Toll样受体5的激动剂在小鼠和灵长类动物模型中具有辐射防护活性。
An agonist of toll-like receptor 5 has radioprotective activity in mouse and primate models.
作者信息
Burdelya Lyudmila G, Krivokrysenko Vadim I, Tallant Thomas C, Strom Evguenia, Gleiberman Anatoly S, Gupta Damodar, Kurnasov Oleg V, Fort Farrel L, Osterman Andrei L, Didonato Joseph A, Feinstein Elena, Gudkov Andrei V
机构信息
Department of Cell Stress Biology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
出版信息
Science. 2008 Apr 11;320(5873):226-30. doi: 10.1126/science.1154986.
The toxicity of ionizing radiation is associated with massive apoptosis in radiosensitive organs. Here, we investigate whether a drug that activates a signaling mechanism used by tumor cells to suppress apoptosis can protect healthy cells from the harmful effects of radiation. We studied CBLB502, a polypeptide drug derived from Salmonella flagellin that binds to Toll-like receptor 5 (TLR5) and activates nuclear factor-kappaB signaling. A single injection of CBLB502 before lethal total-body irradiation protected mice from both gastrointestinal and hematopoietic acute radiation syndromes and resulted in improved survival. CBLB502 injected after irradiation also enhanced survival, but at lower radiation doses. It is noteworthy that the drug did not decrease tumor radiosensitivity in mouse models. CBLB502 also showed radioprotective activity in lethally irradiated rhesus monkeys. Thus, TLR5 agonists could potentially improve the therapeutic index of cancer radiotherapy and serve as biological protectants in radiation emergencies.
电离辐射的毒性与放射敏感器官中的大量细胞凋亡相关。在此,我们研究一种激活肿瘤细胞用于抑制细胞凋亡的信号传导机制的药物是否能保护健康细胞免受辐射的有害影响。我们研究了CBLB502,一种源自沙门氏菌鞭毛蛋白的多肽药物,它与Toll样受体5(TLR5)结合并激活核因子-κB信号传导。在致死性全身照射前单次注射CBLB502可保护小鼠免受胃肠道和造血系统急性放射综合征的影响,并提高生存率。照射后注射CBLB502也能提高生存率,但辐射剂量较低。值得注意的是,该药物在小鼠模型中并未降低肿瘤放射敏感性。CBLB502在接受致死性照射的恒河猴中也显示出辐射防护活性。因此,TLR5激动剂有可能提高癌症放疗的治疗指数,并在辐射紧急情况下用作生物保护剂。