Prophylactic and Therapeutic Efficacy of Avian Antibodies Against Influenza Virus H5N1 and H1N1 in Mice

H5N1亚型流感病毒 病毒学 病毒 大流行 免疫 接种疫苗 甲型流感病毒 生物 抗体 微生物学 医学 免疫学 传染病(医学专业) 疾病 2019年冠状病毒病(COVID-19) 病理
作者
Huan Huu Nguyen,Terrence M. Tumpey,Hae-Jung Park,Young-Ho Byun,Linh Tran,Nguyễn Văn Dũng,Paul E. Kilgore,Cécil Czerkinsky,Jacqueline M. Katz,Baik Lin Seong,Jae Min Song,Young Bong Kim,Hoa Do,Tung Nguyen,Cam V. Nguyen
出处
期刊:PLOS ONE [Public Library of Science]
卷期号:5 (4): e10152-e10152 被引量:84
标识
DOI:10.1371/journal.pone.0010152
摘要

Pandemic influenza poses a serious threat to global health and the world economy. While vaccines are currently under development, passive immunization could offer an alternative strategy to prevent and treat influenza virus infection. Attempts to develop monoclonal antibodies (mAbs) have been made. However, passive immunization based on mAbs may require a cocktail of mAbs with broader specificity in order to provide full protection since mAbs are generally specific for single epitopes. Chicken immunoglobulins (IgY) found in egg yolk have been used mainly for treatment of infectious diseases of the gastrointestinal tract. Because the recent epidemic of highly pathogenic avian influenza virus (HPAIV) strain H5N1 has resulted in serious economic losses to the poultry industry, many countries including Vietnam have introduced mass vaccination of poultry with H5N1 virus vaccines. We reasoned that IgY from consumable eggs available in supermarkets in Vietnam could provide protection against infections with HPAIV H5N1.We found that H5N1-specific IgY that are prepared from eggs available in supermarkets in Vietnam by a rapid and simple water dilution method cross-protect against infections with HPAIV H5N1 and related H5N2 strains in mice. When administered intranasally before or after lethal infection, the IgY prevent the infection or significantly reduce viral replication resulting in complete recovery from the disease, respectively. We further generated H1N1 virus-specific IgY by immunization of hens with inactivated H1N1 A/PR/8/34 as a model virus for the current pandemic H1N1/09 and found that such H1N1-specific IgY protect mice from lethal influenza virus infection.The findings suggest that readily available H5N1-specific IgY offer an enormous source of valuable biological material to combat a potential H5N1 pandemic. In addition, our study provides a proof-of-concept for the approach using virus-specific IgY as affordable, safe, and effective alternative for the control of influenza outbreaks, including the current H1N1 pandemic.
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