New method facilitates development of antibody-based drugs

New method facilitates development of antibody-based drugs
In recent years, therapeutic antibodies have transformed the treatment of cancer and autoimmune diseases. Now, researchers at Lund University in Sweden have developed a new, efficient method based on the genetic scissors CRISPR-Cas9, that facilitates antibody development. The discovery is published in Nature Communications.


Antibody drugs are the fastest growing class of drug, and several therapeutic antibodies are used to treat cancer. They are effective, often have few side effects and benefit from the body s own immune system by identifying foreign substances in the body. By binding to a specific target molecule on a cell, the antibody can either activate the immune system, or cause the cell to self-destruct.

However, most antibody drugs used today have been developed against an antibody target chosen beforehand. This approach is limited by the knowledge of cancer we have today and restricts the discovery of new medicines to currently known targets.

"Many antibody drugs currently target the same molecule, which is a bit limiting. Antibodies targeting new molecules could give more patients access to effective treatment," says Jenny Mattsson, doctoral student at the Department of Hematology and Transfusion Medicine at Lund University.

Another route -- that pharmaceutical companies would like to go down -- would be to search for antibodies against cancer cells without being limited to a pre-specified target molecule. In this way, new, unexpected target molecules could be identified. The problem is that this method (so-called "phenotypic antibody development") requires that the target molecule be identified at a later stage, which has so far been technically difficult and time-consuming.

"Using the CRISPR-Cas9 gene scissors, we were able to quickly identify the target molecules for 38 of 39 test antibodies. Although we were certain that the method would be effective, we were surprised that the results would be this precise. With previous methods, it has been difficult to find the target molecule even for a single antibody," says Jenny Mattsson.

The research project is a collaboration between Lund University, BioInvent International and the Foundation for Strategic Research. The researchers method has already been put into practical use in BioInvent s ongoing research projects.

"We believe the method can help antibody developers and hopefully contribute to the development of new antibody-based drugs in the future," concludes Professor Björn Nilsson, who led the project.

Materials provided by Lund University . Note: Content may be edited for style and length.

Lund University. "New method facilitates development of antibody-based drugs." ScienceDaily. ScienceDaily, 5 March 2021. .

Lund University. "New method facilitates development of antibody-based drugs." ScienceDaily. (accessed March 5, 2021).



Nov. 18, 2020 — Researchers have demonstrated that the CRISPR/Cas9 system is very effective in treating metastatic cancers, a significant step on the way to finding a cure for cancer. The researchers developed a ...

Apr. 1, 2019 — Therapeutic antibodies are increasingly being used in the clinic for the treatment of various diseases. Yet, oral to gut targeting of antibodies remains a challenge due to their incapability to ...

Sep. 28, 2017 — A research group has found out how CRISPR-Cas9 -- also known as molecular scissors -- can search the genome for a specific DNA sequence. Cas9 already has many applications in ...

Feb. 7, 2017 — The new gene-editing tool CRISPR/Cas9 holds promise for new treatment of such genetic diseases as cystic fibrosis, muscular dystrophy and hemophilia. But to work well, it must be delivered across the ...
News Topics :
Scientists at the University of Southampton s Centre for Cancer Immunology have gained new insight into how the immune system can be better used to find and kill cancer cells....
Researchers from the University of Illinois Chicago have discovered a new gene editing technique that allows for the programming of sequential cuts or edits over time. advertisement CRISPR is...
Researchers used single molecule imaging to compare the genome editing tools CRISPR Cas9 and TALEN. Their experiments revealed that TALEN is up to five times more efficient than CRISPR Cas9 in parts of the...
Researchers injected gold nanoparticles upper right carrying CRISPR Cas9 into the brains of mice with fragile X syndrome to edit DNA scissors and knock out a neurotransmitter receptor, which reduced exaggerated...
Researchers at Tel Aviv University TAU have demonstrated that the CRISPR/Cas9 system is very effective in treating metastatic cancers, a significant step on the way to finding a cure for...