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Research Article

Agonist antibody that induces human malignant cells to kill one another

Kyungmoo Yea, Hongkai Zhang, Jia Xie, Teresa M. Jones, Chih-Wei Lin, Walter Francesconi, Fulvia Berton, Mohammad Fallahi, Karsten Sauer, and Richard A. Lerner
  1. aShanghai Institute for Advanced Immunological Studies, ShanghaiTech University, Shanghai 200031, China;
  2. bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
  3. cDepartment of Molecular and Cellular Neuroscience, The Scripps Research Institute, La Jolla, CA 92037;
  4. dDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037;
  5. eBioInformatics Core, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458;
  6. fDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037

See allHide authors and affiliations

PNAS first published October 20, 2015; https://doi.org/10.1073/pnas.1519079112
Kyungmoo Yea
aShanghai Institute for Advanced Immunological Studies, ShanghaiTech University, Shanghai 200031, China;
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Hongkai Zhang
bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
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Jia Xie
bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
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Teresa M. Jones
bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
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Chih-Wei Lin
bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
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Walter Francesconi
cDepartment of Molecular and Cellular Neuroscience, The Scripps Research Institute, La Jolla, CA 92037;
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Fulvia Berton
dDepartment of Chemical Physiology, The Scripps Research Institute, La Jolla, CA 92037;
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Mohammad Fallahi
eBioInformatics Core, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458;
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Karsten Sauer
bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
fDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037
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Richard A. Lerner
bDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037;
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  • For correspondence: rlerner@scripps.edu
  1. Contributed by Richard A. Lerner, September 25, 2015 (sent for review September 14, 2015; reviewed by Terence H. Rabbitts and Owen N. Witte

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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.

  • agonist antibody
  • natural killer cell
  • differentiation
  • combinatorial antibody libraries

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.

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Converting cancer cells to killer cells
Kyungmoo Yea, Hongkai Zhang, Jia Xie, Teresa M. Jones, Chih-Wei Lin, Walter Francesconi, Fulvia Berton, Mohammad Fallahi, Karsten Sauer, Richard A. Lerner
Proceedings of the National Academy of Sciences Oct 2015, 201519079; DOI: 10.1073/pnas.1519079112

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Converting cancer cells to killer cells
Kyungmoo Yea, Hongkai Zhang, Jia Xie, Teresa M. Jones, Chih-Wei Lin, Walter Francesconi, Fulvia Berton, Mohammad Fallahi, Karsten Sauer, Richard A. Lerner
Proceedings of the National Academy of Sciences Oct 2015, 201519079; DOI: 10.1073/pnas.1519079112
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