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Immunogenicity and safety of an intradermal ChAdOx1 nCoV-19 boost in a healthy population.

Nawamin PinpathomratPorntip IntapiboonPurilap SeepathomnarongJomkwan OngarjRatchanon SophonmaneeJariya HengprakopSmonrapat SurasombatpattanaSupattra UppanisakornSurakameth MahasirimongkolWaritta SawaengdeeSupaporn PhumiamornSompong SapsutthipasChanon KongkamolThammasin IngviyaPasuree SangsupawanichSarunyou Chusri
Published in: NPJ vaccines (2022)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a global pandemic. Two doses of an inactivated SARS-CoV-2 vaccine (CoronaVac) have been shown to be insufficient to protect against variants of concern (VOCs), while viral vector vaccines remain protective against the infection. Herein, we conducted a preliminary study to evaluate the safety and immunity in an adult population who received the conventional 2 dosage-regimen of inactivated SARS-CoV-2 vaccine; with an additional intradermal ChAdOx1 nCoV-19 reciprocal dosage (1:5). An Intramuscular ChAdOx1 nCoV-19 booster was also included as a control. Immediate and delayed local reactions were frequently observed in the fractional intradermal boost, but systemic side effects were significantly decreased compared to the conventional intramuscular boost. The anti-RBD-IgG levels, the neutralising function against delta variants, and T cell responses were significantly increased after boosting via both routes. Interestingly, the shorter interval elicited higher immunogenicity compared to the extended interval. Taken together, a reciprocal dosage of intradermal ChAdOx1 nCoV-19 booster reduces systemic adverse reactions and enhances non inferiority humoral and cellular immune responses compared to a full dose of intramuscular boosting. These findings provide for an effective vaccine management during the shortages of vaccine supply.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • immune response
  • coronavirus disease
  • copy number
  • toll like receptor
  • emergency department
  • dendritic cells
  • inflammatory response