ENDOGENOUS PRODUCTION OF TUMOR-NECROSIS-FACTOR IN NORMAL MICE ORALLY TREATED WITH DEODAN - A PREPARATION FROM LACTOBACILLUS-BULGARICUS LB51

被引:17
作者
DAVIDKOVA, G
POPOVA, P
GUENCHEVA, G
BOGDANOV, A
PACELLI, E
AUTERI, A
MINCHEVA, V
机构
[1] INST STATE CONTROL DRUGS,26 BLVD YANKO SAKAZOV,BU-1504 SOFIA,BULGARIA
[2] UNIV SIENA,POLYCLIN LE SCOTTE,IMMUNOL & ALLERGOL CLIN,I-53100 SIENA,ITALY
[3] DEODAN LABS,BU-1000 SOFIA,BULGARIA
来源
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY | 1992年 / 14卷 / 08期
关键词
D O I
10.1016/0192-0561(92)90006-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ability of orally administered Deodan, a product from the cell wall of Lactobacillus bulgaricus strain "I. Bogdanov patent strain tumoronecroticance B51" ATCC #21815, shortly called "LB51", to induce endogenous tumor necrosis factor-alpha (TNFalpha) production in normal mice was evaluated. The priming and triggering activities of the preparation were investigated in combination with lipopolysaccharide (LPS) and live BCG vaccine. Deodan was applied at a dose of 150 mg/kg and various treatment schedules were employed. The serum levels of TNFalpha in treated mice were quantified by ELISA. Oral administration of Deodan at a dose of 150 mg/kg for 1, 3, 10 or 20 consecutive days only enhanced serum TNFalpha levels in treated mice. Maximal TNFalpha levels were reached 6 h after the last application of Deodan. Deodan was effective in priming TNFalpha in mice triggered intravenously (i.v.) with LPS. Deodan triggered the production of TNFalpha in BCG-primed mice. The preparation, however, was not an effective trigger of mice primed intradermally (i.d.) with 1 mug/mouse LPS. These findings suggest that Deodan is both a primer and trigger of endogenous TNFalpha. The advantages of treatment of neoplastic disease with agents which induce endogenous TNFalpha is discussed.
引用
收藏
页码:1355 / 1362
页数:8
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