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Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection
BACKGROUND: Recent studies in adults have characterized differences in systemic inflammation between adults with and without latent tuberculosis infection (LTBI+ vs. LTBI−). Potential differences in systemic inflammation by LTBI status has not been assess in pregnant women. METHODS: We conducted a c...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873478/ https://www.ncbi.nlm.nih.gov/pubmed/33584652 http://dx.doi.org/10.3389/fimmu.2020.587617 |
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author | Naik, Shilpa Alexander, Mallika Kumar, Pavan Kulkarni, Vandana Deshpande, Prasad Yadana, Su Leu, Cheng-Shiun Araújo-Pereira, Mariana Andrade, Bruno B. Bhosale, Ramesh Babu, Subash Gupta, Amita Mathad, Jyoti S. Shivakoti, Rupak |
author_facet | Naik, Shilpa Alexander, Mallika Kumar, Pavan Kulkarni, Vandana Deshpande, Prasad Yadana, Su Leu, Cheng-Shiun Araújo-Pereira, Mariana Andrade, Bruno B. Bhosale, Ramesh Babu, Subash Gupta, Amita Mathad, Jyoti S. Shivakoti, Rupak |
author_sort | Naik, Shilpa |
collection | PubMed |
description | BACKGROUND: Recent studies in adults have characterized differences in systemic inflammation between adults with and without latent tuberculosis infection (LTBI+ vs. LTBI−). Potential differences in systemic inflammation by LTBI status has not been assess in pregnant women. METHODS: We conducted a cohort study of 155 LTBI+ and 65 LTBI− pregnant women, stratified by HIV status, attending an antenatal clinic in Pune, India. LTBI status was assessed by interferon gamma release assay. Plasma was used to measure systemic inflammation markers using immunoassays: IFNβ, CRP, AGP, I-FABP, IFNγ, IL-1β, soluble CD14 (sCD14), sCD163, TNF, IL-6, IL-17a and IL-13. Linear regression models were fit to test the association of LTBI status with each inflammation marker. We also conducted an exploratory analysis using logistic regression to test the association of inflammatory markers with TB progression. RESULTS: Study population was a median age of 23 (Interquartile range: 21–27), 28% undernourished (mid-upper arm circumference (MUAC) <23 cm), 12% were vegetarian, 10% with gestational diabetes and 32% with HIV. In multivariable models, LTBI+ women had significantly lower levels of third trimester AGP, IL1β, sCD163, IL-6 and IL-17a. Interestingly, in exploratory analysis, LTBI+ TB progressors had significantly higher levels of IL1β, IL-6 and IL-13 in multivariable models compared to LTBI+ non-progressors. CONCLUSIONS: Our data shows a distinct systemic immune profile in LTBI+ pregnant women compared to LTBI− women. Data from our exploratory analysis suggest that LTBI+ TB progressors do not have this immune profile, suggesting negative association of this profile with TB progression. If other studies confirm these differences by LTBI status and show a causal relationship with TB progression, this immune profile could identify subsets of LTBI+ pregnant women at high risk for TB progression and who can be targeted for preventative therapy. |
format | Online Article Text |
id | pubmed-7873478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78734782021-02-11 Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection Naik, Shilpa Alexander, Mallika Kumar, Pavan Kulkarni, Vandana Deshpande, Prasad Yadana, Su Leu, Cheng-Shiun Araújo-Pereira, Mariana Andrade, Bruno B. Bhosale, Ramesh Babu, Subash Gupta, Amita Mathad, Jyoti S. Shivakoti, Rupak Front Immunol Immunology BACKGROUND: Recent studies in adults have characterized differences in systemic inflammation between adults with and without latent tuberculosis infection (LTBI+ vs. LTBI−). Potential differences in systemic inflammation by LTBI status has not been assess in pregnant women. METHODS: We conducted a cohort study of 155 LTBI+ and 65 LTBI− pregnant women, stratified by HIV status, attending an antenatal clinic in Pune, India. LTBI status was assessed by interferon gamma release assay. Plasma was used to measure systemic inflammation markers using immunoassays: IFNβ, CRP, AGP, I-FABP, IFNγ, IL-1β, soluble CD14 (sCD14), sCD163, TNF, IL-6, IL-17a and IL-13. Linear regression models were fit to test the association of LTBI status with each inflammation marker. We also conducted an exploratory analysis using logistic regression to test the association of inflammatory markers with TB progression. RESULTS: Study population was a median age of 23 (Interquartile range: 21–27), 28% undernourished (mid-upper arm circumference (MUAC) <23 cm), 12% were vegetarian, 10% with gestational diabetes and 32% with HIV. In multivariable models, LTBI+ women had significantly lower levels of third trimester AGP, IL1β, sCD163, IL-6 and IL-17a. Interestingly, in exploratory analysis, LTBI+ TB progressors had significantly higher levels of IL1β, IL-6 and IL-13 in multivariable models compared to LTBI+ non-progressors. CONCLUSIONS: Our data shows a distinct systemic immune profile in LTBI+ pregnant women compared to LTBI− women. Data from our exploratory analysis suggest that LTBI+ TB progressors do not have this immune profile, suggesting negative association of this profile with TB progression. If other studies confirm these differences by LTBI status and show a causal relationship with TB progression, this immune profile could identify subsets of LTBI+ pregnant women at high risk for TB progression and who can be targeted for preventative therapy. Frontiers Media S.A. 2021-01-27 /pmc/articles/PMC7873478/ /pubmed/33584652 http://dx.doi.org/10.3389/fimmu.2020.587617 Text en Copyright © 2021 Naik, Alexander, Kumar, Kulkarni, Deshpande, Yadana, Leu, Araújo-Pereira, Andrade, Bhosale, Babu, Gupta, Mathad and Shivakoti http://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 | Immunology Naik, Shilpa Alexander, Mallika Kumar, Pavan Kulkarni, Vandana Deshpande, Prasad Yadana, Su Leu, Cheng-Shiun Araújo-Pereira, Mariana Andrade, Bruno B. Bhosale, Ramesh Babu, Subash Gupta, Amita Mathad, Jyoti S. Shivakoti, Rupak Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection |
title | Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection |
title_full | Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection |
title_fullStr | Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection |
title_full_unstemmed | Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection |
title_short | Systemic Inflammation in Pregnant Women With Latent Tuberculosis Infection |
title_sort | systemic inflammation in pregnant women with latent tuberculosis infection |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873478/ https://www.ncbi.nlm.nih.gov/pubmed/33584652 http://dx.doi.org/10.3389/fimmu.2020.587617 |
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