口腔黏膜的免疫病理学。口腔免疫系统——炎症反应——肿瘤——“标记物”——病毒鉴定。

T Löning
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引用次数: 0

摘要

本研究涉及口腔修复和炎症反应,良性上皮增生和恶性病变及其前期。在对正常口腔黏膜进行检查的基础上,采用光镜和电镜对患病人口腔黏膜的活检和手术标本进行了研究。此外,还建立了口腔创面愈合和癌变的实验模型。结合形态学(免疫荧光、免疫细胞化学、电镜)和生化(SDS -聚丙烯酰胺凝胶电泳)技术对口腔黏膜上皮细胞和非上皮细胞的分化和功能进行了研究。临床病理学。从汉堡大学皮肤科诊所的档案中收集了725例口腔病变。在这些病变中,上皮增生和瘤变是口腔粘膜最常见的病变。癌前病变发生率(3.7%)与文献报道的百分比一致。在冷冻或戊二醛固定的组织样本中,免疫组织学和超微结构方法的价值被检查,特别是关于反应性炎症过程与真正的恶性前病变和恶性病变的区别,并特别参考上皮和非上皮肿瘤的鉴别诊断。举例说明了炎性病变的免疫学特征和肿瘤的组织遗传学分型。正常口腔黏膜。角蛋白丝的生化和形态学研究表明,基底上皮和上基底上皮含有不同的角蛋白多肽,这与细胞分化程度有关。这些细胞骨架修饰被认为与细胞膜分化有关,这是由不同的凝集素对上皮基底室和基底上室的亲和力所证明的。在上皮-间质界面处出现了由基底上皮细胞(如层粘连蛋白)和结缔组织细胞产生的大分子物质(如纤维连接蛋白),导致基底膜区形成。免疫能态细胞是正常口腔黏膜的常规成分。在上皮内,抑制型/细胞毒性表型的朗格汉斯细胞和T淋巴细胞被证明是主要的炎症细胞。B淋巴细胞,T淋巴细胞的抑制/细胞毒性和辅助/诱导表型和典型的巨噬细胞代表结缔组织的细胞元件。所有这些非上皮细胞均含有静脉蛋白丝。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Immunopathology of the oral mucosa. Oral immune system--inflammatory reactions--tumor-"marker"--virus identification].

The present study was concerned with oral reparative and inflammatory reactions, benign epithelial proliferations and malignant lesions including their prestages. Following investigations of normal oral mucosa, biopsy and surgical specimens of diseased human oral mucosa were studied with light and electron microscopical methods. In addition, experimental models of oral wound healing and carcinogenesis were developed. Combining morphological (immunofluorescence, immunocytochemistry, electron microscopy) and biochemical (SDS polyacrylamide gel electrophoresis) techniques differentiation and function of epithelial and non-epithelial cells of the oral mucosa were investigated. Clinical pathology. 725 oral lesions were collected from the files of the Dermatological Clinic of the University of Hamburg. Among these lesions epithelial hyperplasias and neoplasias represented the most frequent alterations of the oral mucosa. The incidence of premalignant lesions (3.7%) was consistent with the percentages reported in the literature. On frozen or glutaraldehyde-fixed tissue samples the value of immunohistological and ultrastructural methods was examined with particular respect to the distinction of reactive inflammatory processes from true premalignant and malignant lesions and with special reference to the differential diagnosis of epithelial and non-epithelial tumours. Examples were given for immunological characterization of inflammatory lesions and for histogenetical typing of neoplasias. Normal oral mucosa. Biochemical and morphological investigations of keratin filaments showed that basal and suprabasal epithelia contain different keratin polypeptides related to the degree of cell differentiation. These cytoskeletal modifications were seen to be associated with cell membrane differentiations which was demonstrated by different lectin affinities to basal and suprabasal compartments of epithelium. At the epithelial-mesenchymal interfaces macromolecular substances appeared (e.g. fibronectin) which are produced by basal epithelia (e.g. laminin) and connective tissue cells leading to the formation of the basement membrane zone. Immune competent cells were seen to be regular components of normal oral mucosa. Within the epithelium Langerhans cells and T lymphocytes of the suppressor/cytotoxic phenotype were shown to be the predominant inflammatory cells. B lymphocytes, T lymphocytes of the suppressor/cytotoxic and helper/inducer phenotypes and typical macrophages represented cellular elements of the connective tissue. All these non-epithelial cells were found to contain vimentin filaments.(ABSTRACT TRUNCATED AT 400 WORDS)

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