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Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis

OBJECTIVE: Brucellosis is a common bacterial zoonotic infection, and greater than half a million new cases are diagnosed annually. This study investigates the expression of Th2 and Th17 immunity-related factors (Th2-LCR lncRNA, IL-25, TRAF3IP2, and IL-17RB) in different stages of Brucella infections...

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Autores principales: Gheitasi, Reza, Keramat, Fariba, Khosravi, Sara, Hajilooi, Mehrdad, Pletz, Mathias W., Makarewicz, Oliwia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777051/
https://www.ncbi.nlm.nih.gov/pubmed/35071039
http://dx.doi.org/10.3389/fcimb.2021.786994
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author Gheitasi, Reza
Keramat, Fariba
Khosravi, Sara
Hajilooi, Mehrdad
Pletz, Mathias W.
Makarewicz, Oliwia
author_facet Gheitasi, Reza
Keramat, Fariba
Khosravi, Sara
Hajilooi, Mehrdad
Pletz, Mathias W.
Makarewicz, Oliwia
author_sort Gheitasi, Reza
collection PubMed
description OBJECTIVE: Brucellosis is a common bacterial zoonotic infection, and greater than half a million new cases are diagnosed annually. This study investigates the expression of Th2 and Th17 immunity-related factors (Th2-LCR lncRNA, IL-25, TRAF3IP2, and IL-17RB) in different stages of Brucella infections. MATERIAL AND METHODS: In total, 99 brucellosis patients were divided into three groups (acute = first infection before treatment, relapse = before treatment, and treated = after treatment for 6–8 weeks with doxycycline and rifampin). Thirty-three healthy volunteers represented the control group. Gene expression levels were assessed by quantitative amplification in reference to the 18S rRNA gene and statistically evaluated. RESULTS: No significant differences in the expression of these genes were observed between the control group and patients after completion of antibiotic treatment. Compared to these two groups, only Th2-LCR lncRNA and TRAF3IP2 were significantly more highly expressed in the acute group. Th2-LCR lncRNA was also significantly elevated in the relapse group. TRAF3IP2 expression was additionally significantly increased in the acute group compared to the relapse group. CONCLUSION: IL-25 and IL-17RB failed to differentiate between the infected and noninfected groups. TRAF3IP2 and Th2-LCR lncRNA might be good indicators of brucellosis during the acute phase, but the expression levels varied strongly among patients. To verify the suitability of these factors as an indicator for brucellosis, acute infection or relapse should be investigated in further studies on larger cohorts with well-defined inclusion criteria.
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spelling pubmed-87770512022-01-22 Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis Gheitasi, Reza Keramat, Fariba Khosravi, Sara Hajilooi, Mehrdad Pletz, Mathias W. Makarewicz, Oliwia Front Cell Infect Microbiol Cellular and Infection Microbiology OBJECTIVE: Brucellosis is a common bacterial zoonotic infection, and greater than half a million new cases are diagnosed annually. This study investigates the expression of Th2 and Th17 immunity-related factors (Th2-LCR lncRNA, IL-25, TRAF3IP2, and IL-17RB) in different stages of Brucella infections. MATERIAL AND METHODS: In total, 99 brucellosis patients were divided into three groups (acute = first infection before treatment, relapse = before treatment, and treated = after treatment for 6–8 weeks with doxycycline and rifampin). Thirty-three healthy volunteers represented the control group. Gene expression levels were assessed by quantitative amplification in reference to the 18S rRNA gene and statistically evaluated. RESULTS: No significant differences in the expression of these genes were observed between the control group and patients after completion of antibiotic treatment. Compared to these two groups, only Th2-LCR lncRNA and TRAF3IP2 were significantly more highly expressed in the acute group. Th2-LCR lncRNA was also significantly elevated in the relapse group. TRAF3IP2 expression was additionally significantly increased in the acute group compared to the relapse group. CONCLUSION: IL-25 and IL-17RB failed to differentiate between the infected and noninfected groups. TRAF3IP2 and Th2-LCR lncRNA might be good indicators of brucellosis during the acute phase, but the expression levels varied strongly among patients. To verify the suitability of these factors as an indicator for brucellosis, acute infection or relapse should be investigated in further studies on larger cohorts with well-defined inclusion criteria. Frontiers Media S.A. 2022-01-07 /pmc/articles/PMC8777051/ /pubmed/35071039 http://dx.doi.org/10.3389/fcimb.2021.786994 Text en Copyright © 2022 Gheitasi, Keramat, Khosravi, Hajilooi, Pletz and Makarewicz https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Gheitasi, Reza
Keramat, Fariba
Khosravi, Sara
Hajilooi, Mehrdad
Pletz, Mathias W.
Makarewicz, Oliwia
Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis
title Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis
title_full Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis
title_fullStr Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis
title_full_unstemmed Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis
title_short Evaluation of Th2 and Th17 Immunity-Related Factors as Indicators of Brucellosis
title_sort evaluation of th2 and th17 immunity-related factors as indicators of brucellosis
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777051/
https://www.ncbi.nlm.nih.gov/pubmed/35071039
http://dx.doi.org/10.3389/fcimb.2021.786994
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