细菌免疫刺激剂(Broncho-Vaxom)对小鼠环磷酰胺免疫抑制的补偿作用。

A Bosch, F Lucena, R Parés, J Jofre
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引用次数: 11

摘要

研究了细菌裂解物Broncho-Vaxom (BV)对环磷酰胺(CY)免疫抑制作用的代偿作用。在CY免疫抑制小鼠中,BV治疗动物血清IgM和IgG以及肠道分泌物IgA和IgG恢复到正常水平的时间明显早于对照组。此外,通过测量胸腺的相对大小来估计,BV治疗小鼠的胸腺正常细胞增殖比对照组小鼠更早实现。口服BV治疗可恢复CY免疫抑制小鼠脾脏中IgM抗SRBC生成细胞的数量。由于CY引起的免疫抑制增加了对各种感染的易感性,我们在免疫抑制的动物身上测试了BV对肺炎链球菌、金黄色葡萄球菌、变ozaenae肺炎克雷伯菌、铜绿假单胞菌和白色念珠菌的IP攻击感染的保护作用。BV导致对肺炎球菌和葡萄球菌攻击感染的抵抗力增强,但对其他攻击微生物没有抵抗力。
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Compensation of cyclophosphamide immunosuppression by a bacterial immunostimulant (Broncho-Vaxom) in mice.

The compensatory effect of a bacterial lysate, Broncho-Vaxom (BV) on the immunosuppressive action of cyclophosphamide (CY) was investigated. In CY immunosuppressed mice, BV treated animals recovered to normal levels of IgM and IgG in serum as well of IgA and IgG in gut secretions significantly earlier than controls. Furthermore, normal cell proliferation in thymus, as estimated by measuring the relative size of this organ was achieved earlier in BV treated mice than in control mice. Oral treatment with BV restores the number of IgM anti SRBC producing cells in spleen, in CY immunosuppressed mice. Since immunosuppression induced by CY increases the susceptibility to various infections, we tested in immunosuppressed animals the protective effect of BV towards IP challenge infections with Streptococcus pneumoniae, Staphylococcus aureus, Klebsiella pneumoniae var ozaenae, Pseudomonas aeruginosa and Candida albicans. BV led to an enhanced resistance towards both pneumococci and staphylococci challenge infections but not to the other challenge microorganisms.

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