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Naslov:Autoimmunity to synovial extracellular matrix proteins in patients with postinfectious Lyme arthritis
Avtorji:ID Kanjana, Korawit (Avtor)
ID Strle, Klemen (Avtor)
ID Lochhead, Robert B. (Avtor)
ID Pianta, Annalisa (Avtor)
ID Mateyka, Laura M. (Avtor)
ID Wang, Qi (Avtor)
ID Arvikar, Sheila (Avtor)
ID Kling, David E. (Avtor)
ID Deangelo, Cameron A. (Avtor)
ID Curham, Lucy (Avtor), et al.
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (2,04 MB)
MD5: 11B53E586C9CBE4F8F4640D6432629CA
 
URL URL - Izvorni URL, za dostop obiščite https://www.jci.org/articles/view/161170
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Background. Autoimmune diseases often have strong genetic associations with specific HLA-DR alleles. The synovial lesion in chronic inflammatory forms of arthritis shows marked upregulation of HLA-DR molecules, including in postinfectious Lyme arthritis (LA). However, the identity of HLA-DR–presented peptides, and therefore the reasons for these associations, has frequently remained elusive. Methods. Using immunopeptidomics to detect HLA-DR–presented peptides from synovial tissue, we identified T cell epitopes from 3 extracellular matrix (ECM) proteins in patients with postinfectious LA, identified potential Borreliella burgdorferi–mimic (Bb-mimic) epitopes, and characterized T and B cell responses to these peptides or proteins. Results. Of 24 postinfectious LA patients, 58% had CD4+ T cell responses to at least 1 epitope of 3 ECM proteins, fibronectin-1, laminin B2, and/or collagen Vα1, and 17% of 52 such patients had antibody responses to at least 1 of these proteins. Patients with autoreactive T cell responses had significantly increased frequencies of HLA-DRB1*04 or -DRB1*1501 alleles and more prolonged arthritis. When tetramer reagents were loaded with ECM or corresponding Bb-mimic peptides, binding was only with the autoreactive T cells. A high percentage of ECM-autoreactive CD4+ T cells in synovial fluid were T-bet–expressing Th1 cells, a small percentage were RoRγt-expressing Th17 cells, and a minimal percentage were FoxP3-expressing Tregs. Conclusion. Autoreactive, proinflammatory CD4+ T cells and autoantibodies develop to ECM proteins in a subgroup of postinfectious LA patients who have specific HLA-DR alleles. Rather than the traditional molecular mimicry model, we propose that epitope spreading provides the best explanation for this example of infection-induced autoimmunity.
Ključne besede:Lyme arthritis, autoimmune diseases, infectious disease
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2023
Št. strani:str. 1-13
Številčenje:Vol. 133, no. 17, [article no.] e161170
PID:20.500.12556/DiRROS-29656 Novo okno
UDK:616.9
ISSN pri članku:1558-8238
DOI:10.1172/JCI161170 Novo okno
COBISS.SI-ID:279244035 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 25. 5. 2026;
Datum objave v DiRROS:02.06.2026
Število ogledov:58
Število prenosov:55
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:The journal of clinical investigation
Skrajšan naslov:J. clin. invest.
Založnik:American Society for Clinical Investigation
ISSN:1558-8238
COBISS.SI-ID:520751129 Novo okno

Gradivo je financirano iz projekta

Financer:NIH - National Institutes of Health
Številka projekta:5R01AI101175-08
Naslov:Borrelia burgdorferi-Induced Autoimmunity in Lyme Disease

Financer:NIH - National Institutes of Health
Številka projekta:1R01AI144365-01
Naslov:Cellular and humoral immunity in Lyme arthritis

Financer:NIH - National Institutes of Health
Številka projekta:1K01AR062098-01
Naslov:Defining Microbial and Host Factors in Innate Immune Responses in Lyme Arthritis

Financer:NIH - National Institutes of Health
Številka projekta:2T32AR007258-46
Naslov:Research Training in Rheumatology at Massachusetts General Hospital

Financer:NIH - National Institutes of Health
Številka projekta:1F32AI126764-01
Naslov:Pathogenic and Diagnostic Implications of MicroRNAs in Lyme Disease.

Financer:NIH - National Institutes of Health
Številka projekta:4P41GM104603-20
Naslov:Mass Spectrometry Resource for Biology and Medicine

Financer:NIH - National Institutes of Health
Številka projekta:1R24GM134210-01
Naslov:Legacy Support During Closure of the Mass Spectrometry Resource for Biology and Medicine

Financer:NIH - National Institutes of Health
Številka projekta:1S10RR020946-01A1
Naslov:LTQ MASS SPECTROMETER: PERIODONTAL HOST-PARASITE INTERACTIONS

Financer:NIH - National Institutes of Health
Številka projekta:1S10OD010724-01
Naslov:MALDI-TOF/TOF MS TO SUPPORT BIOMEDICAL RESEARCH

Financer:NIH - National Institutes of Health
Številka projekta:1S10OD021651-01
Naslov:A Thermo-Fisher Scientific Q-Exactive HF Mass Spectrometry System

Financer:NIH - National Institutes of Health
Številka projekta:1S10OD021728-01A1
Naslov:A Thermo-Fisher Scientific Orbitrap Fusion Lumos Tribrid Mass Spectrometer System

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

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