Abstract

The human population is constantly exposed to multiple influenza A subtypes due to zoonotic spillover and rapid viral evolution driven by intrinsic error-prone replication and immunological pressure. In this context, antibody responses directed against the HA protein are of importance since they have been shown to correlate with protective immunity. Serological techniques, detecting these responses, play a critical role for influenza surveillance, vaccine development, and assessment. As the recent human pandemics and avian influenza outbreaks have demonstrated, there is an urgent need to be better prepared to assess the contribution of the antibody response to protection against newly emerged viruses and to evaluate the extent of preexisting heterosubtypic immunity in populations. In this study, 68 serum samples collected from the Italian population between 1992 and 2007 were found to be positive for antibodies against H5N1 as determined by single radial hemolysis (SRH), but most were negative when evaluated using haemagglutination inhibition (HI) and microneutralisation (MN) assays. As a result of these discordant serological findings, the increased sensitivity of lentiviral pseudotypes was exploited in pseudotype-based neutralisation (pp-NT) assays and the results obtained provide further insight into the complex nature of humoral immunity against influenza A viruses.

Highlights

  • The constant rapid evolution of HPAI H5 and H7 viruses driven by intrinsic error-prone replication and increased by immune pressure significantly influences the sensitivity of available serological assays

  • A subset from the panel of 68 serum samples was tested using influenza pseudotypes bearing the HAs from H3N2 A/Udorn/ 307/1972 and H1N1 A/South Carolina/1/1918

  • The individual components employed for the construction of the pseudotypes used for this assay have been chosen from a set of interchangeable plasmids many of which we have used for serological assay development previously [32, 33]

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Summary

Introduction

The constant rapid evolution of HPAI H5 and H7 viruses driven by intrinsic error-prone replication and increased by immune pressure significantly influences the sensitivity of available serological assays. The human population is constantly exposed, during a lifetime (by natural infection and/or vaccination) to different influenza A subtypes with an associated increase in the memory B cell repertoire. This antibody repertoire may be cross-reactive to closely related variant viruses making it more difficult to develop sensitive and specific serological assays [2,3,4]. It has been shown that exposure to one subtype of influenza A can induce immunity that is cross-protective against other influenza subtypes Such adaptive immune response, called “heterosubtypic” immunity, elicits an antibody response to epitopes that are highly conserved amongst strains [5,6,7].

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