Cross-Reactivity Conferred by Homologous and Heterologous Prime-Boost A/H5 Influenza Vaccination Strategies in Humans: A Literature Review

• Published in: Vaccines (Basel) Vol. 9; no. 12; p. 1465
• Main Authors: Kok, Adinda, Fouchier, Ron A. M., Richard, Mathilde
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 10.12.2021; MDPI
• Subjects: Antibodies; Antigens; Aquatic birds; Avian flu; avian influenza A virus; Coronaviruses; COVID-19; Cross-reactivity; Datasets; Genetic diversity; Glycoproteins; H5 influenza virus; Hemagglutinins; Heterogeneity; Homology; Immune response (humoral); Immunogenicity; Immunology; Infections; Influenza; Literature reviews; pandemic; Pandemics; Review; Vaccination; Vaccines; Viruses; Zoonoses; zoonosis; avian influenza A virus; H5 influenza virus; pandemic; zoonosis; vaccination
• ISSN: 2076-393X; 2076-393X
• DOI: 10.3390/vaccines9121465

Avian influenza viruses from the A/H5 A/goose/Guangdong/1/1996 (GsGd) lineage pose a continuing threat to animal and human health. Since their emergence in 1997, these viruses have spread across multiple continents and have become enzootic in poultry. Additionally, over 800 cases of human infection with A/H5 GsGd viruses have been reported to date, which raises concerns about the potential for a new influenza virus pandemic. The continuous circulation of A/H5 GsGd viruses for over 20 years has resulted in the genetic and antigenic diversification of their hemagglutinin (HA) surface glycoprotein, which poses a serious challenge to pandemic preparedness and vaccine design. In the present article, clinical studies on A/H5 influenza vaccination strategies were reviewed to evaluate the breadth of antibody responses induced upon homologous and heterologous prime-boost vaccination strategies. Clinical data on immunological endpoints were extracted from studies and compiled into a dataset, which was used for the visualization and analysis of the height and breadth of humoral immune responses. Several aspects leading to high immunogenicity and/or cross-reactivity were identified, although the analysis was limited by the heterogeneity in study design and vaccine type used in the included studies. Consequently, crucial questions remain to be addressed in future studies on A/H5 GsGd vaccination strategies.