Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.

Autoimmune hemolytic anemia (AIHA) is a chronic autoimmune disease characterized by the self-destruction of red blood cells (RBCs). For investigating the role molecular mimicry in the onset of AIHA manifestations, we identified the microbial epitopes as precipitating factors in the disease etiopatho...

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Main Authors: Pratyusha Patidar, Arihant Jain, Tulika Prakash
Format: Article
Language:English
Published: Elsevier 2025-03-01
Series:ImmunoInformatics
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Online Access:http://www.sciencedirect.com/science/article/pii/S2667119025000011
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author Pratyusha Patidar
Arihant Jain
Tulika Prakash
author_facet Pratyusha Patidar
Arihant Jain
Tulika Prakash
author_sort Pratyusha Patidar
collection DOAJ
description Autoimmune hemolytic anemia (AIHA) is a chronic autoimmune disease characterized by the self-destruction of red blood cells (RBCs). For investigating the role molecular mimicry in the onset of AIHA manifestations, we identified the microbial epitopes as precipitating factors in the disease etiopathology using an integrated immunoinformatics pipeline which includes sequence homology search between microbial and RBC proteins, followed by B-cell and T-cell epitope prediction. These epitopes were further subjected to a homology search with the human gut microbial proteins. Eight out of the ten analysed infectious agents, including Hepatitis C Virus (HCV), Cytomegalovirus (CMV), Epstein-Barr Virus (EBV), Herpes Simplex Virus (HSV), Human Papillomavirus (HPV), Human Immunodeficiency Virus (HIV), Mycoplasma pneumoniae (MP), and Treponema pallidum (TP), possessed B-cell and T-cell epitopes. Interestingly, EBV, HSV, MP, and TP displayed conformational B-cell epitopes, which overlapped with their linear B-cell epitopes. HLA DRB1_0305 was found to exhibit binding with several bacterial epitopes indicating its predisposing potential to AIHA. Further, we report cross-reactive microbial epitopes against RBC proteins that have been experimentally proven to be associated with AIHA indicating a high possibility of those epitopes causing AIHA. Additionally, many B-cell and T-cell epitopes exhibited exact homologies with various human gut microbial proteins. The functional annotation highlighted the involvement of specialized RBC functions, such as cytoskeleton organization, ammonium homeostasis, signalling transduction, in the underlying disease mechanism. These findings suggest that infection-causing pathogens and gut microbes might have a plausible association with AIHA in the context of molecular mimicry.
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spelling doaj-art-a0e1872471314aeaa1d0c5bd5c0490e72025-08-20T03:12:43ZengElsevierImmunoInformatics2667-11902025-03-011710004710.1016/j.immuno.2025.100047Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.Pratyusha Patidar0Arihant Jain1Tulika Prakash2School of Biosciences and Bioengineering, Indian Institute of Technology (IIT) Mandi, H.P., IndiaDepartment of Clinical Hematology and Medical Oncology, Post Graduate Institute of Medical Education & Research (PGIMER), Chandigarh, IndiaSchool of Biosciences and Bioengineering, Indian Institute of Technology (IIT) Mandi, H.P., India; Corresponding author.Autoimmune hemolytic anemia (AIHA) is a chronic autoimmune disease characterized by the self-destruction of red blood cells (RBCs). For investigating the role molecular mimicry in the onset of AIHA manifestations, we identified the microbial epitopes as precipitating factors in the disease etiopathology using an integrated immunoinformatics pipeline which includes sequence homology search between microbial and RBC proteins, followed by B-cell and T-cell epitope prediction. These epitopes were further subjected to a homology search with the human gut microbial proteins. Eight out of the ten analysed infectious agents, including Hepatitis C Virus (HCV), Cytomegalovirus (CMV), Epstein-Barr Virus (EBV), Herpes Simplex Virus (HSV), Human Papillomavirus (HPV), Human Immunodeficiency Virus (HIV), Mycoplasma pneumoniae (MP), and Treponema pallidum (TP), possessed B-cell and T-cell epitopes. Interestingly, EBV, HSV, MP, and TP displayed conformational B-cell epitopes, which overlapped with their linear B-cell epitopes. HLA DRB1_0305 was found to exhibit binding with several bacterial epitopes indicating its predisposing potential to AIHA. Further, we report cross-reactive microbial epitopes against RBC proteins that have been experimentally proven to be associated with AIHA indicating a high possibility of those epitopes causing AIHA. Additionally, many B-cell and T-cell epitopes exhibited exact homologies with various human gut microbial proteins. The functional annotation highlighted the involvement of specialized RBC functions, such as cytoskeleton organization, ammonium homeostasis, signalling transduction, in the underlying disease mechanism. These findings suggest that infection-causing pathogens and gut microbes might have a plausible association with AIHA in the context of molecular mimicry.http://www.sciencedirect.com/science/article/pii/S2667119025000011AutoimmunityAutoimmune hemolytic anemia (AIHA)EpitopeGut microbiomeMolecular mimicry
spellingShingle Pratyusha Patidar
Arihant Jain
Tulika Prakash
Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.
ImmunoInformatics
Autoimmunity
Autoimmune hemolytic anemia (AIHA)
Epitope
Gut microbiome
Molecular mimicry
title Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.
title_full Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.
title_fullStr Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.
title_full_unstemmed Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.
title_short Deciphering the role of molecular mimicry in the etiopathogenesis of Autoimmune Hemolytic Anemia using an immunoinformatics approach.
title_sort deciphering the role of molecular mimicry in the etiopathogenesis of autoimmune hemolytic anemia using an immunoinformatics approach
topic Autoimmunity
Autoimmune hemolytic anemia (AIHA)
Epitope
Gut microbiome
Molecular mimicry
url http://www.sciencedirect.com/science/article/pii/S2667119025000011
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