Ex vivo expanded human Vγ9vδ2 T-cells can suppress epithelial ovarian cancer cell growth
Journal
International Journal of Molecular Sciences
Journal Volume
20
Journal Issue
5
Pages
1139
Date Issued
2019
Author(s)
Abstract
γδ-T-cells have attracted attention because of their potent cytotoxicity towards tumors. Most γδ-T-cells become activated via a major histocompatibility complex (MHC)-independent pathway by the interaction of their receptor, Natural Killer Group 2 Member D (NKG2D) with the tumor-specific NKG2D ligands, including MHC class I-related chain A/B (MICA/B) and UL16-binding proteins (ULBPs), to kill tumor cells. However, despite their potent antitumor effects, the treatment protocols specifically targeting ovarian tumors require further improvements. Ovarian cancer is one of the most lethal and challenging female malignancies worldwide because of delayed diagnoses and resistance to traditional chemotherapy. In this study, we successfully enriched and expanded γδ-T-cells up to ~78% from peripheral blood mononuclear cells (PBMCs) with mostly the Vγ9Vδ2-T-cell subtype in the circulation. We showed that expanded γδ-T-cells alone exerted significant cytotoxic activities towards specific epithelial-type OVCAR3 and HTB75 cells, whereas the combination of γδ-T cells and pamidronate (PAM), a kind of aminobisphosphonates (NBPs), showed significantly enhanced cytotoxic activities towards all types of ovarian cancer cells in vitro. Furthermore, in tumor xenografts of immunodeficient NSG mice, γδ-T-cells not only suppressed tumor growth but also completely eradicated preexisting tumors with an initial size of ~5 mm. Thus, we concluded that γδ-T-cells alone possess dramatic cytotoxic activities towards epithelial ovarian cancers both in vitro and in vivo. These results strongly support the potential of clinical immunotherapeutic application of γδ-T-cells to treat this serious female malignancy. ? 2019 by the authors. Licensee MDPI, Basel, Switzerland.
Subjects
NSG mice; Ovarian cancer; Pamidronate (PAM); Vγ9Vδ2-T cells; Xenograft
SDGs
Other Subjects
gamma interferon; interleukin 2; natural killer cell receptor NKG2D; pamidronic acid; tumor necrosis factor; lymphocyte antigen receptor; antineoplastic activity; apoptosis; Article; cancer growth; cancer immunotherapy; cell adhesion; controlled study; cytotoxicity; enzyme linked immunosorbent assay; female; flow cytometry; gamma delta T lymphocyte; human; human cell; immunohistochemistry; major histocompatibility complex; mouse; MTT assay; natural killer cell; ovarian cancer cell line; ovary carcinoma; scanning electron microscopy; short tandem repeat; tumor microenvironment; tumor volume; upregulation; xenograft; adoptive immunotherapy; animal; cell proliferation; cell survival; coculture; cytology; drug screening; immunology; metabolism; mononuclear cell; ovary tumor; pathology; T lymphocyte; tumor cell line; Animals; Carcinoma, Ovarian Epithelial; Cell Line, Tumor; Cell Proliferation; Cell Survival; Coculture Techniques; Female; Humans; Immunotherapy, Adoptive; Leukocytes, Mononuclear; Mice; Ovarian Neoplasms; Receptors, Antigen, T-Cell, gamma-delta; T-Lymphocytes; Xenograft Model Antitumor Assays
Publisher
MDPI AG
Type
journal article