From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity

Sequence analyses highlight a massive peptide sharing between immunoreactive Epstein-Barr virus (EBV) epitopes and human proteins that—when mutated, deficient or improperly functioning—associate with tumorigenesis, diabetes, lupus, multiple sclerosis, rheumatoid arthritis, and immunodeficiencies, am...

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Main Authors: Darja Kanduc, Yehuda Shoenfeld
Format: Article
Language:English
Published: Georg Thieme Verlag KG 2020-08-01
Series:Global Medical Genetics
Subjects:
Online Access:http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1715641
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author Darja Kanduc
Yehuda Shoenfeld
author_facet Darja Kanduc
Yehuda Shoenfeld
author_sort Darja Kanduc
collection DOAJ
description Sequence analyses highlight a massive peptide sharing between immunoreactive Epstein-Barr virus (EBV) epitopes and human proteins that—when mutated, deficient or improperly functioning—associate with tumorigenesis, diabetes, lupus, multiple sclerosis, rheumatoid arthritis, and immunodeficiencies, among others. Peptide commonality appears to be the molecular platform capable of linking EBV infection to the vast EBV-associated diseasome via cross-reactivity and questions the hypothesis of the “negative selection” of self-reactive lymphocytes. Of utmost importance, this study warns that using entire antigens in anti-EBV immunotherapies can associate with autoimmune manifestations and further supports the concept of peptide uniqueness for designing safe and effective anti-EBV immunotherapies.
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spelling doaj.art-2ae62966b9d047f5837c1ff605634bb02022-12-22T02:49:48ZengGeorg Thieme Verlag KGGlobal Medical Genetics2699-94042020-08-01070205106310.1055/s-0040-1715641From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivityDarja Kanduc0Yehuda Shoenfeld1Department of Biosciences, Biotechnologies, and Biopharmaceutics, University of Bari, Bari, ItalyZabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel-Aviv University School of Medicine, Tel-Hashomer, IsraelSequence analyses highlight a massive peptide sharing between immunoreactive Epstein-Barr virus (EBV) epitopes and human proteins that—when mutated, deficient or improperly functioning—associate with tumorigenesis, diabetes, lupus, multiple sclerosis, rheumatoid arthritis, and immunodeficiencies, among others. Peptide commonality appears to be the molecular platform capable of linking EBV infection to the vast EBV-associated diseasome via cross-reactivity and questions the hypothesis of the “negative selection” of self-reactive lymphocytes. Of utmost importance, this study warns that using entire antigens in anti-EBV immunotherapies can associate with autoimmune manifestations and further supports the concept of peptide uniqueness for designing safe and effective anti-EBV immunotherapies.http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1715641ebv epitopessystemic lupus erythematosuscross-reactivityautoimmunitynegative selectionself-reactive lymphocytespathogenic autoantibodies
spellingShingle Darja Kanduc
Yehuda Shoenfeld
From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity
Global Medical Genetics
ebv epitopes
systemic lupus erythematosus
cross-reactivity
autoimmunity
negative selection
self-reactive lymphocytes
pathogenic autoantibodies
title From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity
title_full From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity
title_fullStr From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity
title_full_unstemmed From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity
title_short From Anti-EBV Immune Responses to the EBV Diseasome via Cross-reactivity
title_sort from anti ebv immune responses to the ebv diseasome via cross reactivity
topic ebv epitopes
systemic lupus erythematosus
cross-reactivity
autoimmunity
negative selection
self-reactive lymphocytes
pathogenic autoantibodies
url http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1715641
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