Reactogenicity and immunogenicity after a late second dose or a third dose of ChAdOx1 nCoV-19 in the UK: A substudy of two randomised controlled trials (COV001 and COV002)
The Lancet Sep 06, 2021
Flaxman A, Marchevsky NG, Jenkin D, et al. - Increased antibody titres are recorded in correlation with an extended interval before the second dose of ChAdOx1 nCoV-19. A third dose of ChAdOx1 nCoV-19 after the second dose resulted in induction of antibodies to a level that links with high efficacy along with a boost in T-cell responses.
In this sub study, invitation for vaccination was given to volunteers who were enrolled in the phase 1/2 (COV001) controlled trial and received either a single dose or two doses of 5 × 1010 viral particles.
For comparison purposes, researchers used data from volunteers enrolled in either the phase 1/2 (COV001) or phase 2/3 (COV002), single-blinded, randomized controlled trials of ChAdOx1 nCoV-19 and had previously received a single dose or two doses of 5 × 1010 viral particles.
Those with a longer interval between first and second dose had higher antibody titers at 28 days after vaccination relative to those with a short interval.
Antibody titers were significantly higher 28 days after a third dose than 28 days after a second dose.
A third dose also resulted in a boost of T-cell responses.
Relative to reactogenicity after a first dose, a lower reactogenicity was recorded after a late second dose or a third dose.
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