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用链球菌制剂OK-432刺激血液单核细胞产生的细胞因子:通过在培养基中补充异种血清对其产生的影响。

Cytokines produced by blood mononuclear cells stimulated with the streptococcal preparation OK-432: effect on production by supplementing the medium with xenogeneic serum.

作者信息

Fujii M, Abo T, Kumagai K

机构信息

Department of Microbiology, Tohoku University School of Dentistry, Sendai, Japan.

出版信息

Cancer Immunol Immunother. 1988;27(2):97-102. doi: 10.1007/BF00200011.

Abstract

Human blood MNC were stimulated for 7 days with a streptococcal preparation, OK-432, in a medium supplemented with either 10% autologous serum (autoserum) or 10% FCS. Cytokines, including IL-2, IL-1, IFN, and TNF in the supernatants, and antitumor cytotoxicity of MNC were analyzed. None of the IL-2 was detectable during the culture in medium with autoserum, although significant enhancement of cytotoxicity was observed at day 1. On the other hand, production of IL-2 and higher cytotoxicity were induced in the medium with FCS. Even a control culture of MNC unstimulated with OK-432 in the medium with FCS, showed a slight but significant amount of IL-2 and considerable cytotoxicity. However, such a culture in the medium with autoserum showed no such IL-2 production or cytotoxicity. The cytotoxicity induced in the medium with FCS was significantly inhibited by the addition of anti-IL-2 antibody to the culture as well as by the addition of anti-IFN gamma antibody, whereas the cytotoxicity in the medium with autoserum was not inhibited at all by anti-IL-2 antibody. Therefore, the cytotoxicity induced in the medium with FCS included IL-2-induced killer activity, i.e., LAK activity. Similarly, the levels of IL-1, IFN, and TNF production in the supernatants were variable depending on the serum used to supplement the medium. The nonspecific production of IL-2 and the unexpected induction of cytotoxicity were consistently provoked in the medium using several different lots of FCS, but not in the medium with human allogeneic sera or pooled AB serum nor in that with autoserum. It was revealed that the source of sera used to supplement the medium is an important factor affecting the results of analysis of cytokine production and cytotoxicity of MNC induced by certain stimulants.

摘要

人血单核细胞在补充有10%自体血清(自身血清)或10%胎牛血清的培养基中,用链球菌制剂OK-432刺激7天。分析上清液中的细胞因子,包括白细胞介素-2(IL-2)、白细胞介素-1(IL-1)、干扰素(IFN)和肿瘤坏死因子(TNF),以及单核细胞的抗肿瘤细胞毒性。在含有自身血清的培养基培养期间,未检测到任何IL-2,尽管在第1天观察到细胞毒性有显著增强。另一方面,在含有胎牛血清的培养基中诱导产生了IL-2并具有更高的细胞毒性。即使是在含有胎牛血清的培养基中未用OK-432刺激的单核细胞对照培养物,也显示出少量但显著量的IL-2和相当的细胞毒性。然而,在含有自身血清的培养基中的这种培养物未显示出这种IL-2产生或细胞毒性。向含有胎牛血清的培养基中的培养物中添加抗IL-2抗体以及添加抗IFNγ抗体,均可显著抑制其中诱导的细胞毒性,而含有自身血清的培养基中的细胞毒性完全不受抗IL-2抗体的抑制。因此,在含有胎牛血清的培养基中诱导的细胞毒性包括IL-2诱导的杀伤活性,即淋巴因子激活的杀伤细胞(LAK)活性。同样,上清液中IL-1、IFN和TNF的产生水平因用于补充培养基的血清而异。使用几种不同批次的胎牛血清在培养基中持续引发IL-2的非特异性产生和细胞毒性的意外诱导,但在含有人同种异体血清或混合AB血清的培养基中以及含有自身血清的培养基中则未出现这种情况。结果表明,用于补充培养基的血清来源是影响某些刺激物诱导的单核细胞细胞因子产生分析结果和细胞毒性的重要因素。

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