Immunogenicity of mRNA-1273 and BNT162b2 in Immunocompromised Patients: Systematic Review and Meta-analysis Using GRADE

Infect Dis Ther. 2024 Jul;13(7):1419-1438. doi: 10.1007/s40121-024-00987-2. Epub 2024 May 27.

Abstract

Introduction: Immunocompromised (IC) patients mount poor immune responses to vaccination. Higher-dose coronavirus disease 2019 (COVID-19) vaccines may offer increased immunogenicity.

Methods: A pairwise meta-analysis of 98 studies reporting comparisons of mRNA-1273 (50 or 100 mcg/dose) and BNT162b2 (30 mcg/dose) in IC adults was performed. Outcomes were seroconversion, total and neutralizing antibody titers, and cellular immune responses.

Results: mRNA-1273 was associated with a significantly higher seroconversion likelihood [relative risk, 1.11 (95% CI, 1.08, 1.14); P < 0.0001; I2 = 66.8%] and higher total antibody titers [relative increase, 50.45% (95% CI, 34.63%, 66.28%); P < 0.0001; I2 = 89.5%] versus BNT162b2. mRNA-1273 elicited higher but statistically nonsignificant relative increases in neutralizing antibody titers and cellular immune responses versus BNT162b2.

Conclusion: Higher-dose mRNA-1273 had increased immunogenicity versus BNT162b2 in IC patients.

Keywords: BNT162b2; COVID-19; Cellular immunity; Immunocompromised; Neutralizing antibody; Seroconversion; Severe acute respiratory syndrome coronavirus–2; Total antibody; mRNA vaccine; mRNA-1273.

Publication types

  • Review