Public Perception Survey on Inhaled Live Biotherapeutic Products for Cystic Fibrosis
调研导语 | Survey Introduction
您好!我们是iGEM的一支参赛团队,致力于用合成生物学技术解决罕见病患者的治疗困境。
囊性纤维化(CF)是一种遗传性罕见病,患者肺部易被铜绿假单胞菌感染。这些细菌会形成“生物膜”堡垒,使抗生素无法穿透,导致感染反复发作,肺功能逐年下降。
我们正在研发一种“智能吸入式活菌制剂”——改造对人体无害的益生菌,为其设计两道“安全锁”:仅在进入肺部深处且遇到致病菌时才启动治疗,分泌酶摧毁生物膜。任务完成后,细菌启动“自毁程序”,防止泄漏到环境中。
为确保该技术在未来的落地符合社会伦理与公众期望,我们发起本次调研。您的每一个观点,都将直接影响我们的实验设计与伦理决策。感谢您对生命科学进步的贡献!
Hello! We are an iGEM team dedicated to applying synthetic biology to address the treatment challenges faced by patients with rare diseases.
Cystic Fibrosis (CF) is a rare genetic disorder. Patients' lungs are vulnerable to Pseudomonas aeruginosa infection. These bacteria build "biofilm" fortresses that block antibiotics, causing recurrent infections and progressive lung decline.
We're developing a "smart inhaled live biotherapeutic"—engineered harmless probiotics with two safety locks: they activate only upon reaching the deep lung AND detecting pathogens, then secrete enzymes to dismantle biofilms. Upon task completion, they self-destruct to prevent environmental release.
To ensure that this technology aligns with social ethics and public expectations, we are conducting this survey. Your perspectives will directly inform our experimental design and ethical decision-making. Thank you for supporting the advancement of life sciences!