Thermostable;
Peste des petits ruminants;
PPR;
Rinderpest;
Lyophilization;
Eradication;
ADAPTED RINDERPEST VACCINE;
CHEMICAL STABILIZERS;
CULTURE VACCINE;
VIRUS;
GOATS;
D O I:
10.1016/j.vaccine.2017.05.040
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The research objective was to develop a thermostable vaccine against peste des petits ruminants (PPR), a morbilliviral disease of small ruminants targeted for eradication that is a major constraint on the livelihoods of the rural poor throughout much of Africa and Asia. Although existing PPR vaccines provide lifelong immunity, they require continuous refrigeration. This limits their utility in developing countries. Methods for the lyophilization of a related morbillivirus, rinderpest (RP), resulted in vaccine that could be used in the field for up to 30 days without refrigeration which was a major contribution to the global eradication of RP completed in 2011. The present research applied the rinderpest lyophilization method to the attenuated Nigeria 75/1 PPR vaccine strain, and measured thermostability in accelerated stability tests (AST) at 37 degrees C. The shelf-life of the vaccine was determined as the time a vial retained the minimum dose required as a 25-dose presentation at the specified temperature. A lactalbumin hydrolysate and sucrose (LS) stabilizer was compared to stabilizers based on trehalose. PPR vaccine produced using the Xerovac drying method was compared to vaccine produced using the rinderpest lyophilization method in AST. LS vaccine was evaluated in AST at 37, 45 and 56 degrees C and an Arrhenius plot was constructed for estimation of stability at temperatures not tested. Vaccines produced using LS and the rinderpest method of lyophilization were the most stable. The shelf-life of the Xerovac preparation was 22.2 days at 37 degrees C. The three LS vaccine batches had shelf-lives at 37 degrees C of 177.6, 105.0 and 148.9 days, respectively, at 37 degrees C. At 56 degrees C, the shelf-life was 13.7 days. The projected half-life at 25 degrees C was 1.3 years. This is sufficient thermostability for use without a cold chain for up to 30 days which will greatly facilitate the delivery of vaccination in the global eradication of PPR. (C) 2017 The Authors. Published by Elsevier Ltd.
机构:
Division of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
National Institute of Veterinary Epidemiology and Disease Informatics (NIVEDI) (formerly Project Directorate on Animal Disease Monitoring and Surveillance-PD_ADMAS), Hebbal, Bangalore, 560 024, KarnatakaDivision of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Balamurugan V.
Sen A.
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Division of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Animal Health Division, ICAR-NEH Region, Umiam, 793 103, MeghalayaDivision of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Sen A.
Venkatesan G.
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Division of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, UttarakhandDivision of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Venkatesan G.
Bhanuprakash V.
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Division of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Indian Veterinary Research Institute, Bangalore Campus, Bangalore, 560 024, KarnatakaDivision of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Bhanuprakash V.
Singh R.K.
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Division of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
Indian Veterinary Research Institute, Izatnagar, 243 122, Uttar PradeshDivision of Virology, Indian Veterinary Research Institute, Mukteswar Campus 263 138, Nainital District, Uttarakhand
机构:
Indian Vet Res Inst, FMD QC&QA Unit, Bangalore 560024, Karnataka, India
Indian Vet Res Inst, Div Virol, Natl Morbillivirus Referral Lab, Naini Tal 263138, Uttaranchal, IndiaIndian Vet Res Inst, FMD QC&QA Unit, Bangalore 560024, Karnataka, India
Saravanan, P.
Sen, A.
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Indian Vet Res Inst, Div Virol, Natl Morbillivirus Referral Lab, Naini Tal 263138, Uttaranchal, IndiaIndian Vet Res Inst, FMD QC&QA Unit, Bangalore 560024, Karnataka, India
Sen, A.
Balamurugan, V.
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Indian Vet Res Inst, Div Virol, Natl Morbillivirus Referral Lab, Naini Tal 263138, Uttaranchal, IndiaIndian Vet Res Inst, FMD QC&QA Unit, Bangalore 560024, Karnataka, India
Balamurugan, V.
Bandyopadhyay, S. K.
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Government India, Minist Agr, Anim Husbandry Commiss, New Delhi 110001, IndiaIndian Vet Res Inst, FMD QC&QA Unit, Bangalore 560024, Karnataka, India
Bandyopadhyay, S. K.
Singh, R. K.
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Indian Vet Res Inst, Div Virol, Natl Morbillivirus Referral Lab, Naini Tal 263138, Uttaranchal, IndiaIndian Vet Res Inst, FMD QC&QA Unit, Bangalore 560024, Karnataka, India