HBV reactivation in patients with rheumatoid arthritis treated with anti-interleukin-6: a systematic review and meta-analysis

Author:

Katelani Stamatia1ORCID,Fragoulis George E23ORCID,Bakasis Athanasios-Dimitrios1ORCID,Pouliakis Abraham4,Nikiphorou Elena5,Atzeni Fabiola6,Androutsakos Theodoros1ORCID

Affiliation:

1. Department of Pathophysiology, Medical School, National and Kapodistrian University of Athens , Athens, Greece

2. First Department of Internal Medicine, Propedeutic Clinic, “Laiko” Hospital, National and Kapodistrian University of Athens , Athens, Greece

3. Institute of Infection, Immunity and Inflammation, University of Glasgow , Scotland, UK

4. 2nd Department of Pathology, National and Kapodistrian University of Athens, Medical School, University General Hospital Attikon , Athens, Greece

5. Centre for Rheumatic Diseases, King’s College London , London, UK

6. Rheumatology Unit, Department of Experimental and Internal Medicine, University of Messina , Messina, Italy

Abstract

Abstract Objective The objective of this study was to assess the possibility of HBV reactivation (HBVr) in patients with RA under anti-IL-6 treatment. Methods Using PubMed, Scopus and EMBASE, we performed a systematic literature search for articles related to HBVr in RA patients under anti-IL-6 treatment. The search was performed with no date limits and was last updated 28 January 2023. The results from all the databases were combined and duplicates were excluded, as were non-English articles, case reports, position articles, comments, and paediatric studies. Results Our initial search led to 427 articles; 28 were duplicates, 46 non-English, 169 reviews, 31 books/letters, 25 case reports, and 88 irrelevant to the meta-analysis aim; 21 were excluded due to inadequate information, leaving 19 articles, with a sum of 372 RA patients with chronic HBV (CHB) or resolved HBV infection, for further analysis. The overall risk for HBVr in RA patients with CHB was 6.7%, increasing to 37% when only RA patients with CHB and no antiviral prophylaxis were included. On the contrary, HBVr was close to 0% in RA patients with resolved HBV infection, irrespective of antiviral prophylaxis. All RA patients experiencing HBVr in these studies were successfully managed with antiviral treatment and/or drug withdrawal. Conclusion Overall, anti-IL-6 treatment comes with a significant risk of HBVr in RA patients with CHB; risk is diminished when antiviral prophylaxis is used. In contrast, in RA patients with resolved HBV infection, the risk of HBVr seems to be extremely low. Large, well-designed studies (either controlled trials or multicentre/international observational studies) are warranted to further validate these results.

Funder

Pfizer and Lilly

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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