Enhancement of anti-tumor immunity by lipoteichoic acid-related molecule isolated from OK-432, a streptococcal agent, in athymic nude mice bearing human salivary adenocarcinoma: Role of natural killer cells

被引:0
作者
Okamoto, M
Ohe, G
Furuichi, S
Nishikawa, H
Oshikawa, T
Tano, T
Ahmed, SU
Yoshida, H
Moriya, Y
Matsubara, S
Ryoma, Y
Saito, M
Sato, M
机构
[1] Univ Tokushima, Sch Med, Dept Oral & Maxillofacial Surg 2, Tokushima 1108504, Japan
[2] Chugai Pharmaceut Co Ltd, Prod Res Labs, Toshima Ku, Tokyo 1718545, Japan
关键词
OK-432; lipoteichoic acid; nude mice; NK cells; anti-tumor immunity;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: OK-PSA, a lipoteichoic acid (LTA)-related molecule isolated from a streptococcal agent OK-432, enhances anti-tumor immunity as a potent inducer of Th1-type cytokines. Recently, we obtained the data suggesting that natural killer (NK) cells may play a significant role for OK-PSA-induced cytokine production in vitro. Materials and Methods: We conducted the animal experiments using athymic nude mice beating human salivary adenocarcinoma to examine the role of NK cells in OK-PSA-induced anti-tumor immunity. OK-PSA was peritumorally injected into the mice. Cytokines in the sera were analyzed by ELISA. mRNAs for cytokines were detected by RT-PCR. Cr-51 release test was performed to measure killer cell acticities. Results: OK-PSA markedly increased the amounts of IFN-gamma, tumor necrosis factor (TNF)-alpha, interleukin (IL)-2, IL-12 and IL-18 that are generally called "Th1-type cytokines" in the sera derived from tumor-beating nude mice, and also accelerated the killing activities of tumor-infiltrating lymphocytes as well as of draining lymph node cells. Furthermore, OK-PSA administration resulted in significant inhibition of tumor growth, but the effect of OK-PSA was almost completely inhibited by the deletion of NK cells using anti-asialo GM(1) antibody. Conclusion: These findings strongly suggested that NK cells are closely involved in OK-PSA-mediated anti-tumor immunity.
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页码:3229 / 3239
页数:11
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