Antibody response to hepatitis B virus vaccine is impaired in patients with inflammatory bowel disease on infliximab therapy

PK Pratt Jr, N David, HC Weber, FF Little… - Inflammatory bowel …, 2018 - academic.oup.com
PK Pratt Jr, N David, HC Weber, FF Little, T Kourkoumpetis, GJ Patts, J Weinberg…
Inflammatory bowel diseases, 2018academic.oup.com
Background Studies have demonstrated an association between anti-TNF/
immunomodulator agents used in inflammatory bowel disease (IBD) and impaired hepatitis
B virus (HBV) vaccine immunogenicity, but little data exist on whether specific medication
types affect protective HBsAb titers. Our aim was to analyze this association. Methods This is
a retrospective cohort study. Inclusion criteria: age≥ 18, diagnosis of Crohn's disease (CD)
or ulcerative colitis (UC), previous HBV vaccination series and/or≥ 1 positive HBsAb, and …
Background
Studies have demonstrated an association between anti-TNF/immunomodulator agents used in inflammatory bowel disease (IBD) and impaired hepatitis B virus (HBV) vaccine immunogenicity, but little data exist on whether specific medication types affect protective HBsAb titers. Our aim was to analyze this association.
Methods
This is a retrospective cohort study. Inclusion criteria: age ≥18, diagnosis of Crohn’s disease (CD) or ulcerative colitis (UC), previous HBV vaccination series and/or ≥1 positive HBsAb, and record of IBD therapy in 6 months before titer level. Patients were stratified based upon medication exposures: anti-TNF, immunomodulator, combination anti-TNF and immunomodulatory, and a reference arm. Titer levels following vaccination and specific medication types given in the 6 months before titer were recorded. Seroprotection was defined as HBsAb ≥10 IU/l and ≥100 IU/l.
Results
The study cohort (N = 391) was 70.8% white, 51.4% female and 64.2% had CD and 35.8% had UC. The mean age was 45.8 years. A significantly lower percentage of patients exposed to anti-TNF, immunomodulator or dual therapy had titers ≥10 (P < 0.01). Regarding specific medications, only patients exposed to infliximab (P < 0.01) were less likely to have titer levels ≥10, after controlling for other medication exposures, age at titer level, and interval time between vaccination/titer level. This was not found for patients exposed to adalimumab, methotrexate, 6-mercaptopurine, or azathioprine.
Conclusions
Patients exposed to infliximab were significantly less likely to have protective HBsAb titer levels following vaccination, a trend not seen in patients on adalimumab. Efforts to vaccinate IBD patients against HBV before use of immunomodulators and anti-TNFs, infliximab specifically, and screen periodically thereafter must be reinforced.
Oxford University Press