IMMUNOLOGICAL ANALYSIS OF ENHANCED SPONTANEOUS METASTASIS IN WKA RATSFOLLOWING CRYOSURGERY

Citation
T. Shibata et al., IMMUNOLOGICAL ANALYSIS OF ENHANCED SPONTANEOUS METASTASIS IN WKA RATSFOLLOWING CRYOSURGERY, Anticancer research, 18(4A), 1998, pp. 2483-2486
Citations number
21
Categorie Soggetti
Oncology
Journal title
ISSN journal
02507005
Volume
18
Issue
4A
Year of publication
1998
Pages
2483 - 2486
Database
ISI
SICI code
0250-7005(1998)18:4A<2483:IAOESM>2.0.ZU;2-8
Abstract
We have previously reported that inhibition of anti-tumor immune respo nses and enhancement of metastatic tumor growth occurred in rats follo wing cryosurgery of the transplantable 3-methlcholanthrene-induced rat fibrosarcoma KMT-17. In this study, to elucidate the immunological re sponses in rats following cryosurgery, we examined whether rat serum o btained from rats which underwent cryosurgery (c-serum) might affect t he in vivo neutralizing activity of the Winn assay. In this assay, c-s erum did not reduce the anti-tumor immunity, though spleen cells obtai ned from rats undergoing surgical excision indicated strong anti-tumor immunity as compared with cryosurgery. Thus, we examined the anti-tum or responses of spleen cells. Macrophages were obtained from the glass adherent fraction of rat spleen cells following cryosurgery and these macrophages were used for cytostatic activity against KMT-17 cells. C ytostatic activity was not reduced by cryosurgery The spleen cells obt ained from rats receiving cryosurgery were intravenously transferred i nto other rats that were previously immunized with 80 Gy-irradiated KM T-17 cells, end an alteration of tumor growth modulated by this adopti ve cell transfusion was observed. The anti-tumor resistance of rats wa s diminished by the adoptive transfusion of spleen cells treated with cryosurgery, though this diminution disappeared following anti-T serum and immune complement treatment of spleen cells. These results sugges t that immune-suppression following cryosurgery may be mainly caused b y suppressor T cells.