Across rheumatic diseases

Humoral and cellular immunity in patients with rare autoimmune rheumatic diseases following SARS-CoV-2 vaccination

Rheumatology (Oxford)Published Observational study

Authors' conclusion

Following two doses, most RAIRD patients have lower antibody levels than the lowest HC and lower anti-spike T cells. RAIRD patients with no/low antibodies have diminished numbers and poor quality of memory T cells that lack proliferative and functional capacities.

Study context

Population
Patients with rare autoimmune rheumatic diseases (RAIRDs) (AAV, other systemic vasculitis, SLE, myositis) after the second SARS-CoV-2 vaccine dose
Participants
50 RAIRD patients
Exposure
RAIRD patients vs healthy controls after the second SARS-CoV-2 vaccine dose
  • RAIRDn = 50
Outcome
Short-term humoral (anti-spike, anti-nucleocapsid antibody) and cell-mediated T cell response after the second SARS-CoV-2 vaccination
Follow-up
After the second dose

Main finding

As reported in the abstract

Median anti-spike antibody levels

Undetectable anti-spike levels in RAIRD patients

15

33%

Anti-spike levels lower than the lowest HC in RAIRD patients

26

57%

Observational data: associations, not effects.

Further findings

OutcomeP value
Immunogenicity by rituximab in the last 12 months vs a longer pre-vaccination periodAssociated with reduced immunogenicityP = 0.003
B cell percentages, no/low vs high antibodySignificant differenceP = 0.03
Spike-specific CD4+ T cells, no/low vs high antibodySignificant differenceP = 0.02

Terminally differentiated (exhausted) T cells

Higher percentage in the no/low antibody group

Original publication

Humoral and cellular immunity in patients with rare autoimmune rheumatic diseases following SARS-CoV-2 vaccination. Rheumatology (Oxford). Published 17 October 2022. doi:10.1093/rheumatology/keac574

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