Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jun 24;12(1):e003008.
doi: 10.1136/bmjresp-2024-003008.

Association of vaccination status and immunosuppression with mortality of SARS-CoV-2 infection in patients with fibrotic interstitial lung disease

Affiliations

Association of vaccination status and immunosuppression with mortality of SARS-CoV-2 infection in patients with fibrotic interstitial lung disease

Kathryn Donohoe et al. BMJ Open Respir Res. .

Abstract

Background: There are limited data exploring the outcome following SARS-CoV-2 infection in fibrotic interstitial lung disease (fILD). Our goal was to determine the association of vaccination for SARS-CoV-2 with both SARS-CoV-2 infection and subsequent 90-day mortality in fILD. Our second objective was to determine the association of immunosuppressive use with both SARS-CoV-2 infection and subsequent 90-day mortality in fILD.

Methods: Patients with fILD enrolled in the Canadian Registry for Pulmonary Fibrosis with comprehensive access to data on SARS-CoV-2 vaccination and PCR-confirmed infection were included. Associations of vaccination status and current immunosuppressant use with SARS-CoV-2 infection and subsequent 90-day mortality were tested using Fisher's exact test and subsequently multivariable logistic regression adjusting for age, sex, pre-identified comorbidities, forced vital capacity and diffusing capacity of the lung for carbon monoxide.

Results: Of 1452 total patients with fILD, 138 tested positive for SARS-CoV-2. On adjusted analysis, vaccination for SARS-CoV-2 was associated with a 60% reduction in the odds of infection (OR 0.40, 95% CI 0.24 to 0.67 p<0.001) and a 97% reduction in the odds of 90-day mortality following infection (OR 0.03, 95% CI 0.0007 to 0.26, p=0.01). SARS-CoV-2 was diagnosed in 13% of patients on an immunosuppressant and 9% of those not (OR 1.4, 95% CI 1.0 to 2.1, p=0.04). Immunosuppressant use was not associated with 90-day mortality after SARS-CoV-2 infection on adjusted analysis.

Conclusion: In patients with fILD, vaccination against SARS-CoV-2 was associated with decreased frequency of SARS-CoV-2 infection and subsequent 90-day mortality, while current use of immunosuppressive medication was associated with risk of infection but only a trend for subsequent 90-day mortality.

Keywords: COVID-19; Idiopathic Pulmonary Fibrosis; Interstitial Fibrosis.

PubMed Disclaimer

Conflict of interest statement

Competing interests: KDonohoe reports no conflicts of interest relevant to this manuscript. KAJ reports personal fees from Boehringer Ingelheim and Abbvie, and consulting grants from Boehringer Ingelheim, Pliant Therapeutics, Hoffman-La Roche and Brainomix. KJ reports grants from the University of Calgary Foundation and Three Lakes Foundation. HM reports personal fees from Boehringer Ingelheim Canada and grants from Boehringer Ingelheim Canada, BMS, Galapagos and Endeavor Biomedicines Inc. VM reports consulting fees from Boehringer Ingelheim Canada and Hoffman-La Roche, grants from Astra Zeneca, Boehringer Ingelheim, the University of Saskatchewan and the Respiratory Research Center-Saskatchewan. CJR reports personal fees from Boehringer Ingelheim and consulting fees from Boehringer Ingelheim, Pliant Therapeutics, Astra Zeneca, Trevi Therapeutics and Veracyte. CJR reports grants from Boehringer Ingelheim.

Figures

Figure 1
Figure 1. Survival stratified by vaccination and immunosuppression status in fILD.
Figure 2
Figure 2. SARS-CoV-2 infection and 90-day mortality in fILD.

Similar articles

  • Antibody tests for identification of current and past infection with SARS-CoV-2.
    Fox T, Geppert J, Dinnes J, Scandrett K, Bigio J, Sulis G, Hettiarachchi D, Mathangasinghe Y, Weeratunga P, Wickramasinghe D, Bergman H, Buckley BS, Probyn K, Sguassero Y, Davenport C, Cunningham J, Dittrich S, Emperador D, Hooft L, Leeflang MM, McInnes MD, Spijker R, Struyf T, Van den Bruel A, Verbakel JY, Takwoingi Y, Taylor-Phillips S, Deeks JJ; Cochrane COVID-19 Diagnostic Test Accuracy Group. Fox T, et al. Cochrane Database Syst Rev. 2022 Nov 17;11(11):CD013652. doi: 10.1002/14651858.CD013652.pub2. Cochrane Database Syst Rev. 2022. PMID: 36394900 Free PMC article.
  • Cyclophosphamide for connective tissue disease-associated interstitial lung disease.
    Barnes H, Holland AE, Westall GP, Goh NS, Glaspole IN. Barnes H, et al. Cochrane Database Syst Rev. 2018 Jan 3;1(1):CD010908. doi: 10.1002/14651858.CD010908.pub2. Cochrane Database Syst Rev. 2018. PMID: 29297205 Free PMC article.
  • Dynamics of interstitial lung disease following immunosuppressive treatment differ between antisynthetase syndrome and systemic sclerosis.
    Freund O, Eviatar T, Meidan R, Shalmon T, Stav D, Hershko T, Perluk TM, Wand O, Schneer S, Adir Y, Shitrit D, Elkayam O, Bar-Shai A, Unterman A. Freund O, et al. Ther Adv Respir Dis. 2025 Jan-Dec;19:17534666251336896. doi: 10.1177/17534666251336896. Epub 2025 May 8. Ther Adv Respir Dis. 2025. PMID: 40337907 Free PMC article.
  • Rapid, point-of-care antigen tests for diagnosis of SARS-CoV-2 infection.
    Dinnes J, Sharma P, Berhane S, van Wyk SS, Nyaaba N, Domen J, Taylor M, Cunningham J, Davenport C, Dittrich S, Emperador D, Hooft L, Leeflang MM, McInnes MD, Spijker R, Verbakel JY, Takwoingi Y, Taylor-Phillips S, Van den Bruel A, Deeks JJ; Cochrane COVID-19 Diagnostic Test Accuracy Group. Dinnes J, et al. Cochrane Database Syst Rev. 2022 Jul 22;7(7):CD013705. doi: 10.1002/14651858.CD013705.pub3. Cochrane Database Syst Rev. 2022. PMID: 35866452 Free PMC article.
  • SARS-CoV-2-neutralising monoclonal antibodies to prevent COVID-19.
    Hirsch C, Park YS, Piechotta V, Chai KL, Estcourt LJ, Monsef I, Salomon S, Wood EM, So-Osman C, McQuilten Z, Spinner CD, Malin JJ, Stegemann M, Skoetz N, Kreuzberger N. Hirsch C, et al. Cochrane Database Syst Rev. 2022 Jun 17;6(6):CD014945. doi: 10.1002/14651858.CD014945.pub2. Cochrane Database Syst Rev. 2022. PMID: 35713300 Free PMC article.

References

    1. Collard HR, Ryerson CJ, Corte TJ, et al. Acute Exacerbation of Idiopathic Pulmonary Fibrosis. An International Working Group Report. Am J Respir Crit Care Med. 2016;194:265–75. doi: 10.1164/rccm.201604-0801CI. - DOI - PubMed
    1. Drake TM, Docherty AB, Harrison EM, et al. Outcome of Hospitalization for COVID-19 in Patients with Interstitial Lung Disease. An International Multicenter Study. Am J Respir Crit Care Med. 2020;202:1656–65. doi: 10.1164/rccm.202007-2794OC. - DOI - PMC - PubMed
    1. Gallay L, Uzunhan Y, Borie R, et al. Risk Factors for Mortality after COVID-19 in Patients with Preexisting Interstitial Lung Disease. Am J Respir Crit Care Med. 2021;203:245–9. doi: 10.1164/rccm.202007-2638LE. - DOI - PMC - PubMed
    1. Shao C, Shi Y, Chen R, et al. Risk factors associated with COVID-19 pneumonia in Chinese patients with pre-existing interstitial lung disease during the SARS-CoV-2 pandemic. J Med Virol. 2023;95:e29098. doi: 10.1002/jmv.29098. - DOI - PubMed
    1. Beltramo G, Cottenet J, Mariet A-S, et al. Chronic respiratory diseases are predictors of severe outcome in COVID-19 hospitalised patients: a nationwide study. Eur Respir J. 2021;58:2004474. doi: 10.1183/13993003.04474-2020. - DOI - PMC - PubMed

MeSH terms

LinkOut - more resources