lps处理的肿瘤患者巨噬细胞的干扰素释放。

R A Merendino, A Arena, S Zummo, M Mesiti, S Chillemi, L Bonina
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引用次数: 0

摘要

针对LPS对免疫活性细胞的调节作用,研究了人γ干扰素(HUIFN γ)诱导巨噬细胞产生干扰素的过程。特别是,在自体血清或健康供体血清中分化的乳腺癌患者的引物巨噬细胞产生的IFN与健康供体巨噬细胞产生的IFN进行了比较。内毒素诱导的IFN水平通过注入HUIFN γ增强。大肠杆菌LPS的“体外”治疗恢复了从乳腺癌患者获得的巨噬细胞的干扰素产生,这些巨噬细胞在健康供体血清的存在下分化。此外,LPS处理来自患者的巨噬细胞,在自体血清中分化,不影响这些细胞的干扰素产生。然而,与来自乳腺癌患者的巨噬细胞相比,来自健康供体的巨噬细胞似乎对LPS治疗更敏感。
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Interferon release by LPS-treated macrophages from patients affected by neoplasia.

Concerning the modulatory role of LPS on immunocompetent cells, the production of interferon by macrophages primed with human gamma interferon (HUIFN gamma), was studied. In particular the production of IFN from primed macrophages of patients affected by breast cancer, differentiated in presence of autologous serum or in serum from healthy donors, was compared with the IFN production from macrophages of healthy donors. The levels of endotoxin-induced IFN were enhanced by priming macrophages with HUIFN gamma. The "in vitro" treatment with Escherichia coli LPS restores the interferon production of primed macrophages, obtained from patients affected by breast cancer, differentiated in presence of serum from healthy donors. Moreover, LPS treatment of primed macrophages from patients, differentiated in autologous serum, did not influence the interferon production of these cells. Nevertheless, primed macrophages from healthy donors appeared to be more sensitive to LPS treatment in comparison with primed macrophages from patients affected by breast cancer.

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