Chumachenko Petr V, Ivanova Alexandra G, Bagheri Ekta Mariam, Omelchenko Andrey V, Sukhorukov Vasily N, Markin Alexander M, Markina Yuliya V, Postnov Anton Y
Petrovsky National Russian Research Center of Surgery, Lane Abrikosovsky, 2, 119991 Moscow, Russia.
National Medical Research Center of Cardiology, Academician Chazova St., 15a, 121552 Moscow, Russia.
J Clin Med. 2023 May 20;12(10):3578. doi: 10.3390/jcm12103578.
It is known that vasa vasorum contributes substantially to the blood supply and nutrition of one-third of the wall of the ascending thoracic aorta. Therefore, we focused on studying the relationship between inflammatory cells and vasa vasorum vessels in patients with aortic aneurysm. The material for the study was biopsies of thoracic aortic aneurysms taken from patients during an aneurysmectomy (34 men, 14 women, aged 33 to 79 years). The biopsies belonged to patients with non-hereditary thoracic aortic aneurysm. An immunohistochemical study was carried out using antibodies to antigens of T cells (CD3, CD4, CD8); macrophages (CD68); B cells (CD20); endothelium (CD31, CD34, von Willebrand factor (vWF)); and smooth muscle cells (alpha actin). Samples without inflammatory infiltrates contained less vasa vasorum in the tunica adventitia than samples with inflammatory infiltrates, and this difference was statistically significant < 0.05. T cell infiltrates in the adventitia of aortic aneurysms were found in 28 of 48 patients. In the vessels of the vasa vasorum, surrounded by inflammatory infiltrates, T cells that adhered to the endothelium were found. The same cells were also localized in the subendothelial area. The number of adherent T cells in patients with inflammatory infiltrates in the aortic wall dominated the number of these cells in patients without inflammation of the aortic wall. This difference was statistically significant, < 0.0006. Hypertrophy and sclerosis of the arteries of the vasa vasorum system, the narrowing of their lumen, and, as a result, impaired blood supply to the aortic wall, were found in 34 patients with hypertension. In 18 patients (both in patients with hypertension and in patients without hypertension), T cells that adhered to the vasa vasorum endothelium were found. In nine cases, massive infiltrates of T cells and macrophages were found, which surrounded and squeezed the vasa vasorum, preventing blood circulation. In six patients, parietal and obturating blood clots were found in the vasa vasorum vessels, which disrupted the normal blood supply to the aortic wall. We believe that this indicates the importance of the state of the vessels of the vasa vasorum in the development of an aortic aneurysm. In addition, pathological changes in these vessels may not always play a primary role, but always a very important role, in the pathogenesis of this disease.
已知滋养血管对胸主动脉升部三分之一管壁的血液供应和营养起着重要作用。因此,我们着重研究主动脉瘤患者炎症细胞与滋养血管之间的关系。研究材料为在动脉瘤切除术中取自患者的胸主动脉瘤活检组织(34名男性,14名女性,年龄33至79岁)。这些活检组织来自非遗传性胸主动脉瘤患者。使用针对T细胞(CD3、CD4、CD8)、巨噬细胞(CD68)、B细胞(CD20)、内皮(CD31、CD34、血管性血友病因子(vWF))和平滑肌细胞(α肌动蛋白)抗原的抗体进行免疫组织化学研究。无炎症浸润的样本外膜中滋养血管比有炎症浸润的样本少,且这种差异具有统计学意义(<0.05)。48例患者中有28例在主动脉瘤外膜发现T细胞浸润。在被炎症浸润包围的滋养血管中,发现了黏附在内皮上的T细胞。同样的细胞也定位于内皮下区域。主动脉壁有炎症浸润患者中黏附T细胞的数量多于无主动脉壁炎症患者中这些细胞的数量。这种差异具有统计学意义(<0.0006)。34例高血压患者发现滋养血管系统动脉肥大和硬化,管腔狭窄,进而导致主动脉壁血液供应受损。18例患者(包括高血压患者和非高血压患者)在滋养血管内皮发现黏附的T细胞。9例发现大量T细胞和巨噬细胞浸润,它们包围并挤压滋养血管,阻碍血液循环。6例患者在滋养血管中发现壁层和闭塞性血凝块,破坏了主动脉壁的正常血液供应。我们认为这表明滋养血管状态在主动脉瘤发生发展中的重要性。此外,这些血管的病理变化在该疾病的发病机制中可能并不总是起主要作用,但始终起着非常重要的作用。