{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Packard TA"],"funding":["JDRF","NIH"],"pagination":["E98"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5126795"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["5(11)"],"pubmed_abstract":["B cells have been strongly implicated in the development of human type 1 diabetes and are required for disease in the NOD mouse model. These functions are dependent on B cell antigen receptor (BCR) specificity and expression of MHC, implicating linked autoantigen recognition and presentation to effector T cells. BCR-antigen affinity requirements for participation in disease are unclear. We hypothesized that BCR affinity for the autoantigen insulin differentially affects lymphocyte functionality, including tolerance modality and the ability to acquire and become activated in the diabetogenic environment. Using combined transgenic and retrogenic heavy and light chain to create multiple insulin-binding BCRs, we demonstrate that affinity for insulin is a critical determinant of the function of"],"journal":["Journal of clinical medicine"],"pubmed_title":["B Cell Receptor Affinity for Insulin Dictates Autoantigen Acquisition and B Cell Functionality in Autoimmune Diabetes."],"pmcid":["PMC5126795"],"funding_grant_id":["R01DK096492-05","AI051448","27-2012-450","P01AI022295","T32AI007405"],"pubmed_authors":["Smith MJ","Lindsay RS","Conrad FJ","Thomas JW","Packard TA","Johnson SA","Getahun A","Friedman RS","Hinman RM","Cambier JC"],"additional_accession":[]},"is_claimable":false,"name":"B Cell Receptor Affinity for Insulin Dictates Autoantigen Acquisition and B Cell Functionality in Autoimmune Diabetes.","description":"B cells have been strongly implicated in the development of human type 1 diabetes and are required for disease in the NOD mouse model. These functions are dependent on B cell antigen receptor (BCR) specificity and expression of MHC, implicating linked autoantigen recognition and presentation to effector T cells. BCR-antigen affinity requirements for participation in disease are unclear. We hypothesized that BCR affinity for the autoantigen insulin differentially affects lymphocyte functionality, including tolerance modality and the ability to acquire and become activated in the diabetogenic environment. Using combined transgenic and retrogenic heavy and light chain to create multiple insulin-binding BCRs, we demonstrate that affinity for insulin is a critical determinant of the function of","dates":{"release":"2016-01-01T00:00:00Z","publication":"2016 Nov","modification":"2025-04-18T18:36:11.51Z","creation":"2019-03-27T02:30:03Z"},"accession":"S-EPMC5126795","cross_references":{"pubmed":["27834793"],"doi":["10.3390/jcm5110098"]}}