Abstract
CD22 is an attractive target for the development of immunotherapeutic approaches for the therapy of B-cell malignancies. In particular, an m971 antibody-derived, second generation chimeric antigen receptor (CAR) that targets CD22 holds significant therapeutic promise. The key aspect for the development of such a highly-active CAR was its ability to target a membrane-proximal epitope of CD22 © 2013 Landes Bioscience.
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Long, A. H., Haso, W. M., & Orentas, R. J. (2013). Lessons learned from a highly-active CD22-specific chimeric antigen receptor. OncoImmunology, 2(4). https://doi.org/10.4161/onci.23621
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