ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2019

Incidence of Coronavirus Disease 2019 in Participants with IgG4-Related Disease Treated with Inebilizumab in the MITIGATE Study

Arezou Khosroshahi1, Emma Culver2, Wen Zhang3, Kazuichi Okazaki4, Yoshiya Tanaka5, Matthias Lohr6, nicolas schleinitz7, Xinxin Dong8, Sue Cheng8, Daniel Cimbora8 and John Stone9, 1Emory University, Atlanta, GA, 2John Radcliffe Hospital; University of Oxford, Oxford, United Kingdom, 3Peking Union Medical College Hospital, Dong Cheng Qu, China (People's Republic), 4Kansai Medical University Kori Hospital, Osaka, Japan, 5University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 6Karolinska Institutet, Stockholm, Sweden, 7Aix Marseille university, AP-HM, Marseille, France, 8Amgen, Thousand Oaks, CA, 9Massachusetts General Hospital , Harvard Medical School, Concord, MA

Meeting: ACR Convergence 2025

Keywords: B-Cell Targets, COVID-19, Fibrosing syndromes, IgG4 Related Disease, immunology

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, October 28, 2025

Title: (2015–2051) Miscellaneous Rheumatic & Inflammatory Diseases Poster III

Session Type: Poster Session C

Session Time: 10:30AM-12:30PM

Background/Purpose: The potential of B-cell-depleting therapies to diminish humoral responses is recognized, but whether this leads to an increased risk of Coronavirus Disease 2019 (COVID-19) remains unknown. Inebilizumab (INEB) is a humanized, glycoengineered, CD19-directed, monoclonal antibody that depletes B cells, including plasmablasts and some plasma cells, effectively in a targeted manner. MITIGATE (NCT04540497) is an international, randomized, blinded, placebo (PBO)-controlled Phase 3 trial that evaluates the safety and efficacy of INEB as treatment for IgG4 related disease (IgG4-RD). This ad hoc analysis examined whether INEB treatment is associated with an increased risk of COVID-19 infection in adult participants with IgG4-RD.

Methods: Primary results of the MITIGATE trial have been previously reported (Stone et al, 2024). Eligible participants were randomized 1:1 to inebilizumab or placebo and were treated on day 1, day 15, and week 26 of the 1-year randomized controlled period (RCP). Ad hoc analyses were performed to assess the risk of COVID-19 infections with INEB treatment, as COVID-related endpoints were not prespecified. First participant was enrolled October 26, 2020, after COVID-19 was initially reported (December 2019) and before the first vaccine received approval (December 2020). To determine the relationship between COVID-19 infections and immune response, the lowest recorded values of IgG, IgM, and IgA were measured and compared among participants with COVID-19 infections. Vaccination status, incidence of COVID-19, and safety were evaluated.

Results: In the trial population, 28.4% (n=19/67) of PBO-treated and 29.4% (n=20/68) of INEB-treated participants had received a COVID-19 vaccination. COVID-19 infection was reported in 13 (19.4%) PBO-treated and in 17 (25.0%) INEB-treated participants. Most infections were in participants < 65 years of age (84.6% PBO, 58.9% INEB). The majority of infections were mild [Grade 1; PBO: 7/13 (53.8%); INEB: 11/17 (64.7%)] or moderate [Grade 2; PBO: 6/13 (46.2%); INEB: 5/17 (29.4%)]. Serious COVID-19 occurred in 0 PBO-treated and 2 INEB-treated participants, both requiring hospitalizations, but were not life-threatening (Table 1). Both of these subjects had been vaccinated for COVID-19 prior to COVID-19 infection. There was no significant association between immunoglobulin reductions and occurrence of serious COVID.

Conclusion: Treatment with INEB was not associated with a higher incidence or severity of COVID-19 compared with placebo. Despite B-cell depletion, infections were mostly mild, and serious infections were infrequent. These findings support the safety of INEB in the context of the COVID-19 pandemic.

Supporting image 1


Disclosures: A. Khosroshahi: Amgen, 1, 2; E. Culver: Amgen, 1, 2, Zenus, 2; W. Zhang: None; K. Okazaki: Amgen, 1; Y. Tanaka: AbbVie, 6, AstraZeneca, 6, BMS, 6, Boehringer Ingelheim, 6, Chugai, 6, Daiichi Sankyo, 6, Eisai, 6, Eli Lilly & Co., 6, Gilead, 6, GSK, 6, IQVIA, 6, Otsuka, 6, Taisho, 6, UCB, 6; M. Lohr: Amgen, 1; n. schleinitz: Amgen, 1, 2; X. Dong: Amgen, 3, 11; S. Cheng: Amgen, 3, 11; D. Cimbora: Amgen, 3, 11; J. Stone: Acepodia, 2, Amgen, 1, 2, argenx, 2, Bristol-Myers Squibb, 2, Novartis, 2, Q32 Bio, 2, Sanofi, 2, Zenas, 2.

To cite this abstract in AMA style:

Khosroshahi A, Culver E, Zhang W, Okazaki K, Tanaka Y, Lohr M, schleinitz n, Dong X, Cheng S, Cimbora D, Stone J. Incidence of Coronavirus Disease 2019 in Participants with IgG4-Related Disease Treated with Inebilizumab in the MITIGATE Study [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/incidence-of-coronavirus-disease-2019-in-participants-with-igg4-related-disease-treated-with-inebilizumab-in-the-mitigate-study/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2025

ACR Meeting Abstracts - https://acrabstracts.org/abstract/incidence-of-coronavirus-disease-2019-in-participants-with-igg4-related-disease-treated-with-inebilizumab-in-the-mitigate-study/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology