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中药免疫疗法。II. 体内给予黄芪提取物逆转环磷酰胺诱导的免疫抑制作用

Immunotherapy with Chinese medicinal herbs. II. Reversal of cyclophosphamide-induced immune suppression by administration of fractionated Astragalus membranaceus in vivo.

作者信息

Chu D T, Wong W L, Mavligit G M

机构信息

Department of Clinical Immunology and Biological Therapy, University of Texas System Cancer Center, M.D. Anderson Hospital and Tumor Institute, Houston 77030.

出版信息

J Clin Lab Immunol. 1988 Mar;25(3):125-9.

PMID:3260961
Abstract

A partially purified fraction (F3) with an estimated molecular weight of 20,000 to 25,000 derived from the traditional Chinese medicinal herb Astragalus membranaceus, was found to possess a potent immunorestorative activity in vitro. Its capacity to aborogate the local xenogeneic graft versus host reaction (XGVHR) following injection in vivo was further studied in a newly developed animal model designed for preclinical evaluation of various biological response modifiers. F3 was injected intravenously into cyclophosphamide-primed rats at varied concentrations and schedules prior to grafting of mononuclear cells from healthy normal donors. Maximal abrogation of the local XGVHR mounted by the mononuclear cells, was observed following injection of 5.55 mg of F3 daily for eight days. This abrogation of XGVHR indicates a reversal of the immunosuppressive effect of cyclophosphamide as manifested by a significant decline in the local XGVHR volume from 99.42 +/- 9.2 mm3 (positive control) to 39.78 +/- 8.3 mm3 (p less than 0.001). This reversal of cyclophosphamide-induced immunosuppression by the administration of F3 was complete, since the volume of the abrogated local XGVHR (39.78 +/- 8.3 mm3) was comparable to 34.79 +/- 5.69 mm3 (p greater than 0.1) in the negative control group (no cyclophosphamide-priming; saline injection only). These data indicate that F3 administration markedly enhances the rats' ability to reject the xenogeneic graft and therefore possesses a strong immune potentiating activity in vivo. These preclinical data also provide the rational basis for the use of extracts of Astragalus membranaceus in phase I clinical trials among patients suffering from iatrogenic or inherent immune deficiency states.

摘要

从传统中药黄芪中提取的一种部分纯化组分(F3),估计分子量为20,000至25,000,在体外具有强大的免疫恢复活性。在一种新开发的用于各种生物反应调节剂临床前评估的动物模型中,进一步研究了其在体内注射后消除局部异种移植物抗宿主反应(XGVHR)的能力。在将来自健康正常供体的单核细胞移植之前,以不同浓度和给药方案将F3静脉注射到经环磷酰胺预处理的大鼠体内。在连续八天每天注射5.55 mg F3后,观察到单核细胞引发的局部XGVHR得到最大程度的消除。XGVHR的这种消除表明环磷酰胺免疫抑制作用的逆转,表现为局部XGVHR体积从99.42±9.2 mm3(阳性对照)显著下降至39.78±8.3 mm3(p<0.001)。通过给予F3使环磷酰胺诱导的免疫抑制逆转是完全的,因为消除后的局部XGVHR体积(39.78±8.3 mm3)与阴性对照组(未用环磷酰胺预处理;仅注射生理盐水)中的34.79±5.69 mm3(p>0.1)相当。这些数据表明,给予F3可显著增强大鼠排斥异种移植物的能力,因此在体内具有强大的免疫增强活性。这些临床前数据也为黄芪提取物在医源性或先天性免疫缺陷状态患者的I期临床试验中的应用提供了合理依据。

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