論文 - 大家　基嗣

Laparoscopic surgical correction ofcircuivicaval ureter

Baba Shiro, Oya Mototsugu, Miyahara Makoto, Deguchi Nobuhiro, Tazaki Hiroshi

Urology 44 （ 1 ） 122 - 126 1994年

ISSN  0090-4295

　概要を見る

<p>Laparoscopic transposition and reanastomosis of a circumcaval ureter were performed in a 52-year-old man with right flank pain. A preoperative perfusion pressure study revealed abnormally high intrapelvic pressure. Under laparoscopy, the renal pelvis was divided above the ureteropelvic junction and the ureter was relocated from behind the vena cava. A 5 cm segment of redundant ureter containing the postcaval segment was resected and the ureteral end and renal pelvis were reapproximated with interrupted.</p>

• Access to Document (DOI)

Antitumor effect of interleukin-2 entrapped in liposomes on murine renal cell carcinoma

Oya M.

Keio Journal of Medicine 43 （ 1 ） 37 - 44 1994年

ISSN  0022-9717

　概要を見る

<p>Antitumor effects of interleukin-2 entrapped in liposomes (IL-2 liposomes) on Renca, murine renal cell carcinoma of spontaneous origin, were evaluated by in vivo and in vitro experiments. As a local treatment model, IL-2 liposomes at a dose of 1.0 x 10⁴ units were for 7 days injected adjacent to the Renca tumors inoculated in the back of BALB/c mice. The treatment inhibited the tumor growth and prolonged the survival time of mice significantly compared to the control (p&lt;0.01). Serum IL-2 levels after subcutaneous administration of IL-2 liposomes confirmed its slow releasing mechanism into blood circulation. The spleen cells from mice following the IL-2 liposome treatment showed higher cytotoxicity in vitro than that of IL-2 alone using Renca, YAC-1, and P-815 cells, which was determined by ⁵¹Cr-release assay. Indirect immunoperoxidase staining of tumor-infiltrating lymphocytes (TILs) showed that accumulation of Lyt-2⁺ and L3T4⁺ cells were seen in the tumor treated with IL-2 liposomes. These results indicate that IL-2 liposomes have a long-acting cytotoxicity against renal cell carcinoma caused by a slow release mechanism generated through the efficient local immune response mediated by TILs.</p>