Autologous dendritic cells and activated cytotoxic T‑cells as combination therapy for breast cancer

• Published in: Oncology reports Vol. 43; no. 2; pp. 671 - 680
• Main Authors: Shevchenko, Julia A, Khristin, Alexander A, Kurilin, Vasily V, Kuznetsova, Maria S, Blinova, Darya D, Starostina, Natalya M, Sidorov, Sergey V, Sennikov, Sergey V
• Format: Journal Article
• Language: English
• Published: Greece Spandidos Publications 01-02-2020; Spandidos Publications UK Ltd
• Subjects: Antigens; Breast cancer; Cancer cells; Cancer metastasis; Cancer prevention; Cancer research; Cancer therapies; Care and treatment; Chemotherapy; Cloning; Combination therapy; Cytotoxicity; Dendritic cells; Deoxyribonucleic acid; Development and progression; Disease; Diseases; DNA; Family medical history; Health aspects; Immunology; Immunotherapy; Lung cancer; Lymphocytes; Medical equipment industry; Metastasis; Mortality; Neutrophils; Patients; Recurrence (Disease); Surgery; T cells; Tumors; Vaccines; Canada; United States; Russia
• ISSN: 1021-335X; 1791-2431
• DOI: 10.3892/or.2019.7435

Breast cancer is the most common oncological pathology in women worldwide. Techniques for improving the clinical parameters of patients undergoing combination therapy for breast cancer are currently under development. A type of treatment employing dendritic cells (DCs) and cytotoxic DC‑induced antigen‑specific T lymphocytes efficiently eliminates residual cancer cells that are the key cause of tumor recurrence and metastasis. In the present study, DCs and activated lymphocytes (treated with IL‑12 and IL‑18) were isolated from the peripheral blood of patients with breast cancer, using a lysate of tumor tissue as antigen. The patients received the cells as part of adjuvant or neoadjuvant regimens (stage IV disease or progression). Evaluation of immunity was performed at 3 and 6 months after terminating immunotherapy. Evaluation of the disease‑free period was performed for 3 years after surgery. The use of antigen‑loaded autologous DCs combined with mononuclear cells with increased cytotoxic activity following Th1 polarization reduced the populations of immunosuppressive cells. The results of the present study demonstrated that the investigated cellular immunotherapy for breast cancer is safe, reduces the risk of relapse and metastasis, and improves immunity by reducing the number of regulatory T cells. Therefore, this therapeutic strategy may represent a novel approach to combating distant metastases of breast cancer.