2011
DOI: 10.1093/rheumatology/ker223
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Risk of infections in rheumatoid arthritis patients treated with tocilizumab

Abstract: The rate of infection in RA patients treated with tocilizumab in clinical practice is higher than in the clinical trial populations. Increased attention should especially be given to patients with longer disease duration, previous exposure to multiple DMARDs, i.e. previous exposure to rituximab and those receiving concomitant LEF, prednisone or proton-pump inhibitor treatment.

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Cited by 105 publications
(78 citation statements)
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“…Such infections may cause severe morbidity and even mortality (14). Recently, not only post-transplant patients, but also those taking biological agents (i.e., RA patients) such as tocilizumab and anti-TNF-α antibodies (which are widely recognized to be safe and efficacious), have been shown to be at risk of various infections (15). When such agents are pre- scribed, surveillance for infection with, for example, Mycobacterium tuberculosis is essential (16).…”
Section: Discussionmentioning
confidence: 99%
“…Such infections may cause severe morbidity and even mortality (14). Recently, not only post-transplant patients, but also those taking biological agents (i.e., RA patients) such as tocilizumab and anti-TNF-α antibodies (which are widely recognized to be safe and efficacious), have been shown to be at risk of various infections (15). When such agents are pre- scribed, surveillance for infection with, for example, Mycobacterium tuberculosis is essential (16).…”
Section: Discussionmentioning
confidence: 99%
“…Treatment with a small molecule STAT3 inhibitor (AG490) also decreased hepcidin and increased serum iron in healthy mice. 86 Although anti-cytokine therapies are effective in lowering hepcidin production, their side effects include increased risk of infection due to impaired host defense, 87,88 thus these types of therapies may be confined to the treatment of severe inflammatory diseases.…”
Section: E Fung Et Almentioning
confidence: 99%
“…Consequently, infections are at risk of a late diagnosis because of the masking effect. Despite the therapy with TCZ at the moment of infection, the reported patient had an actual and past of immunosuppressors that rise the cumulative risk of serious infection in association to a longer disease duration and previous use of rituximab which are identified as predictors of infection [9]. The actual contribution of TCZ to infection susceptibility is yet to know, as its use experience rises.…”
Section: Discussionmentioning
confidence: 99%
“…Most of the serious infections described are bacterial and viral, with no uncommon pathogens. Also, a longer disease duration, higher number of previous DMARDs and previous use of rituximab are identified as predictors of infection [9].…”
Section: Introductionmentioning
confidence: 98%