Evaluation of Immune Response and Disease Status in Systemic Lupus Erythematosus Patients Following SARS-CoV-2 Vaccination.
2019-nCoV Vaccine mRNA-1273
/ therapeutic use
Ad26COVS1
/ therapeutic use
Adult
Antibodies, Viral
/ immunology
Antirheumatic Agents
/ therapeutic use
B-Lymphocytes
/ immunology
BNT162 Vaccine
/ therapeutic use
COVID-19
/ prevention & control
COVID-19 Vaccines
/ immunology
Case-Control Studies
Cohort Studies
Enzyme-Linked Immunospot Assay
Female
Glucocorticoids
/ therapeutic use
Humans
Immunocompromised Host
Immunogenicity, Vaccine
Immunoglobulin G
/ immunology
Immunosuppressive Agents
/ therapeutic use
Interferon-gamma
/ immunology
Lupus Erythematosus, Systemic
/ drug therapy
Male
Middle Aged
Neutralization Tests
Prednisone
/ therapeutic use
SARS-CoV-2
Spike Glycoprotein, Coronavirus
/ immunology
Symptom Flare Up
Journal
Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795
Informations de publication
Date de publication:
02 2022
02 2022
Historique:
revised:
09
07
2021
received:
04
06
2021
accepted:
29
07
2021
pubmed:
5
8
2021
medline:
4
2
2022
entrez:
4
8
2021
Statut:
ppublish
Résumé
To evaluate seroreactivity and disease flares after COVID-19 vaccination in a multiethnic/multiracial cohort of patients with systemic lupus erythematosus (SLE). Ninety SLE patients and 20 healthy controls receiving a complete COVID-19 vaccine regimen were included. IgG seroreactivity to the SARS-CoV-2 spike receptor-binding domain (RBD) and SARS-CoV-2 microneutralization were used to evaluate B cell responses; interferon-γ (IFNγ) production was measured by enzyme-linked immunospot (ELISpot) assay in order to assess T cell responses. Disease activity was measured by the hybrid SLE Disease Activity Index (SLEDAI), and flares were identified according to the Safety of Estrogens in Lupus Erythematosus National Assessment-SLEDAI flare index. Overall, fully vaccinated SLE patients produced significantly lower IgG antibodies against SARS-CoV-2 spike RBD compared to fully vaccinated controls. Twenty-six SLE patients (28.8%) generated an IgG response below that of the lowest control (<100 units/ml). In logistic regression analyses, the use of any immunosuppressant or prednisone and a normal anti-double-stranded DNA antibody level prior to vaccination were associated with decreased vaccine responses. IgG seroreactivity to the SARS-CoV-2 spike RBD strongly correlated with the SARS-CoV-2 microneutralization titers and correlated with antigen-specific IFNγ production determined by ELISpot. In a subset of patients with poor antibody responses, IFNγ production was similarly diminished. Pre- and postvaccination SLEDAI scores were similar in both groups. Postvaccination flares occurred in 11.4% of patients; 1.3% of these were severe. In a multiethnic/multiracial study of SLE patients, 29% had a low response to the COVID-19 vaccine which was associated with receiving immunosuppressive therapy. Reassuringly, severe disease flares were rare. While minimal protective levels remain unknown, these data suggest that protocol development is needed to assess the efficacy of booster vaccination.
Identifiants
pubmed: 34347939
doi: 10.1002/art.41937
pmc: PMC8426963
doi:
Substances chimiques
Ad26COVS1
JT2NS6183B
Antibodies, Viral
0
Antirheumatic Agents
0
COVID-19 Vaccines
0
Glucocorticoids
0
Immunoglobulin G
0
Immunosuppressive Agents
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Interferon-gamma
82115-62-6
2019-nCoV Vaccine mRNA-1273
EPK39PL4R4
BNT162 Vaccine
N38TVC63NU
Prednisone
VB0R961HZT
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
284-294Subventions
Organisme : NIAID NIH HHS
ID : K23 AI163359
Pays : United States
Organisme : NIAMS NIH HHS
ID : AR07059
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI074492
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI148574
Pays : United States
Informations de copyright
© 2021, American College of Rheumatology.
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