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慢性过敏性肺炎中支气管相关淋巴组织的发育

Development of bronchus-associated lymphoid tissue in chronic hypersensitivity pneumonitis.

作者信息

Suda T, Chida K, Hayakawa H, Imokawa S, Iwata M, Nakamura H, Sato A

机构信息

2nd Division of Internal Medicine, Hamamatsu University School of Medicine, Japan.

出版信息

Chest. 1999 Feb;115(2):357-63. doi: 10.1378/chest.115.2.357.

Abstract

STUDY OBJECTIVES

Bronchus-associated lymphoid tissue (BALT) is well defined in animals. In humans, however, BALT has been reported to be inducible under pathologic conditions, such as chronic respiratory infection, although it is not present in healthy adults. Thus, induced BALT is considered to be involved in the mucosal immunity of the human lung under these conditions. However, there have been few studies to investigate BALT development in hypersensitivity pneumonitis. The aim of this study was to examine the presence of BALT in hypersensitivity pneumonitis, especially in its chronic form.

METHODS

The subjects included five patients with chronic hypersensitivity pneumonitis (CHP) diagnosed from clinical and histologic findings. We investigated histologically the development of BALT in these patients. Further, the cellular distribution of BALT was also examined by immunohistochemistry.

RESULTS

BALT was present in three of five patients with CHP. Immunohistochemical examination revealed the follicular area of BALT to be composed mainly of B cells, while the parafollicular area comprised predominantly T cells. Centroblasts located in the germinal center of BALT expressed Ki-67 antigen, a marker of cell proliferation, suggesting that these cells were actively proliferating after antigenic stimulation. Cells expressing bcl-2, which is present primarily on memory B cells, were confined to the follicular area, devoid of any germinal centers. S-100-positive, CD1a-negative interdigitating dendritic cells were observed in the dome area of BALT.

CONCLUSIONS

These observations suggest that chronic antigenic stimulation and/or inflammation in CHP may cause BALT development, which, in turn, is likely to play an important role in the mucosal immune response of this disease.

摘要

研究目的

支气管相关淋巴组织(BALT)在动物中已有明确界定。然而,在人类中,尽管健康成年人不存在BALT,但据报道在诸如慢性呼吸道感染等病理条件下可诱导产生BALT。因此,在这些情况下,诱导产生的BALT被认为参与了人类肺部的黏膜免疫。然而,关于超敏性肺炎中BALT发育的研究较少。本研究的目的是检查超敏性肺炎,尤其是慢性形式的超敏性肺炎中BALT的存在情况。

方法

研究对象包括5例根据临床和组织学检查结果诊断为慢性超敏性肺炎(CHP)的患者。我们对这些患者的BALT发育进行了组织学研究。此外,还通过免疫组织化学检查了BALT的细胞分布。

结果

5例CHP患者中有3例存在BALT。免疫组织化学检查显示,BALT的滤泡区主要由B细胞组成,而滤泡旁区主要由T细胞组成。位于BALT生发中心的中心母细胞表达细胞增殖标志物Ki-67抗原,表明这些细胞在抗原刺激后正在积极增殖。主要存在于记忆B细胞上的bcl-2表达细胞局限于滤泡区,没有任何生发中心。在BALT的圆顶区观察到S-100阳性、CD1a阴性的交错突细胞。

结论

这些观察结果表明,CHP中的慢性抗原刺激和/或炎症可能导致BALT发育,而BALT反过来可能在该疾病的黏膜免疫反应中发挥重要作用。

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