Reduced antiviral seropositivity among patients with inflammatory bowel disease treated with immunosuppressive agents.


Journal

Scandinavian journal of gastroenterology
ISSN: 1502-7708
Titre abrégé: Scand J Gastroenterol
Pays: England
ID NLM: 0060105

Informations de publication

Date de publication:
04 2023
Historique:
pubmed: 13 10 2022
medline: 10 3 2023
entrez: 12 10 2022
Statut: ppublish

Résumé

Although live-attenuated vaccines are contraindicated under immunosuppression, the immune status of patients with inflammatory bowel disease (IBD) has not been fully assessed prior to immunosuppressive therapy. To investigate antiviral serostatus against viruses requiring live vaccines for prevention in IBD patients undergoing immunosuppressive therapy. This multicenter study included IBD patients who were aged <40 years and were treated with thiopurine monotherapy, molecular-targeted monotherapy, or combination therapy. Gender- and age-matched healthy subjects (HS) living in the same areas were included as control group. Antibody titers against measles, rubella, mumps, and varicella were measured by enzyme-linked immunosorbent assays. A total of 437 IBD patients (163 ulcerative colitis [UC] and 274 Crohn's disease [CD]) and 225 HS were included in the final analysis. Compared with HS, IBD patients had lower seropositivity rates for measles (IBD vs. HS = 83.91% vs. 85.33%), rubella (77.55% vs. 84.89%), mumps (37.50% vs. 37.78%), and varicella (91.26% vs. 96.44%). Gender- and age-adjusted seropositivity rates were lower in UC patients than in both CD patients and HS for measles (UC, CD, and HS = 81.60%, 85.29%, and 85.33%), rubella (76.40%, 78.23%, and 84.89%), mumps (27.16%, 43.70%, and 37.78%), and varicella (90.80%, 91.54%, and 96.44%); the difference was significant for all viruses except measles. Divided by the degree of immunosuppression, there were no significant differences in seropositivity rates among IBD patients. IBD patients, especially those with UC, exhibit reduced seropositivity rates and may benefit from screening prior to the initiation of immunosuppressive therapy.

Sections du résumé

BACKGROUND
Although live-attenuated vaccines are contraindicated under immunosuppression, the immune status of patients with inflammatory bowel disease (IBD) has not been fully assessed prior to immunosuppressive therapy.
AIMS
To investigate antiviral serostatus against viruses requiring live vaccines for prevention in IBD patients undergoing immunosuppressive therapy.
METHODS
This multicenter study included IBD patients who were aged <40 years and were treated with thiopurine monotherapy, molecular-targeted monotherapy, or combination therapy. Gender- and age-matched healthy subjects (HS) living in the same areas were included as control group. Antibody titers against measles, rubella, mumps, and varicella were measured by enzyme-linked immunosorbent assays.
RESULTS
A total of 437 IBD patients (163 ulcerative colitis [UC] and 274 Crohn's disease [CD]) and 225 HS were included in the final analysis. Compared with HS, IBD patients had lower seropositivity rates for measles (IBD vs. HS = 83.91% vs. 85.33%), rubella (77.55% vs. 84.89%), mumps (37.50% vs. 37.78%), and varicella (91.26% vs. 96.44%). Gender- and age-adjusted seropositivity rates were lower in UC patients than in both CD patients and HS for measles (UC, CD, and HS = 81.60%, 85.29%, and 85.33%), rubella (76.40%, 78.23%, and 84.89%), mumps (27.16%, 43.70%, and 37.78%), and varicella (90.80%, 91.54%, and 96.44%); the difference was significant for all viruses except measles. Divided by the degree of immunosuppression, there were no significant differences in seropositivity rates among IBD patients.
CONCLUSIONS
IBD patients, especially those with UC, exhibit reduced seropositivity rates and may benefit from screening prior to the initiation of immunosuppressive therapy.

Identifiants

pubmed: 36222610
doi: 10.1080/00365521.2022.2132831
doi:

Substances chimiques

Antiviral Agents 0
Immunosuppressive Agents 0
Measles-Mumps-Rubella Vaccine 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

360-367

Auteurs

Hisashi Shiga (H)

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Takahiro Takahashi (T)

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Manabu Shiraki (M)

Department of Gastroenterology, Tohoku Rosai Hospital, Sendai, Japan.

Yasuhiro Kojima (Y)

Department of Gastroenterology, Tohoku Rosai Hospital, Sendai, Japan.

Tsuyotoshi Tsuji (T)

Department of Gastroenterology, Akita City Hospital, Akita, Japan.

Sho Takagi (S)

Takagi Clinic, Sendai, Japan.

Keiichiro Hiramoto (K)

Department of Gastroenterology, South Miyagi Medical Center, Ohgawara, Japan.

Naonobu Yokoyama (N)

Department of Gastroenterology, Iwate Prefectural Iwai Hospital, Ichinoseki, Japan.

Mikako Sugimura (M)

Department of Gastroenterology, NHO Sendai Medical Center, Sendai, Japan.

Masahiro Iwabuchi (M)

Department of Gastroenterology, NHO Sendai Medical Center, Sendai, Japan.

Katsuya Endo (K)

Department of Gastroenterology, Tohoku Medical and Pharmaceutical University, Sendai, Japan.

Motoyuki Onodera (M)

Department of Gastroenterology, Osaki Citizen Hospital, Osaki, Japan.

Yuichirou Sato (Y)

Department of Gastroenterology, Osaki Citizen Hospital, Osaki, Japan.

Yosuke Shimodaira (Y)

Department of Gastroenterology and Neurology, Akita University Graduate School of Medicine, Akita, Japan.

Eiki Nomura (E)

Department of Gastroenterology, Sendai City Hospital, Sendai, Japan.

Tatsuya Kikuchi (T)

Department of Gastroenterology, Sendai City Hospital, Sendai, Japan.

Hirofumi Chiba (H)

Department of Gastroenterology, Iwate Prefectural Isawa Hospital, Oshu, Japan.

Shinya Oomori (S)

Department of Gastroenterology, Japanese Red Cross Sendai Hospital, Sendai, Japan.

Hisaaki Kudo (H)

Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.

Kazuki Kumada (K)

Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Advanced Research Center for Innovations in Next-Generation Medicine, Tohoku University, Sendai, Japan.

Satoshi Nagaie (S)

Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.

Soichi Ogishima (S)

Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Advanced Research Center for Innovations in Next-Generation Medicine, Tohoku University, Sendai, Japan.

Fuji Nagami (F)

Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
Advanced Research Center for Innovations in Next-Generation Medicine, Tohoku University, Sendai, Japan.

Yusuke Shimoyama (Y)

Department of Gastroenterology, Iwate Prefectural Isawa Hospital, Oshu, Japan.

Rintaro Moroi (R)

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Masatake Kuroha (M)

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Yoichi Kakuta (Y)

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Takashi Ishige (T)

Department of Pediatrics, Gunma University Graduate School of Medicine, Maebashi, Japan.

Yoshitaka Kinouchi (Y)

Student Health Care Center, Institute for Excellence in Higher Education, Tohoku University, Sendai, Japan.

Atsushi Masamune (A)

Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.

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