Accelerated waning of immunity to SARS-CoV-2 mRNA vaccines in patients with immune-mediated inflammatory diseases

Thumbnail image

Download files

DOI

https://doi.org/10.1172/jci.insight.159721

Language of the publication
English
Date
2022-06-08
Type
Article
Author(s)
  • Dayam, Roya M.
  • Law, Jaclyn C.
  • Goetgebuer, Rogier L.
  • Chao, Gary Y.C.
  • Abe, Kento T.
  • Sutton, Mitchell
  • Finkelstein, Naomi
  • Stempak, Joanne M.
  • Pereira, Daniel
  • Croitoru, David
  • Acheampong, Lily
  • Rizwan, Saima
  • Rymaszewski, Klaudia
  • Milgrom, Raquel
  • Ganatra, Darshini
  • Batista, Nathalia V.
  • Girard, Melanie
  • Lau, Irene
  • Law, Ryan
  • Cheung, Michelle W.
  • Rathod, Bhavisha
  • Kitaygorodsky, Julia
  • Samson, Reuben
  • Hu, Queenie
  • Hardy, W. Rod
  • Haroon, Nigil
  • Inman, Robert D.
  • Piguet, Vincent
  • Chandran, Vinod
  • Silverberg, Mark S.
  • Gingras, Anne-Claude
  • Watts, Tania H.
Publisher
American Society for Clinical Investigation

Abstract

BACKGROUND: Limited information is available on the impact of immunosuppressants on COVID-19 vaccination in patients with immune-mediated inflammatory diseases (IMID). METHODS: This observational cohort study examined the immunogenicity of SARS-CoV-2 mRNA vaccines in adult patients with inflammatory bowel disease, rheumatoid arthritis, ankylosing spondylitis, or psoriatic disease, with or without maintenance immunosuppressive therapies. Ab and T cell responses to SARS-CoV-2, including neutralization against SARS-CoV-2 variants, were determined before and after 1 and 2 vaccine doses. RESULTS: We prospectively followed 150 subjects, 26 healthy controls, 9 patients with IMID on no treatment, 44 on anti-TNF, 16 on anti-TNF with methotrexate/azathioprine (MTX/AZA), 10 on anti–IL-23, 28 on anti–IL-12/23, 9 on anti–IL-17, and 8 on MTX/AZA. Ab and T cell responses to SARS-CoV-2 were detected in all participants, increasing from dose 1 to dose 2 and declining 3 months later, with greater attrition in patients with IMID compared with healthy controls. Ab levels and neutralization efficacy against variants of concern were substantially lower in anti-TNF–treated patients than in healthy controls and were undetectable against Omicron by 3 months after dose 2. CONCLUSIONS: Our findings support the need for a third dose of the mRNA vaccine and for continued monitoring of immunity in these patient groups.

Subject

  • Health

Keywords

  • Antibodies, Viral,
  • COVID-19 Vaccines*,
  • COVID-19* / prevention & control,
  • Canada,
  • Humans,
  • SARS-CoV-2,
  • Tumor Necrosis Factor Inhibitors,
  • Vaccines, Synthetic,
  • mRNA Vaccines,
  • BNT162 Vaccine

Rights

Pagination

1-14

Peer review

Yes

Open access level

Gold

Identifiers

PubMed ID
35471956
ISSN
2379-3708

Article

Journal title
JCI Insight
Journal volume
7
Journal issue
11
Article number
e159721

Sponsors

Funded by a donation from Juan and Stefania Speck and by Canadian Institutes of Health (CIHR)/COVID-Immunity Task Force (CITF) grants VR-1 172711 and VS1-175545 (to THW and ACG), CIHR FDN-143250 (to THW), GA2-177716 (to VC, ACG, and THW), and GA1-177703 (to ACG) and the CIHR rapid response network to SARS-CoV-2 variants, CoVaRR-Net (to ACG).

Download(s)

URI

Collection(s)

Communicable diseases

Full item page

Full item page

Page details

Date modified: