| Literature DB >> 35452603 |
Mark B Leick1, Harrison Silva2, Irene Scarfò3, Rebecca Larson3, Bryan D Choi4, Amanda A Bouffard2, Kathleen Gallagher5, Andrea Schmidts3, Stefanie R Bailey3, Michael C Kann2, Max Jan6, Marc Wehrli2, Korneel Grauwet2, Nora Horick7, Matthew J Frigault1, Marcela V Maus8.
Abstract
Chimeric antigen receptor (CAR) T cell therapy is effective in lymphoid malignancies, but there has been limited data in myeloid cancers. Here, we start with a CD27-based CAR to target CD70 ("native") in acute myeloid leukemia (AML), and we find modest efficacy in vivo, consistent with prior reports. We then use orthogonal approaches to increase binding on both the tumor and CAR-T cell sides of the immune synapse: a pharmacologic approach (azacitidine) to increase antigen density of CD70 in myeloid tumors, and an engineering approach to stabilize binding of the CAR to CD70. To accomplish the latter, we design a panel of hinge-modified regions to mitigate cleavage of the extracellular portion of CD27. Our CD8 hinge and transmembrane-modified CD70 CAR-T cells are less prone to cleavage, have enhanced binding avidity, and increased expansion, leading to more potent in vivo activity. This enhanced CD70-targeted CAR is a promising candidate for further clinical development.Entities:
Keywords: acute myeloid leukemia; adoptive T cell therapy; cell engineering; cellular immunity; chimeric antigen receptors; combined modality therapy; hematologic neoplasms
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Year: 2022 PMID: 35452603 PMCID: PMC9107929 DOI: 10.1016/j.ccell.2022.04.001
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 38.585