Distinct roles of ICOS and CD40L in human T-B cell adhesion and antibody production

Adult CD4-Positive T-Lymphocytes Male 0301 basic medicine B-Lymphocytes Adolescent CD40 Ligand Cell Communication Middle Aged Lymphocyte Activation Inducible T-Cell Co-Stimulator Protein Young Adult 03 medical and health sciences Focal Adhesion Kinase 2 Immunoglobulin M Immunoglobulin G Antibody Formation Cell Adhesion Humans Lupus Erythematosus, Systemic Female Cells, Cultured
DOI: 10.1016/j.cellimm.2021.104420 Publication Date: 2021-08-06T15:06:33Z
ABSTRACT
CD40-CD40L and inducible co-stimulatory molecule (ICOS)-ICOSL ligations are demonstrated to play critical roles in CD4+ T-B interaction for B cell activation differentiation mouse models. Herein, by using a micropipette adhesion assay an vitro coculture system simultaneously, we intended dissect their human IgG/IgM production. With the upregulation of CD40L ICOS expressions on T cells upon TCR/CD28 stimulation vitro, activated exhibited enhanced with autologous at single level when compared resting counterparts. Blockade dramatically damped between whereas less effect blockade was observed. On contrary, led dramatic decrease production were cocultured together induction CD19hi cells. However, displayed attenuation Distinct ICOS-ICOSL also observed lupus erythematosus patients. The CD40L, rather than ICOS, phosphorylation Pyk2 total Our study thus provides evidence that either or pathogenic state function diversely during interactions. While ligation is more likely be engaged adhesion, indispensable signal results indicative segregating costimulation differentiation, which might helpful dissection SLE pathogenesis.
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