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Identifying Potent and Broadly-neutralizing Henipaviral Antigens and Epitopes

Principal Investigator: Hector Aguilar-Carreno

Department of Microbiology and Immunology
Sponsor: NIH-National Institute of Allergy and Infectious Diseases (NIAID)
Grant Number: 1R21AI142377-01
Title: Identifying Potent and Broadly-neutralizing Henipaviral Antigens and Epitopes
Project Amount: $227,938
Project Period: December 2018 to November 2019

DESCRIPTION (provided by applicant): 

The henipaviruses are a growing new genus of viruses that include the emerging and highly lethal Nipah virus (NiV) and Hendra virus (HeV). NiV and HeV cause encephalitis and pneumonia, yielding mortality rates of 40- 100% in humans. NiV is a NIAID priority pathogen listed by the World Health Organization as likely to cause future pandemics and necessitating “urgent action”. Making matters worse, an additional ~20 new henipaviruses were recently discovered, raising the possibility that new henipaviruses will emerge in the human population. Unfortunately, we currently do not have approved human vaccines or therapeutic agents to protect individuals from natural outbreaks, laboratory accidents, or bioterrorism. An ideal solution would be to create potent and broadly-protective henipavirus vaccines. Although neutralizing antibodies are known to be vital for protection against henipaviral infections, a major obstacle hindering progress towards developing henipaviral vaccines is that we currently do not know what viral antigens or epitopes elicit potent and broadly-neutralizing antihenipaviral antibodies. To fill this gap, we designed experiments that will allow us to identify such antigens and epitopes. The obtained results will aid vaccine development, future immunological studies, and the basic field of henipavirus entry. We believe it is possible to elicit broadly-neutralizing antibodies for henipaviruses because: 1) they all share structurally and functionally conserved glycoproteins required for viral entry, and 2) published and our preliminary data indicate that cross-neutralization is achievable. Further, our preliminary data indicates that distinct combinations of henipaviral antigens elicit distinct neutralizing antibody potencies and breadth of neutralization. The main goal of this R21 proposal is to understand the combination(s) of henipaviral antigens and epitopes that elicits potent and broadly-neutralizing antibody responses against henipaviruses. We are in a unique position to accomplish this goal because our laboratory has already developed a novel set of tools needed to assess and map the neutralization capabilities of antisera and monoclonal antibodies (mAbs). We will use these tools to address the following specific aims. Aim 1. Identify the optimal henipaviral protein combinations that elicit high potency and broadly-neutralizing antibody responses in a rodent model of disease. Aim 2. Identify the specific epitopes responsible for eliciting highly-potent and broadly-neutralizing antibody responses and determine where in the viral entry pathway they work. The obtained results will identify highly potent and broadlyneutralizing antibodies and their specific epitopes to best protect against future emerging henipaviral outbreaks. The knowledge gained will be useful for: vaccine development, future immunological studies, and an understanding of the role of viral glycoprotein epitopes in viral entry. In turn, such understanding will aid the development of new therapeutic strategies.

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