生物制剂在儿童结缔组织病相关间质性肺病中的应用研究进展
Research Progress of Biologics and Antifibrosis Therapy in Children with Connective Tissue Disease-Associated Interstitial Lung Disease
DOI: 10.12677/ACM.2023.132322, PDF,   
作者: 龚 玲*, 舒 畅#:重庆医科大学附属儿童医院呼吸科,国家儿童健康与疾病临床医学研究中心,儿童发育疾病研究教育部重点实验室,儿科学重庆市重点实验室,重庆
关键词: 结缔组织病间质性肺病生物制剂儿童Connective Tissue Disease Interstitial Lung Disease Biologics Children
摘要: 间质性肺病(ILD)可源于多种不同病因,较常见于结缔组织病(CTD)的肺部并发症,这类并发症可统称为结缔组织病相关间质性肺病(CTD-ILD)。在儿童患者中,CTD-ILD早期症状不明显,容易被忽视,可能进展为肺纤维化,从而降低患儿生存质量、影响预后。目前儿童CTD-ILD尚无明确统一的诊疗指南,但多数研究者认为对于激素联合免疫抑制剂治疗效果欠佳或无效的CTD-ILD患儿,生物制剂将是一种安全有效的治疗选择,且可延缓病情进展及肺功能的恶化。本文总结了现有的生物制剂在成人及儿童CTD-ILD的相关研究,为其在儿童CTD-ILD中的进一步应用提供参考依据。
Abstract: Interstitial lung disease (ILD) can be derived from many different etiologies, and is common in the lung complications of connective tissue disease (CTD), which can be collectively referred to as con-nective tissue disease-associated interstitial lung disease (CTD-ILD). In children, the early symp-toms of CTD-ILD are not obvious and easy to be ignored, which may lead to the progression of pul-monary fibrosis, reduce the quality of life of children and affect the prognosis. At present, there are no clear and unified guidelines for the diagnosis and treatment of pediatric CTD-ILD, but most re-searchers believe that biologics will be a safe and effective treatment option for children with poor or ineffective glucocorticoids combined immunosuppressor on CTD-ILD, and can delay the progres-sion of the disease and the deterioration of lung function. In this paper, the relevant studies of ex-isting biologics in adult and children CTD-ILD were summarized, in order to provide reference for their further application in pediatric CTD-ILD.
文章引用:龚玲, 舒畅. 生物制剂在儿童结缔组织病相关间质性肺病中的应用研究进展[J]. 临床医学进展, 2023, 13(2): 2305-2312. https://doi.org/10.12677/ACM.2023.132322

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