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COPD 肺组织中的嗜酸性粒细胞、嗜碱性粒细胞和 2 型免疫微环境。

Eosinophils, basophils and type 2 immune microenvironments in COPD-affected lung tissue.

机构信息

Dept of Experimental Medical Science, Lund University, Lund, Sweden.

Medetect AB, Lund, Sweden.

出版信息

Eur Respir J. 2020 May 7;55(5). doi: 10.1183/13993003.00110-2019. Print 2020 May.

Abstract

Although elevated blood or sputum eosinophils are present in many patients with COPD, uncertainties remain regarding the anatomical distribution pattern of lung-infiltrating eosinophils. Basophils have remained virtually unexplored in COPD. This study mapped tissue-infiltrating eosinophils, basophils and eosinophil-promoting immune mechanisms in COPD-affected lungs.Surgical lung tissue and biopsies from major anatomical compartments were obtained from COPD patients with severity grades Global Initiative for Chronic Obstructive Lung Disease stages I-IV; never-smokers/smokers served as controls. Automated immunohistochemistry and hybridisation identified immune cells, the type 2 immunity marker GATA3 and eotaxins (CCL11, CCL24).Eosinophils and basophils were present in all anatomical compartments of COPD-affected lungs and increased significantly in very severe COPD. The eosinophilia was strikingly patchy, and focal eosinophil-rich microenvironments were spatially linked with GATA3 cells, including type 2 helper T-cell lymphocytes and type 2 innate lymphoid cells. A similarly localised and interleukin-33/ST2-dependent eosinophilia was demonstrated in influenza-infected mice. Both mice and patients displayed spatially confined eotaxin signatures with CCL11 fibroblasts and CCL24 macrophages.In addition to identifying tissue basophilia as a novel feature of advanced COPD, the identification of spatially confined eosinophil-rich type 2 microenvironments represents a novel type of heterogeneity in the immunopathology of COPD that is likely to have implications for personalised treatment.

摘要

虽然许多 COPD 患者的血液或痰液中存在嗜酸性粒细胞升高,但肺浸润嗜酸性粒细胞的解剖分布模式仍存在不确定性。嗜碱性粒细胞在 COPD 中几乎未被探索。本研究描绘了 COPD 受累肺组织中浸润性嗜酸性粒细胞、嗜碱性粒细胞和嗜酸性粒细胞促进免疫机制的分布。从 COPD 患者(全球慢性阻塞性肺疾病倡议分期 I-IV 级)的主要解剖部位获得手术肺组织和活检,从不吸烟者/吸烟者中获得对照。自动化免疫组织化学和杂交鉴定了免疫细胞、2 型免疫标志物 GATA3 和嗜酸性粒细胞趋化因子(CCL11、CCL24)。嗜酸性粒细胞和嗜碱性粒细胞存在于 COPD 受累肺的所有解剖部位,在非常严重的 COPD 中显著增加。嗜酸性粒细胞增多呈明显斑片状,富含嗜酸性粒细胞的局灶性微环境与 GATA3 细胞(包括 2 型辅助 T 细胞和 2 型固有淋巴细胞)空间相关。在流感感染的小鼠中也观察到类似的局部和白细胞介素-33/ST2 依赖性嗜酸性粒细胞增多。小鼠和患者均显示出空间受限的嗜酸性粒细胞趋化因子特征,与成纤维细胞的 CCL11 和巨噬细胞的 CCL24 相关。除了将组织嗜碱性粒细胞鉴定为晚期 COPD 的一个新特征外,鉴定空间受限的富含嗜酸性粒细胞的 2 型微环境代表了 COPD 免疫病理学中的一种新型异质性,这可能对个体化治疗具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7562/7236868/63927170d9cc/ERJ-00110-2019.01.jpg

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