Intradermal Fractional ChAdOx1 nCoV-19 Booster Vaccine Induces Memory T Cells: A Follow-Up Study

Author:

Sophonmanee Ratchanon1,Preampruchcha Perawas1,Ongarj Jomkwan1,Seeyankem Bunya1,Intapiboon Porntip2ORCID,Surasombatpattana Smonrapat3,Uppanisakorn Supattra4,Sangsupawanich Pasuree4,Chusri Sarunyou2ORCID,Pinpathomrat Nawamin1ORCID

Affiliation:

1. Department of Biomedical Sciences and Biomedical Engineering, Faculty of Medicine, Prince of Songkla University, Songkhla 90110, Thailand

2. Department of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Songkhla 90110, Thailand

3. Department of Pathology, Faculty of Medicine, Prince of Songkla University, Songkhla 90110, Thailand

4. Clinical Research Center, Faculty of Medicine, Prince of Songkla University, Songkhla 90110, Thailand

Abstract

The administration of viral vector and mRNA vaccine booster effectively induces humoral and cellular immune responses. Effector T cell responses after fractional intradermal (ID) vaccination are comparable to those after intramuscular (IM) boosters. Here, we quantified T cell responses after booster vaccination. ChAdOx1 nCoV-19 vaccination induced higher numbers of S1-specific CD8+ memory T cells, consistent with the antibody responses. Effector memory T cell phenotypes elicited by mRNA vaccination showed a similar trend to those elicited by the viral vector vaccine booster. Three months post-vaccination, cytokine responses remained detectable, confirming effector T cell responses induced by both vaccines. The ID fractional dose of ChAdOx1 nCoV-19 elicited higher effector CD8+ T cell responses than IM vaccination. This study confirmed that an ID dose-reduction vaccination strategy effectively stimulates effector memory T cell responses. ID injection could be an improved approach for effective vaccination programs.

Funder

National Vaccine Institute

National Research Council of Thailand

Faculty of Medicine, and Prince of Songkhla University

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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