4.5 Article

IgG Anti-Citrullinated Protein Antibody Variable Domain Glycosylation Increases Before the Onset of Rheumatoid Arthritis and Stabilizes Thereafter: A Cross-Sectional Study Encompassing ∼1,500 Samples

期刊

ARTHRITIS & RHEUMATOLOGY
卷 74, 期 7, 页码 1147-1158

出版社

WILEY
DOI: 10.1002/art.42098

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资金

  1. ReumaNederland [17-1-402, 08-1-34]
  2. IMI [777357]
  3. ZonMw TOP [91214031]
  4. Target to B! [LSHM18055-5GF]
  5. Swedish Research Council [VR 2017-00650]
  6. King Gustaf V's 80-Year Fund
  7. King Gustaf V's and Queen Victoria's Fund
  8. Swedish Rheumatism Association
  9. Canadian Institutes of Health Research MOP grant [77700]
  10. NWO-ZonMW clinical fellowship [90714509]
  11. NWO-ZonMW VENI grant [91617107]
  12. NWO-ZonMW VIDI grant [09150172010067]
  13. ZonMW Enabling Technology Hotels grant [435002030]
  14. Dutch Arthritis Foundation [15-2-402, 18-1-205]
  15. European Research Council (ERC) [AdG2019-884796]

向作者/读者索取更多资源

The abundance of N-linked glycans in the variable domain of IgG ACPA increases towards the onset of rheumatoid arthritis (RA), and is associated with the maturation of the ACPA response and disease development.
Objective. The autoimmune response in rheumatoid arthritis (RA) is marked by the presence of anti-citrullinated protein antibodies (ACPAs). A notable feature of IgG ACPA is the abundant expression of N-linked glycans in the variable domain. However, the presence of ACPA variable domain glycosylation (VDG) across disease stages, and its response to therapy, are poorly described. To understand its dynamics, we investigated the abundance of IgG ACPA VDG in 1,498 samples from individuals in different clinical stages. Methods. Using liquid chromatography, we analyzed IgG ACPA VDG profiles in 7 different cohorts from Japan, Canada, The Netherlands, and Sweden. We assessed 106 healthy individuals, 228 individuals with presymptomatic RA, 277 individuals with arthralgia, 307 patients with new-onset/early RA, and 117 RA patients after prespecified treatment regimens. Additionally, we measured VDG in 234 samples from patients with RA who did or did not achieve long-term drug-free remission (DFR) during up to 16 years follow-up. Results. IgG ACPA VDG significantly increased (P < 0.0001) toward disease onset and was associated with ACPA levels and epitope spreading prior to diagnosis. A slight increase in VDG was observed in patients with established RA, with a moderate influence of treatment (P = 0.007). In patients in whom DFR was later achieved, IgG ACPA VDG was already reduced at the time of RA onset. Conclusion. The abundance of IgG ACPA VDG increases toward RA onset and correlates with maturation of the ACPA response. While IgG ACPA VDG levels are fairly stable in established disease, a lower degree of VDG at RA onset correlates with DFR. Although the underlying biologic mechanisms remain elusive, our data support the concept that VDG relates to an expansion of the ACPA response in the pre-disease phase and contributes to disease development.

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