Serologic Response of 2 Versus 3 Doses and Intradermal Versus Intramuscular Administration of a Licensed Rabies Vaccine for Preexposure Prophylaxis

Author:

Endy Timothy P1,Keiser Paul B2,Wang Dongliang3,Jarman Richard G2,Cibula Don3,Fang Hengsheng1,Ware Lisa4,Abbott Mark4,Thomas Stephen J4,Polhemus Mark E4

Affiliation:

1. Departments of Microbiology and Immunology, State University of New York Upstate Medical University, Syracuse, New York, USA

2. Walter Reed Army Institute of Research, Silver Spring, Maryland, USA

3. Department of Public Health, State University of New York Upstate Medical University, Syracuse, New York, USA

4. Institute for Global Heath and Translational Sciences, State University of New York Upstate Medical University, Syracuse, New York, USA

Abstract

Abstract Background The World Health Organization recommends intradermal (ID) administration of rabies vaccine for preexposure prophylaxis. Methods In a randomized trial in adults assigned to 1 of 6 treatment groups (ID vs intramuscular [IM], 2 vs 3 doses, and controls), rabies neutralizing antibody titers were measured to 1 year postvaccination. Results ID vaccination produced acceptable antibody levels in all subjects (2- and 3-dose groups). At day 365, acceptable levels were 40% for IM and 50% for ID 2-dose schedule, and 70% for IM and 60% for ID 3-dose schedule. Conclusions ID rabies vaccination induces acceptable antibody titers at a fraction of the dose. Clinical Trials Registration NCT02374814.

Funder

US Department of Defense

Defense Health Agency

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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