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Mistletoe lectin I-induced effects on human cytotoxic lymphocytes. I. Synergism with IL-2 in the induction of enhanced LAK cytotoxicity.

作者信息

Baxevanis C N, Voutsas I F, Soler M H, Gritzapis A D, Tsitsilonis O E, Stoeva S, Voelter W, Arsenis P, Papamichail M

机构信息

Cancer Immunology and Immunotherapy Center, St. Savas Cancer Hospital, Athens, Greece.

出版信息

Immunopharmacol Immunotoxicol. 1998 Aug;20(3):355-72. doi: 10.3109/08923979809034819.

DOI:10.3109/08923979809034819
PMID:9736441
Abstract

This report demonstrates that in vitro activation of human cells with the beta-galactoside-specific lectin from mistletoe (ML-I) or interleukin-2 (IL-2) results in different patterns of activation and function of cytotoxic cells. It is now well established that natural killer (NK) and lymphokine-activated killer (LAK) cytotoxicity is mainly mediated by resting (NK) and IL-2-activated (LAK) CD56-positive (+) cells respectively. Culture of peripheral blood lymphocytes (PBL) for 3 days with ML-I led to expansion and activation of T cells which demonstrated NK- and LAK-like cytotoxicity. T lymphocyte subset analysis revealed that in total PBL, ML-I preferentially stimulated and expanded CD8+ T cells which mediated the cytotoxic effect. Incubation of highly purified CD8+ T cells alone with ML-I did not lead to induction of cytotoxicity, which required the presence of both CD4+ and CD14+ (monocytes) cells, suggesting that ML-I does not exert a direct effect on CD8+ T cells. Activation of PBL with both ML-I and IL-2 resulted in simultaneous induction of T and CD56+ cell-mediated NK and LAK cytotoxicity. These data suggest that treatment with ML-I and IL-2 might provide an approach to induce maximum cytotoxicity against tumors and to recruit both T and NK cells for tumor therapy.

摘要

相似文献

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引用本文的文献

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Evid Based Complement Alternat Med. 2005 Mar;2(1):59-67. doi: 10.1093/ecam/neh058. Epub 2005 Jan 28.
2
Recombinant mistletoe lectin induces p53-independent apoptosis in tumour cells and cooperates with ionising radiation.重组槲寄生凝集素可诱导肿瘤细胞发生不依赖p53的凋亡,并与电离辐射协同作用。
Br J Cancer. 2003 Jun 2;88(11):1785-92. doi: 10.1038/sj.bjc.6600982.