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Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients

BACKGROUND: The etiology of Multiple sclerosis (MS) is complicated and can be affected by several environmental factors, such as Mycobacterium avium subspecies paratuberculosis (MAP) infection in genetically predisposed individuals. The link between MAP and MS depends on host genetic and epigenetic...

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Autores principales: Asgari, Negar, Ghaemi, Ezzat Allah, Naeimi, Mohammad Hasan, Tahamtan, Alireza, Sechi, Leonardo Antonio, Zamani, Samin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686849/
https://www.ncbi.nlm.nih.gov/pubmed/38034802
http://dx.doi.org/10.1016/j.heliyon.2023.e22137
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author Asgari, Negar
Ghaemi, Ezzat Allah
Naeimi, Mohammad Hasan
Tahamtan, Alireza
Sechi, Leonardo Antonio
Zamani, Samin
author_facet Asgari, Negar
Ghaemi, Ezzat Allah
Naeimi, Mohammad Hasan
Tahamtan, Alireza
Sechi, Leonardo Antonio
Zamani, Samin
author_sort Asgari, Negar
collection PubMed
description BACKGROUND: The etiology of Multiple sclerosis (MS) is complicated and can be affected by several environmental factors, such as Mycobacterium avium subspecies paratuberculosis (MAP) infection in genetically predisposed individuals. The link between MAP and MS depends on host genetic and epigenetic aspects and population-based features that require further investigation. We aimed to study the possible role of MAP in triggering MS using molecular and serological methods. MATERIALS AND METHODS: This case-control study examined 200 blood samples (100 MS patients and 100 HCs) to search for the MAP-specific IS900 gene. In addition, ELISA was conducted to determine the humoral response against MAP_4027(18-32) and its human IRF5(424–434) peptide homolog. RESULTS: The frequency of MAP detection based on the molecular method in MS patients and HCs was 48 % and 13 %, respectively (p < 0.0001). The presence of antibodies against MAP_4027(18-32) and IRF5(424–434) was 55 % and 65 % in MS patients versus 9 % and 7 % in HCs, respectively (p < 0.0001). A good correlation was observed between MAP_4027 and IRF5 antibodies (r = 0.5782, p < 0.0001), indicating that the same antibodies recognized common peptide epitopes. CONCLUSION: Our research revealed a significant association between MAP and MS, highlighting the possible role of MAP as an important infection trigger factor of MS. It is hypothesized that cross-reactivity between MAP4027 and IRF5 may dysregulate immune homeostasis.
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spelling pubmed-106868492023-11-30 Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients Asgari, Negar Ghaemi, Ezzat Allah Naeimi, Mohammad Hasan Tahamtan, Alireza Sechi, Leonardo Antonio Zamani, Samin Heliyon Research Article BACKGROUND: The etiology of Multiple sclerosis (MS) is complicated and can be affected by several environmental factors, such as Mycobacterium avium subspecies paratuberculosis (MAP) infection in genetically predisposed individuals. The link between MAP and MS depends on host genetic and epigenetic aspects and population-based features that require further investigation. We aimed to study the possible role of MAP in triggering MS using molecular and serological methods. MATERIALS AND METHODS: This case-control study examined 200 blood samples (100 MS patients and 100 HCs) to search for the MAP-specific IS900 gene. In addition, ELISA was conducted to determine the humoral response against MAP_4027(18-32) and its human IRF5(424–434) peptide homolog. RESULTS: The frequency of MAP detection based on the molecular method in MS patients and HCs was 48 % and 13 %, respectively (p < 0.0001). The presence of antibodies against MAP_4027(18-32) and IRF5(424–434) was 55 % and 65 % in MS patients versus 9 % and 7 % in HCs, respectively (p < 0.0001). A good correlation was observed between MAP_4027 and IRF5 antibodies (r = 0.5782, p < 0.0001), indicating that the same antibodies recognized common peptide epitopes. CONCLUSION: Our research revealed a significant association between MAP and MS, highlighting the possible role of MAP as an important infection trigger factor of MS. It is hypothesized that cross-reactivity between MAP4027 and IRF5 may dysregulate immune homeostasis. Elsevier 2023-11-19 /pmc/articles/PMC10686849/ /pubmed/38034802 http://dx.doi.org/10.1016/j.heliyon.2023.e22137 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Asgari, Negar
Ghaemi, Ezzat Allah
Naeimi, Mohammad Hasan
Tahamtan, Alireza
Sechi, Leonardo Antonio
Zamani, Samin
Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients
title Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients
title_full Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients
title_fullStr Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients
title_full_unstemmed Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients
title_short Cross-reactivity between Mycobacterium avium subspecies paratuberculosis 4027 peptide and Human IRF5 may contribute to Multiple Sclerosis in Iranian patients
title_sort cross-reactivity between mycobacterium avium subspecies paratuberculosis 4027 peptide and human irf5 may contribute to multiple sclerosis in iranian patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10686849/
https://www.ncbi.nlm.nih.gov/pubmed/38034802
http://dx.doi.org/10.1016/j.heliyon.2023.e22137
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