PMID- 14572581 OWN - NLM STAT- MEDLINE DCOM- 20031126 LR - 20071114 IS - 0002-9270 (Print) IS - 0002-9270 (Linking) VI - 98 IP - 10 DP - 2003 Oct TI - Hepatitis B vaccine nonresponse and celiac disease. PG - 2289-92 AB - OBJECTIVES: There is a genetic predisposition to hepatitis B vaccine nonresponse. The link between human leukocyte antigen (HLA) genotype and ineffective development of immunity to the hepatitis B vaccine has been characterized in multiple studies. Celiac disease has a strong association with a particular HLA genotype of DQ2; interestingly, this HLA genotype is seen in association with nonresponders to the hepatitis B vaccine. We report a disproportionate number of patients with celiac disease who are nonresponders to the hepatitis B vaccine series. METHODS: We reviewed the hepatitis B vaccine records, serological tests for anti-hepatitis B surface antigen antibody (anti-HBs), and HLA genotypes of celiac disease patients identified as nonresponders to hepatitis B vaccine. Subjects were identified from a database of patients diagnosed with celiac disease at our institution or referred to our center for evaluation and management of celiac disease between November, 2000, and October, 2002. RESULTS: A total of 23 subjects were reviewed. All had a clinical and pathological diagnosis of celiac disease. All subjects reported receiving the full series of hepatitis B vaccinations. Of the subjects, 19 had testing for hepatitis B vaccine response. Of these 19 subjects, 13 did not achieve long-term immunity as seen by the negative qualitative or quantitative anti-HBs antibody titer. All tested subjects were either homozygous or heterozygous for DQ2. CONCLUSIONS: We postulate that celiac disease patients may have a significant predisposition to hepatitis B vaccine nonresponse. Both celiac disease and hepatitis B vaccine nonresponse is genetically mediated. Celiac disease patients may have a failure of induction of humoral immune response needed for development of long term immunity; the mechanism for this is unclear. FAU - Noh, Kyung W AU - Noh KW AD - Department of Internal Medicine, Mayo Vaccine Research Group, and Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, USA. FAU - Poland, Gregory A AU - Poland GA FAU - Murray, Joseph A AU - Murray JA LA - eng GR - DK 57982/DK/NIDDK NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Am J Gastroenterol JT - The American journal of gastroenterology JID - 0421030 RN - 0 (HLA Antigens) RN - 0 (Hepatitis B Surface Antigens) RN - 0 (Hepatitis B Vaccines) SB - IM MH - Adolescent MH - Adult MH - Aged MH - Celiac Disease/*diagnosis/epidemiology/genetics MH - Female MH - Follow-Up Studies MH - HLA Antigens/*genetics/immunology MH - Hepatitis B/epidemiology/*immunology/prevention & control MH - Hepatitis B Surface Antigens/analysis MH - Hepatitis B Vaccines/*administration & dosage/immunology MH - Humans MH - Immunity/*physiology MH - Incidence MH - Male MH - Middle Aged MH - Phenotype MH - Retrospective Studies MH - Risk Assessment MH - Sampling Studies EDAT- 2003/10/24 05:00 MHDA- 2003/12/03 05:00 CRDT- 2003/10/24 05:00 PHST- 2003/10/24 05:00 [pubmed] PHST- 2003/12/03 05:00 [medline] PHST- 2003/10/24 05:00 [entrez] AID - S000292700300707X [pii] AID - 10.1111/j.1572-0241.2003.07701.x [doi] PST - ppublish SO - Am J Gastroenterol. 2003 Oct;98(10):2289-92. doi: 10.1111/j.1572-0241.2003.07701.x.