Mycobacterium tuberculosis-Specific T-Cell Responses Are Impaired During Late Pregnancy With Elevated Biomarkers of Tuberculosis Risk Postpartum

Abstract Background Pregnancy is a risk factor for progression from latent tuberculosis infection to symptomatic tuberculosis. However, how pregnancy influences T-cell responses to Mycobacterium tuberculosis is unknown. Methods We measured M. tuberculosis-specific cytokines, T-cell memory markers, a...

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Veröffentlicht in:The Journal of infectious diseases 2022-05, Vol.225 (9), p.1663-1674
Hauptverfasser: Saha, Aparajita, Escuduero, Jaclyn, Layouni, Troy, Richardson, Barbra, Hou, Sharon, Mugo, Nelly, Mujugira, Andrew, Celum, Connie, Baeten, Jared M, Lingappa, Jairam, John-Stewart, Grace C, LaCourse, Sylvia M, Shah, Javeed A
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container_end_page 1674
container_issue 9
container_start_page 1663
container_title The Journal of infectious diseases
container_volume 225
creator Saha, Aparajita
Escuduero, Jaclyn
Layouni, Troy
Richardson, Barbra
Hou, Sharon
Mugo, Nelly
Mujugira, Andrew
Celum, Connie
Baeten, Jared M
Lingappa, Jairam
John-Stewart, Grace C
LaCourse, Sylvia M
Shah, Javeed A
description Abstract Background Pregnancy is a risk factor for progression from latent tuberculosis infection to symptomatic tuberculosis. However, how pregnancy influences T-cell responses to Mycobacterium tuberculosis is unknown. Methods We measured M. tuberculosis-specific cytokines, T-cell memory markers, and overall CD4+ and CD8+ T-cell activation by flow cytometry from 49 women (18 with and 31 without HIV) who became pregnant while enrolled in a randomized controlled trial of preexposure prophylaxis for HIV. We analyzed data using COMPASS, an established statistical method for evaluating overall antigen-specific T-cell responses. Results Pregnant women with latent tuberculosis infection demonstrated significantly diminished M. tuberculosis-specific CD4+ cytokine responses in the third trimester (COMPASS polyfunctional score [PFS], 0.07) compared before (PFS, 0.15), during (PFS, 0.13 and 0.16), and after pregnancy (PFS, 0.14; P = .0084, Kruskal-Wallis test). Paradoxically, M. tuberculosis-specific CD8+ cytokines and nonspecifically activated T-cells increased during late pregnancy. Nonspecific T-cell activation, a validated biomarker for progression from latent tuberculosis infection to tuberculosis disease, increased in latent tuberculosis infection-positive women postpartum, compared with latent tuberculosis infection-negative women. Conclusions Pregnancy-related functional T-cell changes were most pronounced during late pregnancy. Both M. tuberculosis-specific T-cell changes during pregnancy and increases in immune activation postpartum may contribute to increased risk for tuberculosis progression. Clinical Trials Registration NCT0557245. Pregnancy is a risk factor for tuberculosis disease. The influence of pregnancy on Mycobacterium tuberculosis-specific T-cell responses is unknown. M. tuberculosis-specific CD4+T-cell responses were selectively diminished and simplified in the third trimester of pregnancy.
doi_str_mv 10.1093/infdis/jiab614
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However, how pregnancy influences T-cell responses to Mycobacterium tuberculosis is unknown. Methods We measured M. tuberculosis-specific cytokines, T-cell memory markers, and overall CD4+ and CD8+ T-cell activation by flow cytometry from 49 women (18 with and 31 without HIV) who became pregnant while enrolled in a randomized controlled trial of preexposure prophylaxis for HIV. We analyzed data using COMPASS, an established statistical method for evaluating overall antigen-specific T-cell responses. Results Pregnant women with latent tuberculosis infection demonstrated significantly diminished M. tuberculosis-specific CD4+ cytokine responses in the third trimester (COMPASS polyfunctional score [PFS], 0.07) compared before (PFS, 0.15), during (PFS, 0.13 and 0.16), and after pregnancy (PFS, 0.14; P = .0084, Kruskal-Wallis test). Paradoxically, M. tuberculosis-specific CD8+ cytokines and nonspecifically activated T-cells increased during late pregnancy. Nonspecific T-cell activation, a validated biomarker for progression from latent tuberculosis infection to tuberculosis disease, increased in latent tuberculosis infection-positive women postpartum, compared with latent tuberculosis infection-negative women. Conclusions Pregnancy-related functional T-cell changes were most pronounced during late pregnancy. Both M. tuberculosis-specific T-cell changes during pregnancy and increases in immune activation postpartum may contribute to increased risk for tuberculosis progression. Clinical Trials Registration NCT0557245. Pregnancy is a risk factor for tuberculosis disease. The influence of pregnancy on Mycobacterium tuberculosis-specific T-cell responses is unknown. M. tuberculosis-specific CD4+T-cell responses were selectively diminished and simplified in the third trimester of pregnancy.</description><identifier>ISSN: 0022-1899</identifier><identifier>ISSN: 1537-6613</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiab614</identifier><identifier>PMID: 34929030</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Biomarkers ; CD4 antigen ; CD4-Positive T-Lymphocytes ; CD8 antigen ; Cell activation ; Clinical trials ; Cytokines ; Female ; Flow cytometry ; HIV ; HIV Infections ; Human immunodeficiency virus ; Humans ; Immune response ; Immunological memory ; Infections ; Latent Tuberculosis ; Lymphocytes T ; Major and Brief Reports ; Mycobacterium tuberculosis ; Postpartum ; Postpartum Period ; Pregnancy ; Prophylaxis ; Risk factors ; Tuberculosis</subject><ispartof>The Journal of infectious diseases, 2022-05, Vol.225 (9), p.1663-1674</ispartof><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-cbc67c875a1385a76d1cfb257ee694c34d8c24a9cc134f62a0263160bad5466a3</citedby><cites>FETCH-LOGICAL-c452t-cbc67c875a1385a76d1cfb257ee694c34d8c24a9cc134f62a0263160bad5466a3</cites><orcidid>0000-0002-2997-7988 ; 0000-0002-9809-5997 ; 0000-0002-5014-6687</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,1583,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34929030$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saha, Aparajita</creatorcontrib><creatorcontrib>Escuduero, Jaclyn</creatorcontrib><creatorcontrib>Layouni, Troy</creatorcontrib><creatorcontrib>Richardson, Barbra</creatorcontrib><creatorcontrib>Hou, Sharon</creatorcontrib><creatorcontrib>Mugo, Nelly</creatorcontrib><creatorcontrib>Mujugira, Andrew</creatorcontrib><creatorcontrib>Celum, Connie</creatorcontrib><creatorcontrib>Baeten, Jared M</creatorcontrib><creatorcontrib>Lingappa, Jairam</creatorcontrib><creatorcontrib>John-Stewart, Grace C</creatorcontrib><creatorcontrib>LaCourse, Sylvia M</creatorcontrib><creatorcontrib>Shah, Javeed A</creatorcontrib><title>Mycobacterium tuberculosis-Specific T-Cell Responses Are Impaired During Late Pregnancy With Elevated Biomarkers of Tuberculosis Risk Postpartum</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Abstract Background Pregnancy is a risk factor for progression from latent tuberculosis infection to symptomatic tuberculosis. However, how pregnancy influences T-cell responses to Mycobacterium tuberculosis is unknown. Methods We measured M. tuberculosis-specific cytokines, T-cell memory markers, and overall CD4+ and CD8+ T-cell activation by flow cytometry from 49 women (18 with and 31 without HIV) who became pregnant while enrolled in a randomized controlled trial of preexposure prophylaxis for HIV. We analyzed data using COMPASS, an established statistical method for evaluating overall antigen-specific T-cell responses. Results Pregnant women with latent tuberculosis infection demonstrated significantly diminished M. tuberculosis-specific CD4+ cytokine responses in the third trimester (COMPASS polyfunctional score [PFS], 0.07) compared before (PFS, 0.15), during (PFS, 0.13 and 0.16), and after pregnancy (PFS, 0.14; P = .0084, Kruskal-Wallis test). Paradoxically, M. tuberculosis-specific CD8+ cytokines and nonspecifically activated T-cells increased during late pregnancy. Nonspecific T-cell activation, a validated biomarker for progression from latent tuberculosis infection to tuberculosis disease, increased in latent tuberculosis infection-positive women postpartum, compared with latent tuberculosis infection-negative women. Conclusions Pregnancy-related functional T-cell changes were most pronounced during late pregnancy. Both M. tuberculosis-specific T-cell changes during pregnancy and increases in immune activation postpartum may contribute to increased risk for tuberculosis progression. Clinical Trials Registration NCT0557245. Pregnancy is a risk factor for tuberculosis disease. The influence of pregnancy on Mycobacterium tuberculosis-specific T-cell responses is unknown. M. tuberculosis-specific CD4+T-cell responses were selectively diminished and simplified in the third trimester of pregnancy.</description><subject>Biomarkers</subject><subject>CD4 antigen</subject><subject>CD4-Positive T-Lymphocytes</subject><subject>CD8 antigen</subject><subject>Cell activation</subject><subject>Clinical trials</subject><subject>Cytokines</subject><subject>Female</subject><subject>Flow cytometry</subject><subject>HIV</subject><subject>HIV Infections</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunological memory</subject><subject>Infections</subject><subject>Latent Tuberculosis</subject><subject>Lymphocytes T</subject><subject>Major and Brief Reports</subject><subject>Mycobacterium tuberculosis</subject><subject>Postpartum</subject><subject>Postpartum Period</subject><subject>Pregnancy</subject><subject>Prophylaxis</subject><subject>Risk factors</subject><subject>Tuberculosis</subject><issn>0022-1899</issn><issn>1537-6613</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EokvhyhFZ4gKHtP6InfiCVJYClRZRlUUcLceZbL1N4tSOK-2_4CdjtEtVuHAaaeaZdz5ehF5SckKJ4qdu7FoXT7fONJKWj9CCCl4VUlL-GC0IYaygtVJH6FmMW0JIyWX1FB3xUjFFOFmgn1921jfGzhBcGvCcGgg29T66WHybwLrOWbwultD3-Ari5McIEZ8FwBfDZFyAFn9IwY0bvDIz4MsAm9GMdod_uPkan_dwl9Mtfu_8YMINhIh9h9cPpuArF2_wpY_zZMKchufoSWf6CC8O8Rh9_3i-Xn4uVl8_XSzPVoUtBZsL21hZ2boShvJamEq21HYNExWAVKXlZVtbVhplLeVlJ5khTHIqSWNaUUpp-DF6t9edUjNAa2Gcg-n1FFxedKe9cfrvyuiu9cbfaUUqyiqZBd4cBIK_TRBnPbho85_MCD5FzSRlvOZUsIy-_gfd-hTGfF6mJBFUCSUydbKnbPAxBujul6FE_zZb783WB7Nzw6uHJ9zjf9zNwNs94NP0P7FfAdO5bA</recordid><startdate>20220504</startdate><enddate>20220504</enddate><creator>Saha, Aparajita</creator><creator>Escuduero, Jaclyn</creator><creator>Layouni, Troy</creator><creator>Richardson, Barbra</creator><creator>Hou, Sharon</creator><creator>Mugo, Nelly</creator><creator>Mujugira, Andrew</creator><creator>Celum, Connie</creator><creator>Baeten, Jared M</creator><creator>Lingappa, Jairam</creator><creator>John-Stewart, Grace C</creator><creator>LaCourse, Sylvia M</creator><creator>Shah, Javeed A</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2997-7988</orcidid><orcidid>https://orcid.org/0000-0002-9809-5997</orcidid><orcidid>https://orcid.org/0000-0002-5014-6687</orcidid></search><sort><creationdate>20220504</creationdate><title>Mycobacterium tuberculosis-Specific T-Cell Responses Are Impaired During Late Pregnancy With Elevated Biomarkers of Tuberculosis Risk Postpartum</title><author>Saha, Aparajita ; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saha, Aparajita</au><au>Escuduero, Jaclyn</au><au>Layouni, Troy</au><au>Richardson, Barbra</au><au>Hou, Sharon</au><au>Mugo, Nelly</au><au>Mujugira, Andrew</au><au>Celum, Connie</au><au>Baeten, Jared M</au><au>Lingappa, Jairam</au><au>John-Stewart, Grace C</au><au>LaCourse, Sylvia M</au><au>Shah, Javeed A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mycobacterium tuberculosis-Specific T-Cell Responses Are Impaired During Late Pregnancy With Elevated Biomarkers of Tuberculosis Risk Postpartum</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2022-05-04</date><risdate>2022</risdate><volume>225</volume><issue>9</issue><spage>1663</spage><epage>1674</epage><pages>1663-1674</pages><issn>0022-1899</issn><issn>1537-6613</issn><eissn>1537-6613</eissn><abstract>Abstract Background Pregnancy is a risk factor for progression from latent tuberculosis infection to symptomatic tuberculosis. However, how pregnancy influences T-cell responses to Mycobacterium tuberculosis is unknown. Methods We measured M. tuberculosis-specific cytokines, T-cell memory markers, and overall CD4+ and CD8+ T-cell activation by flow cytometry from 49 women (18 with and 31 without HIV) who became pregnant while enrolled in a randomized controlled trial of preexposure prophylaxis for HIV. We analyzed data using COMPASS, an established statistical method for evaluating overall antigen-specific T-cell responses. Results Pregnant women with latent tuberculosis infection demonstrated significantly diminished M. tuberculosis-specific CD4+ cytokine responses in the third trimester (COMPASS polyfunctional score [PFS], 0.07) compared before (PFS, 0.15), during (PFS, 0.13 and 0.16), and after pregnancy (PFS, 0.14; P = .0084, Kruskal-Wallis test). Paradoxically, M. tuberculosis-specific CD8+ cytokines and nonspecifically activated T-cells increased during late pregnancy. Nonspecific T-cell activation, a validated biomarker for progression from latent tuberculosis infection to tuberculosis disease, increased in latent tuberculosis infection-positive women postpartum, compared with latent tuberculosis infection-negative women. Conclusions Pregnancy-related functional T-cell changes were most pronounced during late pregnancy. Both M. tuberculosis-specific T-cell changes during pregnancy and increases in immune activation postpartum may contribute to increased risk for tuberculosis progression. Clinical Trials Registration NCT0557245. Pregnancy is a risk factor for tuberculosis disease. The influence of pregnancy on Mycobacterium tuberculosis-specific T-cell responses is unknown. 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subjects Biomarkers
CD4 antigen
CD4-Positive T-Lymphocytes
CD8 antigen
Cell activation
Clinical trials
Cytokines
Female
Flow cytometry
HIV
HIV Infections
Human immunodeficiency virus
Humans
Immune response
Immunological memory
Infections
Latent Tuberculosis
Lymphocytes T
Major and Brief Reports
Mycobacterium tuberculosis
Postpartum
Postpartum Period
Pregnancy
Prophylaxis
Risk factors
Tuberculosis
title Mycobacterium tuberculosis-Specific T-Cell Responses Are Impaired During Late Pregnancy With Elevated Biomarkers of Tuberculosis Risk Postpartum
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