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Evaluation of hepatitis B vaccine efficacy and factors affecting vaccine nonresponse in patients receiving anti-tumor necrosis factor agents

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MEG.0000000000001849

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anti-tumor necrosis factors therapy; hepatitis B vaccine efficacy; response

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This study evaluated the efficacy of HBV vaccination in patients with chronic inflammatory diseases (CIDs) receiving anti-TNF agents and healthy controls. Results showed that male sex, use of specific medications, and vaccination after anti-TNF treatment were identified as risk factors of nonresponse to HBV vaccine. Vigilance and HBV vaccination prior to initiating anti-TNF treatment in patients with CIDs are recommended.
Objectives The response rate of patients to hepatitis B virus (HBV) vaccination receiving anti-tumor necrosis factor (TNF) agents is quite low. We aimed to assess the efficiency of HBV vaccination in patients with chronic inflammatory diseases (CIDs) receiving anti-TNF agents as well as in healthy controls. We also evaluated the impact of different factors on the efficacy of HBV vaccination. Methods Patients with CIDs receiving anti-TNF agents and healthy controls vaccinated for HBV were included in the study during 2018-2019. An adequate immune response and an effective immune response to HBV were defined as >10 IU/L and > 100 IU/L, respectively. Results Among 274 participants, 187 were patients with CID and 87 were healthy controls. The mean age of the patients with CID (43.9 +/- 11.7 years) was significantly higher than that of the healthy controls (31.4 +/- 7 years) (P = 0.000). Adequate immune response was 60.8 and 94.3% in patients with CID and healthy controls (P = 0.000), respectively, whereas effective immune response was 37.9 and 75.9% (P = 0.000), respectively. In logistic regression analysis, male sex [odds ratio (OR), 0.408; 95% confidence interval (CI), 0.201-0.830; P = 0.013), use of infliximab (OR, 2.694; 95% CI, 1.203-6.035; P = 0.016) and sertoluzimab (OR, 3.307; 95% CI, 1.287-8.498; P = 0.013), vaccination after anti-TNF treatment (OR, 0.224; 95% CI, 0.083-0.602; P = 0.003) were identified as risk factors of nonresponse to HBV vaccine. Conclusions Infliximab and sertoluzimab usage, male sex, and vaccination after anti-TNF treatment were risk factors of nonresponse. HBV vaccination should be given to patients with CID before initiation of anti-TNF treatment and awareness should be spread on this subject.

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