Abstract

IntroductionThe aim of this study was to explore the persistence of an antibody response 1.5 years after vaccination with 7-valent pneumococcal conjugate vaccine in patients with rheumatoid arthritis (RA) or spondyloarthropathy (SpA) treated with different antirheumatic drugs.MethodsOf 505 patients initially recruited, data on current antirheumatic treatment and blood samples were obtained from 398 (79%) subjects after mean (SD, range) 1.4 (0.5; 1 to 2) years. Antibody levels against pneumococcal serotypes 23F and 6B were analyzed by using enzyme-linked immunosorbent assay (ELISA). Original treatment groups were as follows: (a) RA receiving methotrexate (MTX); (b) RA taking anti-TNF monotherapy; (c) RA taking anti-TNF+MTX; (d) SpA with anti-TNF monotherapy; (e) SpA taking anti-TNF+MTX; and (f) SpA taking NSAID/analgesics. Geometric mean levels (GMLs; 95% CI) and proportion (percentage) of patients with putative protective antibody levels ≥1 mg/L for both serotypes, calculated in different treatment groups, were compared with results 4 to 6 weeks after vaccination. Patients remaining on initial treatment were included in the analysis. Possible predictors of persistence of protective antibody response were analysed by using logistic regression analysis.ResultsOf 398 patients participating in the 1.5-year follow up, 302 patients (RA, 163, and SpA, 139) had unchanged medication. Compared with postvaccination levels at 1.5 years, GMLs for each serotype were significantly lower in all groups (P between 0.035 and <0.001; paired-sample t test), as were the proportions of patients with protective antibody levels for both serotypes (P < 0.001; χ2 test). Higher prevaccination antibody levels for both serotypes 23F and 6B were associated with better persistence of protective antibodies (P < 0.001). Compared with patients with protective antibody levels at 1.5 years, those not having protective antibody levels were older, more often women, had longer disease duration and higher HAQ and DAS, and had a lower proportion of initial responders to both serotypes.Concomitant anti-TNF treatment and MTX were identified as negative predictors of the persistence of protective antibodies among RA patients (P = 0.024 and P = 0.065, respectively). Only age 65 years or older (P = 0.017) and not antirheumatic treatment was found to be a negative predictor of protective antibodies in patients with SpA.ConclusionsAfter initial increase, 1.5 years after pneumococcal vaccination with 7-valent conjugate vaccine, postvaccination antibody levels decreased significantly, reaching levels before vaccination in this cohort of patients with established arthritis treated with different antirheumatic drugs. MTX and anti-TNF treatment predicted low persistence of protective immunity among patients with RA. To boost antibody response, early revaccination with conjugate vaccine might be needed in patients receiving potent immunosuppressive remedies.Trial registration numberEudraCT EU 2007-006539-29 and NCT00828997.

Highlights

  • The aim of this study was to explore the persistence of an antibody response 1.5 years after vaccination with 7-valent pneumococcal conjugate vaccine in patients with rheumatoid arthritis (RA) or spondyloarthropathy (SpA) treated with different antirheumatic drugs

  • The aim of the present study was to investigate the 1.5year persistence of serotype-specific antibodies after conjugate pneumococcal vaccination in patients with RA and spondyloarthropathy (SpA) treated with different antiinflammatory remedies, including tumor necrosis factor (TNF) blockers, compared with spondyloarthropathy patients treated with nonsteroidal antiinflammatory drug (NSAID)/ analgesics

  • Of 398 patients participating in the 1.5-year follow-up, 302 patients (RA, 163; and SpA, 139) did not change their antirheumatic treatment during follow-up, and these patients were included in the analysis

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Summary

Introduction

The aim of this study was to explore the persistence of an antibody response 1.5 years after vaccination with 7-valent pneumococcal conjugate vaccine in patients with rheumatoid arthritis (RA) or spondyloarthropathy (SpA) treated with different antirheumatic drugs. Available 23-valent pneumococcal polysaccharide vaccine covers 85% to 90% of the serotypes causing invasive pneumococcal disease, such as pneumonia, pneumococcal bacteremia, or meningitis [7]. A suboptimal rate of pneumococcal vaccination among rheumatology outpatients receiving different immunosuppressive remedies has been reported [8]. One important issue is the limited evidence of efficacy of the polysaccharide vaccine in preventing infections in this high-risk group of patients, a recent study reported an increased risk of developing pneumonia in pneumococcal nonvaccinated compared with vaccinated rheumatoid arthritis (RA) patients receiving methotrexate (MTX) (180 patients followed up for 10 years) [9].

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