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临床有效的单克隆抗体3F8介导多形核白细胞对人神经外胚层肿瘤细胞的非氧化裂解。

Clinically effective monoclonal antibody 3F8 mediates nonoxidative lysis of human neuroectodermal tumor cells by polymorphonuclear leukocytes.

作者信息

Kushner B H, Cheung N K

机构信息

Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

Cancer Res. 1991 Sep 15;51(18):4865-70.

PMID:1654202
Abstract

Most studies of antibody-dependent cellular cytotoxicity (ADCC) by polymorphonuclear leukocytes (PMN) have supported oxidative lytic processes. This may be because the studies used nonhuman or nonneoplastic cells that were highly sensitive to reactive oxygen species or were small enough to be phagocytosed by PMN. We therefore investigated whether oxygen radicals participate in PMN cytotoxicity toward human neuroectodermal solid tumor cells sensitized by 3F8, which is an anti-ganglioside GD2 murine IgG3 monoclonal antibody with documented anticancer activity in humans. A 4-h 51Cr release assay was used to assess tumor cell lysis by hydrogen peroxide, superoxide, and hypochlorite. Nine of 11 GD2(+) human melanoma and neuroblastoma cell lines had equal or greater resistance to these oxidants as compared to a GD2(-) human carcinoma line (SKBr1-III) found by others (and confirmed by us) to be significantly more resistant to oxidative lysis than a murine cell line (P388D1) representative of those commonly used in cytotoxicity assays. To facilitate detection of oxidant-mediated lysis, subsequent studies of 3F8-mediated ADCC used GD2(+) targets that were relatively sensitive and others that were relatively resistant to oxygen radicals. Normal PMN and PMN obtained from children with chronic granulomatous disease, which do not generate reactive oxygen species, were equally effective in ADCC. Granulocyte-macrophage colony-stimulating factor, which primes oxidative responses of normal but not of chronic granulomatous disease PMN, enhanced ADCC by both kinds of PMN. During ADCC of 3F8-sensitized targets, with or without granulocyte-macrophage colony-stimulating factor, GD2(-) "innocent bystander" tumor cells (including P388D1) were not lysed, a finding consistent with unimportant extracellular release of cytotoxic mediators. Finally, antioxidant and antimyeloperoxidase moieties did not block ADCC. We conclude that oxidants are not key factors in 3F8-mediated lysis by PMN of human neuroectodermal tumor cells.

摘要

大多数关于多形核白细胞(PMN)介导的抗体依赖性细胞毒性(ADCC)的研究都支持氧化溶解过程。这可能是因为这些研究使用的是非人类或非肿瘤细胞,它们对活性氧高度敏感,或者小到足以被PMN吞噬。因此,我们研究了氧自由基是否参与PMN对经3F8致敏的人神经外胚层实体瘤细胞的细胞毒性作用,3F8是一种抗神经节苷脂GD2的鼠IgG3单克隆抗体,在人类中具有已证实的抗癌活性。采用4小时51Cr释放试验来评估过氧化氢、超氧化物和次氯酸盐对肿瘤细胞的裂解作用。与其他人(并经我们证实)发现的一种GD2(-)人癌细胞系(SKBr1-III)相比,11种GD2(+)人黑色素瘤和神经母细胞瘤细胞系中有9种对这些氧化剂具有同等或更高的抗性,该GD2(-)人癌细胞系对氧化溶解的抗性明显高于一种常用于细胞毒性试验的鼠细胞系(P388D1)。为便于检测氧化剂介导的裂解作用,随后对3F8介导的ADCC的研究使用了对氧自由基相对敏感和相对抗性的GD2(+)靶细胞。正常PMN和从慢性肉芽肿病患儿获得的不产生活性氧的PMN在ADCC中同样有效。粒细胞巨噬细胞集落刺激因子可引发正常PMN而非慢性肉芽肿病PMN的氧化反应,它增强了这两种PMN的ADCC作用。在对3F8致敏靶细胞进行ADCC的过程中,无论有无粒细胞巨噬细胞集落刺激因子,GD2(-)“无辜旁观者”肿瘤细胞(包括P388D1)均未被裂解,这一发现与细胞毒性介质的细胞外释放不重要一致。最后,抗氧化剂和抗髓过氧化物酶部分并未阻断ADCC。我们得出结论,氧化剂不是PMN对人神经外胚层肿瘤细胞进行3F8介导的裂解作用的关键因素。

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