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Higher Cell-Mediated Immune Responses in Patients With Inflammatory Bowel Disease on Anti-TNF Therapy After COVID-19 Vaccination.
Caldera, Freddy; Farraye, Francis A; Necela, Brian M; Cogen, Davitte; Saha, Sumona; Wald, Arnold; Daoud, Nader D; Chun, Kelly; Grimes, Ian; Lutz, Megan; Van Helden, Sean R; Swift, Melanie D; Virk, Abinash; Bharucha, Adil E; Patel, Tushar C; Gores, Gregory J; Chumsri, Saranya; Hayney, Mary S; Knutson, Keith L.
Affiliation
  • Caldera F; Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Farraye FA; Inflammatory Bowel Disease Center, Department of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
  • Necela BM; Department of Immunology, Mayo Clinic, Jacksonville, FL, USA.
  • Cogen D; Department of Immunology, Mayo Clinic, Jacksonville, FL, USA.
  • Saha S; Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Wald A; Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Daoud ND; Inflammatory Bowel Disease Center, Department of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
  • Chun K; R&D and Specialty Medicine, LabCorp, Calabasas, CA, USA.
  • Grimes I; Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Lutz M; Division of Gastroenterology and Hepatology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Van Helden SR; School of Pharmacy, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Swift MD; Division of Public Health, Infectious Diseases and Occupational Medicine, Mayo Clinic, Rochester, MN, USA.
  • Virk A; Division of Infectious Diseases, Mayo Clinic, Rochester, MN, USA.
  • Bharucha AE; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  • Patel TC; Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, FL, USA.
  • Gores GJ; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
  • Chumsri S; Division of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, USA.
  • Hayney MS; School of Pharmacy, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
  • Knutson KL; Department of Immunology, Mayo Clinic, Jacksonville, FL, USA.
Inflamm Bowel Dis ; 29(8): 1202-1209, 2023 08 01.
Article in En | MEDLINE | ID: mdl-36103273
ABSTRACT

BACKGROUND:

Some patients with inflammatory bowel disease (IBD) on immunosuppressive therapies may have a blunted response to certain vaccines, including the messenger RNA (mRNA) coronavirus disease 2019 (COVID-19) vaccines. However, few studies have evaluated the cell-mediated immune response (CMIR), which is critical to host defense after COVID-19 infection. The aim of this study was to evaluate the humoral immune response and CMIR after mRNA COVID-19 vaccination in patients with IBD.

METHODS:

This prospective study (HERCULES [HumoRal and CellULar initial and Sustained immunogenicity in patients with IBD] study) evaluated humoral immune response and CMIR after completion of 2 doses of mRNA COVID-19 vaccines in 158 IBD patients and 20 healthy control (HC) subjects. The primary outcome was the CMIR to mRNA COVID-19 vaccines in patients with IBD. The secondary outcomes were a comparison of (1) the CMIR in patients with IBD and HC subjects, (2) CMIR and humoral immune response in all participants, and (3) correlation between CMIR and humoral immune response.

RESULTS:

The majority (89%) of patients with IBD developed a CMIR, which was not different vs HC subjects (94%) (P = .6667). There was no significant difference (P = .5488) in CMIR between immunocompetent (median 255 [interquartile range, 146-958] spike T cells per million peripheral blood mononuclear cells) and immunosuppressed patients (median 377 [interquartile range, 123-1440]). There was no correlation between humoral and cell-mediated immunity after vaccination (P = .5215). In univariable analysis, anti-tumor necrosis factor therapy was associated with a higher CMIRs (P = .02) and confirmed in a multivariable model (P = .02). No other variables were associated with CMIR.

CONCLUSIONS:

Most patients with IBD achieved CMIR to a COVID-19 vaccine. Future studies are needed evaluating sustained CMIR and clinical outcomes.
Antibody and T cell responses to coronavirus disease 2019 vaccines in patients with inflammatory bowel disease do not correlate. Most patients with inflammatory bowel disease mount a T cell response despite being on biologic therapies, those on anti-tumor necrosis factor may have a higher T cell response. Anti-tumor necrosis factor therapy has been associated with a lower antibody response to coronavirus disease 2019 vaccines, but the T cell response is augmented.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Inflammatory Bowel Diseases / COVID-19 Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Inflamm Bowel Dis Journal subject: GASTROENTEROLOGIA Year: 2023 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Inflammatory Bowel Diseases / COVID-19 Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Inflamm Bowel Dis Journal subject: GASTROENTEROLOGIA Year: 2023 Document type: Article Affiliation country: United States