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对聚乙醇酸植入物的免疫反应。

Immune response to polyglycolic acid implants.

作者信息

Santavirta S, Konttinen Y T, Saito T, Grönblad M, Partio E, Kemppinen P, Rokkanen P

机构信息

Helsinki University, Central Hospital, Finland.

出版信息

J Bone Joint Surg Br. 1990 Jul;72(4):597-600. doi: 10.1302/0301-620X.72B4.2166048.

Abstract

Cytological analysis of material aspirated from the effusion which occasionally develops around a polyglycolic acid (PGA) osteosynthesis implant showed a predominance of inflammatory monocytes and in particular lymphocytes. In order to discover whether PGA implants are immunologically inert, density gradient-isolated peripheral blood mononuclear cells were cultured in 0.2 ml of 10% delta FCS-RPMI 1640 culture medium supplemented with 10 mg PGA. Phytohaemagglutinin (PHA) lectin, a purified protein derivate of tuberculin (PPD) antigen and culture medium alone were used as positive and negative controls. We studied lymphocyte activation kinetics on days 0, 1, 3 and 5. Major histocompatibility complex locus II antigen (MHC locus II antigen) and interleukin-2 receptor (IL-2R) expression were analysed using the avidin-biotin-peroxidase complex (ABC) method and lymphocyte DNA synthesis by using 3H-thymidine incorporation and beta-scintillation counting. Especially on culture days 0 and 1, lymphocytes and monocytes were seen by light microscopy to be attached to PGA particles. However, our results show no PGA-induced lymphocyte DNA synthesis, but PGA-induced MHC locus II antigen and IL-2R activation marker expression was seen, greater than in negative controls, but less than that seen in PPD antigen driven lymphocyte response. This suggests that PGA is an immunologically inert implant material, but it does seem to induce inflammatory mononuclear cell migration and adhesion, leading to a slight non-specific lymphocyte activation. This activation is lower than that seen in mitogen and antigen-driven lymphocyte responses.

摘要

对偶尔在聚乙醇酸(PGA)骨合成植入物周围形成的积液进行抽吸物的细胞学分析显示,炎症单核细胞尤其是淋巴细胞占主导。为了探究PGA植入物是否在免疫上呈惰性,将密度梯度分离的外周血单核细胞在0.2 ml添加了10 mg PGA的10% δ胎牛血清 - RPMI 1640培养基中培养。植物血凝素(PHA)凝集素、结核菌素纯化蛋白衍生物(PPD)抗原和仅培养基分别用作阳性和阴性对照。我们在第0、1、3和5天研究淋巴细胞激活动力学。使用抗生物素蛋白 - 生物素 - 过氧化物酶复合物(ABC)方法分析主要组织相容性复合体II类抗原(MHC II类抗原)和白细胞介素 - 2受体(IL - 2R)表达,并通过3H - 胸腺嘧啶核苷掺入和β闪烁计数分析淋巴细胞DNA合成。特别是在培养的第0天和第1天,通过光学显微镜观察到淋巴细胞和单核细胞附着在PGA颗粒上。然而,我们的结果显示没有PGA诱导的淋巴细胞DNA合成,但观察到PGA诱导的MHC II类抗原和IL - 2R激活标志物表达,高于阴性对照,但低于PPD抗原驱动的淋巴细胞反应中的表达。这表明PGA是一种免疫惰性植入材料,但它似乎确实诱导炎症单核细胞迁移和黏附,导致轻微的非特异性淋巴细胞激活。这种激活低于有丝分裂原和抗原驱动的淋巴细胞反应中的激活。

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