Ebola virus-induced eye sequelae: a murine model for evaluating glycoprotein-targeting therapeutics

EBioMedicine. 2024 Jun:104:105170. doi: 10.1016/j.ebiom.2024.105170. Epub 2024 Jun 1.

Abstract

Background: Ebola virus disease (EVD) survivors experience ocular sequelae including retinal lesions, cataracts, and vision loss. While monoclonal antibodies targeting the Ebola virus glycoprotein (EBOV-GP) have shown promise in improving prognosis, their effectiveness in mitigating ocular sequelae remains uncertain.

Methods: We developed and characterized a BSL-2-compatible immunocompetent mouse model to evaluate therapeutics targeting EBOV-GP by inoculating neonatal mice with vesicular stomatitis virus expressing EBOV-GP (VSV-EBOV). To examine the impact of anti-EBOV-GP antibody treatment on acute retinitis and ocular sequelae, VSV-EBOV-infected mice were treated with polyclonal antibodies or monoclonal antibody preparations with antibody-dependent cellular cytotoxicity (ADCC-mAb) or neutralizing activity (NEUT-mAb).

Findings: Treatment with all anti-EBOV-GP antibodies tested dramatically reduced viremia and improved survival. Further, all treatments reduced the incidence of cataracts. However, NEUT-mAb alone or in combination with ADCC-mAb reduced viral load in the eyes, downregulated the ocular immune and inflammatory responses, and minimized retinal damage more effectively.

Interpretation: Anti-EBOV-GP antibodies can improve survival among EVD patients, but improved therapeutics are needed to reduce life altering sequelae. This animal model offers a new platform to examine the acute and long-term effect of the virus in the eye and the relative impact of therapeutic candidates targeting EBOV-GP. Results indicate that even antibodies that improve systemic viral clearance and survival can differ in their capacity to reduce acute ocular inflammation, and long-term retinal pathology and corneal degeneration.

Funding: This study was partly supported by Postgraduate Research Fellowship Awards from ORISE through an interagency agreement between the US DOE and the US FDA.

Keywords: Anti-EBOV-GP antibodies; BSL-2 model; EBOV glycoprotein (EBOV-GP); EBOV-GP pseudotyped vesicular stomatitis virus (VSV-EBOV); Ebola virus (EBOV); Ocular sequelae; Retinitis.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Neutralizing / immunology
  • Antibodies, Neutralizing / pharmacology
  • Antibodies, Neutralizing / therapeutic use
  • Antibodies, Viral* / immunology
  • Antibody-Dependent Cell Cytotoxicity
  • Disease Models, Animal*
  • Ebolavirus* / immunology
  • Ebolavirus* / pathogenicity
  • Glycoproteins / immunology
  • Glycoproteins / metabolism
  • Hemorrhagic Fever, Ebola* / drug therapy
  • Hemorrhagic Fever, Ebola* / immunology
  • Hemorrhagic Fever, Ebola* / virology
  • Humans
  • Mice
  • Viral Envelope Proteins / immunology
  • Viral Load

Substances

  • Antibodies, Viral
  • Antibodies, Monoclonal
  • Glycoproteins
  • Viral Envelope Proteins
  • Antibodies, Neutralizing