TY - JOUR
T1 - T-cell epitopes and neo-epitopes in type 1 diabetes
T2 - A comprehensive update and reappraisal
AU - James, Eddie A.
AU - Mallone, Roberto
AU - Kent, Sally C.
AU - Dilorenzo, Teresa P.
N1 - Funding Information:
Acknowledgments. The authors thank Nima Salimi (IEDB) for assistance with epitope data curation and for working with IEDB staff to ensure that all of the epitopes in this article were assigned identification numbers. The authors appreciate the Immunology of Diabetes Society T Cell Workshop for fostering discussions that launched this epitope reappraisal. Funding. Work in the laboratory of E.A.J. is supported by grants from JDRF (1-SRA-2017-344-S-B and 2-SRA-2018-551-S-B). Work in the laboratory of R.M. is supported by grants from JDRF (2-SRA-2016-164-Q-R), The Leona M. and Harry B. Helmsley Charitable Trust (1901-03689), Fondation Francophone pour la Recherche sur le Diabète, Agence Nationale de la Recherche (ANR-19-CE15-0014-01), Fondation pour la Recherche Médicale (EQU20193007831), and the Innovative Medicines Initiative 2 Joint Undertaking (INNODIA, 115797), which receives support from the EU Horizon 2020 program, the European Federation of Pharmaceutical Industries and Associations, JDRF, and The Leona M. and Harry B. Helmsley Charitable Trust. Work in the laboratory of S.C.K. is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (UC4 DK116284). S.C.K. is the George F. and Sybil H. Fuller Term Chair in Diabetes. Work in the laboratory of T.P.D. is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK120420 and P30 DK020541, which supports the Einstein–Mount Sinai Diabetes Research Center), the National Institute of Allergy and Infectious Diseases (R01 AI123730), and the American Diabetes Association (1-16-IBS-069). T.P.D. is the Diane Belfer, Cypres & Endelson Families Faculty Scholar in Diabetes Research. Duality of Interest. R.M. holds patents related to some of the antigens reviewed here. No other potential conflicts of interest relevant to this article were reported.
Funding Information:
The authors thank Nima Salimi (IEDB) for assistance with epitope data curation and for working with IEDB staff to ensure that all of the epitopes in this article were assigned identification numbers. The authors appreciate the Immunology of Diabetes Society T Cell Workshop for fostering discussions that launched this epitope reappraisal. Funding. Work in the laboratory of E.A.J. is supported by grants from JDRF (1-SRA- 2017-344-S-B and 2-SRA-2018-551-S-B). Work in the laboratory of R.M. is supported by grants from JDRF (2-SRA-2016-164-Q-R), The Leona M. and Harry B. Helmsley Charitable Trust (1901-03689), Fondation Francophone pour la Recherche sur le Diabète, Agence Nationale de la Recherche (ANR-19-CE15-0014-01), Fondation pour la Recherche Médicale (EQU20193007831), and the Innovative Medicines Initiative 2 Joint Undertaking (INNODIA, 115797), which receives support from the EU Horizon 2020 program, the European Federation of Pharmaceutical Industries and Associations, JDRF, and The Leona M. and Harry B. Helmsley Charitable Trust. Work in the laboratory of S.C.K. is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (UC4 DK116284). S.C.K. is the George F. and Sybil H. Fuller Term Chair in Diabetes. Work in the laboratory of T.P.D. is supported by the National Institute of Diabetes and Digestive and Kidney Diseases (R01 DK120420 and P30 DK020541, which supports the Einstein–Mount Sinai Diabetes Research Center), the National Institute of Allergy and Infectious Diseases (R01 AI123730), and the American Diabetes Association (1-16-IBS-069). T.P.D. is the Diane Belfer, Cypres & Endelson Families Faculty Scholar in Diabetes Research.
Publisher Copyright:
© 2020 by the American Diabetes Association.
PY - 2020/7
Y1 - 2020/7
N2 - The autoimmune disease type 1 diabetes is characterized by effector T-cell responses to pancreatic b-cell– derived peptides presented by HLA class I and class II molecules, leading ultimately to b-cell demise and insulin insufficiency. Although a given HLA molecule presents a vast array of peptides, only those recognized by T cells are designated as epitopes. Given their intimate link to etiology, the discovery and characterization of T-cell epitopes is a critical aspect of type 1 diabetes research. Understanding epitope recognition is also crucial for the pursuit of antigen-specific immunotherapies and implementation of strategies for T-cell monitoring. For these reasons, a cataloging and appraisal of the T-cell epitopes targeted in type 1 diabetes was completed over a decade ago, providing an important resource for both the research and the clinical communities. Here we present a much needed update and reappraisal of this earlier work and include online supplementary material where we cross-index each epitope with its primary references and Immune Epitope Database (IEDB) identifier. Our analysis includes a grading scale to score the degree of evidence available for each epitope, which conveys our perspective on several useful criteria for epitope evaluation. While providing an efficient summary of the arguably impressive current state of knowledge, this work also brings to light several deficiencies. These include the need for improved epitope validation, as few epitopes score highly by the criteria employed, and the dearth of investigations of the epitopes recognized in the context of several understudied type 1 diabetes–associated HLA molecules.
AB - The autoimmune disease type 1 diabetes is characterized by effector T-cell responses to pancreatic b-cell– derived peptides presented by HLA class I and class II molecules, leading ultimately to b-cell demise and insulin insufficiency. Although a given HLA molecule presents a vast array of peptides, only those recognized by T cells are designated as epitopes. Given their intimate link to etiology, the discovery and characterization of T-cell epitopes is a critical aspect of type 1 diabetes research. Understanding epitope recognition is also crucial for the pursuit of antigen-specific immunotherapies and implementation of strategies for T-cell monitoring. For these reasons, a cataloging and appraisal of the T-cell epitopes targeted in type 1 diabetes was completed over a decade ago, providing an important resource for both the research and the clinical communities. Here we present a much needed update and reappraisal of this earlier work and include online supplementary material where we cross-index each epitope with its primary references and Immune Epitope Database (IEDB) identifier. Our analysis includes a grading scale to score the degree of evidence available for each epitope, which conveys our perspective on several useful criteria for epitope evaluation. While providing an efficient summary of the arguably impressive current state of knowledge, this work also brings to light several deficiencies. These include the need for improved epitope validation, as few epitopes score highly by the criteria employed, and the dearth of investigations of the epitopes recognized in the context of several understudied type 1 diabetes–associated HLA molecules.
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U2 - 10.2337/dbi19-0022
DO - 10.2337/dbi19-0022
M3 - Article
C2 - 32561620
AN - SCOPUS:85086752526
SN - 0012-1797
VL - 69
SP - 1311
EP - 1335
JO - Diabetes
JF - Diabetes
IS - 7
ER -