The Jerusalem Post

Pluristem joins CRISPR-IL to develop next-gen genome editing products

- • By MAAYAN HOFFMAN

Haifa-based Pluristem Therapeuti­cs has joined a consortium to help develop next-generation, multi-species genome editing products for human, plant and animal DNA that could improve work being done in the pharma, agricultur­e and aquacultur­e industries.

“We see cell therapy and gene editing as highly synergisti­c methods to treat and cure diseases using advanced technologi­es,” said Pluristem CEO Yaky Yanay.

The CRISPR-IL consortium, funded by the Israeli Innovation Authority, brings together a team of multi-disciplina­ry experts to develop artificial intelligen­ce based end-toend genome-editing solutions. Pluristem is a regenerati­ve medicine company, best known for its PLX cell therapy, which was recently cleared by the US Food and Drug Administra­tion for a Phase II study in the treatment of severe COVID-19 cases complicate­d by Acute Respirator­y Distress Syndrome.

Pluristem’s vice president of research and intellectu­al property, Racheli Ofir, will lead CRISPR-IL’s pharma working group.

Several medical institutio­ns and centers of academia are members of CRISPR-IL, including Sheba Medical Center and Schneider Children’s Medical Center, BarIlan University, Ben-Gurion University of the Negev, Hebrew University of Jerusalem, the Weizmann Institute of Science, IDC Herzliya and Tel-Aviv University. In addition, several companies like Pluristem are part of the team.

The genome editing product is expected to improve on existing technology and should include “the computatio­nal design of on-target DNA modificati­on, with minimal accidental, off-target modificati­ons, improved modificati­on efficiency and provide an accurate measuring tool to ensure the desired modificati­on was made,” a release explained.

Yanay said that “Pluristem is honored to bring its allogeneic cell therapy and manufactur­ing expertise to the CRISPR-IL consortium and to lead the developmen­t of the next generation of allogeneic cell therapies for treating the diseases of today and the future.”

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