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Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis

BACKGROUND: Immune responses play significant roles in protection against leishmaniasis. Polymorphisms within the interleukin 4 receptor alpha chain (IL-4Rα) gene affect the production of cytokines, which is important for the clearance of many pathogens. The aim of the current study was to identify...

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Autores principales: Ahmadi, Alireza, Hajilooi, Mehrdad, Solgi, Ghasem, Abasi, Mohammad, Bazmani, Ahad, Matini, Mohammad, Sardarian, Khosro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616996/
https://www.ncbi.nlm.nih.gov/pubmed/26605234
http://dx.doi.org/10.4103/2277-9175.166131
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author Ahmadi, Alireza
Hajilooi, Mehrdad
Solgi, Ghasem
Abasi, Mohammad
Bazmani, Ahad
Matini, Mohammad
Sardarian, Khosro
author_facet Ahmadi, Alireza
Hajilooi, Mehrdad
Solgi, Ghasem
Abasi, Mohammad
Bazmani, Ahad
Matini, Mohammad
Sardarian, Khosro
author_sort Ahmadi, Alireza
collection PubMed
description BACKGROUND: Immune responses play significant roles in protection against leishmaniasis. Polymorphisms within the interleukin 4 receptor alpha chain (IL-4Rα) gene affect the production of cytokines, which is important for the clearance of many pathogens. The aim of the current study was to identify the relationship between visceral leishmaniasis (VL) infection and polymorphisms at positions T1432C and A1652G of IL-4Rα in an Iranian population. MATERIALS AND METHODS: This cross-sectional study was performed during 2004–2012 and included three groups of participants: VL patients (Group 1, n = 124), seropositive healthy controls (Group 2, n = 101), and seronegative healthy controls (Group 3, n = 55). The IL-4Rα T1432C and A1652G polymorphisms were evaluated using a polymerase chain reaction-restriction fragment length polymorphism technique, and anti-Leishmania antibody titers were determined by using immunofluorescence technique. Alleles and genotypes were compared between groups of the study as well as Groups 1 and 2 based on the titer of antibodies. The validity of the data was analyzed using Hardy–Weinberg equilibrium and one-way analysis of variance, as well as χ(2) tests. RESULTS: The polymorphisms at IL-4Rα positions T1432C and A1652G were significantly associated with active VL infection. These results demonstrated that the IL-4Rα T1432C and A1652G polymorphisms were not associated with anti-Leishmania antibody production. CONCLUSION: Our results indicate that these IL-4Rα polymorphisms may be risk factors for the development of VL.
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spelling pubmed-46169962015-11-24 Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis Ahmadi, Alireza Hajilooi, Mehrdad Solgi, Ghasem Abasi, Mohammad Bazmani, Ahad Matini, Mohammad Sardarian, Khosro Adv Biomed Res Original Article BACKGROUND: Immune responses play significant roles in protection against leishmaniasis. Polymorphisms within the interleukin 4 receptor alpha chain (IL-4Rα) gene affect the production of cytokines, which is important for the clearance of many pathogens. The aim of the current study was to identify the relationship between visceral leishmaniasis (VL) infection and polymorphisms at positions T1432C and A1652G of IL-4Rα in an Iranian population. MATERIALS AND METHODS: This cross-sectional study was performed during 2004–2012 and included three groups of participants: VL patients (Group 1, n = 124), seropositive healthy controls (Group 2, n = 101), and seronegative healthy controls (Group 3, n = 55). The IL-4Rα T1432C and A1652G polymorphisms were evaluated using a polymerase chain reaction-restriction fragment length polymorphism technique, and anti-Leishmania antibody titers were determined by using immunofluorescence technique. Alleles and genotypes were compared between groups of the study as well as Groups 1 and 2 based on the titer of antibodies. The validity of the data was analyzed using Hardy–Weinberg equilibrium and one-way analysis of variance, as well as χ(2) tests. RESULTS: The polymorphisms at IL-4Rα positions T1432C and A1652G were significantly associated with active VL infection. These results demonstrated that the IL-4Rα T1432C and A1652G polymorphisms were not associated with anti-Leishmania antibody production. CONCLUSION: Our results indicate that these IL-4Rα polymorphisms may be risk factors for the development of VL. Medknow Publications & Media Pvt Ltd 2015-09-28 /pmc/articles/PMC4616996/ /pubmed/26605234 http://dx.doi.org/10.4103/2277-9175.166131 Text en Copyright: © 2015 Advanced Biomedical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Ahmadi, Alireza
Hajilooi, Mehrdad
Solgi, Ghasem
Abasi, Mohammad
Bazmani, Ahad
Matini, Mohammad
Sardarian, Khosro
Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis
title Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis
title_full Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis
title_fullStr Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis
title_full_unstemmed Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis
title_short Interleukin-4 receptor alpha T1432C and A1652G polymorphisms are associated with risk of visceral leishmaniasis
title_sort interleukin-4 receptor alpha t1432c and a1652g polymorphisms are associated with risk of visceral leishmaniasis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616996/
https://www.ncbi.nlm.nih.gov/pubmed/26605234
http://dx.doi.org/10.4103/2277-9175.166131
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