Making Cell Therapy Affordable and Accessible: Off-the-Shelf CAR γδT Cells Generated Using CRISPR/AAV

Speaker

Meisam Naeimi, PhD

• Assistant Professor of Pediatrics, The Ohio State University

• Principal Investigator, Nationwide Children’s Hospital

• Chief Scientific Officer, CARTx Therapeutics

 

In this Webinar, You Will Learn:

• The importance of off-the-shelf CAR-T cells in making therapies more affordable and accessible
• Next-generation engineering: the development of CRISPR/AAV-based off-the-shelf CAR γδT cells to overcome the limitations of traditional CAR-T therapies
• Preclinical efficacy: the potent antitumor activity of CAR γδT cells demonstrated across multiple tumor types

 

About this Webinar:

Cell therapy has transformed cancer treatment but remains costly and inaccessible for many patients. Using a novel γδT cell and CRISPR/AAV platform, we have developed off-the-shelf CAR γδT cells that combine strong antitumor activity with global scalability. I will share recent data on the CD38-CAR for hematological malignancies, as well as the GD2- and Nucleolin-CAR γδT cells. This work paves the way for affordable and accessible cell therapies worldwide.

 

About Meisam Naeimi, PhD:

Dr. Meisam Naeimi’s mission is to bring cellular therapies to low- and middle-income countries. At Nationwide Children’s Hospital and The Ohio State University, he leads a translational research program focused on gene-edited T and γδT cell therapies for high-grade gliomas, T-ALL, and other hard-to-treat malignancies. He currently serves as Chief Scientific Officer at CARTx Therapeutics, where he drives the development of next-generation allogeneic CAR γδT cell therapies for both pediatric and adult cancers.

Dr. Naeimi has pioneered CRISPR/AAV-based engineering platforms to generate potent off-the-shelf CAR γδT cells, including CD38-, GD2-, and Nucleolin-directed constructs, and has advanced multiple collaborations to scale these therapies globally. His work bridges academic innovation with industry translation, supported by a strong track record in preclinical development, grant funding, and strategic partnerships.

 

We look forward to welcoming you to our event. By filling in these details we can better plan your participation. You will receive a copy of the request by e-mail.