EFFECTS ON ANTITUMOR-ACTIVITY AND CYTOKINE PRODUCTION IN THE THORACICCAVITY BY INTRAPLEURAL ADMINISTRATION OF LACTOBACILLUS-CASEI IN TUMOR-BEARING MICE

Citation
T. Matsuzaki et al., EFFECTS ON ANTITUMOR-ACTIVITY AND CYTOKINE PRODUCTION IN THE THORACICCAVITY BY INTRAPLEURAL ADMINISTRATION OF LACTOBACILLUS-CASEI IN TUMOR-BEARING MICE, Medical microbiology and immunology, 185(3), 1996, pp. 157-161
Citations number
26
Categorie Soggetti
Microbiology,Immunology
ISSN journal
03008584
Volume
185
Issue
3
Year of publication
1996
Pages
157 - 161
Database
ISI
SICI code
0300-8584(1996)185:3<157:EOAACP>2.0.ZU;2-3
Abstract
The effects Lactobacillus casei Y1T9108 (LC 9018) on antitumor activit y and cytokine production in Meth A fibrosarcoma (Meth Al-bearing BALB /c mice were examined. Intrapleural (i.pl.) administration of LC 9018 was effective in prolonging the survival of Meth A-bearing mice, and f requently cured mice of the tumor. However, the results also indicated that the effect of LC 9018 was in part inhibited in mice treated with anti-CD3 or anti-CD8 antibody, but not affected in anti-CD4 antibody- treated mice. In contrast, LC 9018 had little effect on Meth A-bearing SCID or nude mice. These results demonstrated that CD8(+) T cells par ticipated in prolonging the survival of Meth A-bearing mice. Moreover, the examination of the production of several cytokines revealed that the production of interferon-gamma and interleukin-6 was, in particula r, augmented in the exudated fluid of the thoracic cavity in BALB/c mi ce injected with LC 9018 i.pl. These results suggested that i.pl. admi nistration of LC 9018 induced those cytokines which had the potential to activate the thoracic macrophages or proliferate the thoracic lymph ocytes to the cytotoxic T cells. Taken together, these findings demons trated that the prolonging effects on survival by i.pl. administration of LC 9018 depended on CD8+ T cells, and the i.pl. administration of LC 9018 into i.pl. Meth A-bearing mice induced several cytokines which participated in the subsequent immunoresponses.