Comparing Intradermal (ID) Rabies Vaccination with Conventional IM Regimen on Humoral Response of New Zealand White Rabbits for the Production of Animal-Derived Polyclonal Antibodies

Author:

Najam Amina1ORCID,Abid Rameesha23ORCID,Ali Hussain1ORCID,Hafeez Hamza4ORCID,Arif Amna5ORCID,Ahmed Safia2ORCID,Di Cerbo Alessandro6ORCID,Ghazanfar Shakira3ORCID

Affiliation:

1. Biological Production Division, National Institute of Health, Islamabad 45500, Pakistan

2. Department of Microbiology, Quaid-I-Azam University, Islamabad 44100, Pakistan

3. National Institute for Genomics and Advanced Biotechnology (NIGAB), National Agricultural Research Centre, Park Road, Islamabad 45500, Pakistan

4. Department of Biological Sciences, University of Sialkot, Sialkot 51310, Pakistan

5. Department of Applied Microbiology, University of Veterinary and Animal Sciences, Lahore 05499, Pakistan

6. School of Biosciences and Veterinary Medicine, University of Camerino, Matelica 62024, Italy

Abstract

In developing countries, it is imperative to implement cost-effective strategies for animal humoral response development in the production of antiserum. This study compared the effect of immunization regimens on the humoral immune response of New Zealand White (NZW) rabbits (N = 24) using cell culture rabies vaccine (CCRV) through intradermal (ID) and traditional intramuscular (IM) routes. The rabbits were divided into three experimental groups: (a) IPC-R2 with a two-site one-week regimen; (b) TRC-R3 with a two-site twenty-eight-day regimen; and (c) Alternate-R4 with a four-site one-week regimen. These regimens were then compared to the standard IM schedule of five doses of rabies vaccine administered at days 0, 3, 7, 14, and 28 in control group R-1. The results were evaluated at days 14 and 35 postvaccination using rabies-specific Platelia II™ ELISA kit method. The results showed a better response to the ID regimen than the IM route regarding immunogenicity and volume consumption of the vaccine. The three selected ID regimes showed significantly higher mean titer values than the control IM regimen group R-1 (p<0.001). The study aims to explore simple immunization strategies to enhance the RV-specific antibody titers for immunization donor animals. This method would produce polyclonal antibodies and strengthen local production of polyclonal antibodies in Pakistan to deal with vaccine and rabies immunoglobulin (RIG) shortage, thus providing effective postexposure prophylaxis (PEP) for better control of rabies in developing countries.

Publisher

Hindawi Limited

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