Objectives: To analyze the effects of
tocilizumab on peripheral B-cell subpopulation and its ability to produce anti-
cyclic citrullinated peptide (CCP) antibody in patients with
rheumatoid arthritis (RA).Methods: Thirteen consecutive RA patients initiated with
tocilizumab were enrolled in our prospective study.
Anti-CCP antibody titers and clinical parameters were evaluated during treatment. Peripheral blood B-cell subsets were analyzed using flow cytometry according to the Human Immunology Project.Results: Disease activity was significantly improved and
anti-CCP antibody titers significantly decreased at week 24 compared to baseline. The percentages of post-switch memory B cells in CD19+ cells transiently increased at week 12, but there was no significant difference in any of the investigated B-cell subpopulations at week 24 compared to baseline. The ratios of post-switch memory to naïve B cells (post-switch/naïve) correlated negatively with
anti-CCP antibody titers regardless of the time-points.Conclusion: Our study indicated that
tocilizumab has a potential to reduce
anti-CCP antibody production presumably by affecting post-switch/naïve ratio, and that
anti-CCP antibody titers reflect B-cell distribution/subpopulation. As
anti-CCP antibodies are produced in lymph nodes or ectopic lymphoid structures in synovial tissues, not in circulation, transient increment of post-switch memory B cells after
tocilizumab treatment may reflect the altered balance of B-cell distribution between circulation and arthritic joints, resulting in suppressed production of
anti-CCP antibody in situ.