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Engineered mouse could advance cancer drugs
Scientists have engineered a mouse with a full set of human antibodies.
Scientists have engineered a mouse with a full set of human antibodies.

Scientists claim antibodies breakthrough

Scientists have engineered a mouse with the full set of genes encoding the human antibody repertoire.

They have demonstrated that these mice develop an enormous range of human antibodies which can be developed as potent drugs to treat a variety of human diseases such as cancer, autoimmune and infectious diseases.

"This is a remarkable achievement in our journey towards delivering therapeutic antibodies and to facilitate vaccine development," said Professor Allan Bradley, founder and chief scientific officer of Kymab, a monoclonal antibody biopharmaceutical company founded on research from the Wellcome Trust Sanger Institute.

"Kymab scientists have completed the most ambitious humanisation project of the mouse genome ever undertaken, with 5.4 million bases of human DNA, representing 0.1% of the human genome into the appropriate place in the mouse genome."

Antibodies represent five of the top ten best-selling drugs today. This is because they are natural products, are specific, potent and generally more safe.

Scientists say the challenge has been to capture the full human antibody repertoire and to recapitulate all its attributes.

Mice with portions of the human antibody repertoire have been developed previously. However, the technology used at the time proved unsuitable for moving the very large stretches of DNA from the human genome into the mouse. As a result, their antibody gene repertoires were both incomplete and in the wrong location in the genome.

Kymab scientists took a different approach and moved these vast stretches of DNA into the mouse genome in a series of steps each with a smaller segment of DNA, carefully re-joining them and thereby re-constructing the complete human repertoire in the correct place in the mouse genome.


Dr Christian Grøndahl, Chief Executive Officer of Kymab said: "Antibodies discovered using Kymouse™ strains are essentially ready to be developed as drugs.

"We are building a rich pipeline of first-in-class therapeutics in five areas: haematology, oncology, auto-immunity, pain and cardiovascular disease.

"This technology offers great potential to advance patient care in diseases with significant unmet medical need."

By using the Kymouse™ technology, Kymab can pursue the targeting of the most challenging drug targets ranging from complicated ion channels and GPCRs to deeply hidden epitopes in heavily glycosylated virus proteins.

Dr David Chiswell, former CEO of Cambridge Antibody Technology and Chairman of Kymab's Board of Directors says: "Kymab's highly innovative and technically advanced Kymouse™ platform has overcome the problems which limited previous generations of human antibody generating mice and is a strong foundation on which we can build a global biotechnology company."

 

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FIVP launches CMA remedies survey

News Story 1
 FIVP has shared a survey, inviting those working in independent practice to share their views on the CMA's proposed remedies.

The Impact Assessment will help inform the group's response to the CMA, as it prepares to submit further evidence to the Inquiry Group. FIVP will also be attending a hearing in November.

Data will be anonymised and used solely for FIVP's response to the CMA. The survey will close on Friday, 31 October 2025. 

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News Shorts
CMA to host webinar exploring provisional decisions

The Competition and Markets Authority (CMA) is to host a webinar for veterinary professionals to explain the details of its provisional decisions, released on 15 October 2025.

The webinar will take place on Wednesday, 29 October 2025 from 1.00pm to 2.00pm.

Officials will discuss the changes which those in practice may need to make if the provisional remedies go ahead. They will also share what happens next with the investigation.

The CMA will be answering questions from the main parties of the investigation, as well as other questions submitted ahead of the webinar.

Attendees can register here before Wednesday, 29 October at 11am. Questions must be submitted before 10am on 27 October.

A recording of the webinar will be accessible after the event.