Division of Respiratory Disease, Department of Internal Medicine, Jikei University School of Medicine, Tokyo 105-8461, Japan.
Annu Rev Pathol. 2010;5:77-98. doi: 10.1146/annurev.pathol.4.110807.092217.
Fibrogenic lung reactions occur as a common phenotype shared among disorders of heterogeneous etiologies. Even with a common etiology, the extent and pattern of fibrosis vary greatly among individuals, even within families, suggesting complex gene-environment interactions. The search for mechanisms shared among all fibrotic lung diseases would represent a major advance in the identification of therapeutic targets that could have a broad impact on lung health. Although it is difficult to grasp all of the complexities of the varied cell types and cytokine networks involved in lung fibrogenic responses, and to predict the biologic responses to the overexpression or deficiency of individual cytokines, a large body of evidence converges on a single common theme: the central importance of the transforming growth factor beta (TGF-beta) pathway. Therapies that act upstream or downstream of TGF-beta activation have the therapeutic potential to treat all fibrogenic responses in the lung.
纤维生成性肺反应是多种病因所致疾病的共同表型。即使病因相同,纤维化的程度和模式在个体之间也有很大差异,甚至在家族内也是如此,这表明存在复杂的基因-环境相互作用。寻找所有纤维性肺疾病共有的机制将是在确定治疗靶点方面的重大进展,这些靶点可能对肺部健康产生广泛影响。尽管很难理解参与肺纤维生成反应的各种细胞类型和细胞因子网络的所有复杂性,也很难预测个别细胞因子过表达或缺乏时的生物学反应,但大量证据集中在一个共同主题上:转化生长因子β(TGF-β)途径的核心重要性。作用于 TGF-β激活的上游或下游的治疗方法具有治疗肺部所有纤维生成反应的治疗潜力。