CD4+ T Responses Other Than Th1 Type Are Preferentially Induced by Latency-Associated Antigens in the State of Latent Mycobacterium tuberculosis Infection
( ) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4 T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial...
Saved in:
Published in | Frontiers in immunology Vol. 10; p. 2807 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
29.11.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | (
) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4
T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated
antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of
infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of
-infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4
T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated
antigens, specifically IL-10 response against Acr in latent
infection. From these results, we surmise a shift in the CD4
T cell response from mixed non-Th1 to Th1 dominant type during TB progression. |
---|---|
AbstractList | Mycobacterium tuberculosis (M. tuberculosis) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4+ T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated M. tuberculosis antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of M. tuberculosis infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of M. tuberculosis-infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4+ T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated M. tuberculosis antigens, specifically IL-10 response against Acr in latent M. tuberculosis infection. From these results, we surmise a shift in the CD4+ T cell response from mixed non-Th1 to Th1 dominant type during TB progression. ( ) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4 T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of -infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4 T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated antigens, specifically IL-10 response against Acr in latent infection. From these results, we surmise a shift in the CD4 T cell response from mixed non-Th1 to Th1 dominant type during TB progression. Mycobacterium tuberculosis (M. tuberculosis) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4+ T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated M. tuberculosis antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of M. tuberculosis infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of M. tuberculosis-infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4+ T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated M. tuberculosis antigens, specifically IL-10 response against Acr in latent M. tuberculosis infection. From these results, we surmise a shift in the CD4+ T cell response from mixed non-Th1 to Th1 dominant type during TB progression.Mycobacterium tuberculosis (M. tuberculosis) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4+ T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated M. tuberculosis antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of M. tuberculosis infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of M. tuberculosis-infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4+ T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated M. tuberculosis antigens, specifically IL-10 response against Acr in latent M. tuberculosis infection. From these results, we surmise a shift in the CD4+ T cell response from mixed non-Th1 to Th1 dominant type during TB progression. Mycobacterium tuberculosis ( M. tuberculosis ) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4 + T cell responses, especially subsets other than Th1 type (non-Th1 type), against these latency-associated M. tuberculosis antigens such as α-crystallin (Acr), heparin-binding hemagglutinin (HBHA), and mycobacterial DNA-binding protein 1 (MDP-1) remain elusive in relation to the clinical stage of M. tuberculosis infection. In the present study, peripheral blood mononuclear cells (PBMCs) collected from different stages of M. tuberculosis -infected cases and control PBMCs were stimulated with these antigens and ESAT-6/CFP-10. Cytokine profiles of CD4 + T cells were evaluated by intracellular cytokine staining using multicolor flow cytometry. Our results demonstrate that Th1 cytokine responses were predominant after TB onset independent of the type of antigen stimulation. On the contrary, non-Th1 cytokine responses were preferentially induced by latency-associated M. tuberculosis antigens, specifically IL-10 response against Acr in latent M. tuberculosis infection. From these results, we surmise a shift in the CD4 + T cell response from mixed non-Th1 to Th1 dominant type during TB progression. |
Author | Osada-Oka, Mayuko Ozeki, Yuriko Terahara, Kazutaka Yamashita, Yoshiro Oe, Toshiyuki Edwards, Tansy Tsunetsugu-Yokota, Yasuko Yasuda, Ikkoh Kawakami, Kenji Matsumoto, Sohkichi Ariyoshi, Koya Tanaka, Takeshi |
AuthorAffiliation | 5 Department of Bacteriology, Niigata University Graduate School of Medicine , Niigata , Japan 7 Tropical Epidemiology Group, London School of Hygiene and Tropical Medicine , London , United Kingdom 2 Department of Respiratory Medicine, National Hospital Organization Higashi-Saga Hospital , Miyaki , Japan 10 Laboratory of Tuberculosis, Institute of Tropical Disease, Universitas Airlangga , Surabaya , Indonesia 1 Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University , Nagasaki , Japan 4 Food Hygiene and Environmental Health, Graduate School of Life and Environmental Science, Kyoto Prefectural University , Kyoto , Japan 6 Department of Immunology, National Institute of Infectious Diseases , Tokyo , Japan 3 Department of Respiratory Medicine, National Hospital Organization Nagasaki-Kawatana Medical Center , Kawatana , Japan 9 Department of Medical Technology, School of Health Science, Tokyo University of Technology , Tokyo , Japan 11 Department of Global Health, Scho |
AuthorAffiliation_xml | – name: 8 Infection Control and Education Center, Nagasaki University Hospital , Nagasaki , Japan – name: 10 Laboratory of Tuberculosis, Institute of Tropical Disease, Universitas Airlangga , Surabaya , Indonesia – name: 4 Food Hygiene and Environmental Health, Graduate School of Life and Environmental Science, Kyoto Prefectural University , Kyoto , Japan – name: 11 Department of Global Health, School of Tropical Medicine and Global Health , Nagasaki , Japan – name: 2 Department of Respiratory Medicine, National Hospital Organization Higashi-Saga Hospital , Miyaki , Japan – name: 3 Department of Respiratory Medicine, National Hospital Organization Nagasaki-Kawatana Medical Center , Kawatana , Japan – name: 5 Department of Bacteriology, Niigata University Graduate School of Medicine , Niigata , Japan – name: 9 Department of Medical Technology, School of Health Science, Tokyo University of Technology , Tokyo , Japan – name: 1 Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University , Nagasaki , Japan – name: 6 Department of Immunology, National Institute of Infectious Diseases , Tokyo , Japan – name: 7 Tropical Epidemiology Group, London School of Hygiene and Tropical Medicine , London , United Kingdom |
Author_xml | – sequence: 1 givenname: Yoshiro surname: Yamashita fullname: Yamashita, Yoshiro – sequence: 2 givenname: Toshiyuki surname: Oe fullname: Oe, Toshiyuki – sequence: 3 givenname: Kenji surname: Kawakami fullname: Kawakami, Kenji – sequence: 4 givenname: Mayuko surname: Osada-Oka fullname: Osada-Oka, Mayuko – sequence: 5 givenname: Yuriko surname: Ozeki fullname: Ozeki, Yuriko – sequence: 6 givenname: Kazutaka surname: Terahara fullname: Terahara, Kazutaka – sequence: 7 givenname: Ikkoh surname: Yasuda fullname: Yasuda, Ikkoh – sequence: 8 givenname: Tansy surname: Edwards fullname: Edwards, Tansy – sequence: 9 givenname: Takeshi surname: Tanaka fullname: Tanaka, Takeshi – sequence: 10 givenname: Yasuko surname: Tsunetsugu-Yokota fullname: Tsunetsugu-Yokota, Yasuko – sequence: 11 givenname: Sohkichi surname: Matsumoto fullname: Matsumoto, Sohkichi – sequence: 12 givenname: Koya surname: Ariyoshi fullname: Ariyoshi, Koya |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31849981$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kstu1DAUhiNUREvpnhXyEglliC9J7A3SaLiNNKgIhrXl2MczrhJ7sBOkvApPiztTqhYJL3w5_s93bP3neXHmg4eieImrBaVcvLVuGKYFqbBYVIRX7ZPiAjcNKykh7OzB_ry4SummyoMJSmn9rDinmDMhOL4ofq_eszdoi75BOgSfIKHrcQ8RbffK5wmj7XwAtIyAvkawEMGPTvX9jNbeTBoM6ma0USN4PZfLlIJ2-WDQMst24BNyHmUe-j7mMAr2pB3Rl1mHTukRopsGNE4dRD31IbmUwRb06IJ_UTy1qk9wdbdeFj8-ftiuPpeb60_r1XJT6rolY1mbtu0obTtCcK0wMzU32taWQ4ttyyqulOlEIzTnnRZUcWMt1cxa0tQaGKaXxfrENUHdyEN0g4qzDMrJYyDEnVRxdLoHaU0mEqFbpRirKqyIIpR0lJiOGcVpZr07sQ5TN4DR-a9R9Y-gj2-828td-CUbLlraiAx4fQeI4ecEaZSDSxr6XnkIU5K5HKesZXWdpa8e1rov8tfcLKhOAh1DStm-ewmu5G0LyWMLydsWkscWyinNPynaZeuyG_m1rv9_4h_xuM8F |
CitedBy_id | crossref_primary_10_1021_acs_bioconjchem_3c00273 crossref_primary_10_1016_j_tube_2025_102615 crossref_primary_10_15616_BSL_2024_30_4_335 crossref_primary_10_1016_j_tube_2020_101966 crossref_primary_10_3389_fimmu_2023_1222428 crossref_primary_10_3389_fimmu_2024_1330796 crossref_primary_10_1016_j_micres_2021_126853 crossref_primary_10_3390_cells9122673 crossref_primary_10_3389_fimmu_2024_1422700 |
Cites_doi | 10.1111/j.1348-0421.1999.tb01232.x 10.1038/nature01152 10.3389/fimmu.2017.00624 10.1016/j.cell.2006.07.035 10.1038/ni.3053 10.1186/1471-2458-8-15 10.1084/jem.184.3.993 10.4049/jimmunol.178.8.5217 10.1146/annurev.iy.07.040189.001045 10.1378/chest.11-3157 10.1371/journal.pone.0051747 10.1056/NEJMsa031667 10.1038/nri1840 10.1128/jb.178.15.4484-4492.1996 10.1371/journal.pone.0042403 10.1038/nri2274 10.1002/eji.201040391 10.4049/jimmunol.176.6.3470 10.1111/j.1365-3083.2012.02776.x 10.1016/S1473-3099(04)01206-X 10.4049/jimmunol.162.4.2347 10.1016/j.immuni.2008.05.007 10.1128/IAI.00614-08 10.1002/eji.201040455 10.1111/j.1365-2958.2009.06959.x 10.1016/j.neulet.2012.10.057 10.1111/j.1462-5822.2007.00892.x 10.1001/jama.282.7.677 10.1038/nri3211 10.1097/01.aids.0000194808.20035.c1 10.1016/j.tube.2006.01.016 10.1146/annurev.immunol.19.1.683 10.1084/jem.20101376 10.1073/pnas.1635213100 10.1038/nri2711 10.1038/nm.3179 10.1183/09031936.00114810 10.1128/JB.180.4.801-808.1998 10.4049/jimmunol.175.1.441 10.1371/journal.pone.0102178 10.4049/jimmunol.1101122 10.7883/yoken.66.207 10.1002/eji.200838693 10.1016/j.micpath.2018.11.029 |
ContentType | Journal Article |
Copyright | Copyright © 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi. Copyright © 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi. 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi |
Copyright_xml | – notice: Copyright © 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi. – notice: Copyright © 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi. 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fimmu.2019.02807 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | PubMed MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1664-3224 |
ExternalDocumentID | oai_doaj_org_article_fdf7429c7aa44001a2a232b32db4da83 PMC6897369 31849981 10_3389_fimmu_2019_02807 |
Genre | Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: Japan Society for the Promotion of Science – fundername: Japan Agency for Medical Research and Development |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AENEX AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK EBS EMOBN GROUPED_DOAJ GX1 HYE KQ8 M48 M~E OK1 PGMZT RNS RPM IPNFZ NPM RIG 7X8 5PM |
ID | FETCH-LOGICAL-c572t-5d77b337b2215a14d58dcf5f8e71f7408aadb969c88bc93a8dff3c4ff265ce413 |
IEDL.DBID | DOA |
ISSN | 1664-3224 |
IngestDate | Wed Aug 27 01:31:27 EDT 2025 Thu Aug 21 13:53:23 EDT 2025 Thu Jul 10 19:11:51 EDT 2025 Mon Jul 21 05:47:38 EDT 2025 Tue Jul 01 00:39:53 EDT 2025 Thu Apr 24 23:04:55 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | MDP-1 Acr latent M. tuberculosis infection HBHA CD4+ T cells non-Th1 |
Language | English |
License | Copyright © 2019 Yamashita, Oe, Kawakami, Osada-Oka, Ozeki, Terahara, Yasuda, Edwards, Tanaka, Tsunetsugu-Yokota, Matsumoto and Ariyoshi. 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. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c572t-5d77b337b2215a14d58dcf5f8e71f7408aadb969c88bc93a8dff3c4ff265ce413 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Sadhna Sharma, Miranda House - University College for Women, India; Roberta Olmo Pinheiro, Oswaldo Cruz Foundation (Fiocruz), Brazil This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology Edited by: Mario Alberto Flores-Valdez, CONACYT Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ), Mexico |
OpenAccessLink | https://doaj.org/article/fdf7429c7aa44001a2a232b32db4da83 |
PMID | 31849981 |
PQID | 2328347455 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_fdf7429c7aa44001a2a232b32db4da83 pubmedcentral_primary_oai_pubmedcentral_nih_gov_6897369 proquest_miscellaneous_2328347455 pubmed_primary_31849981 crossref_primary_10_3389_fimmu_2019_02807 crossref_citationtrail_10_3389_fimmu_2019_02807 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2019-11-29 |
PublicationDateYYYYMMDD | 2019-11-29 |
PublicationDate_xml | – month: 11 year: 2019 text: 2019-11-29 day: 29 |
PublicationDecade | 2010 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in immunology |
PublicationTitleAlternate | Front Immunol |
PublicationYear | 2019 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Horsburgh (B2) 2004; 350 Locht (B11) 2006; 86 Storla (B3) 2008; 8 Pai (B4) 2004; 4 Riou (B43) 2014; 9 Menozzi (B9) 1996; 184 Kinhikar (B39) 2010; 75 Matsumoto (B25) 2005; 175 Caccamo (B42) 2010; 40 Seder (B45) 2008; 8 Ivanov (B15) 2006; 126 Wang (B24) 2012; 531 Larsen (B18) 2012; 7 Laan (B27) 1999; 162 Kim (B31) 2012; 76 Belkaid (B16) 2002; 420 Wachstein (B23) 2012; 7 Shoemaker (B34) 2006; 176 Moore (B21) 2001; 19 Kimura (B30) 2010; 40 Derrick (B40) 2007; 9 Matsumoto (B10) 1999; 43 Mosmann (B14) 1989; 7 Yu (B33) 2015; 16 Yamashita (B36) 2013; 66 Yuan (B8) 1996; 178 Lawn (B13) 2005; 19 Pandey (B20) 2019; 126 Ramakrishnan (B12) 2012; 12 Cunningham (B28) 1998; 180 Yang (B32) 2008; 29 Diel (B7) 2012; 142 Millington (B19) 2007; 178 Wang (B35) 2010; 207 (B6) 2011 Smith (B38) 2008; 76 Gagliani (B26) 2013; 19 Hsu (B37) 2003; 100 Day (B17) 2011; 187 Dye (B1) 1999; 282 Sester (B5) 2011; 37 Pantaleo (B44) 2006; 6 Saraiva (B22) 2010; 10 Amir (B29) 2017; 8 Sutherland (B41) 2009; 39 |
References_xml | – volume: 43 start-page: 1027 year: 1999 ident: B10 article-title: Identification of a novel DNA-binding protein from Mycobacterium bovis bacillus Calmette-Guerin publication-title: Microbiol Immunol. doi: 10.1111/j.1348-0421.1999.tb01232.x – volume: 420 start-page: 502 year: 2002 ident: B16 article-title: CD4+CD25+ regulatory T cells control Leishmania major persistence and immunity publication-title: Nature. doi: 10.1038/nature01152 – volume: 8 start-page: 624 year: 2017 ident: B29 article-title: Diametric role of the latency-associated protein Acr1 of Mycobacterium tuberculosis in modulating the functionality of pre- and post-maturational stages of dendritic cells publication-title: Front Immunol. doi: 10.3389/fimmu.2017.00624 – volume: 126 start-page: 1121 year: 2006 ident: B15 article-title: The orphan nuclear receptor RORgammat directs the differentiation program of proinflammatory IL-17+ T helper cells publication-title: Cell. doi: 10.1016/j.cell.2006.07.035 – volume: 16 start-page: 197 year: 2015 ident: B33 article-title: Dynamic expression of transcription factors T-bet and GATA-3 by regulatory T cells maintains immunotolerance publication-title: Nat Immunol. doi: 10.1038/ni.3053 – volume: 8 start-page: 15 year: 2008 ident: B3 article-title: A systematic review of delay in the diagnosis and treatment of tuberculosis publication-title: BMC Public Health. doi: 10.1186/1471-2458-8-15 – volume: 184 start-page: 993 year: 1996 ident: B9 article-title: Identification of a heparin-binding hemagglutinin present in mycobacteria publication-title: J Exp Med. doi: 10.1084/jem.184.3.993 – volume: 178 start-page: 5217 year: 2007 ident: B19 article-title: Dynamic relationship between IFN-gamma and IL-2 profile of Mycobacterium tuberculosis-specific T cells and antigen load publication-title: J Immunol. doi: 10.4049/jimmunol.178.8.5217 – volume: 7 start-page: 145 year: 1989 ident: B14 article-title: TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties publication-title: Annu Rev Immunol. doi: 10.1146/annurev.iy.07.040189.001045 – volume: 142 start-page: 63 year: 2012 ident: B7 article-title: Predictive value of interferon-gamma release assays and tuberculin skin testing for progression from latent TB infection to disease state: a meta-analysis publication-title: Chest. doi: 10.1378/chest.11-3157 – volume: 7 start-page: e51747 year: 2012 ident: B23 article-title: HSP70 enhances immunosuppressive function of CD4(+)CD25(+)FoxP3(+) T regulatory cells and cytotoxicity in CD4(+)CD25(-) T cells publication-title: PLoS ONE. doi: 10.1371/journal.pone.0051747 – volume: 350 start-page: 2060 year: 2004 ident: B2 article-title: Priorities for the treatment of latent tuberculosis infection in the United States publication-title: N Engl J Med. doi: 10.1056/NEJMsa031667 – volume: 6 start-page: 417 year: 2006 ident: B44 article-title: Functional signatures in antiviral T-cell immunity for monitoring virus-associated diseases publication-title: Nat Rev Immunol. doi: 10.1038/nri1840 – volume: 178 start-page: 4484 year: 1996 ident: B8 article-title: Stationary phase-associated protein expression in Mycobacterium tuberculosis: function of the mycobacterial alpha-crystallin homolog publication-title: J Bacteriol. doi: 10.1128/jb.178.15.4484-4492.1996 – volume: 7 start-page: e42403 year: 2012 ident: B18 article-title: Evaluating cellular polyfunctionality with a novel polyfunctionality index publication-title: PLoS ONE. doi: 10.1371/journal.pone.0042403 – volume: 8 start-page: 247 year: 2008 ident: B45 article-title: T-cell quality in memory and protection: implications for vaccine design publication-title: Nat Rev Immunol. doi: 10.1038/nri2274 – volume: 40 start-page: 1830 year: 2010 ident: B30 article-title: IL-6: regulator of Treg/Th17 balance publication-title: Eur J Immunol. doi: 10.1002/eji.201040391 – volume: 176 start-page: 3470 year: 2006 ident: B34 article-title: GATA-3 directly remodels the IL-10 locus independently of IL-4 in CD4+ T cells publication-title: J Immunol. doi: 10.4049/jimmunol.176.6.3470 – volume: 76 start-page: 580 year: 2012 ident: B31 article-title: The responses of multiple cytokines following incubation of whole blood from TB patients, latently infected individuals and controls with the TB antigens ESAT-6, CFP-10 and TB7.7 publication-title: Scand J Immunol. doi: 10.1111/j.1365-3083.2012.02776.x – volume: 4 start-page: 761 year: 2004 ident: B4 article-title: Interferon-gamma assays in the immunodiagnosis of tuberculosis: a systematic review publication-title: Lancet Infect Dis. doi: 10.1016/S1473-3099(04)01206-X – volume-title: Use of Tuberculosis Interferon-Gamma Release Assays (IGRAs) in Low- and Middle-Income Countries year: 2011 ident: B6 – volume: 162 start-page: 2347 year: 1999 ident: B27 article-title: Neutrophil recruitment by human IL-17 via C-X-C chemokine release in the airways publication-title: J Immunol. doi: 10.4049/jimmunol.162.4.2347 – volume: 29 start-page: 44 year: 2008 ident: B32 article-title: Molecular antagonism and plasticity of regulatory and inflammatory T cell programs publication-title: Immunity. doi: 10.1016/j.immuni.2008.05.007 – volume: 76 start-page: 5478 year: 2008 ident: B38 article-title: Evidence for pore formation in host cell membranes by ESX-1-secreted ESAT-6 and its role in Mycobacterium marinum escape from the vacuole publication-title: Infect Immun. doi: 10.1128/IAI.00614-08 – volume: 40 start-page: 2211 year: 2010 ident: B42 article-title: Multifunctional CD4(+) T cells correlate with active Mycobacterium tuberculosis infection publication-title: Eur J Immunol. doi: 10.1002/eji.201040455 – volume: 75 start-page: 92 year: 2010 ident: B39 article-title: Potential role for ESAT6 in dissemination of M. tuberculosis via human lung epithelial cells publication-title: Mol Microbiol. doi: 10.1111/j.1365-2958.2009.06959.x – volume: 531 start-page: 170 year: 2012 ident: B24 article-title: Alpha-crystallin promotes rat olfactory ensheathing cells survival and proliferation through regulation of PI3K/Akt/mTOR signaling pathways publication-title: Neurosci Lett. doi: 10.1016/j.neulet.2012.10.057 – volume: 9 start-page: 1547 year: 2007 ident: B40 article-title: The ESAT6 protein of Mycobacterium tuberculosis induces apoptosis of macrophages by activating caspase expression publication-title: Cell Microbiol. doi: 10.1111/j.1462-5822.2007.00892.x – volume: 282 start-page: 677 year: 1999 ident: B1 article-title: Consensus statement. Global burden of tuberculosis: estimated incidence, prevalence, and mortality by country WHO Global Surveillance and Monitoring Project publication-title: JAMA. doi: 10.1001/jama.282.7.677 – volume: 12 start-page: 352 year: 2012 ident: B12 article-title: Revisiting the role of the granuloma in tuberculosis publication-title: Nat Rev Immunol. doi: 10.1038/nri3211 – volume: 19 start-page: 2109 year: 2005 ident: B13 article-title: Tuberculosis among HIV-infected patients receiving HAART: long term incidence and risk factors in a South African cohort publication-title: AIDS. doi: 10.1097/01.aids.0000194808.20035.c1 – volume: 86 start-page: 303 year: 2006 ident: B11 article-title: Heparin-binding hemagglutinin, from an extrapulmonary dissemination factor to a powerful diagnostic and protective antigen against tuberculosis publication-title: Tuberculosis. doi: 10.1016/j.tube.2006.01.016 – volume: 19 start-page: 683 year: 2001 ident: B21 article-title: Interleukin-10 and the interleukin-10 receptor publication-title: Annu Rev Immunol. doi: 10.1146/annurev.immunol.19.1.683 – volume: 207 start-page: 2479 year: 2010 ident: B35 article-title: A novel subset of CD4(+) T(H)2 memory/effector cells that produce inflammatory IL-17 cytokine and promote the exacerbation of chronic allergic asthma publication-title: J Exp Med. doi: 10.1084/jem.20101376 – volume: 100 start-page: 12420 year: 2003 ident: B37 article-title: The primary mechanism of attenuation of bacillus Calmette-Guerin is a loss of secreted lytic function required for invasion of lung interstitial tissue publication-title: Proc Natl Acad Sci USA. doi: 10.1073/pnas.1635213100 – volume: 10 start-page: 170 year: 2010 ident: B22 article-title: The regulation of IL-10 production by immune cells publication-title: Nat Rev Immunol. doi: 10.1038/nri2711 – volume: 19 start-page: 739 year: 2013 ident: B26 article-title: Coexpression of CD49b and LAG-3 identifies human and mouse T regulatory type 1 cells publication-title: Nat Med. doi: 10.1038/nm.3179 – volume: 37 start-page: 100 year: 2011 ident: B5 article-title: Interferon-gamma release assays for the diagnosis of active tuberculosis: a systematic review and meta-analysis publication-title: Eur Respir J. doi: 10.1183/09031936.00114810 – volume: 180 start-page: 801 year: 1998 ident: B28 article-title: Mycobacterial stationary phase induced by low oxygen tension: cell wall thickening and localization of the 16-kilodalton alpha-crystallin homolog publication-title: J Bacteriol. doi: 10.1128/JB.180.4.801-808.1998 – volume: 175 start-page: 441 year: 2005 ident: B25 article-title: DNA augments antigenicity of mycobacterial DNA-binding protein 1 and confers protection against Mycobacterium tuberculosis infection in mice publication-title: J Immunol. doi: 10.4049/jimmunol.175.1.441 – volume: 9 start-page: e102178 year: 2014 ident: B43 article-title: A subset of circulating blood mycobacteria-specific CD4 T cells can predict the time to Mycobacterium tuberculosis sputum culture conversion publication-title: PLoS ONE. doi: 10.1371/journal.pone.0102178 – volume: 187 start-page: 2222 year: 2011 ident: B17 article-title: Functional capacity of Mycobacterium tuberculosis-specific T cell responses in humans is associated with mycobacterial load publication-title: J Immunol. doi: 10.4049/jimmunol.1101122 – volume: 66 start-page: 207 year: 2013 ident: B36 article-title: Multicolor flow cytometric analyses of CD4+ T cell responses to Mycobacterium tuberculosis-related latent antigens publication-title: Jpn J Infect Dis. doi: 10.7883/yoken.66.207 – volume: 39 start-page: 723 year: 2009 ident: B41 article-title: Pattern and diversity of cytokine production differentiates between Mycobacterium tuberculosis infection and disease publication-title: Eur J Immunol. doi: 10.1002/eji.200838693 – volume: 126 start-page: 399 year: 2019 ident: B20 article-title: DosR proteins of Mycobacterium tuberculosis upregulate effector T cells and down regulate T regulatory cells in TB patients and their healthy contacts publication-title: Microb Pathog. doi: 10.1016/j.micpath.2018.11.029 |
SSID | ssj0000493335 |
Score | 2.2810543 |
Snippet | (
) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4
T cell responses, especially subsets other than Th1 type... Mycobacterium tuberculosis (M. tuberculosis) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4+ T cell... Mycobacterium tuberculosis ( M. tuberculosis ) produces a diverse range of antigenic proteins in its dormant phase. The cytokine profiles of CD4 + T cell... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 2807 |
SubjectTerms | Acr CD4+ T cells HBHA Immunology latent M. tuberculosis infection MDP-1 non-Th1 |
SummonAdditionalLinks | – databaseName: Scholars Portal Journals: Open Access dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Li9RAEG50RfAivo0vWvAikt2kH-nOQWRdXRZxVGQG9hb66Y5kEp0kYP6Kv9bqJDM6MnjykkOnOul0dXV9laquQugZMSbLNc9iqxIZgz4m4bAyi63UlCubscSHXwOzD9nZgr075-e_j0dPE9jsNe1CPanFujz88b1_BQL_MlicoG-P_HK16kKUVn4YHIXiMroCekkEMZ1NYP_riIUppXz0Ve7tuKObhhT--3Dn3-GTf-ij0xvo-gQk8fHI-Zvokqtuoatjacn-Nvp58oa9wHP8eYyBdQ3-GKAenl-oCi4pDgYo9Hb401RpBES9LHscankYZ7Hu8XsVAHUfb1gIrcdABkuuwcsKw_PwgFVx7UfaFs96AxvEkAC6W-G2025turJulg08eAz7qu6gxenb-clZPNVhiA0XpI25FUJTKjQBfKBSZrm0xnMvnUi9YIlUyuo8y42U2uRUSes9Ncx7knHjQEveRQdVXbn7CDMwyDIvTGI4Ydo5xUUSPN_cEQXIyUXoaMOBwkxJykOtjLIAYyXwrBh4VgSeFQPPIvR82-PbmKDjH7SvA1O3dCG19tBQr78Uk6QW3sI3kdwIpRhscKkiClCnpsRqZpWkEXq6WRIFiGLwr6jK1V1TAJmkTDDOI3RvXCLbV8HWCbalTCMkdhbPzlh271TLiyHddyZzQbP8wf8Y_EN0LUxHOExJ8kfooF137jGgqlY_GYTlF9tLJGM priority: 102 providerName: Scholars Portal |
Title | CD4+ T Responses Other Than Th1 Type Are Preferentially Induced by Latency-Associated Antigens in the State of Latent Mycobacterium tuberculosis Infection |
URI | https://www.ncbi.nlm.nih.gov/pubmed/31849981 https://www.proquest.com/docview/2328347455 https://pubmed.ncbi.nlm.nih.gov/PMC6897369 https://doaj.org/article/fdf7429c7aa44001a2a232b32db4da83 |
Volume | 10 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lj9MwELbQSkhcEG8KCzISF4RCEz9i-7gsLCtEAaGu1Fvkp7arNkWb5JC_sr-WcZxWLUJw4eKDM04sz9jzTWY8g9BrYm2pDC8zp3OZgT4m8bIyy5w0lGtXsjzEXwOzr-X5Bfu84Iu9Ul8xJiylB04LNw0ugPWmrNCagbwVmmgAAYYSZ5jTcsjzCTpvz5i6SriXUsqTXxKsMDUNy_W6i6Fc6l30JooDPTSk6_8Txvw9VHJP95zdQ3dH0IhP0mTvo1u-foBupzKS_UN0c_qBvcVz_CPFu_oGf4uwDs8vdQ1NgaOxCaM9_j5WFYFtvVr1ONbtsN5h0-MvOoLnPtuyC3pPgAzEq8HLGsP78IBL8SYk2hbPeguHwZDsuVvjtjP-2narTbNs4MUpxKt-hC7OPs5Pz7Ox5kJmuSBtxp0QhlJhCGABXTDHpbOBB-lFAYzIpdbOqFJZKY1VVEsXArUsBFJy60EjPkZH9ab2TxFmYHyVQdjccsKM95qLPHq5uScaUJKfoOmWA5UdE5LHuhirCgyTyLNq4FkVeVYNPJugN7sRP1Myjr_Qvo9M3dHFNNpDBwhXNQpX9S_hmqBXW5GoYNtFX4qu_aZrKiCTlAnG-QQ9SSKy-xQck2BHymKCxIHwHMzl8Em9vBxSe5dSCVqqZ_9j8s_Rnbgc8eIkUcfoqL3u_AtAUK15OWwWaD8tCmhnTP4Cst4eHg |
linkProvider | Directory of Open Access Journals |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=CD4%2B+T+Responses+Other+Than+Th1+Type+Are+Preferentially+Induced+by+Latency-Associated+Antigens+in+the+State+of+Latent+Mycobacterium+tuberculosis+Infection&rft.jtitle=Frontiers+in+immunology&rft.au=Yoshiro+Yamashita&rft.au=Toshiyuki+Oe&rft.au=Kenji+Kawakami&rft.au=Mayuko+Osada-Oka&rft.date=2019-11-29&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-3224&rft.volume=10&rft_id=info:doi/10.3389%2Ffimmu.2019.02807&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_fdf7429c7aa44001a2a232b32db4da83 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-3224&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-3224&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-3224&client=summon |