The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina

Th17 lymphocytes, that produce IL17A, IL17F, and IL22, play a crucial role during the immune response against Mycobacterium tuberculosis (Mtb) infection. Whereas, the contribution of IL17A in immunity to tuberculosis is usually accepted, the role of IL17F has been scarcely studied so far. The aim of...

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Main Authors: Agustín Rolandelli, Joaquín Miguel Pellegrini, Rodrigo Emanuel Hernández Del Pino, Nancy Liliana Tateosian, Nicolás Oscar Amiano, María Paula Morelli, Florencia Andrea Castello, Nicolás Casco, Alberto Levi, Domingo Juan Palmero, Verónica Edith García
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-09-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.02248/full
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author Agustín Rolandelli
Agustín Rolandelli
Joaquín Miguel Pellegrini
Joaquín Miguel Pellegrini
Rodrigo Emanuel Hernández Del Pino
Nancy Liliana Tateosian
Nancy Liliana Tateosian
Nicolás Oscar Amiano
Nicolás Oscar Amiano
María Paula Morelli
María Paula Morelli
Florencia Andrea Castello
Florencia Andrea Castello
Nicolás Casco
Alberto Levi
Domingo Juan Palmero
Verónica Edith García
Verónica Edith García
spellingShingle Agustín Rolandelli
Agustín Rolandelli
Joaquín Miguel Pellegrini
Joaquín Miguel Pellegrini
Rodrigo Emanuel Hernández Del Pino
Nancy Liliana Tateosian
Nancy Liliana Tateosian
Nicolás Oscar Amiano
Nicolás Oscar Amiano
María Paula Morelli
María Paula Morelli
Florencia Andrea Castello
Florencia Andrea Castello
Nicolás Casco
Alberto Levi
Domingo Juan Palmero
Verónica Edith García
Verónica Edith García
The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
Frontiers in Immunology
tuberculosis
Th17
IL17F
single-nucleotide polymorphism
rs763780
immunogenetics
author_facet Agustín Rolandelli
Agustín Rolandelli
Joaquín Miguel Pellegrini
Joaquín Miguel Pellegrini
Rodrigo Emanuel Hernández Del Pino
Nancy Liliana Tateosian
Nancy Liliana Tateosian
Nicolás Oscar Amiano
Nicolás Oscar Amiano
María Paula Morelli
María Paula Morelli
Florencia Andrea Castello
Florencia Andrea Castello
Nicolás Casco
Alberto Levi
Domingo Juan Palmero
Verónica Edith García
Verónica Edith García
author_sort Agustín Rolandelli
title The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
title_short The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
title_full The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
title_fullStr The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
title_full_unstemmed The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in Argentina
title_sort non-synonymous rs763780 single-nucleotide polymorphism in il17f gene is associated with susceptibility to tuberculosis and advanced disease severity in argentina
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-09-01
description Th17 lymphocytes, that produce IL17A, IL17F, and IL22, play a crucial role during the immune response against Mycobacterium tuberculosis (Mtb) infection. Whereas, the contribution of IL17A in immunity to tuberculosis is usually accepted, the role of IL17F has been scarcely studied so far. The aim of this work was to evaluate the existence of a potential association of the non-synonymous variant rs763780 SNP of the IL17F gene with human tuberculosis. Accordingly, by comparing healthy donors (HD) and tuberculosis patients (TB) populations we demonstrated an association between the C allele of the SNP and the susceptibility to tuberculosis disease in Argentina. Furthermore, we found that peripheral blood mononuclear cells (PBMCs) from individuals with a more effective immune response against Mtb secreted the highest levels of IL17F when stimulated with a lysate of Mtb (Mtb-Ag). Besides, we evidenced that Mtb-Ag-stimulated PBMCs from HD carrying the C variant of the SNP displayed the lowest IFNG secretion, proliferation index, and SLAM expression as compared to TT carriers. Moreover, Mtb-Ag-stimulated PBMCs from TB carrying the C allele produced the lowest levels of IFNG, the highest level of IL17A, and the minimum proliferation indexes as compared to TT TB, suggesting a relationship between the C allele and tuberculosis severity. In fact, TB carrying the C allele presented a more severe disease, with the highest bacilli burden in sputum. Together, our findings identify the IL17F rs763780 SNP as a biomarker of tuberculosis susceptibility and advanced disease severity in Argentina, suggesting that IL17F could be a critical cytokine in tuberculosis immunity.
topic tuberculosis
Th17
IL17F
single-nucleotide polymorphism
rs763780
immunogenetics
url https://www.frontiersin.org/article/10.3389/fimmu.2019.02248/full
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spelling doaj-618ddf7308e843f5a3b6169fb90a47662020-11-24T20:53:50ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-09-011010.3389/fimmu.2019.02248459888The Non-synonymous rs763780 Single-Nucleotide Polymorphism in IL17F Gene Is Associated With Susceptibility to Tuberculosis and Advanced Disease Severity in ArgentinaAgustín Rolandelli0Agustín Rolandelli1Joaquín Miguel Pellegrini2Joaquín Miguel Pellegrini3Rodrigo Emanuel Hernández Del Pino4Nancy Liliana Tateosian5Nancy Liliana Tateosian6Nicolás Oscar Amiano7Nicolás Oscar Amiano8María Paula Morelli9María Paula Morelli10Florencia Andrea Castello11Florencia Andrea Castello12Nicolás Casco13Alberto Levi14Domingo Juan Palmero15Verónica Edith García16Verónica Edith García17Department of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaDepartment of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaCenter of Investigation and Transference of National Northwest University of Buenos Aires (CITNOBA), The National Northwest University of Buenos Aires (UNNOBA)-CONICET, Buenos Aires, ArgentinaDepartment of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaDepartment of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaDepartment of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaDepartment of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaTisioneumonology Division, F. J. Muñiz Hospital, Buenos Aires, ArgentinaTisioneumonology Division, F. J. Muñiz Hospital, Buenos Aires, ArgentinaTisioneumonology Division, F. J. Muñiz Hospital, Buenos Aires, ArgentinaDepartment of Biological Chemistry, University of Buenos Aires (UBA), School of Sciences, Buenos Aires, ArgentinaInstitute of Biological Chemistry of Exact and Natural Sciences (IQUIBICEN), National Council of Science and Technology (CONICET), Buenos Aires, ArgentinaTh17 lymphocytes, that produce IL17A, IL17F, and IL22, play a crucial role during the immune response against Mycobacterium tuberculosis (Mtb) infection. Whereas, the contribution of IL17A in immunity to tuberculosis is usually accepted, the role of IL17F has been scarcely studied so far. The aim of this work was to evaluate the existence of a potential association of the non-synonymous variant rs763780 SNP of the IL17F gene with human tuberculosis. Accordingly, by comparing healthy donors (HD) and tuberculosis patients (TB) populations we demonstrated an association between the C allele of the SNP and the susceptibility to tuberculosis disease in Argentina. Furthermore, we found that peripheral blood mononuclear cells (PBMCs) from individuals with a more effective immune response against Mtb secreted the highest levels of IL17F when stimulated with a lysate of Mtb (Mtb-Ag). Besides, we evidenced that Mtb-Ag-stimulated PBMCs from HD carrying the C variant of the SNP displayed the lowest IFNG secretion, proliferation index, and SLAM expression as compared to TT carriers. Moreover, Mtb-Ag-stimulated PBMCs from TB carrying the C allele produced the lowest levels of IFNG, the highest level of IL17A, and the minimum proliferation indexes as compared to TT TB, suggesting a relationship between the C allele and tuberculosis severity. In fact, TB carrying the C allele presented a more severe disease, with the highest bacilli burden in sputum. Together, our findings identify the IL17F rs763780 SNP as a biomarker of tuberculosis susceptibility and advanced disease severity in Argentina, suggesting that IL17F could be a critical cytokine in tuberculosis immunity.https://www.frontiersin.org/article/10.3389/fimmu.2019.02248/fulltuberculosisTh17IL17Fsingle-nucleotide polymorphismrs763780immunogenetics