Department of Medicine, St George Clinical School, University of New South Wales, Sydney, NSW, Australia ; Inflammation and Infection Research Centre, School of Medical Sciences, Wallace Wurth Building, University of New South Wales, Gate 9 High Street, Sydney, NSW 2052, Australia.
Biol Proced Online. 2014 Jun 13;16:10. doi: 10.1186/1480-9222-16-10. eCollection 2014.
The appendix contains copious lymphoid tissue and is constantly exposed to gut flora. Appendicitis and appendectomy (AA) has been shown to prevent or significantly ameliorate ulcerative colitis. In our novel murine AA model, the only existing experimental model of AA, the appendiceal pathology closely resembles that of human appendicitis; and AA offers an age-, bacteria- and antigen-dependent protection against colitis. Appendicitis and appendectomy performed in the most proximal colon curbs T helper 17 cell activity, curtails autophagy, modulates interferon activity-associated molecules, and suppresses endothelin vasoactivity-mediated immunopathology/vascular remodelling in the most distal colon . These AA-induced changes contribute to the limitation/amelioration of colitis pathology. Investigating strategies to manipulate and modulate different aspects of these pathways (using monoclonal antibodies, combinatorial peptides, and small molecules) would offer novel insight into inflammatory bowel disease pathogenesis, and will augment the development of new therapeutic options to manage recalcitrant colitis.
阑尾含有丰富的淋巴组织,并且经常接触肠道菌群。阑尾炎和阑尾切除术 (AA) 已被证明可以预防或显著改善溃疡性结肠炎。在我们新颖的小鼠 AA 模型中,这是唯一现有的 AA 实验模型,阑尾病理学与人类阑尾炎非常相似;AA 为结肠炎提供了年龄、细菌和抗原依赖性保护。在最近端结肠进行的阑尾炎和阑尾切除术可以抑制 T 辅助 17 细胞的活性,限制自噬,调节干扰素活性相关分子,并抑制最远端结肠中的内皮素血管活性介导的免疫病理学/血管重塑。这些 AA 引起的变化有助于限制/改善结肠炎的病理学。研究操纵和调节这些途径的不同方面的策略(使用单克隆抗体、组合肽和小分子)将为炎症性肠病的发病机制提供新的见解,并将增强开发新的治疗选择来治疗顽固的结肠炎。