School of Chemical & Biomolecular Engineering, Georgia Institute of Technology , 950 Atlantic Drive NW, Atlanta, Georgia 30332, United States.
Department of Pathology, Emory University School of Medicine , Whitehead Bldg., 615 Michael Street, Atlanta, Georgia 30322, United States.
ACS Nano. 2017 Oct 24;11(10):9650-9662. doi: 10.1021/acsnano.7b03239. Epub 2017 Sep 5.
Bacterial enteric pathogens have evolved efficient mechanisms to suppress mammalian inflammatory and immunoregulatory pathways. By exploiting the evolutionary relationship between the gut and pathogenic bacteria, we have developed a potential mucosal therapeutic. Our findings suggest that engineered preparations of the Salmonella acetyltransferase, AvrA, suppress acute inflammatory responses such as those observed in inflammatory bowel disease (IBD). We created 125 nm diameter cross-linked protein nanoparticles directly from AvrA and carrier protein to deliver AvrA in the absence of Salmonella. AvrA nanoparticles are internalized in vitro and in vivo into barrier epithelial and lamina propria monocytic cells. AvrA nanoparticles inhibit inflammatory signaling and confer cytoprotection in vitro, and in murine colitis models, we observe decreased clinical and histological indices of inflammation. Thus, we have combined naturally evolved immunomodulatory proteins with modern bioengineering to produce AvrA nanoparticles, a potential treatment for IBD.
肠道细菌病原体已进化出有效的机制来抑制哺乳动物的炎症和免疫调节途径。通过利用肠道与致病性细菌之间的进化关系,我们开发出了一种有潜力的黏膜治疗方法。我们的研究结果表明,经过工程设计的沙门氏菌乙酰转移酶 AvrA 制剂可抑制急性炎症反应,如炎症性肠病(IBD)中观察到的反应。我们直接从 AvrA 和载体蛋白中构建出 125nm 直径的交联蛋白纳米颗粒,在没有沙门氏菌的情况下递送 AvrA。AvrA 纳米颗粒在体外和体内被屏障上皮和固有层单核细胞内化。AvrA 纳米颗粒可抑制炎症信号转导,并在体外赋予细胞保护作用,在小鼠结肠炎模型中,我们观察到炎症的临床和组织学指标降低。因此,我们将天然进化的免疫调节蛋白与现代生物工程相结合,产生了 AvrA 纳米颗粒,这可能是 IBD 的一种治疗方法。