Urban Particulate Matter–Activated Human Dendritic Cells Induce the Expansion of Potent Inflammatory Th1, Th2, and Th17 Effector Cells

Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPM in enhancing primary immune responses by naive...

Full description

Saved in:
Bibliographic Details
Published inAmerican journal of respiratory cell and molecular biology Vol. 54; no. 2; pp. 250 - 262
Main Authors Matthews, Nick C., Pfeffer, Paul E., Mann, Elizabeth H., Kelly, Frank J., Corrigan, Christopher J., Hawrylowicz, Catherine M., Lee, Tak H.
Format Journal Article
LanguageEnglish
Published United States American Thoracic Society 01.02.2016
Subjects
Online AccessGet full text
ISSN1044-1549
1535-4989
1535-4989
DOI10.1165/rcmb.2015-0084OC

Cover

Abstract Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPM in enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tms), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c(+) DCs were purified and activated with UPM in the presence or absence of house dust mite or tetanus toxoid control antigen. 5-(and -6)-Carboxyfluorescein diacetate succinimidyl ester-labeled blood Tms were cocultured with autologous DCs, T cell proliferation and effector function were assessed using flow cytometry, and secreted cytokines were measured by combined bead array. UPM-DCs elicited IFN-γ and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite-loaded DCs. UPM-DCs drove the expansion and differentiation of a mixed population of Th1, Th2, and Th17 cell effectors through a mechanism that was dependent on major histocompatibility class II but not on cytokine-driven expansion. The data suggest that UPM not only has adjuvant properties but is also a source of antigen that stimulates the generation of Th2, Th1, and Th17 effector phenotypes, which have been implicated in both exacerbations of asthma and chronic inflammatory diseases.
AbstractList Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPM in enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tms), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c(+) DCs were purified and activated with UPM in the presence or absence of house dust mite or tetanus toxoid control antigen. 5-(and -6)-Carboxyfluorescein diacetate succinimidyl ester-labeled blood Tms were cocultured with autologous DCs, T cell proliferation and effector function were assessed using flow cytometry, and secreted cytokines were measured by combined bead array. UPM-DCs elicited IFN-γ and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite-loaded DCs. UPM-DCs drove the expansion and differentiation of a mixed population of Th1, Th2, and Th17 cell effectors through a mechanism that was dependent on major histocompatibility class II but not on cytokine-driven expansion. The data suggest that UPM not only has adjuvant properties but is also a source of antigen that stimulates the generation of Th2, Th1, and Th17 effector phenotypes, which have been implicated in both exacerbations of asthma and chronic inflammatory diseases.Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPM in enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tms), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c(+) DCs were purified and activated with UPM in the presence or absence of house dust mite or tetanus toxoid control antigen. 5-(and -6)-Carboxyfluorescein diacetate succinimidyl ester-labeled blood Tms were cocultured with autologous DCs, T cell proliferation and effector function were assessed using flow cytometry, and secreted cytokines were measured by combined bead array. UPM-DCs elicited IFN-γ and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite-loaded DCs. UPM-DCs drove the expansion and differentiation of a mixed population of Th1, Th2, and Th17 cell effectors through a mechanism that was dependent on major histocompatibility class II but not on cytokine-driven expansion. The data suggest that UPM not only has adjuvant properties but is also a source of antigen that stimulates the generation of Th2, Th1, and Th17 effector phenotypes, which have been implicated in both exacerbations of asthma and chronic inflammatory diseases.
Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPM in enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tms), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c + DCs were purified and activated with UPM in the presence or absence of house dust mite or tetanus toxoid control antigen. 5-(and -6)-Carboxyfluorescein diacetate succinimidyl ester–labeled blood Tms were cocultured with autologous DCs, T cell proliferation and effector function were assessed using flow cytometry, and secreted cytokines were measured by combined bead array. UPM-DCs elicited IFN-γ and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite–loaded DCs. UPM-DCs drove the expansion and differentiation of a mixed population of Th1, Th2, and Th17 cell effectors through a mechanism that was dependent on major histocompatibility class II but not on cytokine-driven expansion. The data suggest that UPM not only has adjuvant properties but is also a source of antigen that stimulates the generation of Th2, Th1, and Th17 effector phenotypes, which have been implicated in both exacerbations of asthma and chronic inflammatory diseases.
Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPM in enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tms), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c(+) DCs were purified and activated with UPM in the presence or absence of house dust mite or tetanus toxoid control antigen. 5-(and -6)-Carboxyfluorescein diacetate succinimidyl ester-labeled blood Tms were cocultured with autologous DCs, T cell proliferation and effector function were assessed using flow cytometry, and secreted cytokines were measured by combined bead array. UPM-DCs elicited IFN-γ and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite-loaded DCs. UPM-DCs drove the expansion and differentiation of a mixed population of Th1, Th2, and Th17 cell effectors through a mechanism that was dependent on major histocompatibility class II but not on cytokine-driven expansion. The data suggest that UPM not only has adjuvant properties but is also a source of antigen that stimulates the generation of Th2, Th1, and Th17 effector phenotypes, which have been implicated in both exacerbations of asthma and chronic inflammatory diseases.
Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DC) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPMin enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tm), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c1 DCs were purified and activated with UPMin the presence or absence of house dustmite or tetanus toxoid control antigen. UPM-DCs elicited IFN-γ and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite-loaded DCs.
Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DC) are critical for stimulating T cell immunity and in maintaining airway tolerance, but they also react to airway UPM. The adjuvant role of UPMin enhancing primary immune responses by naive cells to allergen has been reported, but the direct effects of UPM-activated DCs on the functionality of human memory CD4 T cells (Tm), which constitute the majority of T cells in the lung, has not been investigated. Blood CD1c1 DCs were purified and activated with UPMin the presence or absence of house dustmite or tetanus toxoid control antigen. UPM-DCs elicited IFN- gamma and IL-13 secretion and induced proliferation in Tms isolated from both allergic patients with asthma and healthy control subjects, whereas only IL-13 was produced by Tms from patients with atopic asthma stimulated by house dust mite-loaded DCs.
Author Pfeffer, Paul E.
Lee, Tak H.
Kelly, Frank J.
Matthews, Nick C.
Mann, Elizabeth H.
Corrigan, Christopher J.
Hawrylowicz, Catherine M.
Author_xml – sequence: 1
  givenname: Nick C.
  surname: Matthews
  fullname: Matthews, Nick C.
  organization: Division of Asthma, Allergy, and Lung Biology, Medical Research Council–Asthma United Kingdom Centre for Allergic Mechanisms of Asthma, Guy’s Hospital, King’s College London, London, United Kingdom
– sequence: 2
  givenname: Paul E.
  surname: Pfeffer
  fullname: Pfeffer, Paul E.
  organization: Division of Asthma, Allergy, and Lung Biology, Medical Research Council–Asthma United Kingdom Centre for Allergic Mechanisms of Asthma, Guy’s Hospital, King’s College London, London, United Kingdom
– sequence: 3
  givenname: Elizabeth H.
  surname: Mann
  fullname: Mann, Elizabeth H.
  organization: Division of Asthma, Allergy, and Lung Biology, Medical Research Council–Asthma United Kingdom Centre for Allergic Mechanisms of Asthma, Guy’s Hospital, King’s College London, London, United Kingdom
– sequence: 4
  givenname: Frank J.
  surname: Kelly
  fullname: Kelly, Frank J.
  organization: Environmental Research Group, Medical Research Council–Public Health England Centre for Environment and Health, Franklin Wilkins Building, King’s College London, London, United Kingdom; and
– sequence: 5
  givenname: Christopher J.
  surname: Corrigan
  fullname: Corrigan, Christopher J.
  organization: Division of Asthma, Allergy, and Lung Biology, Medical Research Council–Asthma United Kingdom Centre for Allergic Mechanisms of Asthma, Guy’s Hospital, King’s College London, London, United Kingdom
– sequence: 6
  givenname: Catherine M.
  surname: Hawrylowicz
  fullname: Hawrylowicz, Catherine M.
  organization: Division of Asthma, Allergy, and Lung Biology, Medical Research Council–Asthma United Kingdom Centre for Allergic Mechanisms of Asthma, Guy’s Hospital, King’s College London, London, United Kingdom
– sequence: 7
  givenname: Tak H.
  surname: Lee
  fullname: Lee, Tak H.
  organization: Division of Asthma, Allergy, and Lung Biology, Medical Research Council–Asthma United Kingdom Centre for Allergic Mechanisms of Asthma, Guy’s Hospital, King’s College London, London, United Kingdom, Allergy Centre, Hong Kong Sanatorium and Hospital, Hong Kong, People’s Republic of China
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26196219$$D View this record in MEDLINE/PubMed
BookMark eNqNkjtv1TAUxy1URB-wMyFLLAxNsR07cRak6lJopaJ2aGfLsR2uq8S-2E5FN0Z2viGfhBPdFkElJDz4dX7nr_PaRzshBofQS0qOKG3E22Sm_ogRKipCJL9YPUF7VNSi4p3sduBOOK-o4N0u2s_5hhDKJKXP0C5raNcw2u2h79ep1wFf6lS8mUddHP6kS3Hp57cfx6b4W_ix-HSeAHrvgk0eOLxy45jxWbCzcbisHT75utEh-xhwHPBlLC4UMA-jniZdYrrDV2t6CBs7xDrY5dXik2FwBoxbtefo6aDH7F7cnwfo-sPJ1eq0Or_4eLY6Pq8MF22pejO0vZGmp8S6rtGytm091I63je2EMWzgtiZO9oJZLTWz0hLSOlrDEgRsB-jdVncz95OzBiJNelSb5Ced7lTUXv1tCX6tPsdbxSVb6gkCb-4FUvwyu1zU5LOBFHRwcc6Kto0UbSOY-B-U1ZAWXdDXj9CbOKcAlVgoLjspRQPUqz-D_x31Qz8BaLaASTHn5AZlfNEFGgO5-FFRopbBUcvgqGVw1HZwwJE8cnzQ_qfLLwjsx-s
CitedBy_id crossref_primary_10_1111_pai_12975
crossref_primary_10_1164_rccm_201712_2506OC
crossref_primary_10_3389_fneur_2021_659678
crossref_primary_10_3389_fmicb_2021_688137
crossref_primary_10_1152_ajpgi_00423_2020
crossref_primary_10_1186_s13063_022_06091_5
crossref_primary_10_1177_09612033211061479
crossref_primary_10_1371_journal_pone_0173158
crossref_primary_10_1111_imcb_12425
crossref_primary_10_3390_biology13040247
crossref_primary_10_1016_j_jaci_2022_03_018
crossref_primary_10_1016_j_envres_2023_115449
crossref_primary_10_1016_j_envpol_2022_118892
crossref_primary_10_1165_rcmb_2017_0199ED
crossref_primary_10_1002_ppsc_202300157
crossref_primary_10_1165_rcmb_2018_0346OC
crossref_primary_10_1016_j_chemosphere_2021_131963
crossref_primary_10_1016_j_intimp_2024_113921
crossref_primary_10_1016_j_freeradbiomed_2020_01_179
crossref_primary_10_1016_j_jep_2023_116171
crossref_primary_10_1016_j_jgr_2025_03_001
crossref_primary_10_2337_db16_1416
crossref_primary_10_1016_j_envint_2020_105604
crossref_primary_10_1016_j_envres_2022_112921
crossref_primary_10_1016_j_jep_2021_114789
crossref_primary_10_1038_s41591_022_02073_x
crossref_primary_10_1371_journal_pone_0200040
crossref_primary_10_3390_ijerph192315888
crossref_primary_10_1186_s10020_020_00181_3
crossref_primary_10_1016_j_toxlet_2018_04_020
crossref_primary_10_3390_molecules26195814
crossref_primary_10_4167_jbv_2022_52_3_083
crossref_primary_10_1164_rccm_202112_2668TR
crossref_primary_10_1155_2020_8254909
crossref_primary_10_1016_j_toxlet_2017_03_015
crossref_primary_10_1016_j_cell_2021_01_042
crossref_primary_10_1016_j_envres_2017_10_041
crossref_primary_10_1016_j_chest_2020_10_053
crossref_primary_10_1016_j_intimp_2023_110254
crossref_primary_10_1177_07482337211019172
crossref_primary_10_1002_tox_23476
crossref_primary_10_3390_nu17050829
crossref_primary_10_1016_j_scitotenv_2019_134397
crossref_primary_10_1016_j_chemosphere_2019_124497
crossref_primary_10_3390_ijms21030757
crossref_primary_10_1111_imm_12852
crossref_primary_10_1016_j_freeradbiomed_2020_08_003
crossref_primary_10_1165_rcmb_2016_0409OC
crossref_primary_10_3390_ijerph15010160
Cites_doi 10.1165/rcmb.2012-0465OC
10.1002/eji.201040562
10.1080/10473289.1999.10463879
10.1006/taap.1998.8437
10.1016/j.jaci.2015.01.026
10.1165/ajrcmb.19.3.3143
10.1084/jem.194.12.1711
10.1084/jem.20101376
10.1016/j.immuni.2012.03.027
10.1152/ajplung.00115.2010
10.1111/j.1365-2222.2012.03983.x
10.1111/j.1365-2222.2006.02631.x
10.4049/jimmunol.176.12.7431
10.1371/journal.pone.0016245
10.1016/j.cell.2014.04.048
10.1111/j.1398-9995.2006.01056.x
10.1258/jrsm.2009.090348
10.1289/ehp.99107489
10.1016/j.anai.2014.04.013
10.4049/jimmunol.0902564
10.1038/nature06881
10.1513/AnnalsATS.201407-304AW
10.1371/journal.pone.0082545
10.1080/10590500802494538
10.1016/j.jaci.2013.06.048
10.1164/rccm.200904-0573OC
10.4049/jimmunol.1004062
10.4049/jimmunol.1101380
10.1038/nature10957
10.1016/j.jaci.2013.03.037
10.1164/rccm.201211-2004OC
10.1016/j.immuni.2013.01.013
10.1007/s10875-007-9149-0
10.1084/jem.20130301
10.1038/nm.2684
10.1289/ehp.0901461
10.1016/0022-1759(94)90236-4
10.1016/j.jaci.2006.02.030
10.4049/jimmunol.1000719
10.1016/j.clim.2009.09.013
10.1152/ajplung.00261.2011
10.1016/S0140-6736(14)60617-6
10.1016/j.jaci.2008.08.004
10.1152/jappl.1996.81.5.2203
10.1006/enrs.1994.1005
10.1084/jem.179.4.1109
10.2174/187152806779010909
10.1006/jaut.1996.0087
ContentType Journal Article
Copyright Copyright American Thoracic Society Feb 2016
Copyright © 2016 by the American Thoracic Society 2016
Copyright_xml – notice: Copyright American Thoracic Society Feb 2016
– notice: Copyright © 2016 by the American Thoracic Society 2016
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7T5
7TM
7TO
7X7
7XB
88A
88E
88I
8AF
8AO
8FE
8FH
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BBNVY
BENPR
BHPHI
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
H94
HCIFZ
K9.
LK8
M0S
M1P
M2P
M7P
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
Q9U
S0X
7X8
5PM
DOI 10.1165/rcmb.2015-0084OC
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Immunology Abstracts
Nucleic Acids Abstracts
Oncogenes and Growth Factors Abstracts
ProQuest Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Biology Database (Alumni Edition)
Medical Database (Alumni Edition)
Science Database (Alumni Edition)
STEM Database
ProQuest Pharma Collection
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials - QC
Biological Science Collection
ProQuest Central
Natural Science Collection
ProQuest One Community College
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
AIDS and Cancer Research Abstracts
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
Biological Sciences
ProQuest Health & Medical Collection
PML(ProQuest Medical Library)
Science Database
ProQuest Biological Science
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
SIRS Editorial
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest Central Student
Oncogenes and Growth Factors Abstracts
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
SIRS Editorial
Nucleic Acids Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest AP Science
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Central China
ProQuest Biology Journals (Alumni Edition)
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Biological Science Collection
AIDS and Cancer Research Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Science Journals (Alumni Edition)
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest Science Journals
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
Biological Science Database
ProQuest SciTech Collection
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Immunology Abstracts
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

MEDLINE
ProQuest Central Student
AIDS and Cancer Research Abstracts
Database_xml – sequence: 1
  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: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: http://www.proquest.com/pqcentral?accountid=15518
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Anatomy & Physiology
EISSN 1535-4989
EndPage 262
ExternalDocumentID PMC4821044
3951749951
26196219
10_1165_rcmb_2015_0084OC
Genre Research Support, Non-U.S. Gov't
Journal Article
Feature
GeographicLocations United Kingdom--UK
GeographicLocations_xml – name: United Kingdom--UK
GrantInformation_xml – fundername: Wellcome Trust
– fundername: Medical Research Council
  grantid: G0801056
– fundername: Medical Research Council
  grantid: MR/L01341X/1
– fundername: Medical Research Council
  grantid: G1000758
GroupedDBID ---
0R~
23M
2WC
53G
5GY
5RE
7X7
88E
88I
8AF
8AO
8FE
8FH
8FI
8FJ
8R4
8R5
AAYXX
ABJNI
ABUWG
ACGFO
ACGFS
ACGOD
ACPRK
ADBBV
AENEX
AFFNX
AFKRA
AHMBA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AZQEC
BAWUL
BBNVY
BENPR
BES
BHPHI
BPHCQ
BVXVI
C45
CCPQU
CITATION
CS3
DIK
DWQXO
E3Z
EBS
EJD
EMOBN
F5P
FYUFA
GNUQQ
GX1
H13
HCIFZ
HMCUK
HZ~
J5H
LK8
M1P
M2P
M2Q
M5~
M7P
O9-
OBH
OFXIZ
OK1
OVD
OVIDX
P2P
PHGZM
PHGZT
PQQKQ
PROAC
PSQYO
PZZ
Q2X
RWL
S0X
SJN
TAE
TEORI
THO
TR2
UKHRP
W8F
WOQ
YHG
ZGI
ZXP
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
PQGLB
3V.
7T5
7TM
7TO
7XB
88A
8FK
H94
K9.
PKEHL
PQEST
PQUKI
PRINS
Q9U
7X8
PUEGO
5PM
ID FETCH-LOGICAL-c457t-bcf7bc8cb10de96a83d73f3e476d95cc2f4d30e8b52da8a2d8d007e13333504d3
IEDL.DBID 7X7
ISSN 1044-1549
1535-4989
IngestDate Thu Aug 21 18:38:59 EDT 2025
Fri Sep 05 07:34:47 EDT 2025
Thu Sep 04 16:58:03 EDT 2025
Fri Jul 25 12:15:03 EDT 2025
Mon Jul 21 05:58:45 EDT 2025
Tue Jul 01 03:31:31 EDT 2025
Thu Apr 24 23:13:00 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords memory CD4 T cells
air pollution
cytokines
urban particulate matter
dendritic cells
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c457t-bcf7bc8cb10de96a83d73f3e476d95cc2f4d30e8b52da8a2d8d007e13333504d3
Notes SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/4821044
PMID 26196219
PQID 1764898856
PQPubID 2031371
PageCount 13
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4821044
proquest_miscellaneous_1768576525
proquest_miscellaneous_1762345715
proquest_journals_1764898856
pubmed_primary_26196219
crossref_citationtrail_10_1165_rcmb_2015_0084OC
crossref_primary_10_1165_rcmb_2015_0084OC
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2016-02-00
2016-Feb
20160201
PublicationDateYYYYMMDD 2016-02-01
PublicationDate_xml – month: 02
  year: 2016
  text: 2016-02-00
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: New York
PublicationTitle American journal of respiratory cell and molecular biology
PublicationTitleAlternate Am J Respir Cell Mol Biol
PublicationYear 2016
Publisher American Thoracic Society
Publisher_xml – name: American Thoracic Society
References Li JZ (bib14) 2009; 47
Hopke PK (bib9) 2006; 5
bib36
bib37
bib34
bib35
bib32
bib33
bib30
bib31
bib29
bib27
bib28
bib40
bib47
bib48
bib45
bib46
bib43
bib44
bib41
bib42
bib7
bib8
bib5
bib6
bib3
bib38
bib4
bib39
bib1
bib2
bib50
bib15
bib12
bib13
bib10
bib11
bib49
bib25
Matthews NC (bib23) 2014; 50
bib26
bib24
bib21
bib22
bib20
bib18
bib19
bib16
bib17
References_xml – volume: 50
  start-page: 281
  year: 2014
  ident: bib23
  publication-title: Am J Respir Cell Mol Biol
  doi: 10.1165/rcmb.2012-0465OC
– ident: bib33
  doi: 10.1002/eji.201040562
– ident: bib3
  doi: 10.1080/10473289.1999.10463879
– volume: 47
  start-page: 91
  year: 2009
  ident: bib14
  publication-title: Zhonghua Er Ke Za Zhi
– ident: bib38
  doi: 10.1006/taap.1998.8437
– ident: bib41
  doi: 10.1016/j.jaci.2015.01.026
– ident: bib26
  doi: 10.1165/ajrcmb.19.3.3143
– ident: bib29
  doi: 10.1084/jem.194.12.1711
– ident: bib17
  doi: 10.1084/jem.20101376
– ident: bib22
  doi: 10.1016/j.immuni.2012.03.027
– ident: bib15
  doi: 10.1152/ajplung.00115.2010
– ident: bib18
  doi: 10.1111/j.1365-2222.2012.03983.x
– ident: bib11
  doi: 10.1111/j.1365-2222.2006.02631.x
– ident: bib21
  doi: 10.4049/jimmunol.176.12.7431
– ident: bib24
  doi: 10.1371/journal.pone.0016245
– ident: bib46
  doi: 10.1016/j.cell.2014.04.048
– ident: bib27
  doi: 10.1111/j.1398-9995.2006.01056.x
– ident: bib1
  doi: 10.1258/jrsm.2009.090348
– ident: bib4
  doi: 10.1289/ehp.99107489
– ident: bib42
  doi: 10.1016/j.anai.2014.04.013
– ident: bib12
  doi: 10.4049/jimmunol.0902564
– ident: bib36
  doi: 10.1038/nature06881
– ident: bib48
  doi: 10.1513/AnnalsATS.201407-304AW
– ident: bib37
  doi: 10.1371/journal.pone.0082545
– ident: bib8
  doi: 10.1080/10590500802494538
– ident: bib5
  doi: 10.1016/j.jaci.2013.06.048
– ident: bib13
  doi: 10.1164/rccm.200904-0573OC
– ident: bib35
  doi: 10.4049/jimmunol.1004062
– ident: bib7
  doi: 10.4049/jimmunol.1101380
– ident: bib31
  doi: 10.1038/nature10957
– ident: bib40
  doi: 10.1016/j.jaci.2013.03.037
– ident: bib6
  doi: 10.1164/rccm.201211-2004OC
– ident: bib47
  doi: 10.1016/j.immuni.2013.01.013
– ident: bib19
  doi: 10.1007/s10875-007-9149-0
– ident: bib28
  doi: 10.1084/jem.20130301
– ident: bib39
  doi: 10.1038/nm.2684
– ident: bib16
  doi: 10.1289/ehp.0901461
– ident: bib25
  doi: 10.1016/0022-1759(94)90236-4
– ident: bib49
  doi: 10.1016/j.jaci.2006.02.030
– ident: bib20
  doi: 10.4049/jimmunol.1000719
– ident: bib30
  doi: 10.1016/j.clim.2009.09.013
– ident: bib34
  doi: 10.1152/ajplung.00261.2011
– ident: bib32
  doi: 10.1016/S0140-6736(14)60617-6
– ident: bib45
  doi: 10.1016/j.jaci.2008.08.004
– ident: bib50
  doi: 10.1152/jappl.1996.81.5.2203
– ident: bib2
  doi: 10.1006/enrs.1994.1005
– volume: 5
  start-page: 747
  year: 2006
  ident: bib9
  publication-title: Clin Occup Environ Med
– ident: bib10
  doi: 10.1084/jem.179.4.1109
– ident: bib43
  doi: 10.2174/187152806779010909
– ident: bib44
  doi: 10.1006/jaut.1996.0087
SSID ssj0012811
Score 2.4098592
Snippet Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DCs) are critical for stimulating T cell immunity and...
Exposure to urban particulate matter (UPM) exacerbates asthmatic lung inflammation. Lung dendritic cells (DC) are critical for stimulating T cell immunity and...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 250
SubjectTerms Adult
Air pollution
Allergens - immunology
Animals
Antigens
Asthma
Asthma - immunology
Asthma - metabolism
Case-Control Studies
Cell growth
Cell Proliferation - drug effects
Cells, Cultured
Chronic illnesses
Coculture Techniques
Cytokines
Cytokines - immunology
Cytokines - metabolism
Dendritic cells
Dendritic Cells - drug effects
Dendritic Cells - immunology
Dendritic Cells - metabolism
Disease
Expansion
Female
Gram-positive bacteria
Histocompatibility Antigens Class II - immunology
Histocompatibility Antigens Class II - metabolism
Humans
Immunologic Memory
Inflammation
Inflammation Mediators - immunology
Inflammation Mediators - metabolism
Lymphatic system
Lymphocyte Activation - drug effects
Lymphocytes
Male
Middle Aged
Mortality
Original Research
Outdoor air quality
Particulate Matter - immunology
Particulate Matter - toxicity
Phenotype
Pyroglyphidae - immunology
Receptors, Antigen, T-Cell - immunology
Receptors, Antigen, T-Cell - metabolism
Tetanus Toxin - immunology
Th1 Cells - drug effects
Th1 Cells - immunology
Th1 Cells - metabolism
Th17 Cells - drug effects
Th17 Cells - immunology
Th17 Cells - metabolism
Th2 Cells - drug effects
Th2 Cells - immunology
Th2 Cells - metabolism
Urban Health
Young Adult
Title Urban Particulate Matter–Activated Human Dendritic Cells Induce the Expansion of Potent Inflammatory Th1, Th2, and Th17 Effector Cells
URI https://www.ncbi.nlm.nih.gov/pubmed/26196219
https://www.proquest.com/docview/1764898856
https://www.proquest.com/docview/1762345715
https://www.proquest.com/docview/1768576525
https://pubmed.ncbi.nlm.nih.gov/PMC4821044
Volume 54
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3da9swEBdbC2MvZW33ka4rGozBoCaRJVnK08iylDJIF0YDeTPWh-kgsdskhe4f2N-9O1nxmg3yYrDvbGTdWbov34-QD9bInhC8TGxmwEGRTifGeplIaaxJFdAshgbGV9nlVHybyVkMuK1iWeVmTQwLtastxsi7TGVC97WW2efbuwRRozC7GiE0npJ9BpYIQjeoWetwYZKIbVKTmewu7cJgMZdMsIv89-H2VvSffflvmeSjfefiBTmIBiMdNBI-JE98dUSOBxU4y4tf9CMNJZwhNn5Eno1jpvyY_J4uTVHRSdAMhOjydBxaaSYDGxDNvKMhgE-_-soFvAM69PP5iiKYh_UUDEM6eoC1AsNptC7ppAbzeg3kEpRoEZLz9PqGncMhPadF5fBM0aYdcr1snvaSTC9G18PLJGIuJFZItQZBlcpYbQ3rOd_PCs2d4iX3QmWuL61NS-F4z2sjU1foInXagZXhwdPlHKTu-CuyV9WVf0MoXLXOgbljFTbpd0UpC6adYfj7bb9gHdLdTH9uY0NyxMWY58ExyWSOAstRYHkjsA751N5x2zTj2MF7upFoHj_LVf5XiTrkfUuGDwqzJEXl6_vAk3KYCyZ38mhw1GQKPK8bJWkHhC5pBvtAh6gt9WkZsKH3NqX6eRMaewsNDrgQJ7uH_pY8h_eMpeOnZG-9vPfvwDJam7Og_mdk_8voavLjD1vfEbc
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1bb9MwFD4anQS8INi4dAwwEiAhLWrjxIn7MKHSderYWirUSnsLvkWb1Caj7QT7A_wsfhvHzgUKUt_2EinxSWTnHNvn5vMBvFGStcMwSD0VSTRQmOaeVIZ5jEklaYxtyroGhqNoMA0_nbPzLfhVnYWxaZXVmugWap0r6yNv-XEU8g7nLPpw9c2zqFE2ulpBaIgSWkEfuhJj5cGOU3PzHU245eHJEfL7LaXH_Ulv4JUoA54KWbzCrqWxVFxJv61NJxI80HGQBiaMI91hStE01EHbcMmoFlxQzTXuqwZtuyDAceoAv3sHtkPrQGnA9sf-aPyljmNQ7vtVcDRirYWaS5tOxjxbx_5zb30z_E_D_TdR86-d7_ghPChVVtItZOwRbJlsB3a7GZrr8xvyjrgkUued34G7wzJWvws_pwspMjJ2smlBwgwZumKeXlc5TDWjiQshkCOTaYe4QHpmNlsSCyeiDEHVlPR_4GplHXokT8k4RwV_hc0pivHcpQeQyYV_gBd6QESm7V1MioLM-aL42mOY3go_nkAjyzPzDAg-VVqjwqViCxOgRcqEz7X07QHgjvCb0Kp-f6LKkugWmWOWONMoYollWGIZlhQMa8L7-o2rohzIBtr9iqNJuTAskz9i3ITXdTNOaRunEZnJrx0NDfBf-GwjDUdTkVGkeVoISd0haxRHuBM1IV4Tn5rAlhRfb8kuL1xp8ZBTtM_Dvc1dfwX3BpPhWXJ2Mjp9DvdxzGUi-z40Votr8wL1tJV8WU4GAl9ve_79BiBmVHc
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=Urban+Particulate+Matter-Activated+Human+Dendritic+Cells+Induce+the+Expansion+of+Potent+Inflammatory+Th1%2C+Th2%2C+and+Th17+Effector+Cells&rft.jtitle=American+journal+of+respiratory+cell+and+molecular+biology&rft.au=Matthews%2C+Nick+C&rft.au=Pfeffer%2C+Paul+E&rft.au=Mann%2C+Elizabeth+H&rft.au=Kelly%2C+Frank+J&rft.date=2016-02-01&rft.pub=American+Thoracic+Society&rft.eissn=1535-4989&rft.volume=54&rft.issue=2&rft.spage=250&rft_id=info:doi/10.1165%2Frcmb.2015-0084OC&rft.externalDocID=3951749951
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1044-1549&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1044-1549&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1044-1549&client=summon