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Background: The inflammatory macrophage response contributes to severe Ebola virus disease, with liver and lung injury in humans.

Objective: We sought to further define the activation status of hepatic and pulmonary macrophage populations in Ebola virus disease.

Methods: We compared liver and lung tissue from terminal Ebola virus (EBOV)-infected and uninfected control cynomolgus macaques challenged via the conjunctival route.

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Liquid formulations have been successfully used in many viral vector vaccines including influenza (Flu), hepatitis B, polio (IPV), Ebola, and COVID-19 vaccines. The main advantage of liquid formulations over lyophilized formulations is that they are cost-effective, as well as easier to manufacture and distribute. However, studies have shown that the liquid formulations of enveloped viral vector vaccines are not stable over extended periods of time.

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Sandwich enzyme-linked immunosorbent assays (ELISAs), which quantify antigens captured between two layers of antibodies, are sensitive and fundamental tools used to diagnose diseases, evaluate the effects of countermeasures, and quantify target proteins. Many filoviruses use transcriptional editing to express three different glycoproteins (GPs) from the GP gene. The main product transcribed from the GP gene, the soluble glycoprotein (sGP), is detected at high levels in the blood during the acute phase of infection and correlates with viremia, making it an attractive target for molecular diagnostics.

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Article Synopsis
  • Filoviruses, like Ebola virus (EBOV), cause filovirus disease (FVD) and pose significant global health threats, but studying them has been challenging due to safety restrictions.
  • A new research tool involving a modified vesicular stomatitis virus (VSV-filo GP) allows researchers to safely explore the interactions and immune responses related to filovirus infections outside high-security labs.
  • The study utilizes interferon α/β receptor-deficient (Ifnar) mice to examine different methods of infection and disease progression, providing a cost-effective and manageable way to advance filovirus research.
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