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A Novel Chimeric Anti-PA Neutralizing Antibody for Postexposure Prophylaxis and Treatment of Anthrax

机译:用于预防和治疗炭疽的新型嵌合抗PA中和抗体

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摘要

Anthrax is a highly lethal infectious disease caused by the bacterium Bacillus anthracis, and the associated shock is closely related to the lethal toxin (LeTx) produced by the bacterium. The central role played by the 63 kDa protective antigen (PA63) region of LeTx in the pathophysiology of anthrax makes it an excellent therapeutic target. In the present study, a human/murine chimeric IgG mAb, hmPA6, was developed by inserting murine antibody variable regions into human constant regions using antibody engineering technology. hmPA6 expressed in 293F cells could neutralize LeTx both in vitro and in vivo. At a dose of 0.3 mg/kg, it could protect all tested rats from a lethal dose of LeTx. Even administration of 0.6 mg/kg hmPA6 48 h before LeTx challenge protected all tested rats. The results indicate that hmPA6 is a potential candidate for clinical application in anthrax treatment.
机译:炭疽是由炭疽芽孢杆菌引起的高度致死性传染病,与之相关的休克与细菌产生的致死毒素(LeTx)密切相关。 LeTx的63 kDa保护性抗原(PA63)区在炭疽的病理生理中起着核心作用,使其成为极好的治疗靶标。在本研究中,通过使用抗体工程技术将鼠抗体可变区插入人恒定区,开发了人/鼠嵌合IgG mAb hmPA6。在293F细胞中表达的hmPA6可以在体内和体外中和LeTx。以0.3μmg/ kg的剂量,它可以保护所有受试大鼠免于致命剂量的LeTx。在LeTx攻击前甚至在48 ofh时施用0.6μmg/ kg hmPA6都能保护所有测试的大鼠。结果表明,hmPA6是炭疽治疗中临床应用的潜在候选者。

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