Single-cell T cell receptor sequencing of paired human atherosclerotic plaques and blood reveals autoimmune-like features of expanded effector T cells

Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell sa...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Nature Cardiovascular Research Ročník 2; číslo 2; s. 112 - 125
Hlavní autori: Depuydt, Marie A. C., Schaftenaar, Frank H., Prange, Koen H. M., Boltjes, Arjan, Hemme, Esmeralda, Delfos, Lucie, de Mol, Jill, de Jong, Maaike J. M., Bernabé Kleijn, Mireia N. A., Peeters, Judith A. H. M., Goncalves, Lauren, Wezel, Anouk, Smeets, Harm J., de Borst, Gert J., Foks, Amanda C., Pasterkamp, Gerard, de Winther, Menno P. J., Kuiper, Johan, Bot, Ilze, Slütter, Bram
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England Nature Publishing Group 01.02.2023
Nature Publishing Group UK
Predmet:
ISSN:2731-0590, 2731-0590
On-line prístup:Získať plný text
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Abstract Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell samples to assess the extent of TCR clonality and antigen-specific activation within the various T cell subsets. We observed the highest degree of plaque-specific clonal expansion in effector CD4 + T cells, and these clonally expanded T cells expressed genes such as CD69 , FOS and FOSB , indicative of recent TCR engagement, suggesting antigen-specific stimulation. CellChat analysis suggested multiple potential interactions of these effector CD4 + T cells with foam cells. Finally, we integrated a published scTCR-seq dataset of the autoimmune disease psoriatic arthritis, and we report various commonalities between the two diseases. In conclusion, our data suggest that atherosclerosis has an autoimmune compondent driven by autoreactive CD4 + T cells.
AbstractList Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell samples to assess the extent of TCR clonality and antigen-specific activation within the various T cell subsets. We observed the highest degree of plaque-specific clonal expansion in effector CD4 + T cells, and these clonally expanded T cells expressed genes such as CD69 , FOS and FOSB , indicative of recent TCR engagement, suggesting antigen-specific stimulation. CellChat analysis suggested multiple potential interactions of these effector CD4 + T cells with foam cells. Finally, we integrated a published scTCR-seq dataset of the autoimmune disease psoriatic arthritis, and we report various commonalities between the two diseases. In conclusion, our data suggest that atherosclerosis has an autoimmune compondent driven by autoreactive CD4 + T cells.
Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell samples to assess the extent of TCR clonality and antigen-specific activation within the various T cell subsets. We observed the highest degree of plaque-specific clonal expansion in effector CD4+ T cells, and these clonally expanded T cells expressed genes such as CD69, FOS and FOSB, indicative of recent TCR engagement, suggesting antigen-specific stimulation. CellChat analysis suggested multiple potential interactions of these effector CD4+ T cells with foam cells. Finally, we integrated a published scTCR-seq dataset of the autoimmune disease psoriatic arthritis, and we report various commonalities between the two diseases. In conclusion, our data suggest that atherosclerosis has an autoimmune compondent driven by autoreactive CD4+ T cells. Depuydt and Schaftenaar et al. profile the T cell clonality in patients with atherosclerosis by performing single-cell T cell receptor sequencing on carotid artery plaques and matched peripheral blood mononuclear cell samples. The analyses showed plaque-specific clonal expansion in effector CD4+ T cells, expressing genes indicative of exposure to activating antigens, thus suggesting that atherosclerosis has an autoimmune component driven by autoreactive CD4+ T cells.
Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell samples to assess the extent of TCR clonality and antigen-specific activation within the various T cell subsets. We observed the highest degree of plaque-specific clonal expansion in effector CD4 T cells, and these clonally expanded T cells expressed genes such as , and , indicative of recent TCR engagement, suggesting antigen-specific stimulation. CellChat analysis suggested multiple potential interactions of these effector CD4 T cells with foam cells. Finally, we integrated a published scTCR-seq dataset of the autoimmune disease psoriatic arthritis, and we report various commonalities between the two diseases. In conclusion, our data suggest that atherosclerosis has an autoimmune compondent driven by autoreactive CD4 T cells.
Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell samples to assess the extent of TCR clonality and antigen-specific activation within the various T cell subsets. We observed the highest degree of plaque-specific clonal expansion in effector CD4+ T cells, and these clonally expanded T cells expressed genes such as CD69, FOS and FOSB, indicative of recent TCR engagement, suggesting antigen-specific stimulation. CellChat analysis suggested multiple potential interactions of these effector CD4+ T cells with foam cells. Finally, we integrated a published scTCR-seq dataset of the autoimmune disease psoriatic arthritis, and we report various commonalities between the two diseases. In conclusion, our data suggest that atherosclerosis has an autoimmune compondent driven by autoreactive CD4+ T cells.Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study, we applied single-cell T cell receptor seqencing (scTCR-seq) on human carotid artery plaques and matched peripheral blood mononuclear cell samples to assess the extent of TCR clonality and antigen-specific activation within the various T cell subsets. We observed the highest degree of plaque-specific clonal expansion in effector CD4+ T cells, and these clonally expanded T cells expressed genes such as CD69, FOS and FOSB, indicative of recent TCR engagement, suggesting antigen-specific stimulation. CellChat analysis suggested multiple potential interactions of these effector CD4+ T cells with foam cells. Finally, we integrated a published scTCR-seq dataset of the autoimmune disease psoriatic arthritis, and we report various commonalities between the two diseases. In conclusion, our data suggest that atherosclerosis has an autoimmune compondent driven by autoreactive CD4+ T cells.
Author de Borst, Gert J.
Kuiper, Johan
Smeets, Harm J.
Foks, Amanda C.
Hemme, Esmeralda
Delfos, Lucie
Slütter, Bram
Bernabé Kleijn, Mireia N. A.
Pasterkamp, Gerard
Goncalves, Lauren
Schaftenaar, Frank H.
Peeters, Judith A. H. M.
Depuydt, Marie A. C.
Boltjes, Arjan
de Winther, Menno P. J.
Prange, Koen H. M.
de Jong, Maaike J. M.
Wezel, Anouk
Bot, Ilze
de Mol, Jill
Author_xml – sequence: 1
  givenname: Marie A. C.
  orcidid: 0000-0002-7174-1952
  surname: Depuydt
  fullname: Depuydt, Marie A. C.
– sequence: 2
  givenname: Frank H.
  surname: Schaftenaar
  fullname: Schaftenaar, Frank H.
– sequence: 3
  givenname: Koen H. M.
  orcidid: 0000-0002-9835-1735
  surname: Prange
  fullname: Prange, Koen H. M.
– sequence: 4
  givenname: Arjan
  orcidid: 0000-0002-6338-051X
  surname: Boltjes
  fullname: Boltjes, Arjan
– sequence: 5
  givenname: Esmeralda
  orcidid: 0000-0001-5853-8784
  surname: Hemme
  fullname: Hemme, Esmeralda
– sequence: 6
  givenname: Lucie
  surname: Delfos
  fullname: Delfos, Lucie
– sequence: 7
  givenname: Jill
  orcidid: 0000-0003-3541-9912
  surname: de Mol
  fullname: de Mol, Jill
– sequence: 8
  givenname: Maaike J. M.
  surname: de Jong
  fullname: de Jong, Maaike J. M.
– sequence: 9
  givenname: Mireia N. A.
  surname: Bernabé Kleijn
  fullname: Bernabé Kleijn, Mireia N. A.
– sequence: 10
  givenname: Judith A. H. M.
  orcidid: 0000-0002-0051-9836
  surname: Peeters
  fullname: Peeters, Judith A. H. M.
– sequence: 11
  givenname: Lauren
  surname: Goncalves
  fullname: Goncalves, Lauren
– sequence: 12
  givenname: Anouk
  surname: Wezel
  fullname: Wezel, Anouk
– sequence: 13
  givenname: Harm J.
  surname: Smeets
  fullname: Smeets, Harm J.
– sequence: 14
  givenname: Gert J.
  surname: de Borst
  fullname: de Borst, Gert J.
– sequence: 15
  givenname: Amanda C.
  orcidid: 0000-0002-9747-3458
  surname: Foks
  fullname: Foks, Amanda C.
– sequence: 16
  givenname: Gerard
  orcidid: 0000-0001-5345-1022
  surname: Pasterkamp
  fullname: Pasterkamp, Gerard
– sequence: 17
  givenname: Menno P. J.
  orcidid: 0000-0002-4038-6636
  surname: de Winther
  fullname: de Winther, Menno P. J.
– sequence: 18
  givenname: Johan
  surname: Kuiper
  fullname: Kuiper, Johan
– sequence: 19
  givenname: Ilze
  orcidid: 0000-0002-1242-1959
  surname: Bot
  fullname: Bot, Ilze
– sequence: 20
  givenname: Bram
  orcidid: 0000-0003-3996-0503
  surname: Slütter
  fullname: Slütter, Bram
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38665903$$D View this record in MEDLINE/PubMed
BookMark eNp9Ustu1TAQtVARLaU_wAJZYtNNwK-8VghVvKRKLChry3HGvQbHDnZSlR_p9zLpbVHpgo3Hmjnn-Mx4npODmCIQ8pKzN5zJ7m1Rije8YkJUjAnWVeoJORKtxFTds4MH90NyUoofmGpEV7eyfUYOZdc0WJFH5Oabj5cBKgsh0At6GzJYmJeUaYFfK0SLCJocnY3PMNLdOplIzbKDnIoNeC7e0jkYxBZq4kiHkNKIKldgAmbWJflpWiNUwf8E6sAsa0YoSsL1jAQUBefAbk_uLZQX5KlDMpzcxWPy_eOHi7PP1fnXT1_O3p9XVkm-VM6x3hgu61oyZcVga-ecldALKZVs7Wg6AaoG4cw49AZwJMaNopMNtP2GOibv9rrzOkwwWohLNkHP2U8m_9bJeP1vJfqdvkxXmnOmeFszVDi9U8hpm8CiJ1-2HkyEtBaNxtpeKSUlQl8_gv5Ia47Yn5ZC1H3L63az9Oqhpb9e7v8MAd0eYPEDSganrV_M4tPm0AfNmd42RO83ROOG6NsN0Qqp4hH1Xv0_pD9KCcF6
CitedBy_id crossref_primary_10_1038_s41590_024_02039_w
crossref_primary_10_3389_fimmu_2023_1239148
crossref_primary_10_1038_s44161_023_00376_x
crossref_primary_10_1038_s41577_024_01010_y
crossref_primary_10_1093_cvr_cvae154
crossref_primary_10_1007_s11936_023_01024_0
crossref_primary_10_1038_s44161_025_00652_y
crossref_primary_10_1038_s44161_023_00295_x
crossref_primary_10_1161_CIRCRESAHA_125_325496
crossref_primary_10_3390_cells12172152
crossref_primary_10_1007_s12672_025_03419_w
crossref_primary_10_1038_s41569_024_01111_0
crossref_primary_10_1016_j_atherosclerosis_2023_03_021
crossref_primary_10_1038_s41422_024_00945_0
crossref_primary_10_1161_ATVBAHA_123_320511
crossref_primary_10_3390_ijms25116016
crossref_primary_10_1161_CIRCULATIONAHA_123_067931
crossref_primary_10_1161_CIRCULATIONAHA_124_072384
crossref_primary_10_4049_jimmunol_2300267
crossref_primary_10_1016_j_mvr_2025_104818
crossref_primary_10_1007_s00395_023_01023_z
crossref_primary_10_1161_CIRCRESAHA_123_322791
crossref_primary_10_3389_flupu_2025_1607792
crossref_primary_10_3390_biomedicines13081990
crossref_primary_10_3389_fimmu_2024_1302031
crossref_primary_10_3389_fimmu_2024_1369202
crossref_primary_10_1007_s10557_024_07608_7
crossref_primary_10_1161_ATVBAHA_124_319845
crossref_primary_10_1016_j_jinf_2024_106158
crossref_primary_10_1038_s41590_023_01589_9
crossref_primary_10_1038_s44161_025_00671_9
crossref_primary_10_1038_s44161_023_00230_0
crossref_primary_10_1038_s41422_024_00955_y
crossref_primary_10_2147_IJGM_S418913
crossref_primary_10_1038_s41590_024_02021_6
crossref_primary_10_15829_1560_4071_2024_6017
crossref_primary_10_1016_j_cjca_2023_09_009
crossref_primary_10_1038_s41569_024_01009_x
crossref_primary_10_1016_j_jacbts_2025_101323
crossref_primary_10_1038_s44325_025_00056_8
crossref_primary_10_3389_fcell_2024_1446758
crossref_primary_10_1055_a_2437_6111
crossref_primary_10_1007_s11883_023_01125_y
crossref_primary_10_1038_s42255_024_01015_w
crossref_primary_10_3389_fimmu_2024_1465889
crossref_primary_10_1093_cvr_cvaf098
crossref_primary_10_1016_j_vph_2025_107516
crossref_primary_10_1186_s12979_024_00434_3
crossref_primary_10_1161_ATVBAHA_123_320539
crossref_primary_10_1016_j_ajpath_2023_12_007
crossref_primary_10_3389_fimmu_2024_1350471
Cites_doi 10.1172/jci.insight.149741
10.1038/s41590-019-0444-8
10.1093/nar/gkz874
10.1016/j.jconrel.2018.10.028
10.1056/NEJMoa2021372
10.1161/CIRCRESAHA.122.321116
10.1038/nri1200
10.1016/j.jacc.2017.11.055
10.1038/s41467-021-21246-9
10.1161/ATVBAHA.107.151274
10.1161/CIRCULATIONAHA.119.042863
10.4049/jimmunol.2100522
10.1002/cti2.1005
10.1111/j.1365-2567.2009.03241.x
10.1182/blood-2004-03-1184
10.18632/oncotarget.19892
10.1016/j.immuni.2017.09.008
10.1161/CIRCULATIONAHA.118.039288
10.1126/science.1254536
10.3390/cells9122665
10.1093/cvr/cvr101
10.1038/s41586-019-0969-x
10.1111/joim.12589
10.1111/bph.13802
10.1161/CIRCRESAHA.120.316770
10.1038/emm.2007.20
10.1038/s41587-020-0505-4
10.1038/s44161-022-00063-3
10.1046/j.1365-2567.2000.00964.x
10.1182/blood-2006-05-022798
10.1111/j.1365-2796.2009.02209.x
10.1038/s41586-019-1325-x
10.1161/STROKEAHA.107.496703
10.1016/j.cell.2019.05.031
10.1038/s41467-020-18513-6
10.1056/NEJMoa1707914
10.1038/nature01433
10.1111/j.1365-2133.2009.09552.x
10.1097/MOL.0000000000000025
10.1007/s10564-004-2304-6
10.1161/CIRCRESAHA.121.320090
10.1002/eji.201646837
10.1038/s41467-021-25006-7
10.1038/s41591-019-0590-4
10.1038/s41586-018-0414-6
10.1016/j.smim.2013.10.009
10.1038/ncomms11653
10.1016/j.jacc.2007.06.040
10.1038/nri3862
10.1161/01.CIR.101.25.2883
10.1038/nbt.4096
10.12688/f1000research.22139.1
ContentType Journal Article
Copyright The Author(s) 2023.
Copyright Nature Publishing Group Feb 2023
The Author(s) 2023
Copyright_xml – notice: The Author(s) 2023.
– notice: Copyright Nature Publishing Group Feb 2023
– notice: The Author(s) 2023
DBID AAYXX
CITATION
NPM
3V.
7RV
7X7
7XB
8FI
8FJ
8FK
ABUWG
AFKRA
BENPR
CCPQU
FYUFA
GHDGH
K9.
KB0
M0S
NAPCQ
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOI 10.1038/s44161-022-00208-4
DatabaseName CrossRef
PubMed
ProQuest Central (Corporate)
Nursing & Allied Health Database
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni Edition)
ProQuest Central UK/Ireland
ProQuest Central
ProQuest One Community College
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Database (Alumni Edition)
Health & Medical Collection (Alumni)
Nursing & Allied Health Premium
ProQuest One Academic
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 Academic (retired)
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Nursing & Allied Health Source
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Central China
ProQuest Hospital Collection (Alumni)
ProQuest Central
Nursing & Allied Health Premium
ProQuest Health & Medical Complete
ProQuest Health & Medical Research Collection
Health Research Premium Collection
ProQuest One Academic UKI Edition
Health and Medicine Complete (Alumni Edition)
ProQuest Nursing & Allied Health Source (Alumni)
ProQuest Central (New)
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList CrossRef

ProQuest One Academic Middle East (New)
PubMed
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7RV
  name: Nursing & Allied Health Database
  url: https://search.proquest.com/nahs
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
EISSN 2731-0590
EndPage 125
ExternalDocumentID PMC11041750
38665903
10_1038_s44161_022_00208_4
Genre Journal Article
GroupedDBID 0R~
53G
7RV
7X7
8FI
8FJ
AARCD
AAYXX
ABJNI
ABUWG
ACBWK
AFANA
AFFHD
AFKRA
AFSHS
AFWHJ
AGSTI
ALMA_UNASSIGNED_HOLDINGS
ATHPR
BENPR
CCPQU
CITATION
FYUFA
HMCUK
NAPCQ
NFIDA
PHGZM
PHGZT
PPXIY
SNYQT
SOJ
UKHRP
AAYZH
NPM
ODYON
3V.
7XB
8FK
K9.
PJZUB
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
ID FETCH-LOGICAL-c431t-ff09aa1355304c2bc5fffc3e9233437cda82e45e2fadb9ae731afd2836e79e923
IEDL.DBID BENPR
ISICitedReferencesCount 57
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=001126277600009&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 2731-0590
IngestDate Tue Nov 04 02:05:41 EST 2025
Sun Nov 09 11:35:54 EST 2025
Tue Oct 07 07:18:55 EDT 2025
Mon Jul 21 06:02:00 EDT 2025
Sat Nov 29 06:16:25 EST 2025
Tue Nov 18 22:42:30 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 2
Keywords Autoimmunity
Atherosclerosis
Language English
License The Author(s) 2023.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c431t-ff09aa1355304c2bc5fffc3e9233437cda82e45e2fadb9ae731afd2836e79e923
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0001-5853-8784
0000-0002-1242-1959
0000-0003-3996-0503
0000-0002-6338-051X
0000-0003-3541-9912
0000-0002-4038-6636
0000-0002-0051-9836
0000-0002-9835-1735
0000-0002-7174-1952
0000-0002-9747-3458
0000-0001-5345-1022
OpenAccessLink https://pubmed.ncbi.nlm.nih.gov/PMC11041750
PMID 38665903
PQID 3225971572
PQPubID 7343583
PageCount 14
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_11041750
proquest_miscellaneous_3047944433
proquest_journals_3225971572
pubmed_primary_38665903
crossref_citationtrail_10_1038_s44161_022_00208_4
crossref_primary_10_1038_s44161_022_00208_4
PublicationCentury 2000
PublicationDate 2023-02-01
PublicationDateYYYYMMDD 2023-02-01
PublicationDate_xml – month: 02
  year: 2023
  text: 2023-02-01
  day: 01
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: New York
– name: London
PublicationTitle Nature Cardiovascular Research
PublicationTitleAlternate Nat Cardiovasc Res
PublicationYear 2023
Publisher Nature Publishing Group
Nature Publishing Group UK
Publisher_xml – name: Nature Publishing Group
– name: Nature Publishing Group UK
References S Jin (208_CR25) 2021; 12
D Wolf (208_CR6) 2020; 142
G La Manno (208_CR22) 2018; 560
N Benne (208_CR8) 2018; 291
G Liuzzo (208_CR21) 2007; 50
B Van Wilgenburg (208_CR36) 2016; 7
208_CR50
A Mohr (208_CR14) 2018; 7
D Cibrián (208_CR11) 2017; 47
K Padhan (208_CR17) 2010; 129
PM Ridker (208_CR1) 2017; 377
F D’Acquisto (208_CR30) 2007; 109
GHM Van Puijvelde (208_CR46) 2007; 27
TTP Seijkens (208_CR44) 2018; 71
P Dunér (208_CR47) 2011; 91
R Saigusa (208_CR40) 2022; 1
T Calandra (208_CR29) 2003; 3
SM Nidorf (208_CR2) 2020; 383
208_CR54
A Gisterå (208_CR9) 2017; 281
P Roy (208_CR7) 2022; 131
JM Schenkel (208_CR12) 2014; 346
CK Vorkas (208_CR19) 2022; 208
F Penkava (208_CR31) 2020; 11
DI Godfrey (208_CR35) 2019; 20
E Smeets (208_CR43) 2013; 24
N Borcherding (208_CR53) 2020; 9
DM Fernandez (208_CR4) 2019; 25
K Kranzer (208_CR13) 2000; 99
G Bixel (208_CR28) 2004; 104
MAC Depuydt (208_CR3) 2020; 127
M Kleinewietfeld (208_CR37) 2013; 25
IO Kwon (208_CR27) 2007; 39
A Butler (208_CR51) 2018; 36
S Stemme (208_CR5) 1995; 92
AC Foks (208_CR26) 2017; 174
BAN Verhoeven (208_CR48) 2004; 19
RR Chowdhury (208_CR10) 2022; 130
H Zhang (208_CR39) 2021; 12
WE Hellings (208_CR49) 2008; 39
T Stuart (208_CR52) 2019; 177
DV Bagaev (208_CR18) 2020; 48
X Wang (208_CR24) 2010; 162
O Khan (208_CR16) 2019; 571
G Liuzzo (208_CR20) 2000; 102
H Björkbacka (208_CR32) 2010; 268
M Wigren (208_CR41) 2019; 139
E Treiner (208_CR34) 2003; 422
I Tabas (208_CR42) 2017; 47
J Cao (208_CR55) 2019; 566
EJ Wherry (208_CR15) 2015; 15
AJ Ali (208_CR23) 2020; 9
Z Lin (208_CR33) 2017; 8
H Huang (208_CR38) 2020; 38
KY Chyu (208_CR45) 2022; 7
39196001 - Nat Cardiovasc Res. 2023 Mar;2(3):227-229. doi: 10.1038/s44161-023-00230-0
References_xml – volume: 7
  start-page: e149741
  year: 2022
  ident: 208_CR45
  publication-title: JCI Insight
  doi: 10.1172/jci.insight.149741
– volume: 20
  start-page: 1110
  year: 2019
  ident: 208_CR35
  publication-title: Nat. Immunol.
  doi: 10.1038/s41590-019-0444-8
– volume: 48
  start-page: D1057
  year: 2020
  ident: 208_CR18
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/gkz874
– volume: 291
  start-page: 135
  year: 2018
  ident: 208_CR8
  publication-title: J. Control. Release
  doi: 10.1016/j.jconrel.2018.10.028
– volume: 383
  start-page: 1838
  year: 2020
  ident: 208_CR2
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJMoa2021372
– volume: 131
  start-page: 258
  year: 2022
  ident: 208_CR7
  publication-title: Circ. Res.
  doi: 10.1161/CIRCRESAHA.122.321116
– volume: 3
  start-page: 791
  year: 2003
  ident: 208_CR29
  publication-title: Nat. Rev. Immunol.
  doi: 10.1038/nri1200
– volume: 71
  start-page: 527
  year: 2018
  ident: 208_CR44
  publication-title: J. Am. Coll. Cardiol.
  doi: 10.1016/j.jacc.2017.11.055
– volume: 12
  year: 2021
  ident: 208_CR25
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-021-21246-9
– volume: 27
  start-page: 2677
  year: 2007
  ident: 208_CR46
  publication-title: Arterioscler. Thromb. Vasc. Biol.
  doi: 10.1161/ATVBAHA.107.151274
– volume: 142
  start-page: 1279
  year: 2020
  ident: 208_CR6
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.119.042863
– volume: 208
  start-page: 1042
  year: 2022
  ident: 208_CR19
  publication-title: J. Immunol.
  doi: 10.4049/jimmunol.2100522
– volume: 7
  start-page: e1005
  year: 2018
  ident: 208_CR14
  publication-title: Clin. Transl. Immunol.
  doi: 10.1002/cti2.1005
– volume: 129
  start-page: 322
  year: 2010
  ident: 208_CR17
  publication-title: Immunology
  doi: 10.1111/j.1365-2567.2009.03241.x
– volume: 104
  start-page: 3205
  year: 2004
  ident: 208_CR28
  publication-title: Blood
  doi: 10.1182/blood-2004-03-1184
– volume: 8
  start-page: 99312
  year: 2017
  ident: 208_CR33
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.19892
– volume: 47
  start-page: 621
  year: 2017
  ident: 208_CR42
  publication-title: Immunity
  doi: 10.1016/j.immuni.2017.09.008
– volume: 139
  start-page: 2554
  year: 2019
  ident: 208_CR41
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.118.039288
– volume: 346
  start-page: 98
  year: 2014
  ident: 208_CR12
  publication-title: Science
  doi: 10.1126/science.1254536
– volume: 9
  start-page: 2665
  year: 2020
  ident: 208_CR23
  publication-title: Cells
  doi: 10.3390/cells9122665
– volume: 91
  start-page: 528
  year: 2011
  ident: 208_CR47
  publication-title: Cardiovasc. Res.
  doi: 10.1093/cvr/cvr101
– volume: 566
  start-page: 496
  year: 2019
  ident: 208_CR55
  publication-title: Nature
  doi: 10.1038/s41586-019-0969-x
– volume: 281
  start-page: 383
  year: 2017
  ident: 208_CR9
  publication-title: J. Intern. Med.
  doi: 10.1111/joim.12589
– volume: 174
  start-page: 3940
  year: 2017
  ident: 208_CR26
  publication-title: Br. J. Pharmacol.
  doi: 10.1111/bph.13802
– volume: 127
  start-page: 1437
  year: 2020
  ident: 208_CR3
  publication-title: Circ. Res.
  doi: 10.1161/CIRCRESAHA.120.316770
– volume: 39
  start-page: 176
  year: 2007
  ident: 208_CR27
  publication-title: Exp. Mol. Med.
  doi: 10.1038/emm.2007.20
– volume: 38
  start-page: 1194
  year: 2020
  ident: 208_CR38
  publication-title: Nat. Biotechnol.
  doi: 10.1038/s41587-020-0505-4
– volume: 1
  start-page: 462
  year: 2022
  ident: 208_CR40
  publication-title: Nat. Cardiovasc. Res.
  doi: 10.1038/s44161-022-00063-3
– volume: 99
  start-page: 170
  year: 2000
  ident: 208_CR13
  publication-title: Immunology
  doi: 10.1046/j.1365-2567.2000.00964.x
– volume: 109
  start-page: 1095
  year: 2007
  ident: 208_CR30
  publication-title: Blood
  doi: 10.1182/blood-2006-05-022798
– volume: 268
  start-page: 50
  year: 2010
  ident: 208_CR32
  publication-title: J. Intern. Med.
  doi: 10.1111/j.1365-2796.2009.02209.x
– volume: 571
  start-page: 211
  year: 2019
  ident: 208_CR16
  publication-title: Nature
  doi: 10.1038/s41586-019-1325-x
– volume: 39
  start-page: 1029
  year: 2008
  ident: 208_CR49
  publication-title: Stroke
  doi: 10.1161/STROKEAHA.107.496703
– volume: 177
  start-page: 1888
  year: 2019
  ident: 208_CR52
  publication-title: Cell
  doi: 10.1016/j.cell.2019.05.031
– volume: 11
  year: 2020
  ident: 208_CR31
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-020-18513-6
– volume: 377
  start-page: 1119
  year: 2017
  ident: 208_CR1
  publication-title: N. Engl. J. Med.
  doi: 10.1056/NEJMoa1707914
– volume: 422
  start-page: 164
  year: 2003
  ident: 208_CR34
  publication-title: Nature
  doi: 10.1038/nature01433
– volume: 162
  start-page: 487
  year: 2010
  ident: 208_CR24
  publication-title: Br. J. Dermatol.
  doi: 10.1111/j.1365-2133.2009.09552.x
– volume: 24
  start-page: 518
  year: 2013
  ident: 208_CR43
  publication-title: Curr. Opin. Lipidol.
  doi: 10.1097/MOL.0000000000000025
– volume: 19
  start-page: 1127
  year: 2004
  ident: 208_CR48
  publication-title: Eur. J. Epidemiol.
  doi: 10.1007/s10564-004-2304-6
– volume: 92
  start-page: 3893
  year: 1995
  ident: 208_CR5
  publication-title: Med. Sci.
– volume: 130
  start-page: 1510
  year: 2022
  ident: 208_CR10
  publication-title: Circ. Res.
  doi: 10.1161/CIRCRESAHA.121.320090
– volume: 47
  start-page: 946
  year: 2017
  ident: 208_CR11
  publication-title: Eur. J. Immunol.
  doi: 10.1002/eji.201646837
– volume: 12
  start-page: 4699
  year: 2021
  ident: 208_CR39
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-021-25006-7
– volume: 25
  start-page: 1576
  year: 2019
  ident: 208_CR4
  publication-title: Nat. Med.
  doi: 10.1038/s41591-019-0590-4
– volume: 560
  start-page: 494
  year: 2018
  ident: 208_CR22
  publication-title: Nature
  doi: 10.1038/s41586-018-0414-6
– ident: 208_CR50
– ident: 208_CR54
– volume: 25
  start-page: 305
  year: 2013
  ident: 208_CR37
  publication-title: Semin. Immunol.
  doi: 10.1016/j.smim.2013.10.009
– volume: 7
  year: 2016
  ident: 208_CR36
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms11653
– volume: 50
  start-page: 1450
  year: 2007
  ident: 208_CR21
  publication-title: J. Am. Coll. Cardiol.
  doi: 10.1016/j.jacc.2007.06.040
– volume: 15
  start-page: 486
  year: 2015
  ident: 208_CR15
  publication-title: Nat. Rev. Immunol.
  doi: 10.1038/nri3862
– volume: 102
  start-page: 2883
  year: 2000
  ident: 208_CR20
  publication-title: Circulation
  doi: 10.1161/01.CIR.101.25.2883
– volume: 36
  start-page: 411
  year: 2018
  ident: 208_CR51
  publication-title: Nat. Biotechnol.
  doi: 10.1038/nbt.4096
– volume: 9
  start-page: 47
  year: 2020
  ident: 208_CR53
  publication-title: F1000Res.
  doi: 10.12688/f1000research.22139.1
– reference: 39196001 - Nat Cardiovasc Res. 2023 Mar;2(3):227-229. doi: 10.1038/s44161-023-00230-0
SSID ssib046285737
Score 2.4521217
Snippet Atherosclerosis is a lipid-driven chronic inflammatory disease; however, whether it can be classified as an autoimmune disease remains unclear. In this study,...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 112
SubjectTerms Antigens
Atherosclerosis
Cytomegalovirus
Flow cytometry
Genomics
Leukocytes
Lymphocytes
Patients
Protein expression
Proteins
T cell receptors
Title Single-cell T cell receptor sequencing of paired human atherosclerotic plaques and blood reveals autoimmune-like features of expanded effector T cells
URI https://www.ncbi.nlm.nih.gov/pubmed/38665903
https://www.proquest.com/docview/3225971572
https://www.proquest.com/docview/3047944433
https://pubmed.ncbi.nlm.nih.gov/PMC11041750
Volume 2
WOSCitedRecordID wos001126277600009&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVPQU
  databaseName: Health & Medical Collection
  customDbUrl:
  eissn: 2731-0590
  dateEnd: 20241209
  omitProxy: false
  ssIdentifier: ssib046285737
  issn: 2731-0590
  databaseCode: 7X7
  dateStart: 20220101
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/healthcomplete
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: Nursing & Allied Health Database
  customDbUrl:
  eissn: 2731-0590
  dateEnd: 20241209
  omitProxy: false
  ssIdentifier: ssib046285737
  issn: 2731-0590
  databaseCode: 7RV
  dateStart: 20220101
  isFulltext: true
  titleUrlDefault: https://search.proquest.com/nahs
  providerName: ProQuest
– providerCode: PRVPQU
  databaseName: ProQuest Central
  customDbUrl:
  eissn: 2731-0590
  dateEnd: 20241209
  omitProxy: false
  ssIdentifier: ssib046285737
  issn: 2731-0590
  databaseCode: BENPR
  dateStart: 20220101
  isFulltext: true
  titleUrlDefault: https://www.proquest.com/central
  providerName: ProQuest
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwELbolgMXHuK1UCojcUNWk9iJ7RMC1IoDWlWlVHuLHD_EilUSNrtVfwm_lxnHu7Ag9cLFOXjijDJj-7M9_oaQN4VylarKhmVGwAJFh5IZabC766YxsvAi8hZcfZazmZrP9XnacBtSWOV2TIwDtess7pGfoONpmZeyeNf_YJg1Ck9XUwqNA3KITGViQg4_nM7OL7YehRcvS8llui2TcXUyCIT0DIPYY4JKJvZnpH9g5t_Rkn9MP2cP_lfxh-R-Ap70_egpj8gd3z4mP7_AzLX0DLfv6SWNDxgCfQ8rcZqirEGCdoH2BgZHR2NOPxphYzdAQ6sO2qP90qBK1LSOxlB4isxQ4NnUbNbdAu-geLZcfPc0-MgkOmCT_qbHLWxHx6AS-OSowvCEfD07vfz4iaVMDcwCAFmzEDJtTM4xB5GwRWPLEILlHtAjF1xaZxRYvfRFMK7Rxkuem-AA2VReapR6SiZt1_rnhHoJSzxf2CpruCgyrRolmlw4XrpCOF1NSb61Vm0TjTlm01jW8Tidq3q0cA0WrqOFazElb3fv9COJx63SR1tD1qlDD_VvK07J6101dEX8Lab13QZkIl2_EJxPybPRZ3af48grqDOoUXvetBNAmu_9mnbxLdJ9A0ATAPKyF7fr9ZLcKwCAjRHlR2SyXm38K3LXXq8Xw-qYHMiLKyznMpbqOHWVX-5OHU0
linkProvider ProQuest
linkToHtml http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lb9QwELZKQYILD_FaKGAkOCGrie2s4wNCCKhadVkhWKreghPbYtVVkm6yPP4IP4PfyIyTLCxIvfXAKQdPHGvyeWZsf54h5AlP7TgdJzmLjIQFivYJM8rgdNd5bhR3MuQtOJqo6TQ9PtbvtsjP4S4M0ioHmxgMta0K3CPfReBpFSeKv6hPGVaNwtPVoYRGB4tD9_0rLNma5wev4f8-5XzvzezVPuurCrACnGXLvI-0MbHAejmy4HmReO8L4SDSEVKowpoURpg47o3NtXFKxMZb8MJjpzRKQb8XyEWw4zFSyNT7owG_eM0zUUL1d3Mike42EhcQDCnzoRwmk5v-75-g9m9u5h_Obu_a_6am6-RqH1bTl908uEG2XHmT_PgAfnnhGB5O0BkNDzDwrm6rJe055CBBK09rA6bf0lCxkIaguGqgo2UF_dF6YVAF1JSWBqI_xbxXMG-pWbXVHG_YOLaYnzjqXciT2mCX7luNG_SWdpQZ-GQ3hOYW-XguqrhNtsuqdHcJdQoWsI4X4ygXkkc6zVOZx9KKxHJp9XhE4gEdWdEnacdaIYsskAVEmnWIygBRWUBUJkfk2fqduktRcqb0zgCcrDdXTfYbNSPyeN0MhgbVYkpXrUAmFCOQUogRudNhdP05gVkTdQQt6QZ61wKYxHyzpZx_DsnMIfyUEMJG984e1yNyeX_2dpJNDqaH98kVDqFmx53fIdvtcuUekEvFl3beLB-GKUnJp_MG9y80nngn
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=Single-cell+T+cell+receptor+sequencing+of+paired+human+atherosclerotic+plaques+and+blood+reveals+autoimmune-like+features+of+expanded+effector+T+cells&rft.jtitle=Nature+Cardiovascular+Research&rft.au=Depuydt%2C+Marie+A.+C&rft.au=Schaftenaar%2C+Frank+H&rft.au=Prange%2C+Koen+H.+M&rft.au=Boltjes%2C+Arjan&rft.date=2023-02-01&rft.pub=Nature+Publishing+Group&rft.eissn=2731-0590&rft.volume=2&rft.issue=2&rft.spage=112&rft.epage=125&rft_id=info:doi/10.1038%2Fs44161-022-00208-4
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2731-0590&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2731-0590&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2731-0590&client=summon