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Agonist antibody that induces human malignant cells to kill one another.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2015 Nov 10; Vol. 112 (45), pp. E6158-65. Date of Electronic Publication: 2015 Oct 20. - Publication Year :
- 2015
-
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.
- Subjects :
- Antibodies therapeutic use
Blotting, Western
Cell- and Tissue-Based Therapy trends
Computational Biology
Flow Cytometry
Granzymes
Humans
Immunohistochemistry
Interferon-gamma metabolism
Killer Cells, Natural metabolism
Killer Cells, Natural ultrastructure
Leukemia, Myeloid, Acute immunology
Microscopy, Electron, Scanning
Perforin metabolism
Antibodies immunology
Cell Differentiation genetics
Cell- and Tissue-Based Therapy methods
Killer Cells, Natural immunology
Leukemia, Myeloid, Acute therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 112
- Issue :
- 45
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 26487683
- Full Text :
- https://doi.org/10.1073/pnas.1519079112