Bronchiectasis Is a Model for Chronic Bacterial Infection Inducing Autoimmunity in Rheumatoid Arthritis

Objective To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti–citrullinated protein antibodies (ACPAs), by studying patients with bronchiectasis (BR) alone and BR patients with rheumatoid arthritis (BR/RA). Methods We studied 122 patients with B...

Full description

Saved in:
Bibliographic Details
Published inArthritis & rheumatology (Hoboken, N.J.) Vol. 67; no. 9; pp. 2335 - 2342
Main Authors Quirke, Anne‐Marie, Perry, Elizabeth, Cartwright, Alison, Kelly, Clive, De Soyza, Anthony, Eggleton, Paul, Hutchinson, David, Venables, Patrick J.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.09.2015
John Wiley and Sons Inc
Subjects
Online AccessGet full text
ISSN2326-5191
2326-5205
DOI10.1002/art.39226

Cover

Loading…
Abstract Objective To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti–citrullinated protein antibodies (ACPAs), by studying patients with bronchiectasis (BR) alone and BR patients with rheumatoid arthritis (BR/RA). Methods We studied 122 patients with BR alone, 50 patients with BR/RA, and 50 RA patients without lung disease, as well as 87 patients with asthma and 79 healthy subjects as controls. RF levels were measured using an automated analyzer, and cyclic citrullinated peptide 2 (CCP‐2) was used to detect ACPAs. The fine specificities of citrullinated α‐enolase peptide 1 (CEP‐1), Cit‐vimentin, and Cit‐fibrinogen to their arginine‐containing control peptides (arginine‐containing α‐enolase peptide 1 [REP‐1], vimentin, and fibrinogen) were measured by enzyme‐linked immunosorbent assay. Results Among the BR patients and control subjects, 39% and 42%, respectively, were ever‐smokers. The frequency of RF positivity in serum was increased in BR patients compared with controls (25% versus 10%), as were the frequencies of antibodies to CCP‐2 (5% versus 0%), CEP‐1 (7% versus 4%), Cit‐vimentin (7% versus 4%), and Cit‐fibrinogen (12% versus 4%), although only the differences for RF and Cit‐fibrinogen were significant (P < 0.05). We observed a corresponding increase in the frequency of antibodies to the arginine‐containing control peptides in BR patients compared with controls (for REP‐1, 19% versus 4% [P < 0.01]; for vimentin, 16% versus 4% [P < 0.05]), demonstrating that the ACPA response in patients with BR is not citrulline specific. The lack of citrulline specificity was further confirmed by absorption studies. In BR/RA patients, all ACPA responses were highly citrulline specific. Conclusion Bronchiectasis is an unusual but potent model for the induction of autoimmunity in RA by bacterial infection in the lung. Our study suggests that the ACPA response is not citrulline specific during the early stages of tolerance breakdown but becomes more specific in patients with BR in whom BR/RA develops.
AbstractList To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPAs), by studying patients with bronchiectasis (BR) alone and BR patients with rheumatoid arthritis (BR/RA). We studied 122 patients with BR alone, 50 patients with BR/RA, and 50 RA patients without lung disease, as well as 87 patients with asthma and 79 healthy subjects as controls. RF levels were measured using an automated analyzer, and cyclic citrullinated peptide 2 (CCP-2) was used to detect ACPAs. The fine specificities of citrullinated α-enolase peptide 1 (CEP-1), Cit-vimentin, and Cit-fibrinogen to their arginine-containing control peptides (arginine-containing α-enolase peptide 1 [REP-1], vimentin, and fibrinogen) were measured by enzyme-linked immunosorbent assay. Among the BR patients and control subjects, 39% and 42%, respectively, were ever-smokers. The frequency of RF positivity in serum was increased in BR patients compared with controls (25% versus 10%), as were the frequencies of antibodies to CCP-2 (5% versus 0%), CEP-1 (7% versus 4%), Cit-vimentin (7% versus 4%), and Cit-fibrinogen (12% versus 4%), although only the differences for RF and Cit-fibrinogen were significant (P < 0.05). We observed a corresponding increase in the frequency of antibodies to the arginine-containing control peptides in BR patients compared with controls (for REP-1, 19% versus 4% [P < 0.01]; for vimentin, 16% versus 4% [P < 0.05]), demonstrating that the ACPA response in patients with BR is not citrulline specific. The lack of citrulline specificity was further confirmed by absorption studies. In BR/RA patients, all ACPA responses were highly citrulline specific. Bronchiectasis is an unusual but potent model for the induction of autoimmunity in RA by bacterial infection in the lung. Our study suggests that the ACPA response is not citrulline specific during the early stages of tolerance breakdown but becomes more specific in patients with BR in whom BR/RA develops.
Objective To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPAs), by studying patients with bronchiectasis (BR) alone and BR patients with rheumatoid arthritis (BR/RA). Methods We studied 122 patients with BR alone, 50 patients with BR/RA, and 50 RA patients without lung disease, as well as 87 patients with asthma and 79 healthy subjects as controls. RF levels were measured using an automated analyzer, and cyclic citrullinated peptide 2 (CCP-2) was used to detect ACPAs. The fine specificities of citrullinated [alpha]-enolase peptide 1 (CEP-1), Cit-vimentin, and Cit-fibrinogen to their arginine-containing control peptides (arginine-containing [alpha]-enolase peptide 1 [REP-1], vimentin, and fibrinogen) were measured by enzyme-linked immunosorbent assay. Results Among the BR patients and control subjects, 39% and 42%, respectively, were ever-smokers. The frequency of RF positivity in serum was increased in BR patients compared with controls (25% versus 10%), as were the frequencies of antibodies to CCP-2 (5% versus 0%), CEP-1 (7% versus 4%), Cit-vimentin (7% versus 4%), and Cit-fibrinogen (12% versus 4%), although only the differences for RF and Cit-fibrinogen were significant (P < 0.05). We observed a corresponding increase in the frequency of antibodies to the arginine-containing control peptides in BR patients compared with controls (for REP-1, 19% versus 4% [P < 0.01]; for vimentin, 16% versus 4% [P < 0.05]), demonstrating that the ACPA response in patients with BR is not citrulline specific. The lack of citrulline specificity was further confirmed by absorption studies. In BR/RA patients, all ACPA responses were highly citrulline specific. Conclusion Bronchiectasis is an unusual but potent model for the induction of autoimmunity in RA by bacterial infection in the lung. Our study suggests that the ACPA response is not citrulline specific during the early stages of tolerance breakdown but becomes more specific in patients with BR in whom BR/RA develops.
OBJECTIVETo examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPAs), by studying patients with bronchiectasis (BR) alone and BR patients with rheumatoid arthritis (BR/RA).METHODSWe studied 122 patients with BR alone, 50 patients with BR/RA, and 50 RA patients without lung disease, as well as 87 patients with asthma and 79 healthy subjects as controls. RF levels were measured using an automated analyzer, and cyclic citrullinated peptide 2 (CCP-2) was used to detect ACPAs. The fine specificities of citrullinated α-enolase peptide 1 (CEP-1), Cit-vimentin, and Cit-fibrinogen to their arginine-containing control peptides (arginine-containing α-enolase peptide 1 [REP-1], vimentin, and fibrinogen) were measured by enzyme-linked immunosorbent assay.RESULTSAmong the BR patients and control subjects, 39% and 42%, respectively, were ever-smokers. The frequency of RF positivity in serum was increased in BR patients compared with controls (25% versus 10%), as were the frequencies of antibodies to CCP-2 (5% versus 0%), CEP-1 (7% versus 4%), Cit-vimentin (7% versus 4%), and Cit-fibrinogen (12% versus 4%), although only the differences for RF and Cit-fibrinogen were significant (P < 0.05). We observed a corresponding increase in the frequency of antibodies to the arginine-containing control peptides in BR patients compared with controls (for REP-1, 19% versus 4% [P < 0.01]; for vimentin, 16% versus 4% [P < 0.05]), demonstrating that the ACPA response in patients with BR is not citrulline specific. The lack of citrulline specificity was further confirmed by absorption studies. In BR/RA patients, all ACPA responses were highly citrulline specific.CONCLUSIONBronchiectasis is an unusual but potent model for the induction of autoimmunity in RA by bacterial infection in the lung. Our study suggests that the ACPA response is not citrulline specific during the early stages of tolerance breakdown but becomes more specific in patients with BR in whom BR/RA develops.
Objective To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti–citrullinated protein antibodies (ACPAs), by studying patients with bronchiectasis (BR) alone and BR patients with rheumatoid arthritis (BR/RA). Methods We studied 122 patients with BR alone, 50 patients with BR/RA, and 50 RA patients without lung disease, as well as 87 patients with asthma and 79 healthy subjects as controls. RF levels were measured using an automated analyzer, and cyclic citrullinated peptide 2 (CCP‐2) was used to detect ACPAs. The fine specificities of citrullinated α‐enolase peptide 1 (CEP‐1), Cit‐vimentin, and Cit‐fibrinogen to their arginine‐containing control peptides (arginine‐containing α‐enolase peptide 1 [REP‐1], vimentin, and fibrinogen) were measured by enzyme‐linked immunosorbent assay. Results Among the BR patients and control subjects, 39% and 42%, respectively, were ever‐smokers. The frequency of RF positivity in serum was increased in BR patients compared with controls (25% versus 10%), as were the frequencies of antibodies to CCP‐2 (5% versus 0%), CEP‐1 (7% versus 4%), Cit‐vimentin (7% versus 4%), and Cit‐fibrinogen (12% versus 4%), although only the differences for RF and Cit‐fibrinogen were significant (P < 0.05). We observed a corresponding increase in the frequency of antibodies to the arginine‐containing control peptides in BR patients compared with controls (for REP‐1, 19% versus 4% [P < 0.01]; for vimentin, 16% versus 4% [P < 0.05]), demonstrating that the ACPA response in patients with BR is not citrulline specific. The lack of citrulline specificity was further confirmed by absorption studies. In BR/RA patients, all ACPA responses were highly citrulline specific. Conclusion Bronchiectasis is an unusual but potent model for the induction of autoimmunity in RA by bacterial infection in the lung. Our study suggests that the ACPA response is not citrulline specific during the early stages of tolerance breakdown but becomes more specific in patients with BR in whom BR/RA develops.
Author Quirke, Anne‐Marie
Perry, Elizabeth
Kelly, Clive
Venables, Patrick J.
Eggleton, Paul
Cartwright, Alison
Hutchinson, David
De Soyza, Anthony
AuthorAffiliation 1 Kennedy Institute, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford Oxford UK
4 Newcastle University and The Freeman Hospital Newcastle UK
2 Queen Elizabeth Hospital, Gateshead, UK, and University of Exeter Medical School Exeter UK
6 Royal Cornwall Hospital Truro UK
3 Queen Elizabeth Hospital Gateshead UK
5 University of Exeter Medical School Exeter UK
AuthorAffiliation_xml – name: 4 Newcastle University and The Freeman Hospital Newcastle UK
– name: 2 Queen Elizabeth Hospital, Gateshead, UK, and University of Exeter Medical School Exeter UK
– name: 6 Royal Cornwall Hospital Truro UK
– name: 3 Queen Elizabeth Hospital Gateshead UK
– name: 1 Kennedy Institute, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford Oxford UK
– name: 5 University of Exeter Medical School Exeter UK
Author_xml – sequence: 1
  givenname: Anne‐Marie
  surname: Quirke
  fullname: Quirke, Anne‐Marie
  organization: Kennedy Institute, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford
– sequence: 2
  givenname: Elizabeth
  surname: Perry
  fullname: Perry, Elizabeth
  organization: Queen Elizabeth Hospital, Gateshead, UK, and University of Exeter Medical School
– sequence: 3
  givenname: Alison
  surname: Cartwright
  fullname: Cartwright, Alison
  organization: Kennedy Institute, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford
– sequence: 4
  givenname: Clive
  surname: Kelly
  fullname: Kelly, Clive
  organization: Queen Elizabeth Hospital
– sequence: 5
  givenname: Anthony
  surname: De Soyza
  fullname: De Soyza, Anthony
  organization: Newcastle University and The Freeman Hospital
– sequence: 6
  givenname: Paul
  surname: Eggleton
  fullname: Eggleton, Paul
  organization: University of Exeter Medical School
– sequence: 7
  givenname: David
  surname: Hutchinson
  fullname: Hutchinson, David
  organization: Royal Cornwall Hospital
– sequence: 8
  givenname: Patrick J.
  surname: Venables
  fullname: Venables, Patrick J.
  organization: Kennedy Institute, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26017630$$D View this record in MEDLINE/PubMed
BookMark eNqNkk1rGzEQhkVJaT6aQ_9AEfTSHJzoc3d1KTimH4aUQkjPQitpvQq7UippU_zvK9d2SEIL0UXDzDMvrzRzDA588BaAdxidY4TIhYr5nApCqlfgiFBSzThB_GAfY4EPwWlKt6gcUaMK8TfgkFQI1xVFR2B1GYPXvbM6q-QSXCao4Pdg7AC7EOGiL2Wn4aXS2UanBrj0XWFd8CUyk3Z-BedTDm4cJ-_yGjoPr3s7jarkDJzH3EeXXXoLXndqSPZ0d5-An18-3yy-za5-fF0u5lczzVnx21SmQq0WwlqNK9pyYxhhAjWtaVtGCG9JRynDSiPTCaMswxVinJJGU4p1Q0_Ap63u3dSO1mjrc1SDvItuVHEtg3LyacW7Xq7CvWQNJaQRReDjTiCGX5NNWY4uaTsMytswJYlrXLNGYMpfgKIG85qhDfrhGXobpujLT2yoGgnMaF2o94_NP7jej6sAF1tAx5BStJ3ULqvNNMpb3CAxkpudkGUn5N-dKB1nzzr2ov9id-q_3WDX_wfl_Ppm2_EH8nTFmQ
CitedBy_id crossref_primary_10_1016_j_rdc_2022_06_002
crossref_primary_10_1080_17476348_2021_1886084
crossref_primary_10_1002_art_40858
crossref_primary_10_3389_froh_2022_895753
crossref_primary_10_3899_jrheum_211242
crossref_primary_10_1016_j_jaci_2015_10_024
crossref_primary_10_1155_2019_6363086
crossref_primary_10_1007_s40744_021_00362_4
crossref_primary_10_3390_cells12060842
crossref_primary_10_1016_j_autrev_2018_02_014
crossref_primary_10_1016_j_intimp_2021_108069
crossref_primary_10_1007_s11926_016_0618_4
crossref_primary_10_1136_annrheumdis_2017_211300
crossref_primary_10_1155_2018_6930297
crossref_primary_10_1513_AnnalsATS_202107_876CME
crossref_primary_10_2147_JAA_S342993
crossref_primary_10_1371_journal_pone_0291967
crossref_primary_10_1016_j_biocel_2017_06_013
crossref_primary_10_1097_MCP_0000000000000569
crossref_primary_10_7759_cureus_29628
crossref_primary_10_1002_art_40900
crossref_primary_10_3389_fimmu_2024_1343480
crossref_primary_10_30841_2786_720X_4_2022_274650
crossref_primary_10_1055_a_2311_9450
crossref_primary_10_1016_j_rdc_2017_04_003
crossref_primary_10_3389_fmed_2022_837133
crossref_primary_10_3390_biomedicines11051262
crossref_primary_10_1038_s41584_021_00585_3
crossref_primary_10_1093_mr_roac117
crossref_primary_10_1038_srep26430
crossref_primary_10_3389_fmed_2022_689711
crossref_primary_10_1016_j_jcf_2023_04_011
crossref_primary_10_1007_s10067_019_04845_2
crossref_primary_10_2147_IDR_S343763
crossref_primary_10_1002_jbmr_3745
crossref_primary_10_1016_j_jbspin_2019_12_006
crossref_primary_10_1080_1744666X_2019_1698293
crossref_primary_10_1177_1759720X221074457
crossref_primary_10_1038_s41584_019_0275_x
crossref_primary_10_1111_imr_12842
crossref_primary_10_1016_j_rhum_2020_02_012
crossref_primary_10_1097_BOR_0000000000000703
crossref_primary_10_1016_j_clinthera_2019_04_012
crossref_primary_10_3390_ijms20164046
crossref_primary_10_1097_MD_0000000000021893
crossref_primary_10_1111_1756_185X_14093
crossref_primary_10_1007_s12016_022_08928_y
crossref_primary_10_4078_jrd_2016_23_3_139
crossref_primary_10_3389_fmicb_2016_01296
crossref_primary_10_1002_art_40401
crossref_primary_10_3390_ijms20020408
crossref_primary_10_3390_microorganisms12040665
crossref_primary_10_1093_rheumatology_kez676
crossref_primary_10_1007_s12016_022_08926_0
crossref_primary_10_1016_j_berh_2017_08_002
crossref_primary_10_1136_annrheumdis_2015_208216
crossref_primary_10_3389_fmed_2022_1004550
crossref_primary_10_1002_art_40767
crossref_primary_10_3389_fimmu_2022_961325
crossref_primary_10_1186_s12931_022_02085_8
crossref_primary_10_1097_BOR_0000000000000238
crossref_primary_10_1002_ppul_24290
crossref_primary_10_1136_annrheumdis_2015_208529
crossref_primary_10_1097_BOR_0000000000000356
crossref_primary_10_1136_bmjopen_2020_048409
crossref_primary_10_1111_resp_13615
Cites_doi 10.1038/nrrheum.2009.28
10.1186/s13075-015-0520-x
10.1016/0007-0971(78)90043-8
10.1183/09031936.00064014
10.1002/art.23936
10.1093/rheumatology/keu165
10.1155/2013/726598
10.1136/annrheumdis-2012-202701
10.1002/art.27584
10.1136/annrheumdis-2014-205498
10.1111/j.0105-2896.2009.00850.x
10.1002/art.11223
10.1038/nrrheum.2015.38
10.1016/j.smim.2011.01.014
10.1002/art.34344
10.1002/art.21575
10.1111/jcpe.12138
10.1002/art.33489
10.1007/s10753-004-6641-z
10.1097/BOR.0b013e32801127c8
10.1016/j.rmed.2012.03.006
10.3899/jrheum.131341
ContentType Journal Article
Copyright 2015 The Authors. Arthritis & Rheumatology is published by Wiley Periodicals, Inc. on behalf of the American College of Rheumatology.
2015, American College of Rheumatology
Copyright_xml – notice: 2015 The Authors. Arthritis & Rheumatology is published by Wiley Periodicals, Inc. on behalf of the American College of Rheumatology.
– notice: 2015, American College of Rheumatology
DBID 24P
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7QL
7QP
7T5
7TM
7U7
C1K
H94
K9.
7X8
5PM
DOI 10.1002/art.39226
DatabaseName Wiley Online Library Open Access
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Bacteriology Abstracts (Microbiology B)
Calcium & Calcified Tissue Abstracts
Immunology Abstracts
Nucleic Acids Abstracts
Toxicology Abstracts
Environmental Sciences and Pollution Management
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Toxicology Abstracts
Bacteriology Abstracts (Microbiology B)
Nucleic Acids Abstracts
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Immunology Abstracts
Calcium & Calcified Tissue Abstracts
Environmental Sciences and Pollution Management
MEDLINE - Academic
DatabaseTitleList MEDLINE
Toxicology Abstracts
MEDLINE - Academic
Toxicology Abstracts

Database_xml – sequence: 1
  dbid: 24P
  name: Wiley Online Library Open Access
  url: https://authorservices.wiley.com/open-science/open-access/browse-journals.html
  sourceTypes: Publisher
– 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
DocumentTitleAlternate BRONCHIECTASIS AND AUTOIMMUNITY IN RA
EISSN 2326-5205
EndPage 2342
ExternalDocumentID PMC4832289
3788304951
26017630
10_1002_art_39226
ART39226
Genre article
Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Arthritis Research UK
  funderid: 19894
– fundername: IMI project BTCure
  funderid: 115142‐2
– fundername: European Union
– fundername: 7th Framework Programme project Gums and Joints
  funderid: HEALTH‐F2‐2010‐261460
– fundername: Versus Arthritis
  grantid: 19894
– fundername: 7th Framework Programme project Gums and Joints
  grantid: HEALTH‐F2‐2010‐261460
– fundername: Arthritis Research UK
  grantid: 19894
– fundername: IMI project BTCure
  grantid: 115142‐2
GroupedDBID 0R~
1OC
24P
33P
3SF
4.4
52O
52U
52V
53G
5VS
AAESR
AAEVG
AAHHS
AAHQN
AAIPD
AAMNL
AANHP
AANLZ
AAQQT
AASGY
AAWTL
AAXRX
AAYCA
AAZKR
ABCUV
ABJNI
ABLJU
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACFBH
ACGFS
ACGOF
ACIWK
ACMXC
ACPOU
ACPRK
ACRPL
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AHMBA
AIACR
AITYG
AIURR
AIWBW
AJBDE
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ATUGU
AZFZN
AZVAB
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
DCZOG
DIK
DRFUL
DRMAN
DRSTM
EBS
EJD
EMOBN
EX3
F00
FUBAC
G-S
G.N
GODZA
HGLYW
KBYEO
LATKE
LEEKS
LH4
LITHE
LOXES
LUTES
LW6
LYRES
MEWTI
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
NF~
O66
O9-
OK1
OVD
P2W
PQQKQ
QB0
ROL
SUPJJ
SV3
TEORI
V9Y
WBKPD
WHWMO
WIH
WIJ
WIK
WOHZO
WVDHM
WXSBR
YCJ
AAFWJ
AAYXX
AEYWJ
AGHNM
AGQPQ
AGYGG
CITATION
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
CGR
CUY
CVF
ECM
EIF
NPM
7QL
7QP
7T5
7TM
7U7
C1K
H94
K9.
7X8
5PM
ID FETCH-LOGICAL-c5426-86d60bc99eec163b5dd424908bdbb4225b2f3341ac0df9dae416045328c331c83
IEDL.DBID 24P
ISSN 2326-5191
IngestDate Thu Aug 21 13:33:17 EDT 2025
Fri Jul 11 11:04:33 EDT 2025
Fri Jul 11 16:39:56 EDT 2025
Fri Jul 25 10:34:55 EDT 2025
Mon Jul 21 05:57:33 EDT 2025
Thu Apr 24 22:54:59 EDT 2025
Tue Jul 01 00:33:18 EDT 2025
Wed Jan 22 16:40:30 EST 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 9
Language English
License Attribution
http://creativecommons.org/licenses/by/4.0
2015 The Authors. Arthritis & Rheumatology is published by Wiley Periodicals, Inc. on behalf of the American College of Rheumatology.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c5426-86d60bc99eec163b5dd424908bdbb4225b2f3341ac0df9dae416045328c331c83
Notes Drs. Quirke and Perry contributed equally to this work.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fart.39226
PMID 26017630
PQID 1707091437
PQPubID 946334
PageCount 8
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4832289
proquest_miscellaneous_1717489135
proquest_miscellaneous_1708157405
proquest_journals_1707091437
pubmed_primary_26017630
crossref_citationtrail_10_1002_art_39226
crossref_primary_10_1002_art_39226
wiley_primary_10_1002_art_39226_ART39226
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate September 2015
PublicationDateYYYYMMDD 2015-09-01
PublicationDate_xml – month: 09
  year: 2015
  text: September 2015
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Atlanta
– name: Hoboken
PublicationTitle Arthritis & rheumatology (Hoboken, N.J.)
PublicationTitleAlternate Arthritis Rheumatol
PublicationYear 2015
Publisher Wiley Subscription Services, Inc
John Wiley and Sons Inc
Publisher_xml – name: Wiley Subscription Services, Inc
– name: John Wiley and Sons Inc
References 1971; 8
2007; 19
2015; 17
2006; 54
1997; 64
2013; 35
2004; 28
2013; 40
2010; 233
2015; 11
1978; 72
2008; 58
2003; 48
2011; 23
1967; 36
2009; 5
2014; 41
2014; 73
2012; 106
2014; 44
2010; 62
2012; 64
2014; 53
e_1_2_7_6_1
e_1_2_7_5_1
e_1_2_7_4_1
e_1_2_7_3_1
e_1_2_7_9_1
e_1_2_7_8_1
e_1_2_7_7_1
e_1_2_7_19_1
e_1_2_7_18_1
e_1_2_7_17_1
e_1_2_7_2_1
e_1_2_7_15_1
e_1_2_7_14_1
e_1_2_7_11_1
e_1_2_7_10_1
e_1_2_7_26_1
Waller M (e_1_2_7_16_1) 1971; 8
Allain J (e_1_2_7_13_1) 1997; 64
e_1_2_7_25_1
e_1_2_7_24_1
e_1_2_7_23_1
e_1_2_7_22_1
Walker WC. (e_1_2_7_12_1) 1967; 36
e_1_2_7_21_1
e_1_2_7_20_1
References_xml – volume: 73
  start-page: 580
  year: 2014
  end-page: 6
  article-title: The autoantibody repertoire in periodontitis: a role in the induction of autoimmunity to citrullinated proteins in rheumatoid arthritis?
  publication-title: Ann Rheum Dis
– volume: 48
  start-page: 2741
  year: 2003
  end-page: 9
  article-title: Antibodies against cyclic citrullinated peptide and IgA rheumatoid factor predict the development of rheumatoid arthritis
  publication-title: Arthritis Rheum
– volume: 64
  start-page: 531
  year: 1997
  end-page: 7
  article-title: Prevalence of symptomatic bronchiectasis in patients with rheumatoid arthritis
  publication-title: Rev Rhum Engl Ed
– volume: 106
  start-page: 1040
  year: 2012
  end-page: 7
  article-title: Lung disease with anti‐CCP antibodies but not rheumatoid arthritis or connective tissue disease
  publication-title: Respir Med
– volume: 64
  start-page: 1323
  year: 2012
  end-page: 8
  article-title: Avidity maturation of anti–citrullinated protein antibodies in rheumatoid arthritis
  publication-title: Arthritis Rheum
– volume: 36
  start-page: 239
  year: 1967
  end-page: 51
  article-title: Pulmonary infections and rheumatoid arthritis
  publication-title: Q J Med
– volume: 72
  start-page: 207
  year: 1978
  end-page: 16
  article-title: Immunological abnormalities in bronchiectasis with chronic bronchial suppuration
  publication-title: Br J Dis Chest
– volume: 23
  start-page: 92
  year: 2011
  end-page: 8
  article-title: Smoking, citrullination and genetic variability in the immunopathogenesis of rheumatoid arthritis
  publication-title: Semin Immunol
– volume: 19
  start-page: 49
  year: 2007
  end-page: 54
  article-title: Smoking as a trigger for inflammatory rheumatic diseases
  publication-title: Curr Opin Rheumatol
– volume: 53
  start-page: 1676
  year: 2014
  end-page: 82
  article-title: Rheumatoid arthritis‐related interstitial lung disease: associations, prognostic factors and physiological and radiological characteristics: a large multicentre UK study
  publication-title: Rheumatology (Oxford)
– volume: 62
  start-page: 2569
  year: 2010
  end-page: 81
  article-title: 2010 rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative
  publication-title: Arthritis Rheum
– volume: 41
  start-page: 1282
  year: 2014
  end-page: 9
  article-title: A metaanalysis of the increased risk of rheumatoid arthritis‐related pulmonary disease as a result of serum anticitrullinated protein antibody positivity
  publication-title: J Rheumatol
– volume: 8
  start-page: 451
  year: 1971
  end-page: 9
  article-title: The influence of infection on titres of antiglobulin antibodies
  publication-title: Clin Exp Immunol
– volume: 28
  start-page: 311
  year: 2004
  end-page: 8
  article-title: Hypothesis: the humoral immune response to oral bacteria provides a stimulus for the development of rheumatoid arthritis
  publication-title: Inflammation
– volume: 44
  start-page: 1082
  year: 2014
  end-page: 5
  article-title: RA autoantibodies as predictors of rheumatoid arthritis in non‐cystic fibrosis bronchiectasis patients
  publication-title: Eur Respir J
– volume: 35
  start-page: 727
  year: 2013
  end-page: 34
  article-title: Rheumatoid factors: clinical applications
  publication-title: Dis Markers
– volume: 58
  start-page: 3009
  year: 2008
  end-page: 19
  article-title: Antibodies to citrullinated α‐enolase peptide 1 are specific for rheumatoid arthritis and cross‐react with bacterial enolase
  publication-title: Arthritis Rheum
– volume: 64
  start-page: 1756
  year: 2012
  end-page: 61
  article-title: Airway abnormalities and rheumatoid arthritis–related autoantibodies in subjects without arthritis: early injury or initiating site of autoimmunity?
  publication-title: Arthritis Rheum
– volume: 17
  start-page: 9
  year: 2015
  article-title: Expression of citrulline and homocitrulline residues in the lungs of non‐smokers and smokers: implications for autoimmunity in rheumatoid arthritis
  publication-title: Arthritis Res Ther
– volume: 40
  start-page: 907
  year: 2013
  end-page: 15
  article-title: Influence of periodontal disease, Porphyromonas gingivalis and cigarette smoking on systemic anti‐citrullinated peptide antibody titres
  publication-title: J Clin Periodontol
– volume: 11
  start-page: 261
  year: 2015
  end-page: 2
  article-title: Autoimmunity: lungs and citrullination
  publication-title: Nat Rev Rheumatol
– volume: 5
  start-page: 218
  year: 2009
  end-page: 24
  article-title: Periodontitis in systemic rheumatic diseases
  publication-title: Nat Rev Rheumatol
– volume: 233
  start-page: 34
  year: 2010
  end-page: 54
  article-title: Autoimmunity to specific citrullinated proteins gives the first clues to the etiology of rheumatoid arthritis
  publication-title: Immunol Rev
– volume: 54
  start-page: 38
  year: 2006
  end-page: 46
  article-title: A new model for an etiology of rheumatoid arthritis: smoking may trigger HLA–DR (shared epitope)–restricted immune reactions to autoantigens modified by citrullination
  publication-title: Arthritis Rheum
– volume: 73
  start-page: e46
  year: 2014
  article-title: The autoantibody repertoire in periodontitis: a role in the induction of autoimmunity to citrullinated proteins in rheumatoid arthritis? Antibodies against uncitrullinated peptides seem to occur prior to the antibodies to the corresponding citrullinated peptides
  publication-title: Ann Rheum Dis
– ident: e_1_2_7_9_1
  doi: 10.1038/nrrheum.2009.28
– ident: e_1_2_7_7_1
  doi: 10.1186/s13075-015-0520-x
– ident: e_1_2_7_15_1
  doi: 10.1016/0007-0971(78)90043-8
– ident: e_1_2_7_14_1
  doi: 10.1183/09031936.00064014
– volume: 36
  start-page: 239
  year: 1967
  ident: e_1_2_7_12_1
  article-title: Pulmonary infections and rheumatoid arthritis
  publication-title: Q J Med
– ident: e_1_2_7_18_1
  doi: 10.1002/art.23936
– ident: e_1_2_7_24_1
  doi: 10.1093/rheumatology/keu165
– ident: e_1_2_7_19_1
  doi: 10.1155/2013/726598
– ident: e_1_2_7_11_1
  doi: 10.1136/annrheumdis-2012-202701
– ident: e_1_2_7_17_1
  doi: 10.1002/art.27584
– ident: e_1_2_7_21_1
  doi: 10.1136/annrheumdis-2014-205498
– ident: e_1_2_7_2_1
  doi: 10.1111/j.0105-2896.2009.00850.x
– ident: e_1_2_7_3_1
  doi: 10.1002/art.11223
– ident: e_1_2_7_8_1
  doi: 10.1038/nrrheum.2015.38
– ident: e_1_2_7_6_1
  doi: 10.1016/j.smim.2011.01.014
– ident: e_1_2_7_25_1
  doi: 10.1002/art.34344
– volume: 64
  start-page: 531
  year: 1997
  ident: e_1_2_7_13_1
  article-title: Prevalence of symptomatic bronchiectasis in patients with rheumatoid arthritis
  publication-title: Rev Rhum Engl Ed
– ident: e_1_2_7_4_1
  doi: 10.1002/art.21575
– ident: e_1_2_7_10_1
  doi: 10.1111/jcpe.12138
– ident: e_1_2_7_22_1
  doi: 10.1002/art.33489
– ident: e_1_2_7_5_1
  doi: 10.1007/s10753-004-6641-z
– ident: e_1_2_7_20_1
  doi: 10.1097/BOR.0b013e32801127c8
– ident: e_1_2_7_26_1
  doi: 10.1016/j.rmed.2012.03.006
– volume: 8
  start-page: 451
  year: 1971
  ident: e_1_2_7_16_1
  article-title: The influence of infection on titres of antiglobulin antibodies
  publication-title: Clin Exp Immunol
– ident: e_1_2_7_23_1
  doi: 10.3899/jrheum.131341
SSID ssj0000970605
Score 2.4368472
Snippet Objective To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti–citrullinated protein antibodies (ACPAs),...
To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPAs), by...
Objective To examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPAs),...
OBJECTIVETo examine the potential of chronic severe bacterial infection to generate rheumatoid factor (RF) and anti-citrullinated protein antibodies (ACPAs),...
SourceID pubmedcentral
proquest
pubmed
crossref
wiley
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 2335
SubjectTerms Adult
Aged
Aged, 80 and over
Arthritis, Rheumatoid - immunology
Asthma - immunology
Autoantibodies - immunology
Autoimmunity - immunology
Bacteria
Bacterial infections
Bacterial Infections - immunology
Bronchiectasis - immunology
Case-Control Studies
Chronic Disease
Citrulline - immunology
Citrulline - metabolism
Enzyme-Linked Immunosorbent Assay
Female
Fibrinogen - immunology
Fibrinogen - metabolism
Humans
Immunoglobulins
Infections
Male
Middle Aged
Peptides
Peptides, Cyclic - immunology
Phosphopyruvate Hydratase - immunology
Phosphopyruvate Hydratase - metabolism
Rheumatism
Rheumatoid Arthritis
Rheumatoid Factor - immunology
Smoking - immunology
Vimentin - immunology
Vimentin - metabolism
Title Bronchiectasis Is a Model for Chronic Bacterial Infection Inducing Autoimmunity in Rheumatoid Arthritis
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fart.39226
https://www.ncbi.nlm.nih.gov/pubmed/26017630
https://www.proquest.com/docview/1707091437
https://www.proquest.com/docview/1708157405
https://www.proquest.com/docview/1717489135
https://pubmed.ncbi.nlm.nih.gov/PMC4832289
Volume 67
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1ZS8QwEB48QHwRb9eLKD74UmzTdJvikyeuoogo-FaaY3cL0hW7--C_dybtVhcPfCmFTNN2kpn5cn0DcGC4b7XgODYJTewJ2uYqE196XVqEM0pa4-gYbu_aV0_i-jl6noLj8VmYih-imXAjy3D-mgw8U-XRJ2koahYH7IgepmGWjtZSJ-fivplg8RMiholccjne9hCpBGNmIZ8fNU9PxqNvIPP7XsmvGNYFoctFWKjRIzupmnsJpmyxDHO39fr4CvRwVF3ofo5eLCvzknVKljFKd_bCEJyymgmXnVYUzVhTp96LVTDK4YGV9NjJaDjI3amR4TvLC_bQtyOEtYPc0Hv7jgRpFZ4uLx7Prrw6lYKnI4zBnmybtq90klirEYGpyBjBac1PGaUE2rTi3RADWqZ9001MZhGnIdgLudRhGGgZrsFMMSjsBjAToo3HwsQ2QiyVSAxvNurSaQLh2yBTLTgcKzTVNc84pbt4SSuGZJ6i7lOn-xbsN6KvFbnGT0Lb41ZJa_sq0yBGV5Ug1otbsNcUo2XQckdW2MHIycggihGR_iUTEP1OEKLMetXQzZcQ2Rp6X78F8UQXaASImXuypMj7jqFbkJ-UCarCdZbffy7FUYu72fy_6BbMI2qLqo1u2zAzfBvZHURGQ7XrLACv552bD_CTChg
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LS-RAEC7UBfUirs_xsfYuHrwEk04n6YAXFWVGHVlEwVtIP2YmIBlxZg7-e6s6mbiDD_YW6Mqruqvqq358BXBouG-14JibhCbxBG1zlakvvR4twhklrXF0DN3buP0grh6jxzk4mZ6Fqfghmgk3sgznr8nAaUL6-J01FFWLGTvCh3n4IWKeUOEGLv42Myx-Sswwkasux2MPoUowpRby-XFz92xA-oAyP26W_BfEuih0uQorNXxkp1V__4Q5W67BYrdeIF-HPqbVpR4U6MbyUTFinRHLGdU7e2KITllNhcvOKo5mfFKn3oxVMirigQ_ps9PJeFi4YyPjV1aU7G5gJ4hrh4Wh9w4cC9IGPFxe3J-3vbqWgqcjDMKejE3sK52m1mqEYCoyRnBa9FNGKYFGrXgvxIiWa9_0UpNbBGqI9kIudRgGWoabsFAOS7sNzIRo5IkwiY0QTKUS45uNenScQPg2yFULjqYKzXRNNE71Lp6yiiKZZ6j7zOm-BX8a0eeKXeMzob1pr2S1gY2yIEFflSLYS1rwu2lG06D1jry0w4mTkUGUICT9TiYg_p0gRJmtqqObLyG2NXS_fguSmSHQCBA192xLWQwcRbcgRylTVIUbLF__XIZpi7vY-X_RA1hq33dvspvO7fUuLCOEi6pdb3uwMH6Z2H2ESWP1y1nDGwF_DIs
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1LT9tAEB4BlSIuiJYCgbRdqh64WNjrdbwWp9A2Ii1EESISN8v7MLGEHESSA_-embVjGvFQb5Z2_Jrdmfl2Z_cbgB-G-1YLjnOT0MSeoG2uMvGll1MSzihpjaNjuBx2z8fiz010swany7MwFT9Es-BGluH8NRn4vclPnklDUbM4YUf0sA4fKNlHw5uLUbPA4idEDBO54nK86yFSCZbMQj4_ae5ejUcvQObLvZL_YlgXhPrbsFWjR9aruvsjrNnyE7Qu6_z4DtzirLrUkwK9WDYrZmwwYxmjcmd3DMEpq5lw2VlF0YxPGtR7sUpGNTzwIbest5hPC3dqZP7IipJdTewCYe20MPTeiSNB-gzj_u_rn-deXUrB0xHGYE92TddXOkms1YjAVGSM4JTzU0YpgTateB5iQMu0b_LEZBZxGoK9kEsdhoGW4S5slNPS7gMzIdp4LExsI8RSicTwZqOcThMI3waZasPxUqGprnnGqdzFXVoxJPMUdZ863bfheyN6X5FrvCbUWfZKWtvXLA1idFUJYr24DUdNM1oGpTuy0k4XTkYGUYyI9D2ZgOh3ghBl9qqObr6EyNbQ-_ptiFeGQCNAzNyrLWUxcQzdgvykTFAVbrC8_XMpzlrcxcH_i36D1uhXP70YDP8ewiYCuKja89aBjfnDwn5BkDRXX50xPAFnuwu9
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=Bronchiectasis+Is+a+Model+for+Chronic+Bacterial+Infection+Inducing+Autoimmunity+in+Rheumatoid+Arthritis&rft.jtitle=Arthritis+%26+rheumatology+%28Hoboken%2C+N.J.%29&rft.au=Quirke%2C+Anne%E2%80%90Marie&rft.au=Perry%2C+Elizabeth&rft.au=Cartwright%2C+Alison&rft.au=Kelly%2C+Clive&rft.date=2015-09-01&rft.issn=2326-5191&rft.eissn=2326-5205&rft.volume=67&rft.issue=9&rft.spage=2335&rft.epage=2342&rft_id=info:doi/10.1002%2Fart.39226&rft.externalDBID=n%2Fa&rft.externalDocID=10_1002_art_39226
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2326-5191&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2326-5191&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2326-5191&client=summon