학술논문

Pathogenetic associations of anti-ribosomal P protein antibody titres and their subclasses in patients with systemic lupus erythematosus.
Document Type
Article
Source
Rheumatology. May2024, Vol. 63 Issue 5, p1411-1421. 11p.
Subject
*TRYPTOPHAN metabolism
*PROTEINS
*CROSS-sectional method
*CLINICAL medicine
*RESEARCH funding
*AUTOANTIBODIES
*ENZYME-linked immunosorbent assay
*EXANTHEMA
*KEY performance indicators (Management)
*IMMUNOGLOBULINS
*SYSTEMIC lupus erythematosus
*SEVERITY of illness index
*RETROSPECTIVE studies
*DESCRIPTIVE statistics
*MULTIVARIATE analysis
*PREDNISOLONE
*AGE factors in disease
*MEDICAL records
*ACQUISITION of data
*STATISTICS
*CYTOKINES
*INFLAMMATION
*DISEASE risk factors
Language
ISSN
1462-0324
Abstract
Objectives We evaluated the association between anti-ribosomal P antibody (anti-RibP) titres and disease activity in Japanese SLE patients. Methods Eighty patients admitted and treated in Niigata University Hospital for new-onset or flare-up of SLE were included in this retrospective cross-sectional study. Clinical data were obtained from medical records at admission. The anti-RibP index, and cytokine and tryptophan metabolite levels were determined by ELISA. Results Of the 80 SLE patients, 30 had anti-RibP. Anti-RibP presence was associated with a greater prevalence of skin rash and more severe inflammatory responses, demonstrated by higher inflammatory cytokine levels, hypocomplementemia, and accelerated tryptophan metabolism, in younger patients. The serum anti-RibP index was correlated with age at diagnosis, clinical indicators, initial prednisolone dose, and cytokines and tryptophan metabolite levels in univariate analysis. Multivariate analysis showed that the anti-RibP index was independently associated with the initial prednisolone dose and the prevalence of skin rash. The anti-RibP IgGs were mainly the IgG2 and IgG3 subclasses, and anti-RibP IgG3 was associated with hypocomplementemia, higher DAS, accelerated kynurenine pathway activity, and higher proinflammatory cytokine production. The coexistence of anti-dsDNA IgG and anti-RibP IgG2 or IgG3 accompanied higher IL-10 and IFN-α2 levels; furthermore, anti-RibP IgG3 coexistence with anti-dsDNA antibody contributed to the requirement for higher initial prednisolone doses and accelerated kynurenine pathway activity. Conclusion Anti-RibP was associated with clinical manifestations and parameters in SLE, and its index might be a useful indicator of disease severity. Anti-RibP IgG3 was the IgG subclass most strongly associated with the pathogenesis of SLE. [ABSTRACT FROM AUTHOR]