activity of Recombinant Human Interleukin-15 against Tumor Recurrence and Metastasis in Mice

• Published in: Cellular & molecular immunology Vol. 5; no. 3; pp. 189 - 196
• Main Authors: Tang, Feng, Zhao, Luting, Jiang, Yan, Ba, Denian, Cui, Lianxian, He, Wei
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.06.2008; Nature Publishing Group; Department of Immunology, Institute of Basic Medical Sciences, Chinese Academy of Medical Science & School of Basic Medicine, Peking Union Medical College, Beijing 100005, China
• Subjects: Adenocarcinoma; Adenocarcinoma - drug therapy; Adenocarcinoma - secondary; Animal models; Animals; Antibodies; Antitumor activity; Biomedical and Life Sciences; Biomedicine; Cancer; Cell Line, Tumor; Cytokines; Cytotoxicity; Humans; Immune response; Immunology; Inoculation; Interleukin 15; Interleukin-15 - immunology; Interleukin-15 - metabolism; Interleukin-15 - therapeutic use; LA795; Liver Neoplasms - drug therapy; Liver Neoplasms - secondary; Lung cancer; Lung Neoplasms - drug therapy; Lung Neoplasms - secondary; Lymphocytes T; Male; Medical Microbiology; Metastases; Metastasis; Mice; Mice, Inbred Strains; Microbiology; Natural killer cells; Neoplasm Metastasis - immunology; Neoplasm Metastasis - prevention & control; Neoplasm Recurrence, Local - prevention & control; Neoplasm Transplantation; Random Allocation; Recombinant Proteins - immunology; Recombinant Proteins - metabolism; Recombinant Proteins - therapeutic use; rhIL-15; Splenocytes; Tumor cells; Vaccine; 可移植治疗; 癌细胞转移; 肿瘤治疗; recurrence; transplantable experimental tumor model; LA795; metastasis; rhIL-15; rhlL-15
• ISSN: 1672-7681; 2042-0226
• DOI: 10.1038/cmi.2008.23

Transplantable experimental tumor models were constructed to study the activities of recombinant human interleukin-15 （rhIL-15） against tumor recurrence and metastasis. The results showed that tumor nodule formation was retarded and tumor growth was inhibited in the subcutaneous tumor model of LA795 lung adenocarcinoma after treatment with rhIL-15, and the survival rate of T739 tumor-bearing mice treated with rhIL-15 was much higher than that of mice treated with either saline or with the same dose of rhIL-2. This indicats that rhIL-15 had better antitumor effect than rhIL-2 at the same dose level. In some rhIL-15 treated mice, the tumor cells inoculated subcutaneously were eradicated and there was no tumor formation even 138 days after tumor cell inoculation. The tumor-free mice were rechallenged with live tumor cells and no tumor reoccurred in the following two months in all of these mice, indicating that long-lasting antitumor systemic immunity developed. It was also shown that tumor recurrence and metastasis were inhibited markedly after treatment with rhIL-15, but not with the same dose of rhIL-2, in both subcutaneously and intravenously disseminated tumor models of LA795 lung adenocarcinoma. Simultaneously, the CTL and NK cell activities of the splenocytes obtained from tumor-bearing mice that had been treated with either rhIL-15 or rhIL-2 were both markedly enhanced. However, the enhancement of CTL and NK cell activities was more significant in rhIL-15 treated mice than that in rhIL-2 treated mice. This suggests that the anti-tumor effect of rhIL-15 in vivo was achieved by enhancing the CTL and NK cell activities in tumor immune response.