TY - JOUR
T1 - Reduced antiviral seropositivity among patients with inflammatory bowel disease treated with immunosuppressive agents
AU - Shiga, Hisashi
AU - Takahashi, Takahiro
AU - Shiraki, Manabu
AU - Kojima, Yasuhiro
AU - Tsuji, Tsuyotoshi
AU - Takagi, Sho
AU - Hiramoto, Keiichiro
AU - Yokoyama, Naonobu
AU - Sugimura, Mikako
AU - Iwabuchi, Masahiro
AU - Endo, Katsuya
AU - Onodera, Motoyuki
AU - Sato, Yuichirou
AU - Shimodaira, Yosuke
AU - Nomura, Eiki
AU - Kikuchi, Tatsuya
AU - Chiba, Hirofumi
AU - Oomori, Shinya
AU - Kudo, Hisaaki
AU - Kumada, Kazuki
AU - Nagaie, Satoshi
AU - Ogishima, Soichi
AU - Nagami, Fuji
AU - Shimoyama, Yusuke
AU - Moroi, Rintaro
AU - Kuroha, Masatake
AU - Kakuta, Yoichi
AU - Ishige, Takashi
AU - Kinouchi, Yoshitaka
AU - Masamune, Atsushi
N1 - Funding Information:
HS received lecture fees from Mitsubishi Tanabe Pharma Corp., AbbVie Inc., EA Pharma Co. Ltd., Janssen Pharmaceutical K.K., Takeda Pharmaceutical Co. Ltd., and Pfizer Inc. YKa received research grants from AbbVie Inc., Daiichi Sankyo Co. Ltd., Kyowa Kirin Co. Ltd., PRECISION IBD, and Janssen Pharmaceutical K.K., and received lecture fees from Mitsubishi Tanabe Pharma Corp., and Janssen Pharmaceutical K.K. AM received research grants from Zeria Pharmaceutical Co. Ltd., JIMRO Co. Ltd., Mochida Pharmaceutical Co. Ltd., Mitsubishi Tanabe Pharma Corp., EA Pharma Co. Ltd., and Takeda Pharmaceutical Co. Ltd. and received lecture fees from EA Pharma Co. Ltd. and Takeda Pharmaceutical Co. Ltd. The remaining authors declare no conflicts of interest.
Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
KW - Inflammatory bowel disease
KW - immunosuppressive therapy
KW - measles
KW - mumps
KW - rubella
KW - varicella
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U2 - 10.1080/00365521.2022.2132831
DO - 10.1080/00365521.2022.2132831
M3 - Article
C2 - 36222610
AN - SCOPUS:85139878498
SN - 0036-5521
VL - 58
SP - 360
EP - 367
JO - Scandinavian Journal of Gastroenterology
JF - Scandinavian Journal of Gastroenterology
IS - 4
ER -