根尖周病变发生机制的细菌学和免疫学研究。芽孢杆菌细胞成分在根尖周围病变中的免疫生物学活性和定位。

N Tani
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引用次数: 0

摘要

人们强烈认为,根尖周围病变是免疫病理反应对持续抗原刺激的结果。来自根管系统的细菌可能是最重要的发病机制,能够诱导根尖周围组织的免疫反应。因此,本研究的目的是明确从慢性根尖周病变的根管中分离到的buccae (B. buccae)的免疫潜力。研究了脂多糖(LPS)和细胞蛋白等细胞成分在促进单核细胞迁移、诱导白细胞介素1 (IL-1)产生、有丝分裂性和多克隆B细胞活化方面的生物学活性。采用生物素-亲和素-辣根过氧化物酶法和过氧化物酶抗过氧化物酶单克隆抗体法检测人慢性根尖周病变组织中免疫活性细胞和芽孢杆菌的定位。得到以下结果:1. 在鲎试剂的凝血活性和施瓦兹曼活性方面,布氏杆菌的LPS约为鼠伤寒沙门菌的一半。2. LPS和38K蛋白制剂均能增强人外周血单核细胞的迁移活性,诱导IL-1的产生。3.结果发现,buccae LPS对BALB/c和BALB/c nu/nu小鼠脾细胞的有丝分裂性弱于38K蛋白,而对胸腺细胞的有丝分裂性在两种制剂中均未表现出来。4. 38K蛋白显著诱导BALB/c nu/nu小鼠多克隆B细胞活化BALB/c nu/nu小鼠脾细胞,但LPS诱导的活化作用弱于38K蛋白。5. 由此推测,B. buccae的LPS和38K蛋白可能都依赖于巨噬细胞和淋巴细胞的活性。6. 在结缔组织的巨噬细胞和细胞间隙中发现了最常见的布氏杆菌抗原物质。7. 吞噬性巨噬细胞(泡沫细胞)周围密集聚集T淋巴细胞和B淋巴细胞,巨噬细胞周围B淋巴细胞数量大于T淋巴细胞。8. 这些结果表明,脂多糖和38K蛋白都具有广泛的免疫生物学调控功能。因此,我们认为脂多糖和38K蛋白可能在根尖周病变的发病机制中发挥重要作用。
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[Bacteriological and immunological studies on the mechanism of development of periapical lesion. Immunobiological activities and localization in periapical lesion of the cellular components from Bacteroides buccae].

It has been strongly suggested that the periapical lesion develop as a result of immunopathological response to continuous antigenic stimulation. Bacteria from root canal systems might be most important pathogenesis capable of inducing immunological reactions in periapical tissue. The purpose of this study, therefore, was clarify the immunological potentials of Bacteroides buccae (B. buccae) which was frequently isolated from root canals with chronic periapical lesion. Biological activities of B. buccae cellular components, such as lipopolysaccharides (LPS) and cellular protein were investigated on the enhancement of monocytes migration induction of interleukin 1 (IL-1) production, mitogenicity and polyclonal B cell activation. The localization of immunocompetent cells and B. buccae in human chronic periapical lesions were examined by biotin-avidin-horseradish peroxidase method, and peroxidase antiperoxidase methods using monoclonal antibodies. Following results were obtained. 1. On the lymulus lysafe clotting activity and Shwarzman activity of B. buccae LPS were about half of Salmonella typhimurium (S. typhimurium). 2. Both LPS and 38K protein preparations from B. buccae enhanced the activity of human peripheral monocytes migration and induced IL-1 production. 3. It was found that mitogenicity of LPS from B. buccae on splenocytes of BALB/c and BALB/c nu/nu mice was weaker than that of 38K protein, however mitogenicity on thymocytes were not shown in both preparations. 4. The polyclonal B cell activation on splenocytes of BALB/c nu/nu mice by B. buccae were remarkably induced by 38K protein, but LPS showed less activity elicit than 38K protein. 5. It might be suggested that the both LPS and 38K protein of B. buccae may depend on the activities of macrophage and lymphocytes. 6. Antigenic substance of B. buccae were found most commonly engulfed materials within macrophage and intercellular space in connective tissue. 7. Dense accumulation of T and B lymphocytes were observed gathering around the phagocytic macrophage (foam cell), the number of B lymphocytes around the macrophage was greater than that of T lymphocytes. 8. These findings indicated that both LPS and 38K protein from B. buccae have a wide regulation function of immunobiologic responses. Therefore, it was suggested that both LPS and 38K protein from B. buccae may play significant roles in the pathogenesis of periapical lesion.

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