Improving Gene and Cell Therapy Conditioning Regimens With JSP191


The executive vice president of research and development at Jasper Therapeutics discussed how JSP191 is designed to be better-tolerated than current conditioning regimens.

“JSP 191 is a monoclonal antibody that is directed at CD117. The way this antibody works is it takes away that survival mechanism by blocking the receptor and this results in stem cell depletion. It does so in a manner that is significantly well-tolerated, not the same kind of toxicity associated with other conditioning regimens. And therefore, it offers an opportunity for a safer, gentler conditioning regimen for patients.”

Stem cell therapies require prior, often harsh, conditioning regimens to allow new stem cells to successfully graft. Jasper Therapeutics is aiming to develop a safer, better-tolerated conditioning regimen with their lead program, JSP191, a targeted, first-in-class humanized monoclonal antibody designed to block stem cell factor receptor signaling leading to clearance of hematopoietic stem cells from bone marrow, creating an empty space for donor or gene-corrected transplanted stem cells to engraft.

JSP191 has been evaluated in more than 90 healthy volunteers and patients and is currently in 2 clinical trials for myelodysplastic syndromes/acute myeloid leukemia (NCT04429191) and severe combined immunodeficiency (NCT02963064).

Jasper Therapeutics recently announced a collaboration with Aruvant Sciences to study the use of JSP191 with ARU-1801, an investigational lentiviral gene therapy for the treatment of sickle cell disease, in June 2021.

GeneTherapyLive spoke with Kevin Heller, MD, Jasper’s executive vice president of research and development to learn more about JSP191 and its role in autologous gene therapy and allogeneic hematopoietic stem cell transplantation.

Jasper Therapeutics and Aruvant announce research collaboration to study JSP191, an antibody-based conditioning agent, with ARU-1801, a novel gene therapy for the treatment of sickle cell disease. News release. Jasper Therapeutics. June 21, 2021.
Related Videos
Daniel Hart, PhD, on CRISPR-Mediated, In Vivo Epigenomic Activation
Luke Roberts, MBBS, PhD, on Developing Gene Therapy for Congestive Heart Failure
PJ Brooks, PhD, on Improved Newborn Screening, Non-Viral Gene Editing: New Frontiers for Neuromuscular Disease
Sowmya Viswanathan, PhD, on Translating Cell Therapies to the Clinic at ISCT 2024
Omar Nadeem, MD, on Initial Efficacy of GPRC5D-CAR in R/R Multiple Myeloma
Omer A. Abdul Hamid, MD, on Improving Gene Therapy’s Effect and Accessibility
George Tachas, PhD, on Tackling DMD Treatment From Multiple Angles
David Suhy, PhD, the cofounder and chief scientific officer of Earli
Deepak L. Bhatt, MD, MPH, MBA, on Incorporating AI into Genetic Research for Cardiovascular Disease
Jeffrey Chamberlain, PhD, on Helping Progress Cell and Gene Therapy Development
Related Content
© 2024 MJH Life Sciences

All rights reserved.