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己酮可可碱对单核细胞和T细胞产生肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的不同作用。

Differential effects of pentoxifylline on the production of tumour necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by monocytes and T cells.

作者信息

Schandené L, Vandenbussche P, Crusiaux A, Alègre M L, Abramowicz D, Dupont E, Content J, Goldman M

机构信息

Department of Immunology, Hôpital Erasme, Brussels, Belgium.

出版信息

Immunology. 1992 May;76(1):30-4.

Abstract

Pentoxifylline (PTX) is a methylxanthine compound known to inhibit the production of tumour necrosis factor-alpha (TNF-alpha) by monocytic cells. In this study, we found that PTX differentially regulates the production of TNF-alpha and interleukin-6 (IL-6). Indeed, PTX at high concentrations triggers the production of IL-6 but not of TNF-alpha by peripheral blood mononuclear cells (PBMC). Further experiments indicated that monocytes are responsible for this PTX-induced IL-6 production. When PBMC were stimulated with LPS, PTX was found to inhibit the secretion of TNF-alpha as well as the accumulation of TNF-alpha messenger RNA (mRNA). In contrast, no inhibitory effect was observed on the induction of IL-6. Similar results were obtained when PBMC were stimulated with OKT3 monoclonal antibody (mAb). In addition, the in vivo administration of PTX in transplant patients receiving the first dose of OKT3 allowed to decrease the systemic release of TNF-alpha but not of IL-6. Since monocytes represent a major source of TNF-alpha and IL-6 in these settings, additional experiments were performed in vitro on purified T cells stimulated with the CLB-T3/3, an anti-CD3 mAb which does not require the presence of accessory cells to activate T cells. In this system, PTX was found to inhibit the secretion of both TNF-alpha and IL-6 by T cells. We suggest that cAMP could be involved in these differential effects of PTX on production of TNF-alpha and of IL-6.

摘要

己酮可可碱(PTX)是一种甲基黄嘌呤化合物,已知它可抑制单核细胞产生肿瘤坏死因子-α(TNF-α)。在本研究中,我们发现PTX对TNF-α和白细胞介素-6(IL-6)的产生有不同的调节作用。实际上,高浓度的PTX可触发外周血单核细胞(PBMC)产生IL-6,但不产生TNF-α。进一步的实验表明,单核细胞是PTX诱导IL-6产生的原因。当用脂多糖刺激PBMC时,发现PTX可抑制TNF-α的分泌以及TNF-α信使核糖核酸(mRNA)的积累。相比之下,未观察到对IL-6诱导的抑制作用。当用OKT3单克隆抗体(mAb)刺激PBMC时,也得到了类似的结果。此外,在接受首剂OKT3的移植患者体内给予PTX,可降低TNF-α的全身释放,但不能降低IL-6的全身释放。由于在这些情况下单核细胞是TNF-α和IL-6的主要来源,因此对用CLB-T3/3(一种不需要辅助细胞存在即可激活T细胞的抗CD3 mAb)刺激的纯化T细胞进行了体外额外实验。在这个系统中,发现PTX可抑制T细胞分泌TNF-α和IL-6。我们认为环磷酸腺苷(cAMP)可能参与了PTX对TNF-α和IL-6产生的这些不同作用。

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