Abstract

The pathogenesis of Rheumatoid Arthritis (RA) is not fully understood, probably influenced by genetic and environmental factors. Interstitial Lung Disease (ILD) is an extra-articular manifestation of RA, which contributes significantly to morbidity and mortality. The identification of anti-HLA antibodies has been useful in the transplantation field; however, its contribution to autoimmune diseases as RA has not been fully studied. We aimed to determine the presence of anti-HLA antibodies in RA patients with and without ILD and its possible association with clinical and biochemical markers. One-hundred and forty-seven RA patients, of which 65 had ILD (RA-ILD group), were included. Sera samples for Anti-HLA Class II LABScreen panel-reactive antibodies (PRA) were analyzed. In both groups, women predominated, and lung function was worse in patients with ILD. The anti-CCP+ (UI/mL) was higher in the RA group in comparison to RA-ILD (p < 0.001). Expositional risk factors (tobacco smoking and biomass-burning smoke) were higher in RA-ILD patients. PRA+ was identified in ~25% RA-ILD patients, while ~29% in the RA group. The CRP levels have a positive correlation with the percentage of reactivity (%PRA, p = 0.02, r2 = 0.60) in the RA-ILD group. In conclusion, anti-HLA antibodies correlate with C-reactive protein levels in RA patients with ILD.

Highlights

  • Rheumatoid Arthritis (RA) affects approximately 1% of the population worldwide

  • Once performing correlations between clinical and biological markers of the disease with pulmonary function variables, no statistically significant values were found; we identified a relationship between anti-Human Leukocyte Antigen (HLA) antibodies with the C-reactive protein (CRP) levels, and we found a positive correlation with the percentage of reactivity, (p = 0.02, r2 = 0.60) in the RA-Interstitial Lung Disease (ILD) group

  • Cells 2020, 9, 691between anti-HLA antibodies with the CRP levels, and we found a positive correlation with the percentage of reactivity, (p = 0.02, r2 = 0.60) in the RA-ILD group

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Summary

Introduction

Rheumatoid Arthritis (RA) affects approximately 1% of the population worldwide. It is an inflammatory and autoimmune disease associated with joint destruction, and this can develop extra-articular complications [1,2]. Among genetic factors are several alleles of the Human Leukocyte Antigen (HLA) system [7]. The class I contains the classic genes HLA-A, -B, and -C, while HLA class II comprises the HLA-DRB1, -DPB1 and -DQB1 genes, encoding the β chain of proteins that are expressed as HLA antigens in specialized human cells [8]. The HLA-DRB1*04 allele is the most replicated in association studies with the development of this disease [9]

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