Agonist antibody that induces human malignant cells to kill one another
- aShanghai Institute for Advanced Immunological Studies, ShanghaiTech University, Shanghai 200031, China;
- bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
- cDepartment of Molecular and Cellular Neuroscience, The Scripps Research Institute, La Jolla, CA 92037;
- dDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037;
- eBioInformatics Core, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458;
- fDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037
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Contributed by Richard A. Lerner, September 25, 2015 (sent for review September 14, 2015; reviewed by Terence H. Rabbitts and Owen N. Witte

Significance
A major goal in cancer research is to discover agents that transform malignant cells into benign cells. Here, we report on an agonist antibody that converts leukemic cells into killer cells. This induction has an added benefit: In addition to transforming the cancer cells into other, presumably less aggressive, cells, the newly induced cells have a killer phenotype and kill other as yet unconverted members of the malignant clone.
Abstract
An attractive, but as yet generally unrealized, approach to cancer therapy concerns discovering agents that change the state of differentiation of the cancer cells. Recently, we discovered a phenomenon that we call “receptor pleiotropism” in which agonist antibodies against known receptors induce cell fates that are very different from those induced by the natural agonist to the same receptor. Here, we show that one can take advantage of this phenomenon to convert acute myeloblastic leukemic cells into natural killer cells. Upon induction with the antibody, these leukemic cells enter into a differentiation cascade in which as many as 80% of the starting leukemic cells can be differentiated. The antibody-induced killer cells make large amounts of perforin, IFN-γ, and granzyme B and attack and kill other members of the leukemic cell population. Importantly, induction of killer cells is confined to transformed cells, in that normal bone marrow cells are not induced to form killer cells. Thus, it seems possible to use agonist antibodies to change the differentiation state of cancer cells into those that attack and kill other members of the malignant clone from which they originate.
Footnotes
- ↵1To whom correspondence should be addressed. Email: rlerner{at}scripps.edu.
Author contributions: K.Y., H.Z., J.X., T.M.J., and R.A.L. designed research; K.Y., H.Z., J.X., T.M.J., W.F., and F.B. performed research; K.Y., H.Z., J.X., T.M.J., C.-W.L., and R.A.L. contributed new reagents/analytic tools; K.Y., H.Z., J.X., T.M.J., M.F., K.S., and R.A.L. analyzed data; and R.A.L. wrote the paper.
Reviewers: T.H.R., Weatherall Institute of Molecular Medicine; and O.N.W., Howard Hughes Medical Institute, University of California, Los Angeles.
Conflict of interest statement: R.A.L. is a founder of Zebra biologics.
This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1519079112/-/DCSupplemental.