Immunotherapy against metastatic renal cell carcinoma with mature dendritic cells

• Published in: International journal of urology Vol. 14; no. 4; pp. 277 - 283
• Main Authors: Matsumoto, Akihiko, Haraguchi, Kyoko, Takahashi, Tsuyoshi, Azuma, Takeshi, Kanda, Yoshinobu, Tomita, Kyoichi, Kurokawa, Mineo, Ogawa, Seishi, Takahashi, Koki, Chiba, Shigeru, Kitamura, Tadaichi
• Format: Journal Article
• Language: English
• Published: Melbourne, Australia Blackwell Publishing Asia 01.04.2007
• Subjects: Aged; Cancer Vaccines - therapeutic use; Carcinoma, Renal Cell - secondary; Carcinoma, Renal Cell - therapy; Dendritic Cells; Humans; immunotherapy; Immunotherapy, Active; Kidney Neoplasms - pathology; Lung Neoplasms - secondary; Lung Neoplasms - therapy; Male; mature dendritic cell; Middle Aged; Pancreatic Neoplasms - secondary; Pancreatic Neoplasms - therapy; renal cell carcinoma; Treatment Outcome; tumor lysate
• ISSN: 0919-8172; 1442-2042
• DOI: 10.1111/j.1442-2042.2006.01723.x

Objective:  We performed a clinical trial of immunotherapy using autologous mature dendritic cells (DC) pulsed with autologous tumor lysate, for patients with metastatic renal cell carcinoma (RCC). Methods:  Patients with refractory metastatic RCC were enrolled in the study. All of them received interferon (IFN)‐α treatment after nephrectomy and were followed over 3 months prior to this study. Autologous monocyte‐derived immature DC were pulsed with lysate from autologous primary tumor as the antigen and keyhole limpet hemocyanin (KLH) as immunomodulator, and cultured in the presence of tumor necrosis factor (TNF)‐α, interleukin (IL)‐1β, and prostaglandin (PG)E2 to generate mature DC. Mature DC were injected intradermally near bilateral inguinal lymph nodes of the patients. A delayed‐type hypersensitivity (DTH) test and enzyme‐linked immunospot (ELISPOT) assay were performed to evaluate the immunological response. After 4 months from first injection, the clinical effect was evaluated by diagnostic imaging. Results:  The treatments were well tolerated without significant toxicity by the patients who were an average of 65.7 years old and had multiple metastases in the lung and other organs. One of the two patients developed a positive DTH reaction to tumor lysate and the other patient only to KLH. The patient with a positive DTH reaction to tumor lysate had stable disease in the clinical evaluation. Conclusions:  We confirmed the safety of DC therapy in this clinical trial. The DTH test revealed that the DC therapy induced immunological response to RCC. On the other hand, it was necessary to reconsider the patient selection criteria.