Human antibodies to tick-borne flaviviruses

  • Funded by Swiss National Science Foundation (SNSF)
  • Total publications:4 publications

Grant number: 196866

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Key facts

  • Disease

    Tick-Borne Encephalitis
  • Start & end year

    2021
    2024
  • Known Financial Commitments (USD)

    $647,986.96
  • Funder

    Swiss National Science Foundation (SNSF)
  • Principal Investigator

    Robbiani Davide
  • Research Location

    Switzerland
  • Lead Research Institution

    Università della Svizzera italiana - USI
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Tick-borne encephalitis virus (TBEV) is a flavivirus responsible for thousands of infections every year. TBEV can cause severe disease and death, and no specific treatments exist. Although a TBEV vaccine is available, immunity takes months to achieve and regular boosts to maintain. Moreover, it is not clear whether the TBEV vaccine protects against other tick-borne flaviviruses. There are also gaps in our understanding of TBEV pathogenesis, such as why only a fraction of TBEV infections progress to severe disease. The human antibody response to TBEV has been studied at the level of pools of antibodies circulating in blood. In contrast, the molecular make-up and properties of individual human antibodies that are induced by TBEV during natural infection or vaccination have not been examined. The overall objective of the study is the molecular characterization of the antibodies against TBEV that develop in individuals with exceptional serum neutralizing responses against the virus. In Aim 1, we will discover, characterize and compare the antibodies from the memory B cells of naturally infected and vaccinated individuals. In Aim 2, we will perform a deeper characterization of selected antibodies with stronger virus neutralizing capacity and broader neutralizing profile to investigate their mechanism of neutralization. Finally, since antibodies can play a dual role during flavivirus infection (protective versus disease enhancing), Aim 3 will examine antibody-mediated enhancement of TBEV infection by single monoclonal antibodies and by polyclonal sera from a large cohort of clinical samples.We hypothesize that information gained from the molecular characterization of human anti-TBEV antibodies will advance our understanding of disease pathogenesis. Moreover, we postulate that the discovery and characterization of monoclonal antibodies with potent and broad anti-viral activity against TBEV and related flaviviruses will enable the development of novel countermeasures to comprehensively tackle this group of pathogens, which represent an emerging threat to public health in Europe and elsewhere.

Publicationslinked via Europe PMC

Last Updated:32 minutes ago

View all publications at Europe PMC

Human antibodies in Mexico and Brazil neutralizing tick-borne flaviviruses.

A combination of two resistance mechanisms is critical for tick-borne encephalitis virus escape from a broadly neutralizing human antibody.

Human neutralizing antibodies to cold linear epitopes and subdomain 1 of the SARS-CoV-2 spike glycoprotein.

A dark side to NS1 antibodies?