Higher Cell-Mediated Immune Responses in Patients With Inflammatory Bowel Disease on Anti-TNF Therapy After COVID-19 Vaccination

被引:15
作者
Caldera, Freddy [1 ]
Farraye, Francis A. [2 ]
Necela, Brian M. [3 ]
Cogen, Davitte [3 ]
Saha, Sumona [1 ]
Wald, Arnold [1 ]
Daoud, Nader D. [2 ]
Chun, Kelly [4 ]
Grimes, Ian [1 ]
Lutz, Megan [1 ]
Van Helden, Sean R. [5 ]
Swift, Melanie D. [6 ]
Virk, Abinash [7 ]
Bharucha, Adil E. [8 ]
Patel, Tushar C. [9 ]
Gores, Gregory J. [8 ]
Chumsri, Saranya [10 ]
Hayney, Mary S. [5 ]
Knutson, Keith L. [3 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Div Gastroenterol & Hepatol, Dept Med, Madison, WI USA
[2] Mayo Clin, Inflammatory Bowel Dis Ctr, Dept Gastroenterol & Hepatol, Jacksonville, FL 32224 USA
[3] Mayo Clin, Dept Immunol, Jacksonville, FL 32224 USA
[4] LabCorp, R&D & Specialty Med, Calabasas, CA USA
[5] Univ Wisconsin, Sch Med & Publ Hlth, Sch Pharm, Madison, WI USA
[6] Mayo Clin, Div Publ Hlth Infect Dis & Occupat Med, Rochester, MN USA
[7] Mayo Clin, Div Infect Dis, Rochester, MN USA
[8] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[9] Mayo Clin, Div Gastroenterol & Hepatol, Jacksonville, FL 32224 USA
[10] Mayo Clin, Div Hematol & Med Oncol, Jacksonville, FL 32224 USA
关键词
Crohn's disease; ulcerative colitis; immune response;
D O I
10.1093/ibd/izac193
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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. Lay Summary 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.
引用
收藏
页码:1202 / 1209
页数:8
相关论文
共 38 条
[1]   COVID-19 vaccine-induced antibody responses in immunosuppressed patients with inflammatory bowel disease (VIP): a multicentre, prospective, case-control study [J].
Alexander, James L. ;
Kennedy, Nicholas A. ;
Ibraheim, Hajir ;
Anandabaskaran, Sulak ;
Saifuddin, Aamir ;
Seoane, Rocio Castro ;
Liu, Zhigang ;
Nice, Rachel ;
Bewshea, Claire ;
D'Mello, Andrea ;
Constable, Laura ;
Jones, Gareth R. ;
Balarajah, Sharmili ;
Fiorentino, Francesca ;
Sebastian, Shaji ;
Irving, Peter M. ;
Hicks, Lucy C. ;
Williams, Horace R. T. ;
Kent, Alexandra J. ;
Linger, Rachel ;
Parkes, Miles ;
Kok, Klaartje ;
Patel, Kamal, V ;
Teare, Julian P. ;
Altmann, Daniel M. ;
Boyton, Rosemary J. ;
Goodhand, James R. ;
Hart, Ailsa L. ;
Lees, Charlie W. ;
Ahmad, Tariq ;
Powell, Nick .
LANCET GASTROENTEROLOGY & HEPATOLOGY, 2022, 7 (04) :342-352
[2]   Safety and Immunogenicity of SARS-CoV-2 mRNA-1273 Vaccine in Older Adults [J].
Anderson, E. J. ;
Rouphael, N. G. ;
Widge, A. T. ;
Jackson, L. A. ;
Roberts, P. C. ;
Makhene, M. ;
Chappell, J. D. ;
Denison, M. R. ;
Stevens, L. J. ;
Pruijssers, A. J. ;
McDermott, A. B. ;
Flach, B. ;
Lin, B. C. ;
Doria-Rose, N. A. ;
O'Dell, S. ;
Schmidt, S. D. ;
Corbett, K. S. ;
Swanson, P. A., II ;
Padilla, M. ;
Neuzil, K. M. ;
Bennett, H. ;
Leav, B. ;
Makowski, M. ;
Albert, J. ;
Cross, K. ;
Edara, V. V. ;
Floyd, K. ;
Suthar, M. S. ;
Martinez, D. R. ;
Baric, R. ;
Buchanan, W. ;
Luke, C. J. ;
Phadke, V. K. ;
Rostad, C. A. ;
Ledgerwood, J. E. ;
Graham, B. S. ;
Beigel, J. H. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (25) :2427-2438
[3]   Molnupiravir for Oral Treatment of Covid-19 in Nonhospitalized Patients [J].
Bernal, A. Jayk ;
da Silva, M. M. Gomes ;
Musungaie, D. B. ;
Kovalchuk, E. ;
Gonzalez, A. ;
Delos Reyes, V ;
Martin-Quiros, A. ;
Caraco, Y. ;
Williams-Diaz, A. ;
Brown, M. L. ;
Du, J. ;
Pedley, A. ;
Assaid, C. ;
Strizki, J. ;
Grobler, J. A. ;
Shamsuddin, H. H. ;
Tipping, R. ;
Wan, H. ;
Paschke, A. ;
Butterton, J. R. ;
Johnson, M. G. ;
De Anda, C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2022, 386 (06) :509-520
[4]   Preserved SARS-CoV-2 Vaccine Cell-Mediated Immunogenicity in Patients With Inflammatory Bowel Disease on Immune-Modulating Therapies [J].
Boland, Brigid S. ;
Goodwin, Benjamin ;
Zhang, Zeli ;
Bloom, Nathaniel ;
Kato, Yu ;
Neill, Jennifer ;
Le, Helen ;
Tysl, Tiffani ;
Collins, Angelina E. ;
Dulai, Parambir S. ;
Singh, Siddharth ;
Nguyen, Nghia H. ;
Grifoni, Alba ;
Sette, Alessandro ;
Weiskopf, Daniela ;
Chang, John T. ;
Dan, Jennifer M. .
CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, 2022, 13 (04) :E00484
[5]   Adverse Events After SARS-CoV-2 mRNA Vaccination Among Patients With Inflammatory Bowel Disease [J].
Botwin, Gregory J. ;
Li, Dalin ;
Figueiredo, Jane ;
Cheng, Susan ;
Braun, Jonathan ;
McGovern, Dermot P. B. ;
Melmed, Gil Y. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2021, 116 (08) :1746-1751
[6]   Antibody Response to 2-Dose SARS-CoV-2 mRNA Vaccine Series in Solid Organ Transplant Recipients [J].
Boyarsky, Brian J. ;
Werbel, William A. ;
Avery, Robin K. ;
Tobian, Aaron A. R. ;
Massie, Allan B. ;
Segev, Dorry L. ;
Garonzik-Wang, Jacqueline M. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2021, 325 (21) :2204-2206
[7]   Optimizing Immunization Strategies in Patients with IBD [J].
Caldera, Freddy ;
Ley, Dana ;
Hayney, Mary S. ;
Farraye, Francis A. .
INFLAMMATORY BOWEL DISEASES, 2021, 27 (01) :123-133
[8]   Humoral Immunogenicity of mRNA COVID-19 Vaccines Among Patients With Inflammatory Bowel Disease and Healthy Controls [J].
Caldera, Freddy ;
Knutson, Keith L. ;
Saha, Sumona ;
Wald, Arnold ;
Phan, Hiep S. ;
Chun, Kelly ;
Grimes, Ian ;
Lutz, Megan ;
Hayney, Mary S. ;
Farraye, Francis A. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2022, 117 (01) :176-179
[9]   Immunogenicity of High Dose Influenza Vaccine for Patients with Inflammatory Bowel Disease on Anti-TNF Monotherapy: A Randomized Clinical Trial [J].
Caldera, Freddy ;
Hillman, Luke ;
Saha, Sumona ;
Wald, Arnold ;
Grimes, Ian ;
Zhang, Youqi ;
Sharpe, Abigail R. ;
Reichelderfer, Mark ;
Hayney, Mary S. .
INFLAMMATORY BOWEL DISEASES, 2020, 26 (04) :593-602
[10]  
Centers for Disease Control and Prevention,, Use of COVID-19 vaccines currently authorized in the United States: Interim clinical considerations for