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Potentiation of antitumor CTL response by GM-CSF involves a B7-dependent mechanism.

作者信息

Mokyr M B, Kalinichenko T V, Gorelik L

机构信息

Department of Biochemistry, University of Illinois at Chicago 60680, USA.

出版信息

Cell Immunol. 1997 Jun 15;178(2):152-61. doi: 10.1006/cimm.1997.1130.

DOI:10.1006/cimm.1997.1130
PMID:9225006
Abstract

We have previously demonstrated the importance of endogenous GM-CSF production for the B7-2-dependent potentiating effect of exogenous TNF for CTL generation by stimulation cultures of splenic cells from mice bearing a large MOPC-315 tumor. Here we show that addition of GM-CSF to stimulation cultures of such tumor-bearer splenic cells also leads to the generation of enhanced anti-MOPC-315 CTL activity via a B7-dependent mechanism. However, while the potentiating effect of TNF was previously shown to be IL-2-independent, the potentiating effect of GM-CSF is shown here to be completely IL-2-dependent. Still, the potentiating activity of exogenous GM-CSF for the in vitro generation of CTL activity is shown to depend completely on endogenous TNF production. Finally, TNF and GM-CSF may cooperate in enhancing the in vivo generation of CTL activity in MOPC-315 tumor bearers because low-dose melphalan (L-phenylalanine mustard) therapy, which was previously shown to lead to the rapid up-regulation of TNF production at the tumor site and the subsequent TNF-dependent in vivo acquisition of potent CTL activity, is shown here to lead to the rapid up-regulation of GM-CSF production at the tumor site.

摘要

相似文献

1
Potentiation of antitumor CTL response by GM-CSF involves a B7-dependent mechanism.
Cell Immunol. 1997 Jun 15;178(2):152-61. doi: 10.1006/cimm.1997.1130.
2
Insight into the mechanism(s) through which TNF promotes the generation of T cell-mediated antitumor cytotoxicity by tumor bearer splenic cells.深入了解肿瘤携带者脾细胞中肿瘤坏死因子(TNF)促进T细胞介导的抗肿瘤细胞毒性产生的机制。
J Immunol. 1996 Jun 1;156(11):4298-308.
3
Importance of TNF production for the curative effectiveness of low dose melphalan therapy for mice bearing a large MOPC-315 tumor.肿瘤坏死因子(TNF)产生对低剂量美法仑治疗携带大MOPC - 315肿瘤小鼠疗效的重要性。
J Immunol. 1995 Apr 15;154(8):3941-51.
4
Importance of the B7-2 molecule for low dose melphalan-induced acquisition of tumor-eradicating immunity by mice bearing a large MOPC-315 tumor.B7-2分子对携带大剂量MOPC-315肿瘤的小鼠经低剂量美法仑诱导获得肿瘤根除免疫的重要性。
J Immunol. 1998 Feb 15;160(4):1866-74.
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Norepinephrine-mediated inhibition of antitumor cytotoxic T lymphocyte generation involves a beta-adrenergic receptor mechanism and decreased TNF-alpha gene expression.去甲肾上腺素介导的抗肿瘤细胞毒性T淋巴细胞生成的抑制涉及β-肾上腺素能受体机制和肿瘤坏死因子-α基因表达降低。
J Immunol. 1999 Sep 1;163(5):2492-9.
6
Melphalan-induced enhancement of antitumor immune reactivity in thymocytes of adult BALB/c mice bearing a large MOPC-315 tumor.美法仑诱导携带大型MOPC - 315肿瘤的成年BALB/c小鼠胸腺细胞抗肿瘤免疫反应增强。
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4-1BBL cooperates with B7-1 and B7-2 in converting a B cell lymphoma cell line into a long-lasting antitumor vaccine.4-1BBL与B7-1和B7-2协同作用,将一种B细胞淋巴瘤细胞系转化为长效抗肿瘤疫苗。
J Immunol. 1999 Apr 15;162(8):5003-10.
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Importance of Lyt-2+ T-cells in the resistance of melphalan-cured MOPC-315 tumor bearers to a challenge with MOPC-315 tumor cells.Lyt-2+ T细胞在美法仑治愈的MOPC-315肿瘤荷瘤小鼠对MOPC-315肿瘤细胞攻击的抗性中的重要性。
Cancer Res. 1988 Sep 1;48(17):4834-42.
9
Limited importance of CD40/CD40L interaction in the B7-dependent generation of anti-MOPC-315 cytotoxic T lymphocyte activity by tumor bearer splenic cells stimulated in vitro in the presence of tumor necrosis factor.在肿瘤坏死因子存在的情况下体外刺激荷瘤小鼠脾细胞时,CD40/CD40L相互作用在依赖B7产生抗MOPC - 315细胞毒性T淋巴细胞活性方面的重要性有限。
Cancer Immunol Immunother. 1998 Aug;46(6):293-303. doi: 10.1007/s002620050490.
10
Lysis of antigenically unrelated tumor cells mediated by Lyt 2+ splenic T-cells from melphalan-cured MOPC-315 tumor bearers.来自美法仑治愈的MOPC - 315肿瘤荷瘤小鼠的Lyt 2 + 脾T细胞介导的与抗原无关的肿瘤细胞溶解作用。
Cancer Res. 1989 Sep 15;49(18):5007-15.

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