SARS-CoV-2 Antibody Response by mRNA Vaccine Platform in Incrementally Immunosuppressed Patients
American Journal of Transplantation
; 22(Supplement 3):766, 2022.
Article
in English
| EMBASE | ID: covidwho-2063482
ABSTRACT
Purpose:
This study compares SARS-CoV-2 antibody responses between the twodose mRNA-1273 and BNT162b2 vaccine series across groups of incrementally immunosuppressed patients. Method(s) Semiquantitative testing for antibodies against the receptor binding domain (RBD) of the SARS-CoV-2 spike protein was performed using the Roche Elecsys anti-SARS-CoV-2 S enzyme immunoassay (EIA), 15-45 days after the second vaccine dose for SARS-CoV-2 naive patients with rheumatic and musculoskeletal disease (RMD), and solid organ transplant recipients (SOTRs) from an observational cohort. Anti-RBD titers were divided into categories of >=50, >=100 and >=250 U/mL based on levels associated with plasma neutralizing capacity in COVID-19 convalescent patients. Participants were stratified by increasing intensity of immunosuppression RMD not on immunosuppression, RMD on immunosuppression, SOTR not on mycophenolate (MMF), and SOTR on MMF. Response rates between mRNA-1273 and BNT162b2 recipients were compared using modified Poisson regression weighted for age, time since vaccination, and number of immunosuppressive medications. This analysis was repeated for several thresholds of positive response 50, 100, and 250 U/mL. Result(s) Of 1868 participants, 55.8% of RMD and 52.7% of SOTRs received BNT162b2;the remainder received mRNA-1273. Demographics, diagnoses, and immunosuppressive regimens were similar across vaccine groups. Among RMD participants not on immunosuppression, the chance of anti-RBD >=250U/ml was comparable among BNT162b2 and mRNA-1273 recipients (IRR= 0.91 1.03 1.16 p= 0.67). mRNA-1273 recipients had a higher chance than BNT162b2 recipients to achieve anti-RBD >=250U/ml among RMD participants on immunosuppression (IRR = 1.15 1.241.34, p<0.001);SOTRs not on MMF (IRR = 1.24 1.561.96, p <0.001);and SOTRs on MMF (IRR=1.28 2.625.37, p= 0.01). Similar trends were observed with titer cutoffs of >=100 and >=50 U/mL (Table 1). Conclusion(s) The two-dose mRNA-1273 vaccine series was more likely to induce stronger humoral immunogenicity compared to BNT162b2 in immunosuppressed patients;this effect was more pronounced with greater immunosuppression. These findings suggest importance in the choice of mRNA vaccine platform in optimizing immune responses to SARS-CoV-2 vaccination and can help inform vaccination strategies for booster doses in high-risk, immunosuppressed populations.
adult; antibody response; cohort analysis; conference abstract; controlled study; convalescence; coronavirus disease 2019; demographics; drug therapy; enzyme immunoassay; female; graft recipient; human; human tissue; immune response; immunoassay analyzer; immunogenicity; immunosuppressive treatment; major clinical study; male; musculoskeletal disease; nonhuman; Poisson regression; protein domain; quantitative analysis; receptor binding; rheumatic disease; Severe acute respiratory syndrome coronavirus 2; vaccination; elasomeran; endogenous compound; mycophenolic acid; RNA vaccine; SARS-CoV-2 antibody; tozinameran; virus spike protein
Full text:
Available
Collection:
Databases of international organizations
Database:
EMBASE
Topics:
Vaccines
Language:
English
Journal:
American Journal of Transplantation
Year:
2022
Document Type:
Article
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