news

Protective antibodies identified for rare polio-like disease in children

Researchers isolated monoclonal antibodies from children who has survived infection by EV-D68, the virus linked to acute flaccid myelitis (AFM). These antibodies protected mice against infection.

antibodies on a blue background

Scientists have isolated human monoclonal antibodies that could prevent a rare polio-like illness which affects children.

Acute flaccid myelitis (AFM) causes sudden weakness in the arms and legs following a fever or respiratory illness and has recently been linked to a group of respiratory viruses called enterovirus D68 (EV-D68). Tracking of the disease by the US Centers for Disease Control and Prevention (CDC) began in 2014, since then there have been over 600 cases. AFM, which has been fatal in some instances, currently has no specific treatment.

In order to develop potential treatments for AFM, researchers at the Vanderbilt University Vaccine Center, US, isolated antibody-producing blood cells from the blood of children who had previously been infected by EV-D68. These blood cells were then fused to fast-growing myeloma cells, allowing researchers to generate a panel of monoclonal antibodies that potently neutralised EV-D68 in laboratory studies.

 

Reserve your FREE place

 


Are you advancing promising antibody leads, only to encounter issues with stability, PK or manufacturability later in development?

30 July 2025 | 10:00 AM BST | FREE Webinar

Join us for an expert-led webinar exploring how early-stage developability assessment can help reduce downstream risk and improve candidate selection.

What You’ll Learn:

  • How to identify key developability risks early including aggregation, PK, and manufacturability
  • How to implement high-throughput in vitro assays requiring <1 mg of antibody per test
  • How to combine in silico modeling with wet-lab analytics to guide early optimisation

Don’t miss your chance to learn from Dr Lei Guo.

Register Now – It’s Free!

 

Collaborators at Perdue University, also US, then determined the structure of the antibodies, shedding light o how they interact with EV-D68. One of the antibodies protected mice from respiratory and neurologic disease when given either before or after infection by the enterovirus.

Dr James Crowe, director of the Vanderbilt Vaccine Center and Ann Scott Carell Chair and professor of Pediatrics and Pathology, Microbiology and Immunology in the Vanderbilt University School of Medicine, concluded: “We were excited to isolate potent human antibodies that inhibit this devastating polio-like virus, and these studies will form the basis for taking them forward to clinical trials.”

The paper was published in Science Immunology.

Leave a Reply

Your email address will not be published. Required fields are marked *