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Anti-Leukemia Activity of In Vitro-Expanded Human Gamma Delta T Cells in a Xenogeneic Ph+ Leukemia Model
Author(s) -
Gabrielle M. Siegers,
Tania C. Felizardo,
A. Mark Mathieson,
Yoko Kosaka,
Xinghua Wang,
Jeffrey A. Medin,
Armand Keating
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0016700
Subject(s) - bone marrow , clonogenic assay , cytotoxic t cell , leukemia , spleen , in vitro , immunology , microbiology and biotechnology , biology , chemistry , cancer research , biochemistry
Gamma delta T cells (GDTc) lyse a variety of hematological and solid tumour cells in vitro and in vivo , and are thus promising candidates for cellular immunotherapy. We have developed a protocol to expand human GDTc in vitro , yielding highly cytotoxic Vgamma9/Vdelta2 CD27/CD45RA double negative effector memory cells. These cells express CD16, CD45RO, CD56, CD95 and NKG2D. Flow cytometric, clonogenic, and chromium release assays confirmed their specific cytotoxicity against Ph + cell lines in vitro . We have generated a fluorescent and bioluminescent Ph + cell line, EM-2eGFPluc, and established a novel xenogeneic leukemia model. Intravenous injection of EM-2eGFPluc into NOD.Cg- Prkdcscid Il2rgtm1Wjl /SzJ (NSG) mice resulted in significant dose-dependent bone marrow engraftment; lower levels engrafted in blood, lung, liver and spleen. In vitro -expanded human GDTc injected intraperitoneally were found at higher levels in blood and organs compared to those injected intravenously; GDTc survived at least 33 days post-injection. In therapy experiments, we documented decreased bone marrow leukemia burden in mice treated with GDTc. Live GDTc were found in spleen and bone marrow at endpoint, suggesting the potential usefulness of this therapy.

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