David C. Brice , Konstantin Andreev , Lance Miller , Christopher Patton , Patrick Seiler , Tehui Garcia , Morgan L. LeBlanc , Taylor Hibler , Eda Ozdemir , Alexandra H. Mandarano , Faten Okda , Alejandro García , Richard J. Webby , Ahmed Kandeil
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引用次数: 0
Abstract
The high-pathogenicity avian influenza A (H5N1) viruses of clade 2.3.4.4 b have been detected in domestic poultry and wild birds in Mexico. Vaccination with H5 vaccines has been implemented as a complementary influenza control strategy in poultry in many countries, including Mexico. Continuous reevaluation of the efficacy of licensed vaccines against emerging viruses is required to ensure adequate control of virus transmission and infection. Some commercial poultry H5 vaccines used in Mexico are produced from vaccine seed viruses that are genetically distinct from clade 2.3.4.4 b viruses. Here, we studied the efficacy of four commercial H5 poultry vaccines widely used in the Mexican market and an experimental inactivated, adjuvanted vaccine against a recent North American high-pathogenicity avian influenza A (H5N1) 2.3.4.4 b virus. Chickens in all vaccinated groups developed antibodies to the viral nucleoprotein as detected by enzyme-linked immunosorbent assay. Although some of the commercial vaccines did not elicit detectable hemagglutination inhibition or microneutralization titers, all vaccines provided 80 %–100 % protection from mortality. Immunophenotyping of the peripheral blood mononuclear cells of vaccinated chickens showed that these vaccines did not elicit peripheral T-cell or other non-B cell responses that could explain the observed protection. Accordingly, we recommend continued evaluation of vaccine efficacy against evolving viruses and further efforts to identify non-neutralizing antibody correlates of protection.
期刊介绍:
Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.