IMMUNOLOGY

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MERS Antibodies Produced in Cattle Tolerated in Phase 1 Clinical Trial

 

The first confirmed case of Middle East respiratory syndrome (MERS) was reported in Saudi Arabia in 2012. Since then, the MERS coronavirus has spread to 27 countries and sickened more than 2,000 people, of whom about 35% have died, according to the World Health Organization. There are no licensed treatments for MERS.

 

According to an article published in The Lancet Infectious Diseases (9 January 2018), SAB-301, an experimental treatment developed from cattle plasma for MERS infection, was found to be well-tolerated by healthy volunteers, with only minor reactions. SAB-301 was developed by SAB Biotherapeutics of Sioux Falls, South Dakota, and has been successfully tested in mice. The treatment comes from so-called “transchromosomic cattle.“ These cattle have genes that have been slightly altered to enable them to produce fully human antibodies instead of cow antibodies against killed microbes with which they have been vaccinated — in this case the MERS virus. The clinical trial, was conducted by NIH’s National Institute of Allergy and Infectious Diseases, took place at the NIH Clinical Center.

 

For the study, 28 healthy volunteers were treated with SAB-301 and 10 received a placebo. Six groups of volunteers given different intravenous doses were assessed six times over 90 days. Complaints among the treatment and placebo groups — such as headache and common cold symptoms — were similar and generally mild. The authors stated that they may be able to use these transchromosomic cattle to rapidly produce human antibodies, in as few as three months, against other human pathogens as well,. This means they could conceivably develop antibody treatments against a variety of infectious diseases in a much faster timeframe and in much greater volume than currently possible.

 

SAB Biotherapeutics is planning a larger study of SAB-301 in patients infected with MERS coronavirus.

 

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