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龈沟白细胞迁移的体内测定。其发展与潜在应用。

In vivo assay of crevicular leukocyte migration. Its development and potential applications.

作者信息

Iacono V J, Singh S, Golub L M, Ramamurthy N S, Kaslick R

出版信息

J Periodontol. 1985 Nov;56(11 Suppl):56-62. doi: 10.1902/jop.1985.56.11s.56.

Abstract

Defects in neutrophil or polymorphonuclear leukocyte (PMNL) chemotaxis have been observed in a number of clinical conditions, including Down's syndrome and insulin-dependent diabetes mellitus (IDDM), which tend to be associated with severe forms of periodontal disease. In addition, impaired PMNL chemotaxis is frequently detected in individuals with localized juvenile periodontitis (LJP). The ability to monitor PMNL function in vivo at the gingival sulcus should therefore be useful as a diagnostic test. In this regard, we developed a technique which measures the response of PMNLs to a chemotactic agent, e.g., casein and N-formylmethionylleucylphenylalanine (N-FMLP) placed directly into gingival crevices. The development of the technique and its relationship to in vitro assays of chemotaxis are discussed, and data obtained from tests of the assay on control and streptozotocin-induced diabetic rats and human subjects with various periodontal diseases and IDDM are presented. As compared with healthy subjects and control animals, atypical (double peak) and reduced crevicular PMNL response patterns were observed during oral and systemic diseases. This suggests that the in vivo assay with appropriate modifications can be used diagnostically to assess PMNL migratory dysfunction and to identify individuals who may be susceptible to severe forms of periodontal disease.

摘要

在许多临床病症中都观察到了中性粒细胞或多形核白细胞(PMNL)趋化性的缺陷,包括唐氏综合征和胰岛素依赖型糖尿病(IDDM),这些病症往往与严重形式的牙周病相关。此外,在局限性青少年牙周炎(LJP)患者中经常检测到PMNL趋化性受损。因此,在体内监测牙龈沟处PMNL功能的能力作为一种诊断测试应该是有用的。在这方面,我们开发了一种技术,该技术可测量PMNL对趋化剂(如直接置于牙龈裂隙中的酪蛋白和N-甲酰甲硫氨酰亮氨酰苯丙氨酸(N-FMLP))的反应。本文讨论了该技术的开发及其与趋化性体外测定的关系,并展示了对对照大鼠和链脲佐菌素诱导的糖尿病大鼠以及患有各种牙周病和IDDM的人类受试者进行该测定试验所获得的数据。与健康受试者和对照动物相比,在口腔和全身性疾病期间观察到了非典型(双峰)和龈沟内PMNL反应模式降低的情况。这表明经过适当改进的体内测定法可用于诊断评估PMNL迁移功能障碍,并识别可能易患严重形式牙周病的个体。

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