A recombinant Hendra virus G glycoprotein subunit vaccine protects nonhuman primates against Hendra virus challenge.

Chad E Mire, Joan B Geisbert, Krystle N Agans, Yan-Ru Feng, Karla A Fenton, Katharine N Bossart, Lianying Yan, Yee-Peng Chan, Christopher C Broder, Thomas W Geisbert
Author Information
  1. Chad E Mire: Galveston National Laboratory, University of Texas Medical Branch, Galveston, Texas, USA.

Abstract

Hendra virus (HeV) is a zoonotic emerging virus belonging to the family Paramyxoviridae. HeV causes severe and often fatal respiratory and/or neurologic disease in both animals and humans. Currently, there are no licensed vaccines or antiviral drugs approved for human use. A number of animal models have been developed for studying HeV infection, with the African green monkey (AGM) appearing to most faithfully reproduce the human disease. Here, we assessed the utility of a newly developed recombinant subunit vaccine based on the HeV attachment (G) glycoprotein in the AGM model. Four AGMs were vaccinated with two doses of the HeV vaccine (sGHeV) containing Alhydrogel, four AGMs received the sGHeV with Alhydrogel and CpG, and four control animals did not receive the sGHeV vaccine. Animals were challenged with a high dose of infectious HeV 21 days after the boost vaccination. None of the eight specifically vaccinated animals showed any evidence of clinical illness and survived the challenge. All four controls became severely ill with symptoms consistent with HeV infection, and three of the four animals succumbed 8 days after exposure. Success of the recombinant subunit vaccine in AGMs provides pivotal data in supporting its further preclinical development for potential human use.
IMPORTANCE: A Hendra virus attachment (G) glycoprotein subunit vaccine was tested in nonhuman primates to assess its ability to protect them from a lethal infection with Hendra virus. It was found that all vaccinated African green monkeys were completely protected against subsequent Hendra virus infection and disease. The success of this new subunit vaccine in nonhuman primates provides critical data in support of its further development for future human use.

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Grants

  1. AI054715/NIAID NIH HHS
  2. UC7 AI094660/NIAID NIH HHS
  3. R01 AI054715/NIAID NIH HHS
  4. AI082121/NIAID NIH HHS
  5. U01 AI082121/NIAID NIH HHS
  6. /Intramural NIH HHS
  7. UC7 AI070083/NIAID NIH HHS
  8. AI077995/NIAID NIH HHS
  9. U01 AI077995/NIAID NIH HHS

MeSH Term

Adjuvants, Immunologic
Aluminum Hydroxide
Animals
Chlorocebus aethiops
Disease Models, Animal
Hendra Virus
Henipavirus Infections
Oligodeoxyribonucleotides
Survival Analysis
Vaccination
Vaccines, Subunit
Vaccines, Synthetic
Viral Envelope Proteins
Viral Vaccines

Chemicals

Adjuvants, Immunologic
CPG-oligonucleotide
Oligodeoxyribonucleotides
Vaccines, Subunit
Vaccines, Synthetic
Viral Envelope Proteins
Viral Vaccines
attachment protein G
Aluminum Hydroxide

Word Cloud

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