Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity

Understanding etiology of autoimmune diseases has been a great challenge for designing drugs and vaccines. The pathophysiology of many autoimmune diseases may be attributed to molecular mimicry provoked by microbes. Molecular mimicry hypothesizes that a sequence homology between foreign and self-pep...

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Main Authors: Susanta Pahari, Deepyan Chatterjee, Shikha Negi, Jagdeep Kaur, Balvinder Singh, Javed N. Agrewala
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-10-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2017.01938/full
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author Susanta Pahari
Susanta Pahari
Deepyan Chatterjee
Shikha Negi
Jagdeep Kaur
Balvinder Singh
Javed N. Agrewala
author_facet Susanta Pahari
Susanta Pahari
Deepyan Chatterjee
Shikha Negi
Jagdeep Kaur
Balvinder Singh
Javed N. Agrewala
author_sort Susanta Pahari
collection DOAJ
description Understanding etiology of autoimmune diseases has been a great challenge for designing drugs and vaccines. The pathophysiology of many autoimmune diseases may be attributed to molecular mimicry provoked by microbes. Molecular mimicry hypothesizes that a sequence homology between foreign and self-peptides leads to cross-activation of autoreactive T cells. Different microbial proteins are implicated in various autoimmune diseases, including multiple sclerosis, human type 1 diabetes, primary biliary cirrhosis and rheumatoid arthritis. It may be imperative to identify the microbial epitopes that initiate the activation of autoreactive T cells. Consequently, in the present study, we employed immunoinformatics tools to delineate homologous antigenic regions between microbes and human proteins at not only the sequence level but at the structural level too. Interestingly, many cross-reactive MHC class II binding epitopes were detected from an array of microbes. Further, these peptides possess a potential to skew immune response toward Th1-like patterns. The present study divulges many microbial target proteins, their putative MHC-binding epitopes, and predicted structures to establish the fact that both sequence and structure are two important aspects for understanding the relationship between molecular mimicry and autoimmune diseases. Such findings may enable us in designing potential immunotherapies to tolerize autoreactive T cells.
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spelling doaj.art-82bab89c1504414f9f27569f64f22fc02022-12-21T18:59:33ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2017-10-01810.3389/fmicb.2017.01938282324Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting AutoimmunitySusanta Pahari0Susanta Pahari1Deepyan Chatterjee2Shikha Negi3Jagdeep Kaur4Balvinder Singh5Javed N. Agrewala6Immunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, IndiaDepartment of Biotechnology, Panjab University, Chandigarh, IndiaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, IndiaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, IndiaDepartment of Biotechnology, Panjab University, Chandigarh, IndiaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, IndiaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, IndiaUnderstanding etiology of autoimmune diseases has been a great challenge for designing drugs and vaccines. The pathophysiology of many autoimmune diseases may be attributed to molecular mimicry provoked by microbes. Molecular mimicry hypothesizes that a sequence homology between foreign and self-peptides leads to cross-activation of autoreactive T cells. Different microbial proteins are implicated in various autoimmune diseases, including multiple sclerosis, human type 1 diabetes, primary biliary cirrhosis and rheumatoid arthritis. It may be imperative to identify the microbial epitopes that initiate the activation of autoreactive T cells. Consequently, in the present study, we employed immunoinformatics tools to delineate homologous antigenic regions between microbes and human proteins at not only the sequence level but at the structural level too. Interestingly, many cross-reactive MHC class II binding epitopes were detected from an array of microbes. Further, these peptides possess a potential to skew immune response toward Th1-like patterns. The present study divulges many microbial target proteins, their putative MHC-binding epitopes, and predicted structures to establish the fact that both sequence and structure are two important aspects for understanding the relationship between molecular mimicry and autoimmune diseases. Such findings may enable us in designing potential immunotherapies to tolerize autoreactive T cells.http://journal.frontiersin.org/article/10.3389/fmicb.2017.01938/fullmolecular mimicrymicrobesautoimmunityautoantigensimmunoinformaticsHLA binders
spellingShingle Susanta Pahari
Susanta Pahari
Deepyan Chatterjee
Shikha Negi
Jagdeep Kaur
Balvinder Singh
Javed N. Agrewala
Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity
Frontiers in Microbiology
molecular mimicry
microbes
autoimmunity
autoantigens
immunoinformatics
HLA binders
title Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity
title_full Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity
title_fullStr Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity
title_full_unstemmed Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity
title_short Morbid Sequences Suggest Molecular Mimicry between Microbial Peptides and Self-Antigens: A Possibility of Inciting Autoimmunity
title_sort morbid sequences suggest molecular mimicry between microbial peptides and self antigens a possibility of inciting autoimmunity
topic molecular mimicry
microbes
autoimmunity
autoantigens
immunoinformatics
HLA binders
url http://journal.frontiersin.org/article/10.3389/fmicb.2017.01938/full
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