Antibody responses after documented COVID-19 disease in patients with autoimmune rheumatic disease.
Autoimmune disease
COVID-19 susceptibility
Immune response
Immunosuppressant
Protective antibody
Rheumatic disease
Journal
Clinical rheumatology
ISSN: 1434-9949
Titre abrégé: Clin Rheumatol
Pays: Germany
ID NLM: 8211469
Informations de publication
Date de publication:
Nov 2021
Nov 2021
Historique:
received:
11
03
2021
accepted:
30
05
2021
revised:
27
05
2021
pubmed:
23
6
2021
medline:
21
10
2021
entrez:
22
6
2021
Statut:
ppublish
Résumé
Patients with autoimmune rheumatic diseases (AIRD) are suspected to have less robust immune responses during COVID-19 due to underlying immune dysfunction and the use of immune-suppressive drugs. Fifty consecutive patients with a diagnosis of AIRD on disease-modifying drugs were included at around 30 days after a confirmatory test for COVID-19. Fifty controls matched one to one for age, sex, and severity of COVID-19 were also included at around 30 days after testing positive for COVID-19. Antibody titers for anti-spike protein IgG and anti-nucleocapsid protein IgG were estimated. Cases (mean age 45.9 ± 13; 76% females) and controls (mean age 45.9 ± 13; 76% females) had similar proportion of comorbidities. Of the cases, 4 had moderate and 1 had severe COVID-19, while 3 and 1 of controls had moderate and severe COVID-19 respectively. Positivity of anti-N IgG was similar between patients (80%) and controls (90%) (p = 0.26). Similarly, anti-S IgG was positive in 82% of patients and 86% of controls (p = 0.79). Both the antibodies were negative in seven (14%) patients and five (10%) of controls (p = 0.76, Fischer exact test). Only anti-N IgG titers were lower in patients as compared to controls. In four patients with rheumatoid arthritis, two with spondyloarthritis and one with eosinophilic fasciitis both antibodies were not detectable. They did not differ from the rest of the cohort in clinical characteristics. The patients with AIRD had adequate protective antibody responses to COVID-19 at a median of 30 days post-infection. Thus, the presence of AIRD or the use of immunosuppressants does not seem to influence the development of humoral immune response against COVID-19. Key Points • Patients with autoimmune rheumatic diseases (AIRD) are suspected to have less robust immune responses. • In our cohort of 50 patients with AIRD with confirmed COVID-19, only seven did not have detectable protective antibodies at 30 days post infection. • Patients with AIRD on immunosuppressants have adequate protective antibodies post COVID-19 disease, at rates similar to that in health controls.
Identifiants
pubmed: 34155573
doi: 10.1007/s10067-021-05801-9
pii: 10.1007/s10067-021-05801-9
pmc: PMC8216872
doi:
Substances chimiques
Antibodies, Viral
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
4665-4670Informations de copyright
© 2021. International League of Associations for Rheumatology (ILAR).
Références
Clin Rheumatol. 2020 Sep;39(9):2789-2796
pubmed: 32720259
Clin Rheumatol. 2020 Jul;39(7):2055-2062
pubmed: 32277367
Semin Arthritis Rheum. 1993 Oct;23(2 Suppl 1):82-91
pubmed: 8278823
Ann Rheum Dis. 2020 Jul;79(7):988-990
pubmed: 32503857
Nature. 2020 Aug;584(7821):430-436
pubmed: 32640463
Science. 2020 Dec 4;370(6521):1227-1230
pubmed: 33115920
J Rheumatol. 1994 Nov;21(11):2082-7
pubmed: 7869314
Ann Rheum Dis. 2020 Jul;79(7):859-866
pubmed: 32471903
Rheumatol Int. 2021 Feb;41(2):243-256
pubmed: 33388969
Ann Rheum Dis. 2021 Jan 12;:
pubmed: 33436385
Ann Rheum Dis. 2021 Mar 10;:
pubmed: 33692021
Ann Rheum Dis. 2020 Jul;79(7):986-988
pubmed: 32467245
Clin Rheumatol. 2020 Sep;39(9):2757-2762
pubmed: 32474883
Ann Rheum Dis. 2020 Dec;79(12):1659-1661
pubmed: 32606046
Rheumatol Int. 2020 Sep;40(9):1353-1360
pubmed: 32654078
N Engl J Med. 2021 Feb 11;384(6):533-540
pubmed: 33369366
Nat Rev Immunol. 2020 Jun;20(6):339-341
pubmed: 32317716
Curr Opin Physiol. 2018 Dec;6:16-20
pubmed: 30320243
Ann Rheum Dis. 1995 Apr;54(4):256-62
pubmed: 7763101
Ann Rheum Dis. 2007 Apr;66(4):481-5
pubmed: 16984937