Circulating activated innate lymphoid cells and mucosal-associated invariant T cells are associated with airflow limitation in patients with asthma
A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune resp...
Saved in:
Published in | Allergology international Vol. 66; no. 2; pp. 302 - 309 |
---|---|
Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier B.V
01.04.2017
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 1323-8930 1440-1592 1440-1592 |
DOI | 10.1016/j.alit.2016.07.005 |
Cover
Loading…
Abstract | A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune responses. In the present study, we investigated whether NK cells, ILCs, and MAIT cells in the peripheral blood of patients with asthma would be associated with clinical asthma parameters.
We recruited 75 adult patients with mild to severe asthma. The peripheral blood mononuclear cells in peripheral venous blood samples from the patients were purified and stained with different combinations of appropriate antibodies. The cells were analyzed by flow cytometry.
The percentage of activated (i.e., CD69+) NK cells in the total NK cell population was negatively correlated with FEV1% which is calculated by the forced expiratory volume in 1 s (FEV1)/the forced vital capacity (FVC). The percentages of CD69+ ILC1s and ILC2s were negatively correlated with FEV1% and %FEV1. The percentage of CD69+ ILC3s was positively correlated with BMI, and the percentage of CD69+ MAIT cells was negatively correlated with FEV1%. Moreover, the percentage of CD69+ NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other.
For the first time, our data showed that activated NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other and may be associated with airflow limitation in patients with asthma.
[Display omitted] |
---|---|
AbstractList | A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune responses. In the present study, we investigated whether NK cells, ILCs, and MAIT cells in the peripheral blood of patients with asthma would be associated with clinical asthma parameters.BACKGROUNDA variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune responses. In the present study, we investigated whether NK cells, ILCs, and MAIT cells in the peripheral blood of patients with asthma would be associated with clinical asthma parameters.We recruited 75 adult patients with mild to severe asthma. The peripheral blood mononuclear cells in peripheral venous blood samples from the patients were purified and stained with different combinations of appropriate antibodies. The cells were analyzed by flow cytometry.METHODSWe recruited 75 adult patients with mild to severe asthma. The peripheral blood mononuclear cells in peripheral venous blood samples from the patients were purified and stained with different combinations of appropriate antibodies. The cells were analyzed by flow cytometry.The percentage of activated (i.e., CD69+) NK cells in the total NK cell population was negatively correlated with FEV1% which is calculated by the forced expiratory volume in 1 s (FEV1)/the forced vital capacity (FVC). The percentages of CD69+ ILC1s and ILC2s were negatively correlated with FEV1% and %FEV1. The percentage of CD69+ ILC3s was positively correlated with BMI, and the percentage of CD69+ MAIT cells was negatively correlated with FEV1%. Moreover, the percentage of CD69+ NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other.RESULTSThe percentage of activated (i.e., CD69+) NK cells in the total NK cell population was negatively correlated with FEV1% which is calculated by the forced expiratory volume in 1 s (FEV1)/the forced vital capacity (FVC). The percentages of CD69+ ILC1s and ILC2s were negatively correlated with FEV1% and %FEV1. The percentage of CD69+ ILC3s was positively correlated with BMI, and the percentage of CD69+ MAIT cells was negatively correlated with FEV1%. Moreover, the percentage of CD69+ NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other.For the first time, our data showed that activated NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other and may be associated with airflow limitation in patients with asthma.CONCLUSIONSFor the first time, our data showed that activated NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other and may be associated with airflow limitation in patients with asthma. A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune responses. In the present study, we investigated whether NK cells, ILCs, and MAIT cells in the peripheral blood of patients with asthma would be associated with clinical asthma parameters. We recruited 75 adult patients with mild to severe asthma. The peripheral blood mononuclear cells in peripheral venous blood samples from the patients were purified and stained with different combinations of appropriate antibodies. The cells were analyzed by flow cytometry. The percentage of activated (i.e., CD69 ) NK cells in the total NK cell population was negatively correlated with FEV % which is calculated by the forced expiratory volume in 1 s (FEV )/the forced vital capacity (FVC). The percentages of CD69 ILC1s and ILC2s were negatively correlated with FEV % and %FEV . The percentage of CD69 ILC3s was positively correlated with BMI, and the percentage of CD69 MAIT cells was negatively correlated with FEV %. Moreover, the percentage of CD69 NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other. For the first time, our data showed that activated NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other and may be associated with airflow limitation in patients with asthma. A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune responses. In the present study, we investigated whether NK cells, ILCs, and MAIT cells in the peripheral blood of patients with asthma would be associated with clinical asthma parameters. We recruited 75 adult patients with mild to severe asthma. The peripheral blood mononuclear cells in peripheral venous blood samples from the patients were purified and stained with different combinations of appropriate antibodies. The cells were analyzed by flow cytometry. The percentage of activated (i.e., CD69+) NK cells in the total NK cell population was negatively correlated with FEV1% which is calculated by the forced expiratory volume in 1 s (FEV1)/the forced vital capacity (FVC). The percentages of CD69+ ILC1s and ILC2s were negatively correlated with FEV1% and %FEV1. The percentage of CD69+ ILC3s was positively correlated with BMI, and the percentage of CD69+ MAIT cells was negatively correlated with FEV1%. Moreover, the percentage of CD69+ NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other. For the first time, our data showed that activated NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other and may be associated with airflow limitation in patients with asthma. [Display omitted] Background: A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated invariant T (MAIT) cells as innate-like T lymphocytes are involved in asthma and may have important effector functions in asthmatic immune responses. In the present study, we investigated whether NK cells, ILCs, and MAIT cells in the peripheral blood of patients with asthma would be associated with clinical asthma parameters. Methods: We recruited 75 adult patients with mild to severe asthma. The peripheral blood mononuclear cells in peripheral venous blood samples from the patients were purified and stained with different combinations of appropriate antibodies. The cells were analyzed by flow cytometry. Results: The percentage of activated (i.e., CD69+) NK cells in the total NK cell population was negatively correlated with FEV1% which is calculated by the forced expiratory volume in 1 s (FEV1)/the forced vital capacity (FVC). The percentages of CD69+ ILC1s and ILC2s were negatively correlated with FEV1% and %FEV1. The percentage of CD69+ ILC3s was positively correlated with BMI, and the percentage of CD69+ MAIT cells was negatively correlated with FEV1%. Moreover, the percentage of CD69+ NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other. Conclusions: For the first time, our data showed that activated NK cells, ILC1s, ILC2s, ILC3s, and MAIT cells were positively correlated with each other and may be associated with airflow limitation in patients with asthma. |
Author | Matsuno, Kei Ishimori, Ayako Ito, Jun Atsuta, Ryo Takahashi, Kazuhisa Ono, Junya Harada, Sonoko Ohta, Shoichiro Harada, Norihiro Makino, Fumihiko Miyake, Sachiko Izuhara, Kenji Chiba, Asako |
Author_xml | – sequence: 1 givenname: Ayako surname: Ishimori fullname: Ishimori, Ayako organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 2 givenname: Norihiro surname: Harada fullname: Harada, Norihiro email: nor@juntendo.ac.jp organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 3 givenname: Asako surname: Chiba fullname: Chiba, Asako organization: Department of Immunology, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 4 givenname: Sonoko surname: Harada fullname: Harada, Sonoko organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 5 givenname: Kei surname: Matsuno fullname: Matsuno, Kei organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 6 givenname: Fumihiko surname: Makino fullname: Makino, Fumihiko organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 7 givenname: Jun surname: Ito fullname: Ito, Jun organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 8 givenname: Shoichiro surname: Ohta fullname: Ohta, Shoichiro organization: Department of Laboratory Medicine, Saga Medical School, Saga, Japan – sequence: 9 givenname: Junya surname: Ono fullname: Ono, Junya organization: Shino-Test Corporation, Kanagawa, Japan – sequence: 10 givenname: Ryo surname: Atsuta fullname: Atsuta, Ryo organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 11 givenname: Kenji surname: Izuhara fullname: Izuhara, Kenji organization: Division of Medical Biochemistry, Department of Biomolecular Sciences, Saga Medical School, Saga, Japan – sequence: 12 givenname: Kazuhisa surname: Takahashi fullname: Takahashi, Kazuhisa organization: Department of Respiratory Medicine, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan – sequence: 13 givenname: Sachiko surname: Miyake fullname: Miyake, Sachiko email: s-miyake@juntendo.ac.jp organization: Department of Immunology, Juntendo University Faculty of Medicine and Graduate School of Medicine, Tokyo, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27575652$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kcuO1DAQRSM0iHnAD7BAWbJJKDtOHEtsUIvHSCOxGdZWxY9pt5y4sd09mu_gh3HT3QixmFWVSufeku69ri6WsJiqekugJUCGD5sWvcstLXsLvAXoX1RXhDFoSC_oRdk72jWj6OCyuk5pA0AoF_xVdUl5z_uhp1fVr5WLaucxu-WhRpXdHrPRtVuWMmv_NG_XwelaGe9TjYuu550KCX2DKQXlTvAeo8Ml1_dnMJr6H-DR5XWNLlofHmvvZpfLv7AUYb0tm1lyOjEpr2d8Xb206JN5c5o31Y8vn-9X35q7719vV5_uGjVwyM1ANU4cR8u6ySg7EWaxR0bYNIDp9GDFqC0IEBOMHAgRQ2eIZkQTYS1Q7G6q26OvDriR2-hmjE8yoJN_DiE-SIzZKW8kVawnWoOxY8e0VpNgI2dAQXVUmEEVr_dHr20MP3cmZTm7dAgDFxN2SZKxF5wKGFlB353Q3TQb_ffxuZQCjEdAxZBSNFaqU2I5ovOSgDz0Lzfy0L889C-By9J_kdL_pGf3Z0UfjyJTwt47E2VSpRRltItG5ZKGe07-G2lIzIU |
CitedBy_id | crossref_primary_10_3389_fimmu_2017_01818 crossref_primary_10_3390_biom12040518 crossref_primary_10_1016_j_alit_2023_07_006 crossref_primary_10_1113_JP284686 crossref_primary_10_3390_cimb46100680 crossref_primary_10_1016_j_alit_2017_03_003 crossref_primary_10_1111_imcb_12011 crossref_primary_10_3390_biom15010122 crossref_primary_10_1016_j_intimp_2022_108606 crossref_primary_10_3389_fimmu_2024_1459961 crossref_primary_10_1016_j_jacig_2025_100410 crossref_primary_10_3390_biom13030538 crossref_primary_10_3389_fimmu_2023_1127588 crossref_primary_10_1016_j_clim_2017_11_009 crossref_primary_10_3389_fimmu_2019_01597 crossref_primary_10_4168_aair_2018_10_5_448 crossref_primary_10_1111_all_14017 crossref_primary_10_1183_16000617_0036_2023 crossref_primary_10_1016_j_alit_2023_06_001 crossref_primary_10_1097_ACI_0000000000000515 crossref_primary_10_2147_JAA_S490832 crossref_primary_10_3389_fimmu_2022_1005226 crossref_primary_10_1159_000487057 crossref_primary_10_3389_fimmu_2018_01333 crossref_primary_10_1016_j_intimp_2021_107485 crossref_primary_10_1038_s41577_019_0191_y |
Cites_doi | 10.1164/rccm.201406-1039OC 10.1126/scitranslmed.3004812 10.1038/nm.3423 10.1111/cei.12277 10.1183/09031936.00059810 10.3389/fimmu.2015.00455 10.1016/j.immuni.2014.01.011 10.1371/journal.pone.0021799 10.1007/s11882-014-0500-2 10.1016/j.rmed.2015.09.016 10.3389/fimmu.2015.00303 10.1182/blood.V97.10.3146 10.1371/journal.pntd.0003627 10.1371/journal.ppat.1004210 10.1056/NEJM199201303260504 10.1038/nature11605 10.4049/jimmunol.173.10.6418 10.1038/nm.2768 10.3389/fimmu.2015.00344 10.1126/science.282.5397.2258 10.1126/scitranslmed.3005374 10.1016/j.jaci.2015.05.037 10.1038/nri3365 10.1182/blood-2013-11-427781 10.1182/blood-2013-11-536888 10.4049/jimmunol.1402945 10.1371/journal.pbio.1000054 10.1016/j.it.2010.09.001 10.1016/j.jaci.2015.01.014 10.1371/journal.pbio.1000070 10.1111/sji.12193 10.1016/j.jaci.2013.05.012 10.1093/intimm/dxr047 10.1111/jgh.13242 10.1056/NEJM200102013440507 10.1097/MIB.0000000000000397 10.1016/j.alit.2015.03.004 10.1084/jem.183.1.195 10.1038/ni1370 10.1038/ni.2104 10.1002/eji.201344160 10.1172/JCI119292 10.1002/art.33314 10.1038/ni.1962 10.1182/blood-2010-08-303339 10.1016/j.jaci.2014.06.024 10.1146/annurev.immunol.17.1.255 10.1038/nm.2678 |
ContentType | Journal Article |
Copyright | 2016 Japanese Society of Allergology Copyright © 2016 Japanese Society of Allergology. Production and hosting by Elsevier B.V. All rights reserved. |
Copyright_xml | – notice: 2016 Japanese Society of Allergology – notice: Copyright © 2016 Japanese Society of Allergology. Production and hosting by Elsevier B.V. All rights reserved. |
DBID | 6I. AAFTH AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 DOA |
DOI | 10.1016/j.alit.2016.07.005 |
DatabaseName | ScienceDirect Open Access Titles Elsevier:ScienceDirect:Open Access CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE |
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 – sequence: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1440-1592 |
EndPage | 309 |
ExternalDocumentID | oai_doaj_org_article_2c451dd0ef834ddcb94874020c329e6c 27575652 10_1016_j_alit_2016_07_005 S1323893016301058 |
Genre | Journal Article |
GroupedDBID | --- .55 0R~ 0SF 1OC 23M 2WC 31~ 4.4 457 53G 5GY 5VS 6I. 7.U 8-1 AACTN AAEDW AAFTH AAIKJ AALRI AAXUO ABMAC ACGFO ACGFS ACXQS ADBBV ADEZE AENEX AEXQZ AFTJW AFZJQ AGHFR AHPSJ AITUG AJAOE ALMA_UNASSIGNED_HOLDINGS AMRAJ AZFZN BAWUL BCNDV BFHJK CAG CO8 COF CS3 DIK E3Z EBS EJD F5P FDB FRJ GROUPED_DOAJ GX1 HZ~ IPNFZ JSF JSH KQ8 LH4 LW6 M41 NCXOZ O9- OK1 P2P P6G RIG RJT RNS ROL RZJ SSZ TKC TR2 X7M YFH YUY AAYWO AAYXX ACVFH ADCNI ADVLN AEUPX AFPUW AIGII AKBMS AKRWK AKYEP CITATION OVT CGR CUY CVF ECM EIF NPM 7X8 |
ID | FETCH-LOGICAL-c670t-62dab7a8f43becfb14fa5a414b60e3d6f98df0909b087011963e1d41d19ff02a3 |
IEDL.DBID | DOA |
ISSN | 1323-8930 1440-1592 |
IngestDate | Wed Aug 27 01:16:32 EDT 2025 Fri Jul 11 12:06:01 EDT 2025 Thu Apr 03 07:04:28 EDT 2025 Tue Jul 01 04:11:26 EDT 2025 Thu Apr 24 23:01:26 EDT 2025 Fri Feb 23 02:29:21 EST 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 2 |
Keywords | FeNO ILC TCR Innate lymphoid cell ALX ILC2 ILC3 R20 IFN-γ ILC1 MAIT X5 Airflow limitation IL R5 FOT PBMC Asthma Natural killer cell PEF Mucosal-associated invariant T cell ACT FVC GINA FEV1 Fres NK COPD |
Language | English |
License | This is an open access article under the CC BY-NC-ND license. Copyright © 2016 Japanese Society of Allergology. Production and hosting by Elsevier B.V. All rights reserved. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c670t-62dab7a8f43becfb14fa5a414b60e3d6f98df0909b087011963e1d41d19ff02a3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://doaj.org/article/2c451dd0ef834ddcb94874020c329e6c |
PMID | 27575652 |
PQID | 1859729084 |
PQPubID | 23479 |
PageCount | 8 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_2c451dd0ef834ddcb94874020c329e6c proquest_miscellaneous_1859729084 pubmed_primary_27575652 crossref_citationtrail_10_1016_j_alit_2016_07_005 crossref_primary_10_1016_j_alit_2016_07_005 elsevier_sciencedirect_doi_10_1016_j_alit_2016_07_005 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2017-04-01 |
PublicationDateYYYYMMDD | 2017-04-01 |
PublicationDate_xml | – month: 04 year: 2017 text: 2017-04-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Allergology international |
PublicationTitleAlternate | Allergol Int |
PublicationYear | 2017 |
Publisher | Elsevier B.V Elsevier |
Publisher_xml | – name: Elsevier B.V – name: Elsevier |
References | Jo, Tan, Ussher, Sandalova, Tang, Tan-Garcia (bib22) 2014; 10 Busse, Lemanske (bib1) 2001; 344 Jackson, Makrinioti, Rana, Shamji, Trujillo-Torralbo, Footitt (bib40) 2014; 190 Martin, Treiner, Duban, Guerri, Laude, Toly (bib19) 2009; 7 Spits, Di Santo (bib15) 2011; 12 Novak, Dobrovolny, Novakova, Kozak (bib37) 2014; 80 Global Initiative for Asthma (GINA). Global Strategy for Asthma Management and Prevention. Updated 2014. Available from Halim, Steer, Matha, Gold, Martinez-Gonzalez, McNagny (bib42) 2014; 40 Edwards, McGinley, McGuinness, Mills (bib18) 2015; 6 Barnig, Cernadas, Dutile, Liu, Perrella, Kazani (bib28) 2013; 5 Chiba, Tajima, Tomi, Miyazaki, Yamamura, Miyake (bib10) 2012; 64 Hazenberg, Spits (bib14) 2014; 124 Holt, Sly (bib38) 2012; 18 Wenzel (bib4) 2012; 18 Dalbeth, Gundle, Davies, Lee, McMichael, Callan (bib34) 2004; 173 Kim, Siracusa, Saenz, Noti, Monticelli, Sonnenberg (bib27) 2013; 5 . Spits, Artis, Colonna, Diefenbach, Di Santo, Eberl (bib13) 2013; 13 Mathias (bib39) 2015; 15 Munneke, Bjorklund, Mjosberg, Garming-Legert, Bernink, Blom (bib33) 2014; 124 Taube, Tertilt, Gyulveszi, Dehzad, Kreymborg, Schneeweiss (bib44) 2011; 6 Gapin (bib8) 2009; 7 Croxford, Miyake, Huang, Shimamura, Yamamura (bib11) 2006; 7 Cooper, Fehniger, Turner, Chen, Ghaheri, Ghayur (bib35) 2001; 97 Nausch, Appleby, Sparks, Midzi, Mduluza, Mutapi (bib25) 2015; 9 Willing, Leach, Ufer, Attfield, Steinbach, Kursawe (bib24) 2014; 44 Saenz, Noti, Artis (bib16) 2010; 31 Bartemes, Kephart, Fox, Kita (bib47) 2014; 134 Haga, Chiba, Shibuya, Osada, Ishikawa, Kodani (bib49) 2015; 31 Miyazaki, Miyake, Chiba, Lantz, Yamamura (bib23) 2011; 23 Barlow, Peel, Fox, Panova, Hardman, Camelo (bib41) 2013; 132 Serriari, Eoche, Lamotte, Lion, Fumery, Marcelo (bib50) 2014; 176 Hiejima, Kawai, Nakase, Tsuruyama, Morimoto, Yasumi (bib36) 2015; 21 Foster, Hogan, Ramsay, Matthaei, Young (bib6) 1996; 183 Hinks, Zhou, Staples, Dimitrov, Manta, Petrossian (bib9) 2015; 136 Dusseaux, Martin, Serriari, Peguillet, Premel, Louis (bib20) 2011; 117 Wills-Karp (bib2) 1999; 17 Robinson, Hamid, Ying, Tsicopoulos, Barkans, Bentley (bib3) 1992; 326 Kim, Lee, Chang, Pichavant, Shore, Fitzgerald (bib43) 2014; 20 Kjer-Nielsen, Patel, Corbett, Le Nours, Meehan, Liu (bib21) 2012; 491 Liu, Wu, Zhao, Wang, Zhang, Liu (bib48) 2015; 109 Hogan, Mould, Kikutani, Ramsay, Foster (bib5) 1997; 99 Carolan, Tobin, Mangan, Corrigan, Gaoatswe, Byrne (bib45) 2015; 194 Smith, Chen, Kjarsgaard, Huang, Oliveria, O'Byrne (bib46) 2016; 137 Howson, Salio, Cerundolo (bib12) 2015; 6 Napier, Adams, Gold, Lewinsohn (bib17) 2015; 6 Wills-Karp, Luyimbazi, Xu, Schofield, Neben, Karp (bib7) 1998; 282 Global Initiative for Chronic Obstructive Lung Disease (GOLD). Global Strategy for Diagnosis, Management, and Prevention of COPD. Updated 2006. Available from Okamoto, Hoshino, Kitasato, Sakazaki, Kawayama, Fujimoto (bib32) 2011; 37 Kabata, Moro, Koyasu, Asano (bib29) 2015; 64 Mjosberg, Trifari, Crellin, Peters, van Drunen, Piet (bib26) 2011; 12 Foster (10.1016/j.alit.2016.07.005_bib6) 1996; 183 Halim (10.1016/j.alit.2016.07.005_bib42) 2014; 40 Hazenberg (10.1016/j.alit.2016.07.005_bib14) 2014; 124 Martin (10.1016/j.alit.2016.07.005_bib19) 2009; 7 Kim (10.1016/j.alit.2016.07.005_bib27) 2013; 5 Spits (10.1016/j.alit.2016.07.005_bib13) 2013; 13 Okamoto (10.1016/j.alit.2016.07.005_bib32) 2011; 37 Hinks (10.1016/j.alit.2016.07.005_bib9) 2015; 136 Barnig (10.1016/j.alit.2016.07.005_bib28) 2013; 5 Chiba (10.1016/j.alit.2016.07.005_bib10) 2012; 64 Croxford (10.1016/j.alit.2016.07.005_bib11) 2006; 7 Kjer-Nielsen (10.1016/j.alit.2016.07.005_bib21) 2012; 491 Mathias (10.1016/j.alit.2016.07.005_bib39) 2015; 15 Wills-Karp (10.1016/j.alit.2016.07.005_bib7) 1998; 282 Holt (10.1016/j.alit.2016.07.005_bib38) 2012; 18 Dusseaux (10.1016/j.alit.2016.07.005_bib20) 2011; 117 Wills-Karp (10.1016/j.alit.2016.07.005_bib2) 1999; 17 Kabata (10.1016/j.alit.2016.07.005_bib29) 2015; 64 Saenz (10.1016/j.alit.2016.07.005_bib16) 2010; 31 Carolan (10.1016/j.alit.2016.07.005_bib45) 2015; 194 Edwards (10.1016/j.alit.2016.07.005_bib18) 2015; 6 Willing (10.1016/j.alit.2016.07.005_bib24) 2014; 44 Cooper (10.1016/j.alit.2016.07.005_bib35) 2001; 97 Haga (10.1016/j.alit.2016.07.005_bib49) 2015; 31 Liu (10.1016/j.alit.2016.07.005_bib48) 2015; 109 Miyazaki (10.1016/j.alit.2016.07.005_bib23) 2011; 23 Gapin (10.1016/j.alit.2016.07.005_bib8) 2009; 7 Bartemes (10.1016/j.alit.2016.07.005_bib47) 2014; 134 Taube (10.1016/j.alit.2016.07.005_bib44) 2011; 6 Busse (10.1016/j.alit.2016.07.005_bib1) 2001; 344 Spits (10.1016/j.alit.2016.07.005_bib15) 2011; 12 Munneke (10.1016/j.alit.2016.07.005_bib33) 2014; 124 10.1016/j.alit.2016.07.005_bib30 10.1016/j.alit.2016.07.005_bib31 Hiejima (10.1016/j.alit.2016.07.005_bib36) 2015; 21 Dalbeth (10.1016/j.alit.2016.07.005_bib34) 2004; 173 Novak (10.1016/j.alit.2016.07.005_bib37) 2014; 80 Kim (10.1016/j.alit.2016.07.005_bib43) 2014; 20 Napier (10.1016/j.alit.2016.07.005_bib17) 2015; 6 Barlow (10.1016/j.alit.2016.07.005_bib41) 2013; 132 Mjosberg (10.1016/j.alit.2016.07.005_bib26) 2011; 12 Smith (10.1016/j.alit.2016.07.005_bib46) 2016; 137 Hogan (10.1016/j.alit.2016.07.005_bib5) 1997; 99 Serriari (10.1016/j.alit.2016.07.005_bib50) 2014; 176 Jackson (10.1016/j.alit.2016.07.005_bib40) 2014; 190 Wenzel (10.1016/j.alit.2016.07.005_bib4) 2012; 18 Jo (10.1016/j.alit.2016.07.005_bib22) 2014; 10 Howson (10.1016/j.alit.2016.07.005_bib12) 2015; 6 Nausch (10.1016/j.alit.2016.07.005_bib25) 2015; 9 Robinson (10.1016/j.alit.2016.07.005_bib3) 1992; 326 |
References_xml | – volume: 7 start-page: 987 year: 2006 end-page: 994 ident: bib11 article-title: Invariant V(alpha)19i T cells regulate autoimmune inflammation publication-title: Nat Immunol – volume: 194 start-page: 5775 year: 2015 end-page: 5780 ident: bib45 article-title: Altered distribution and increased IL-17 production by mucosal-associated invariant T cells in adult and childhood obesity publication-title: J Immunol – volume: 282 start-page: 2258 year: 1998 end-page: 2261 ident: bib7 article-title: Interleukin-13: central mediator of allergic asthma publication-title: Science – volume: 12 start-page: 21 year: 2011 end-page: 27 ident: bib15 article-title: The expanding family of innate lymphoid cells: regulators and effectors of immunity and tissue remodeling publication-title: Nat Immunol – volume: 326 start-page: 298 year: 1992 end-page: 304 ident: bib3 article-title: Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma publication-title: N Engl J Med – volume: 134 start-page: 671 year: 2014 end-page: 678.e4 ident: bib47 article-title: Enhanced innate type 2 immune response in peripheral blood from patients with asthma publication-title: J Allergy Clin Immunol – volume: 18 start-page: 716 year: 2012 end-page: 725 ident: bib4 article-title: Asthma phenotypes: the evolution from clinical to molecular approaches publication-title: Nat Med – volume: 9 start-page: e0003627 year: 2015 ident: bib25 article-title: Group 2 innate lymphoid cell proportions are diminished in young helminth infected children and restored by curative anti-helminthic treatment publication-title: PLoS Negl Trop Dis – volume: 183 start-page: 195 year: 1996 end-page: 201 ident: bib6 article-title: Interleukin 5 deficiency abolishes eosinophilia, airways hyperreactivity, and lung damage in a mouse asthma model publication-title: J Exp Med – volume: 20 start-page: 54 year: 2014 end-page: 61 ident: bib43 article-title: Interleukin-17-producing innate lymphoid cells and the NLRP3 inflammasome facilitate obesity-associated airway hyperreactivity publication-title: Nat Med – volume: 6 start-page: 344 year: 2015 ident: bib17 article-title: The role of mucosal associated invariant T cells in antimicrobial immunity publication-title: Front Immunol – volume: 124 start-page: 812 year: 2014 end-page: 821 ident: bib33 article-title: Activated innate lymphoid cells are associated with a reduced susceptibility to graft-versus-host disease publication-title: Blood – volume: 64 start-page: 227 year: 2015 end-page: 234 ident: bib29 article-title: Group 2 innate lymphoid cells and asthma publication-title: Allergol Int – volume: 124 start-page: 700 year: 2014 end-page: 709 ident: bib14 article-title: Human innate lymphoid cells publication-title: Blood – volume: 137 start-page: 75 year: 2016 end-page: 86.e8 ident: bib46 article-title: Increased numbers of activated group 2 innate lymphoid cells in the airways of patients with severe asthma and persistent airway eosinophilia publication-title: J Allergy Clin Immunol – volume: 7 start-page: e54 year: 2009 ident: bib19 article-title: Stepwise development of MAIT cells in mouse and human publication-title: PLoS Biol – volume: 13 start-page: 145 year: 2013 end-page: 149 ident: bib13 article-title: Innate lymphoid cells – a proposal for uniform nomenclature publication-title: Nat Rev Immunol – volume: 37 start-page: 1119 year: 2011 end-page: 1127 ident: bib32 article-title: Periostin, a matrix protein, is a novel biomarker for idiopathic interstitial pneumonias publication-title: Eur Respir J – volume: 6 start-page: 303 year: 2015 ident: bib12 article-title: MR1-restricted mucosal-associated invariant T cells and their activation during infectious diseases publication-title: Front Immunol – volume: 491 start-page: 717 year: 2012 end-page: 723 ident: bib21 article-title: MR1 presents microbial vitamin B metabolites to MAIT cells publication-title: Nature – volume: 344 start-page: 350 year: 2001 end-page: 362 ident: bib1 article-title: Asthma publication-title: N Engl J Med – volume: 136 start-page: 323 year: 2015 end-page: 333 ident: bib9 article-title: Innate and adaptive T cells in asthmatic patients: relationship to severity and disease mechanisms publication-title: J Allergy Clin Immunol – volume: 6 start-page: 455 year: 2015 ident: bib18 article-title: Gammadelta T cells and NK cells – distinct pathogenic roles as innate-like immune cells in CNS autoimmunity publication-title: Front Immunol – volume: 64 start-page: 153 year: 2012 end-page: 161 ident: bib10 article-title: Mucosal-associated invariant T cells promote inflammation and exacerbate disease in murine models of arthritis publication-title: Arthritis Rheum – volume: 190 start-page: 1373 year: 2014 end-page: 1382 ident: bib40 article-title: IL-33-dependent type 2 inflammation during rhinovirus-induced asthma exacerbations in vivo publication-title: Am J Respir Crit Care Med – volume: 12 start-page: 1055 year: 2011 end-page: 1062 ident: bib26 article-title: Human IL-25- and IL-33-responsive type 2 innate lymphoid cells are defined by expression of CRTH2 and CD161 publication-title: Nat Immunol – volume: 15 start-page: 500 year: 2015 ident: bib39 article-title: Natural killer cells in the development of asthma publication-title: Curr Allergy Asthma Rep – volume: 176 start-page: 266 year: 2014 end-page: 274 ident: bib50 article-title: Innate mucosal-associated invariant T (MAIT) cells are activated in inflammatory bowel diseases publication-title: Clin Exp Immunol – volume: 23 start-page: 529 year: 2011 end-page: 535 ident: bib23 article-title: Mucosal-associated invariant T cells regulate Th1 response in multiple sclerosis publication-title: Int Immunol – volume: 10 start-page: e1004210 year: 2014 ident: bib22 article-title: Toll-like receptor 8 agonist and bacteria trigger potent activation of innate immune cells in human liver publication-title: PLoS Pathog – volume: 132 start-page: 933 year: 2013 end-page: 941 ident: bib41 article-title: IL-33 is more potent than IL-25 in provoking IL-13-producing nuocytes (type 2 innate lymphoid cells) and airway contraction publication-title: J Allergy Clin Immunol – volume: 6 start-page: e21799 year: 2011 ident: bib44 article-title: IL-22 is produced by innate lymphoid cells and limits inflammation in allergic airway disease publication-title: PLoS One – volume: 5 start-page: 174ra26 year: 2013 ident: bib28 article-title: Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma publication-title: Sci Transl Med – volume: 5 start-page: 170ra16 year: 2013 ident: bib27 article-title: TSLP elicits IL-33-independent innate lymphoid cell responses to promote skin inflammation publication-title: Sci Transl Med – volume: 117 start-page: 1250 year: 2011 end-page: 1259 ident: bib20 article-title: Human MAIT cells are xenobiotic-resistant, tissue-targeted, CD161hi IL-17-secreting T cells publication-title: Blood – volume: 44 start-page: 3119 year: 2014 end-page: 3128 ident: bib24 article-title: CD8(+) MAIT cells infiltrate into the CNS and alterations in their blood frequencies correlate with IL-18 serum levels in multiple sclerosis publication-title: Eur J Immunol – volume: 173 start-page: 6418 year: 2004 end-page: 6426 ident: bib34 article-title: CD56bright NK cells are enriched at inflammatory sites and can engage with monocytes in a reciprocal program of activation publication-title: J Immunol – volume: 31 start-page: 965 year: 2015 end-page: 972 ident: bib49 article-title: MAIT cells are activated and accumulated in the inflamed mucosa of ulcerative colitis publication-title: J Gastroenterol Hepatol – volume: 99 start-page: 1329 year: 1997 end-page: 1339 ident: bib5 article-title: Aeroallergen-induced eosinophilic inflammation, lung damage, and airways hyperreactivity in mice can occur independently of IL-4 and allergen-specific immunoglobulins publication-title: J Clin Invest – reference: Global Initiative for Chronic Obstructive Lung Disease (GOLD). Global Strategy for Diagnosis, Management, and Prevention of COPD. Updated 2006. Available from: – volume: 18 start-page: 726 year: 2012 end-page: 735 ident: bib38 article-title: Viral infections and atopy in asthma pathogenesis: new rationales for asthma prevention and treatment publication-title: Nat Med – reference: Global Initiative for Asthma (GINA). Global Strategy for Asthma Management and Prevention. Updated 2014. Available from: – volume: 21 start-page: 1529 year: 2015 end-page: 1540 ident: bib36 article-title: Reduced numbers and proapoptotic features of mucosal-associated invariant T cells as a characteristic finding in patients with inflammatory bowel disease publication-title: Inflamm Bowel Dis – volume: 109 start-page: 1391 year: 2015 end-page: 1396 ident: bib48 article-title: Type 2 innate lymphoid cells: a novel biomarker of eosinophilic airway inflammation in patients with mild to moderate asthma publication-title: Respir Med – volume: 31 start-page: 407 year: 2010 end-page: 413 ident: bib16 article-title: Innate immune cell populations function as initiators and effectors in Th2 cytokine responses publication-title: Trends Immunol – volume: 80 start-page: 271 year: 2014 end-page: 275 ident: bib37 article-title: The decrease in number and change in phenotype of mucosal-associated invariant T cells in the elderly and differences in men and women of reproductive age publication-title: Scand J Immunol – volume: 17 start-page: 255 year: 1999 end-page: 281 ident: bib2 article-title: Immunologic basis of antigen-induced airway hyperresponsiveness publication-title: Annu Rev Immunol – reference: . – volume: 97 start-page: 3146 year: 2001 end-page: 3151 ident: bib35 article-title: Human natural killer cells: a unique innate immunoregulatory role for the CD56(bright) subset publication-title: Blood – volume: 7 start-page: e70 year: 2009 ident: bib8 article-title: Where do MAIT cells fit in the family of unconventional T cells? publication-title: PLoS Biol – volume: 40 start-page: 425 year: 2014 end-page: 435 ident: bib42 article-title: Group 2 innate lymphoid cells are critical for the initiation of adaptive T helper 2 cell-mediated allergic lung inflammation publication-title: Immunity – volume: 190 start-page: 1373 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib40 article-title: IL-33-dependent type 2 inflammation during rhinovirus-induced asthma exacerbations in vivo publication-title: Am J Respir Crit Care Med doi: 10.1164/rccm.201406-1039OC – volume: 5 start-page: 174ra26 year: 2013 ident: 10.1016/j.alit.2016.07.005_bib28 article-title: Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma publication-title: Sci Transl Med doi: 10.1126/scitranslmed.3004812 – volume: 20 start-page: 54 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib43 article-title: Interleukin-17-producing innate lymphoid cells and the NLRP3 inflammasome facilitate obesity-associated airway hyperreactivity publication-title: Nat Med doi: 10.1038/nm.3423 – volume: 176 start-page: 266 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib50 article-title: Innate mucosal-associated invariant T (MAIT) cells are activated in inflammatory bowel diseases publication-title: Clin Exp Immunol doi: 10.1111/cei.12277 – volume: 37 start-page: 1119 year: 2011 ident: 10.1016/j.alit.2016.07.005_bib32 article-title: Periostin, a matrix protein, is a novel biomarker for idiopathic interstitial pneumonias publication-title: Eur Respir J doi: 10.1183/09031936.00059810 – volume: 6 start-page: 455 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib18 article-title: Gammadelta T cells and NK cells – distinct pathogenic roles as innate-like immune cells in CNS autoimmunity publication-title: Front Immunol doi: 10.3389/fimmu.2015.00455 – volume: 40 start-page: 425 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib42 article-title: Group 2 innate lymphoid cells are critical for the initiation of adaptive T helper 2 cell-mediated allergic lung inflammation publication-title: Immunity doi: 10.1016/j.immuni.2014.01.011 – volume: 6 start-page: e21799 year: 2011 ident: 10.1016/j.alit.2016.07.005_bib44 article-title: IL-22 is produced by innate lymphoid cells and limits inflammation in allergic airway disease publication-title: PLoS One doi: 10.1371/journal.pone.0021799 – volume: 15 start-page: 500 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib39 article-title: Natural killer cells in the development of asthma publication-title: Curr Allergy Asthma Rep doi: 10.1007/s11882-014-0500-2 – volume: 109 start-page: 1391 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib48 article-title: Type 2 innate lymphoid cells: a novel biomarker of eosinophilic airway inflammation in patients with mild to moderate asthma publication-title: Respir Med doi: 10.1016/j.rmed.2015.09.016 – volume: 6 start-page: 303 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib12 article-title: MR1-restricted mucosal-associated invariant T cells and their activation during infectious diseases publication-title: Front Immunol doi: 10.3389/fimmu.2015.00303 – volume: 97 start-page: 3146 year: 2001 ident: 10.1016/j.alit.2016.07.005_bib35 article-title: Human natural killer cells: a unique innate immunoregulatory role for the CD56(bright) subset publication-title: Blood doi: 10.1182/blood.V97.10.3146 – volume: 9 start-page: e0003627 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib25 article-title: Group 2 innate lymphoid cell proportions are diminished in young helminth infected children and restored by curative anti-helminthic treatment publication-title: PLoS Negl Trop Dis doi: 10.1371/journal.pntd.0003627 – volume: 10 start-page: e1004210 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib22 article-title: Toll-like receptor 8 agonist and bacteria trigger potent activation of innate immune cells in human liver publication-title: PLoS Pathog doi: 10.1371/journal.ppat.1004210 – volume: 326 start-page: 298 year: 1992 ident: 10.1016/j.alit.2016.07.005_bib3 article-title: Predominant TH2-like bronchoalveolar T-lymphocyte population in atopic asthma publication-title: N Engl J Med doi: 10.1056/NEJM199201303260504 – ident: 10.1016/j.alit.2016.07.005_bib31 – volume: 491 start-page: 717 year: 2012 ident: 10.1016/j.alit.2016.07.005_bib21 article-title: MR1 presents microbial vitamin B metabolites to MAIT cells publication-title: Nature doi: 10.1038/nature11605 – volume: 173 start-page: 6418 year: 2004 ident: 10.1016/j.alit.2016.07.005_bib34 article-title: CD56bright NK cells are enriched at inflammatory sites and can engage with monocytes in a reciprocal program of activation publication-title: J Immunol doi: 10.4049/jimmunol.173.10.6418 – volume: 18 start-page: 726 year: 2012 ident: 10.1016/j.alit.2016.07.005_bib38 article-title: Viral infections and atopy in asthma pathogenesis: new rationales for asthma prevention and treatment publication-title: Nat Med doi: 10.1038/nm.2768 – volume: 6 start-page: 344 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib17 article-title: The role of mucosal associated invariant T cells in antimicrobial immunity publication-title: Front Immunol doi: 10.3389/fimmu.2015.00344 – volume: 282 start-page: 2258 year: 1998 ident: 10.1016/j.alit.2016.07.005_bib7 article-title: Interleukin-13: central mediator of allergic asthma publication-title: Science doi: 10.1126/science.282.5397.2258 – volume: 5 start-page: 170ra16 year: 2013 ident: 10.1016/j.alit.2016.07.005_bib27 article-title: TSLP elicits IL-33-independent innate lymphoid cell responses to promote skin inflammation publication-title: Sci Transl Med doi: 10.1126/scitranslmed.3005374 – volume: 137 start-page: 75 year: 2016 ident: 10.1016/j.alit.2016.07.005_bib46 article-title: Increased numbers of activated group 2 innate lymphoid cells in the airways of patients with severe asthma and persistent airway eosinophilia publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2015.05.037 – volume: 13 start-page: 145 year: 2013 ident: 10.1016/j.alit.2016.07.005_bib13 article-title: Innate lymphoid cells – a proposal for uniform nomenclature publication-title: Nat Rev Immunol doi: 10.1038/nri3365 – volume: 124 start-page: 700 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib14 article-title: Human innate lymphoid cells publication-title: Blood doi: 10.1182/blood-2013-11-427781 – volume: 124 start-page: 812 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib33 article-title: Activated innate lymphoid cells are associated with a reduced susceptibility to graft-versus-host disease publication-title: Blood doi: 10.1182/blood-2013-11-536888 – volume: 194 start-page: 5775 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib45 article-title: Altered distribution and increased IL-17 production by mucosal-associated invariant T cells in adult and childhood obesity publication-title: J Immunol doi: 10.4049/jimmunol.1402945 – volume: 7 start-page: e54 year: 2009 ident: 10.1016/j.alit.2016.07.005_bib19 article-title: Stepwise development of MAIT cells in mouse and human publication-title: PLoS Biol doi: 10.1371/journal.pbio.1000054 – volume: 31 start-page: 407 year: 2010 ident: 10.1016/j.alit.2016.07.005_bib16 article-title: Innate immune cell populations function as initiators and effectors in Th2 cytokine responses publication-title: Trends Immunol doi: 10.1016/j.it.2010.09.001 – volume: 136 start-page: 323 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib9 article-title: Innate and adaptive T cells in asthmatic patients: relationship to severity and disease mechanisms publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2015.01.014 – volume: 7 start-page: e70 year: 2009 ident: 10.1016/j.alit.2016.07.005_bib8 article-title: Where do MAIT cells fit in the family of unconventional T cells? publication-title: PLoS Biol doi: 10.1371/journal.pbio.1000070 – volume: 80 start-page: 271 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib37 article-title: The decrease in number and change in phenotype of mucosal-associated invariant T cells in the elderly and differences in men and women of reproductive age publication-title: Scand J Immunol doi: 10.1111/sji.12193 – volume: 132 start-page: 933 year: 2013 ident: 10.1016/j.alit.2016.07.005_bib41 article-title: IL-33 is more potent than IL-25 in provoking IL-13-producing nuocytes (type 2 innate lymphoid cells) and airway contraction publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2013.05.012 – volume: 23 start-page: 529 year: 2011 ident: 10.1016/j.alit.2016.07.005_bib23 article-title: Mucosal-associated invariant T cells regulate Th1 response in multiple sclerosis publication-title: Int Immunol doi: 10.1093/intimm/dxr047 – volume: 31 start-page: 965 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib49 article-title: MAIT cells are activated and accumulated in the inflamed mucosa of ulcerative colitis publication-title: J Gastroenterol Hepatol doi: 10.1111/jgh.13242 – volume: 344 start-page: 350 year: 2001 ident: 10.1016/j.alit.2016.07.005_bib1 article-title: Asthma publication-title: N Engl J Med doi: 10.1056/NEJM200102013440507 – volume: 21 start-page: 1529 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib36 article-title: Reduced numbers and proapoptotic features of mucosal-associated invariant T cells as a characteristic finding in patients with inflammatory bowel disease publication-title: Inflamm Bowel Dis doi: 10.1097/MIB.0000000000000397 – ident: 10.1016/j.alit.2016.07.005_bib30 – volume: 64 start-page: 227 year: 2015 ident: 10.1016/j.alit.2016.07.005_bib29 article-title: Group 2 innate lymphoid cells and asthma publication-title: Allergol Int doi: 10.1016/j.alit.2015.03.004 – volume: 183 start-page: 195 year: 1996 ident: 10.1016/j.alit.2016.07.005_bib6 article-title: Interleukin 5 deficiency abolishes eosinophilia, airways hyperreactivity, and lung damage in a mouse asthma model publication-title: J Exp Med doi: 10.1084/jem.183.1.195 – volume: 7 start-page: 987 year: 2006 ident: 10.1016/j.alit.2016.07.005_bib11 article-title: Invariant V(alpha)19i T cells regulate autoimmune inflammation publication-title: Nat Immunol doi: 10.1038/ni1370 – volume: 12 start-page: 1055 year: 2011 ident: 10.1016/j.alit.2016.07.005_bib26 article-title: Human IL-25- and IL-33-responsive type 2 innate lymphoid cells are defined by expression of CRTH2 and CD161 publication-title: Nat Immunol doi: 10.1038/ni.2104 – volume: 44 start-page: 3119 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib24 article-title: CD8(+) MAIT cells infiltrate into the CNS and alterations in their blood frequencies correlate with IL-18 serum levels in multiple sclerosis publication-title: Eur J Immunol doi: 10.1002/eji.201344160 – volume: 99 start-page: 1329 year: 1997 ident: 10.1016/j.alit.2016.07.005_bib5 article-title: Aeroallergen-induced eosinophilic inflammation, lung damage, and airways hyperreactivity in mice can occur independently of IL-4 and allergen-specific immunoglobulins publication-title: J Clin Invest doi: 10.1172/JCI119292 – volume: 64 start-page: 153 year: 2012 ident: 10.1016/j.alit.2016.07.005_bib10 article-title: Mucosal-associated invariant T cells promote inflammation and exacerbate disease in murine models of arthritis publication-title: Arthritis Rheum doi: 10.1002/art.33314 – volume: 12 start-page: 21 year: 2011 ident: 10.1016/j.alit.2016.07.005_bib15 article-title: The expanding family of innate lymphoid cells: regulators and effectors of immunity and tissue remodeling publication-title: Nat Immunol doi: 10.1038/ni.1962 – volume: 117 start-page: 1250 year: 2011 ident: 10.1016/j.alit.2016.07.005_bib20 article-title: Human MAIT cells are xenobiotic-resistant, tissue-targeted, CD161hi IL-17-secreting T cells publication-title: Blood doi: 10.1182/blood-2010-08-303339 – volume: 134 start-page: 671 year: 2014 ident: 10.1016/j.alit.2016.07.005_bib47 article-title: Enhanced innate type 2 immune response in peripheral blood from patients with asthma publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2014.06.024 – volume: 17 start-page: 255 year: 1999 ident: 10.1016/j.alit.2016.07.005_bib2 article-title: Immunologic basis of antigen-induced airway hyperresponsiveness publication-title: Annu Rev Immunol doi: 10.1146/annurev.immunol.17.1.255 – volume: 18 start-page: 716 year: 2012 ident: 10.1016/j.alit.2016.07.005_bib4 article-title: Asthma phenotypes: the evolution from clinical to molecular approaches publication-title: Nat Med doi: 10.1038/nm.2678 |
SSID | ssj0012797 |
Score | 2.2622726 |
Snippet | A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and mucosal-associated... Background: A variety of innate subsets of lymphoid cells such as natural killer (NK) cells, several populations of innate lymphoid cells (ILCs), and... |
SourceID | doaj proquest pubmed crossref elsevier |
SourceType | Open Website Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 302 |
SubjectTerms | Adult Aged Airflow limitation Asthma Asthma - diagnosis Asthma - drug therapy Asthma - immunology Asthma - physiopathology Biomarkers Cell Adhesion Molecules - blood Female Humans Immunity, Innate Innate lymphoid cell Lymphocyte Count Male Middle Aged Mucosal-associated invariant T cell Mucosal-Associated Invariant T Cells - immunology Mucosal-Associated Invariant T Cells - metabolism Natural killer cell Pulmonary Ventilation Respiratory Function Tests T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism |
Title | Circulating activated innate lymphoid cells and mucosal-associated invariant T cells are associated with airflow limitation in patients with asthma |
URI | https://dx.doi.org/10.1016/j.alit.2016.07.005 https://www.ncbi.nlm.nih.gov/pubmed/27575652 https://www.proquest.com/docview/1859729084 https://doaj.org/article/2c451dd0ef834ddcb94874020c329e6c |
Volume | 66 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQkRAXxJvlURmJG7LwK058LBVVRQUH1IreLCe2ISjNot1tEb-DP8xM7KyWA-XCKVI0TkaeGc9nex6EvNI-RCWCZd43hsHqx1nLq5bFUMtoYlSpmwJkP5rjM_3-vDrfafWFMWG5PHCeuDey05UIgcfUKB1C11qNXeQk75S00XS4-oLPmzdT5f5A1rmtipKKgUfmJV0mR3YhwMWgrly2ExvX7bikqXL_H57pb8hz8kBHd8mdAh3pQWb5HrkRx_vk1odyOf6A_DrsV93UjWv8QjFf4QpwZKD9OMKTDj9Bbss-UDyqX1M_BnqB0ep-YL6IaCK-gs0zzDY9nQlXke4Q4Lkt9f0qDcsfdMDsqEm0MJCWEq3rQrPefL3wD8nZ0bvTw2NWei6wztR8w4wMvq19k7QC6aZW6OQrr4VuDY8qmGSbkLjltuVg6QLtN4qgRRA2JS69ekT2xuUYnxAK3-ARU1lNy3XkxqYAcC0YWERiLSu1IGKedtcVbrEvxuDmyLNvDkXlUFSO4z15tSCvt2O-53Ic11K_RWluKbGU9vQCFMwVBXP_UrAFqWZdcAWVZLQBn-qv_fnLWXEcmCzKzI9xebl2AJEs7Gl4oxfkcdaoLYuyBvxsKvn0f7D-jNyWiEKmQKPnZG-zuowvAENt2n1y8-Dk0-eT_clsfgPCBBv8 |
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=Circulating+activated+innate+lymphoid+cells+and+mucosal-associated+invariant+T+cells+are+associated+with+airflow+limitation+in+patients+with+asthma&rft.jtitle=Allergology+international&rft.au=Ayako+Ishimori&rft.au=Norihiro+Harada&rft.au=Asako+Chiba&rft.au=Sonoko+Harada&rft.date=2017-04-01&rft.pub=Elsevier&rft.issn=1323-8930&rft.volume=66&rft.issue=2&rft.spage=302&rft.epage=309&rft_id=info:doi/10.1016%2Fj.alit.2016.07.005&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_2c451dd0ef834ddcb94874020c329e6c |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1323-8930&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1323-8930&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1323-8930&client=summon |