[特发性肺纤维化(IPF)患者的炎症】。]

Ivon Rodríguez-Rodríguez, Brayan Leonardo Mesa-Gallo, Yubely Rico-Puentes, Mauricio González, Carlos Alberto Parra-López
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引用次数: 0

摘要

方法我们采集了通过活检或临床标准确诊为 IPF 的 60 岁以上成年患者的外周血样本。进行血浆分离,并使用 CBA 测量促炎细胞因子。这项研究获得了哥伦比亚肺病基金会伦理与研究委员会的批准:结果:与健康的老年人相比,IPF 患者的 IL-4、INFy 和 IL-6 等细胞因子有所增加:炎症性疾病与多种慢性非传染性疾病的发生和并存有关,65 岁以后发病率更高。适应性免疫参与了 IPF 的发病机制,这被描述为 Th1/Th2 淋巴细胞反应的失衡。还需要进一步研究,以确定与 IPF 相关的其他免疫衰老标志物。
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[Inflammageing in patients with idiopathic pulmonary fibrosis (IPF)].

Methods: We took Peripheral blood samples from adult patients over 60 years of age with a confirmed diagnosis of IPF through biopsy or clinical criteria. Plasma separation was performed, and proinflammatory cytokines were measured using CBA. This study received approval from the ethics and research committee of the Colombian Pulmonological Foundation.

Results: Patients with IPF exhibited an increase in cytokines such as IL-4, INFy, and IL-6 compared to healthy older adults.

Conclusion: Inflammatory disease has been associated with the development and coexistence of multiple chronic non-communicable diseases that have a higher incidence after 65 years of age. The involvement of adaptive immunity in the pathogenesis of IPF has been described as an imbalance in the Th1/Th2 lymphocyte response. Further studies are required to identify additional markers of immunosenescence that correlate with IPF.

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