Skip to main content

Advertisement

Log in

Multicenter, cross-sectional, observational study on Epstein–Barr viral infection status and thiopurine use by age group in patients with inflammatory bowel disease in Japan (EBISU study)

  • Original Article—Alimentary Tract
  • Published:
Journal of Gastroenterology Aims and scope Submit manuscript

Abstract

Background

The Epstein–Barr virus (EBV) infection status in patients with inflammatory bowel disease (IBD), particularly those using thiopurines, may be associated with the risk of lymphoproliferative disorder and hemophagocytic lymphohistiocytosis. This was the first multicenter survey of EBV infection in Japanese patients with IBD. Factors related to the EBV infection status were also investigated.

Methods

Five tertiary institutions in Japan participated in this study to examine pediatric and adult patients with IBD. Serum EBV anti-viral capsid antigen (VCA) IgG, EBV anti-VCA IgM, and anti-EBV nuclear antigen–antibody were measured in 495 patients with IBD. The patients’ information was obtained from their medical records. Prior EBV infection was defined as anti-VCA IgM negativity and anti-VCA IgG positivity (UMIN000033004).

Results

The patients’ median age was 25 years (range 0–92 years). Of the 495 patients, nine were anti-VCA IgM-positive and 354 were anti-VCA IgG-positive (seroprevalence: 72.8%). The proportion of patients with prior EBV infection was 0% for those aged < 5 years, < 60% for those aged < 30 years, and > 90% for those aged > 30 years. The proportion of EBV-uninfected patients using thiopurines was 28.4% (52/183) for all patients and 51.8% (44/85) for pediatric patients. Age was significantly associated with anti-VCA IgG seropositivity (p < 0.01, odds ratio: 0.902, 95% confidence interval: 0.880–0.925). No cases of lymphoproliferative disorder, hemophagocytic lymphohistiocytosis, or chronic active EBV infection were reported.

Conclusions

Approximately 30% of Japanese patients with IBD were EBV-uninfected, including those using thiopurines. Age was a significant factor for anti-VCA IgG seropositivity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Abbreviations

CD:

Crohn’s disease

EBNA:

Epstein–Barr virus nuclear antigen

EBV:

Epstein–Barr virus

HLH:

Hemophagocytic lymphohistiocytosis

IBD:

Inflammatory bowel disease

IBDU:

Inflammatory bowel disease unclassified

LPD:

Lymphoproliferative disorder

UC:

Ulcerative colitis

VCA:

Viral capsid antigen

References

  1. Odumade OA, Hogquist KA, Balfour HH Jr. Progress and problems in understanding and managing primary Epstein-Barr virus infections. Clin Microbiol Rev. 2011;24:193–209.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Cohen JI. Epstein-Barr virus infection. N Engl J Med. 2000;343:481–92.

    Article  CAS  PubMed  Google Scholar 

  3. Chan HC, Ng SC. Emerging biologics in inflammatory bowel disease. J Gastroenterol. 2017;52:141–50.

    Article  CAS  PubMed  Google Scholar 

  4. Tsai L, Ma C, Dulai PS, et al. Contemporary risk of surgery in patients with ulcerative colitis and Crohn’s disease: a meta-analysis of population-based cohorts. Clin Gastroenterol Hepatol. 2020. https://doi.org/10.1016/j.cgh.2020.10.039.

    Article  PubMed  Google Scholar 

  5. Annese V, Beaugerie L, Egan L, et al. European evidence-based consensus: inflammatory bowel disease and malignancies. J Crohns Colitis. 2015;9:945–65.

    Article  PubMed  Google Scholar 

  6. Beaugerie L, Brousse N, Bouvier AM, CESAME Study Group, et al. Lymphoproliferative disorders in patients receiving thiopurines for inflammatory bowel disease: a prospective observational cohort study. Lancet. 2009;374:1617–25.

    Article  CAS  PubMed  Google Scholar 

  7. Herrinton LJ, Liu L, Weng X, et al. Role of thiopurine and anti-TNF therapy in lymphoma in inflammatory bowel disease. Am J Gastroenterol. 2011;106:2146–53.

    Article  CAS  PubMed  Google Scholar 

  8. Chupin A, Perduca V, Meyer A, et al. Systematic review with meta-analysis: comparative risk of lymphoma with anti-tumour necrosis factor agents and/or thiopurines in patients with inflammatory bowel disease. Aliment Pharmacol Ther. 2020;52:1289–97.

    CAS  PubMed  Google Scholar 

  9. Wisniewski A, Kirchgesner J, Seksik P, et al. Increased incidence of systemic serious viral infections in patients with inflammatory bowel disease associates with active disease and use of thiopurines. United Eur Gastroenterol J. 2020;8:303–13.

    Article  CAS  Google Scholar 

  10. Posthuma EF, Westendorp RG, van der Sluys VA, et al. Fatal infectious mononucleosis: a severe complication in the treatment of Crohn’s disease with azathioprine. Gut. 1995;36:311–3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Biank VF, Sheth MK, Talano J, et al. Association of Crohn’s disease, thiopurines, and primary Epstein-Barr virus infection with hemophagocytic lymphohistiocytosis. J Pediatr. 2011;159:808–12.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Fries W, Cottone M, Cascio A. Systematic review: macrophage activation syndrome in inflammatory bowel disease. Aliment Pharmacol Ther. 2013;37:1033–45.

    Article  CAS  PubMed  Google Scholar 

  13. Hyams JS, Dubinsky MC, Baldassano RN, et al. Infliximab is not associated with increased risk of malignancy or hemophagocytic lymphohistiocytosis in pediatric patients with inflammatory bowel disease. Gastroenterology. 2017;152:1901–14.

    Article  PubMed  Google Scholar 

  14. Fukata N, Okazaki K, Omiya M, et al. Hematologic malignancies in the Japanese patients with inflammatory bowel disease. J Gastroenterol. 2014;49:1299–306.

    Article  PubMed  Google Scholar 

  15. Kobayashi T, Uda A, Udagawa E, et al. Lack of increased risk of lymphoma by thiopurines or biologics in Japanese patients with inflammatory bowel disease: a large-scale administrative database analysis. J Crohns Colitis. 2020;14:617–23.

    Article  PubMed  Google Scholar 

  16. Rahier JF, Magro F, Abreu C, et al. Second European evidence-based consensus on the prevention, diagnosis and management of opportunistic infections in inflammatory bowel disease. J Crohns Colitis. 2014;8:443–68.

    Article  CAS  PubMed  Google Scholar 

  17. Winter JR, Taylor GS, Thomas OG, et al. Predictors of Epstein-Barr virus serostatus in young people in England. BMC Infect Dis. 2019;19:1007.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Takeuchi K, Tanaka-Taya K, Kazuyama Y, et al. Prevalence of Epstein-Barr virus in Japan: trends and future prediction. Pathol Int. 2006;56:112–6.

    Article  PubMed  Google Scholar 

  19. Condon LM, Cederberg LE, Rabinovitch MD, et al. Age-specific prevalence of Epstein-Barr virus infection among Minnesota children: effects of race/ethnicity and family environment. Clin Infect Dis. 2014;59:501–8.

    Article  CAS  PubMed  Google Scholar 

  20. Crawford DH, Macsween KF, Higgins CD, et al. A cohort study among university students: identification of risk factors for Epstein-Barr virus seroconversion and infectious mononucleosis. Clin Infect Dis. 2006;43:276–82.

    Article  PubMed  Google Scholar 

  21. Chen CY, Huang KY, Shen JH, et al. A large-scale seroprevalence of Epstein-Barr virus in Taiwan. PLoS ONE. 2015;10:e0115836.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Love KA, Henderson P, Garrick V, et al. Letter: Epstein-Barr virus status may be especially important in paediatric IBD populations. Aliment Pharmacol Ther. 2014;39:231–2.

    Article  CAS  PubMed  Google Scholar 

  23. Hradsky O, Copova I, Zarubova K, et al. Seroprevalence of Epstein-Barr virus, cytomegalovirus, and polyomaviruses in children with inflammatory bowel disease. Dig Dis Sci. 2015;60:3399–407.

    Article  CAS  PubMed  Google Scholar 

  24. Linton MS, Kroeker K, Fedorak D, et al. Prevalence of Epstein-Barr virus in a population of patients with inflammatory bowel disease: a prospective cohort study. Aliment Pharmacol Ther. 2013;38:1248–54.

    Article  CAS  PubMed  Google Scholar 

  25. de Francisco R, Castaño-García A, Martínez-González S, et al. Impact of Epstein-Barr virus serological status on clinical outcomes in adult patients with inflammatory bowel disease. Aliment Pharmacol Ther. 2018;48:723–30.

    Article  PubMed  Google Scholar 

  26. Gordon J, Ramaswami A, Beuttler M, et al. EBV status and thiopurine use in pediatric IBD. J Pediatr Gastroenterol Nutr. 2016;62:711–4.

    Article  CAS  PubMed  Google Scholar 

  27. El-Matary W. Routine testing for EBV status in children with inflammatory bowel disease: are we overreacting? Inflamm Bowel Dis. 2020;26:e20.

    Article  PubMed  Google Scholar 

  28. Hans AK, Scott FI. Editorial: which inflammatory bowel disease patients should be screened for Epstein-Barr virus infection? Aliment Pharmacol Ther. 2018;48:1158–9.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Traci Raley, MS, ELS and Angela Morben, DVM, ELS, from Edanz Group (https://jp.edanz.com/ac) for editing a draft of this manuscript.

Funding

This work was supported in part by grants from the Japan Sciences Research Grant for Research on Intractable Diseases (Japanese Inflammatory Bowel Disease Research Group) affiliated with the Japan Ministry of Health, Labour and Welfare.

Author information

Authors and Affiliations

Authors

Contributions

Concept and design of the study: TH, MMi, HS, KA, II, HN, and TS; acquisition of data: TH, MMi, HS, DS, TK, DH, MY, KA, II, HN, and TS; analysis and interpretation of data: TH, MMi, JM, MMa, KA, II, HN, and TS; drafting of the manuscript: MMi, TH, JM, and MMa; critical revision of the manuscript for important intellectual content: KA, II, HN, and TS; statistical analyses: JM; study supervision: TH, KA, II, HN, and TS.

Corresponding author

Correspondence to Tadakazu Hisamatsu.

Ethics declarations

Conflict of interest

Tadakazu Hisamatsu has performed joint research with Alfresa Pharma Co., Ltd. and EA Pharma Co., Ltd.; received grant support from Mitsubishi Tanabe Pharma Corporation, EA Pharma Co., Ltd., AbbVie GK, JIMRO Co., Ltd., Zeria Pharmaceutical Co., Ltd., Daiichi-Sankyo, Kyorin Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., Takeda Pharmaceutical Co., Ltd., Pfizer Inc., and Mochida Pharmaceutical Co., Ltd.; and received consulting and lecture fees from Mitsubishi Tanabe Pharma Corporation, AbbVie GK, Celgene K.K., EA Pharma Co., Ltd., Kyorin Pharmaceutical Co. Ltd., JIMRO Co., Janssen Pharmaceutical K.K., Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., and Pfizer Inc. Jun Miyoshi received lecture fees from JIMRO Co. and Takeda Pharmaceutical Co., Ltd. Minoru Matsuura received commercial research funding from AbbVie GK, Mitsubishi Tanabe Pharma Corporation, EA Pharma Co., Ltd., Mochida Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., and JIMRO Co. and received lecture fees from Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, AbbVie GK, Takeda Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., Mochida Pharmaceutical Co., Ltd., Viatris Inc., Sandoz K.K., JIMRO Co., Nippon Kayaku Co., Ltd., Kissei Pharmaceutical Co., Ltd., EA Pharma Co., Ltd., and Zeria Pharmaceutical Co., Ltd. Katsuhiro Arai received grant support from Nippon Kayaku Co., Ltd. and received consulting and lecture fees from Mitsubishi Tanabe Pharma Corporation, Janssen Pharmaceutical K.K., EA Pharma Co., Ltd., AbbVie GK, Zeria Pharmaceutical Co., Ltd., Kyorin Pharmaceutical Co., Ltd., Nippon Kayaku Co., Ltd., Takeda Pharmaceutical Co., Ltd., Alfresa Pharma Corporation, Eli Lilly Japan K.K., and Nobelpharma Co., Ltd. Hirotaka Shimizu received grant support from Nippon Kayaku Co., Ltd. Hiroshi Nakase received honoraria from Mitsubishi Tanabe Pharma Corporation, Mochida Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., and Abbvie GK and commercial research funding from Hoya Group Pentax Medical, Boehringer Ingelheim GmbH, and Daticho-Sankyo Co., Ltd. Toshiaki Shimizu received research grants from Otsuka Pharmaceutical Co., Ltd., Japan Blood Products Organization, EA Pharma Co., Ltd., and Kissei Pharmaceutical Co., Ltd. Miki Miura, Daisuke Saito, Yoshida Masashi, Takahiro Kudo, Daisuke Hirayama, Masashi Yoshida, and Itaru Iwama have no conflicts of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 29 KB)

535_2021_1832_MOESM2_ESM.pptx

Supplementary file2 Supplemental Fig. 1 Flowchart of patients in this study. UC ulcerative colitis; CD Crohn’s disease; IBDU inflammatory bowel disease unclassified; VCA viral capsid antigen (PPTX 42 KB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Miura, M., Shimizu, H., Saito, D. et al. Multicenter, cross-sectional, observational study on Epstein–Barr viral infection status and thiopurine use by age group in patients with inflammatory bowel disease in Japan (EBISU study). J Gastroenterol 56, 1080–1091 (2021). https://doi.org/10.1007/s00535-021-01832-w

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00535-021-01832-w

Keywords

Navigation