,CD86 on CD19+B cells in RA patients and healthy controls.It also decreased the expression levels of CD40L on CD4+T cells and CD40 on CD19+B cells from spleens of collagen-induced arthritis(CIA)mice and reduced IL-17A level in mouse serum.Moreover,administration of IgD-Fc-Ig(1.625-13 mg/kg,iv,twice a week for 4 weeks)in CIA mice dose-dependently decreased the protein expression levels of CD40,CD40L,and IgD in spleens.IgD-Fc-Ig restrains T-cell activation through inhibiting IgD-IgDR-Lck-ZAP70-PI3K-NF-KB signaling,thus inhibiting B-cell activation.Our data provide experimental evidences for application of IgD-Fc-Ig as a highly selective T cell-targeting treatment for RA.
文献关键词:
作者姓名:
Xiao-xi Hu;Ai-jun Zhang;Wen-wen Pan;Qian-ling Xin;Jing-yu Chen;Ling-ling Zhang;Yan Chang;Yu-jing Wu;Wei Wei
作者机构:
Institute of Clinical Pharmacology,Anhui Medical University,Key Laboratory of Anti-inflammatory and Immune Medicine,Ministry of Education,Anhui Collaborative Innovation Center of Anti-inflammatory and Immune Medicine,Hefei 230032,China
引用格式:
[1]Xiao-xi Hu;Ai-jun Zhang;Wen-wen Pan;Qian-ling Xin;Jing-yu Chen;Ling-ling Zhang;Yan Chang;Yu-jing Wu;Wei Wei-.An IgD-Fc-Ig fusion protein restrains the activation of T and B cells by inhibiting IgD-IgDR-Lck signaling in rheumatoid arthritis)[J].中国药理学报(英文版),2022(02):387-400
A类:
IgDR,Lck
B类:
An,Fc,fusion,protein,restrains,activation,cells,by,inhibiting,signaling,rheumatoid,arthritis,Rheumatoid,RA,chronic,systemic,autoimmune,characterized,synovitis,destruction,small,joints,Emerging,shows,that,immunoglobulin,stimulation,induces,which,may,contribute,diseases,pathogenesis,In,this,study,investigated,downstream,pathways,activated,well,possible,role,interaction,Peripheral,blood,mononuclear,were,isolated,from,peripheral,healthy,controls,patients,We,demonstrated,through,receptor,lymphocyte,tyrosine,kinase,zeta,associated,ZAP70,phosphatidylinositol,PI3K,kappa,induced,CD4+T,promoted,proliferation,CD19+B,novel,composed,human,domain,IgG1,specifically,blocked,binding,inhibited,coexpression,phosphorylated,levels,decreased,translocation,Jurkat,Meanwhile,downregulated,CD40L,CD86,It,also,spleens,collagen,CIA,mice,reduced,17A,mouse,serum,Moreover,administration,twice,weeks,dose,dependently,KB,thus,Our,data,provide,experimental,evidences,application,highly,selective,targeting,treatment
AB值:
0.407804
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