(HealthDay News) — For adults who completed a primary COVID-19 vaccine regimen at least 12 weeks earlier, homologous and heterologous booster vaccines are immunogenic, according to a study published online Jan. 26 in the New England Journal of Medicine.
Robert L. Atmar, M.D., from the Baylor College of Medicine in Houston, and colleagues conducted a phase 1-2, open-label clinical trial at 10 U.S. sites involving 458 adults who had completed a COVID-19 vaccine regimen at least 12 weeks earlier, had no reported history of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, and received a booster dose with mRNA-1273, Ad26.COV2.S, or BNT162b2 (154, 150, and 153 participants, respectively; one participant did not receive the assigned vaccine).
The researchers found that reactogenicity was similar to that of the primary series. Injection-site pain, malaise, headache, or myalgia were reported by more than half the recipients.
Antibody neutralizing titers against a SARS-CoV-2 D614G pseudovirus increased by a factor of 4 to 73 for all combinations; binding titers increased by a factor of 5 to 55. Neutralizing antibody titers increased by a factor of 4 to 20 with homologous boosters and by a factor of 6 to 73 with heterologous boosters.
In all but the homologous Ad26.COV2.S-boosted subgroup, spike-specific T-cell responses increased. In the Ad26.COV2.S-primed recipients, CD8+ T-cell levels were more durable; spike-specific CD8+ T cells were increased substantially with heterologous boosting with the Ad26.COV2.S vaccine in mRNA vaccine-primed individuals.
“These data suggest that an immune response will be generated for each of these vaccines used as a booster regardless of the primary COVID-19 vaccination regimen,” the authors write.
Several authors disclosed financial ties to the pharmaceutical industry, including Pfizer, Moderna, and Johnson & Johnson.