Powell Robert M, Hamilton Lynnsey M, Holgate Stephen T, Davies Donna E, Holloway John W
Expert Opin Ther Targets. 2003 Aug;7(4):485-94. doi: 10.1517/14728222.7.4.485.
The incidence of asthma worldwide is increasing, and the disease has a large unmet clinical need. Despite the availability of anti-inflammatory and bronchodilator medication, there is persisting morbidity and mortality. New approaches are needed to understand the role that structural changes in the airways (remodelling) play in this process. Studies of the genetic basis of asthma have identified the ADAM33 (a disintegrase and metalloproteinase 33) gene, a novel member of the ADAM family of zinc-dependent metalloproteases, as a risk factor for the development of asthma and bronchial hyperresponsiveness (BHR). The identification of ADAM33 as a major risk factor involved in the pathogenesis of BHR and airway wall remodelling provides insight into the pathogenesis of asthma and represents a novel therapeutic target.
全球哮喘发病率正在上升,并且该疾病存在大量未满足的临床需求。尽管有抗炎和支气管扩张药物,但仍存在持续的发病率和死亡率。需要新的方法来了解气道结构变化(重塑)在此过程中所起的作用。对哮喘遗传基础的研究已将ADAM33(一种解整合素和金属蛋白酶33)基因确定为哮喘和支气管高反应性(BHR)发展的一个危险因素,ADAM33基因是锌依赖性金属蛋白酶ADAM家族的一个新成员。将ADAM33鉴定为参与BHR发病机制和气道壁重塑的主要危险因素,为哮喘发病机制提供了见解,并代表了一个新的治疗靶点。