Protection from infection with influenza A H7N9 virus in a mouse model by equine neutralizing F(ab')2

Int Immunopharmacol. 2014 Nov;23(1):134-8. doi: 10.1016/j.intimp.2014.08.019. Epub 2014 Sep 2.

Abstract

Influenza A H7N9 virus has demonstrated considerable pandemic potential in China ever since early spring 2013. Until now, there have been no specific medicines to treat influenza A H7N9 virus infected patients. Development of a safe and effective H7N9 therapeutic preparation is urgently needed. To this end, we prepared and evaluated the pepsin-digested F(ab')2 fragments of serum IgGs from the horses inoculated with a inactivated influenza A H7N9 whole virus antigens. The protective effects of the F(ab')2 fragments against H7N9 virus infection were determined in cultured MDCK cells by cytopathic effect (CPE) and evaluated in a BALB/c mouse model by observing death, weight loss and viral load. The in vitro results showed that the F(ab')2 fragments had an HI titer of 1:2048 and a neutralization titer of 1: 31,623. The in vivo assays suggested that 600 U of the preparations could efficiently protect BALB/c mice from a lethal dose of A/Anhui/01/2013 (H7N9) infection even when administered two days post infection. Thus, this highly purified preparation should be a potential candidate for treating severe patients suffering from influenza A H7N9.

Keywords: Equine immunoglobulin F(ab′)(2) fragments;; H7N9; Mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Neutralizing / administration & dosage*
  • Disease Models, Animal
  • Dogs
  • Horses
  • Humans
  • Immunoglobulin Fab Fragments / administration & dosage*
  • Immunotherapy / methods*
  • Influenza A Virus, H7N9 Subtype / immunology*
  • Influenza, Human / immunology
  • Influenza, Human / therapy*
  • Madin Darby Canine Kidney Cells
  • Mice
  • Mice, Inbred BALB C
  • Orthomyxoviridae Infections / immunology
  • Orthomyxoviridae Infections / therapy*
  • Viral Load / drug effects

Substances

  • Antibodies, Neutralizing
  • Immunoglobulin Fab Fragments