Safety and efficacy of an anti–human APC antibody for prophylaxis of congenital factor deficiencies in preclinical models

Author:

Jiang Miao12,Yang Fei1,Jiang Yizhi13,Cheng Lu4,Han Jingjing1,Yi Jiawei4,Zuo Bin1ORCID,Huang Lulu1,Ma Zhenni1,Li Tianyi1,Cao Lijuan J.1,Xia Zhisong4,Bai Xia156,Jia Chenjun7ORCID,Yang Teddy Tat Chi7,Esmon Naomi L.8,Ruan Changgeng156,Xia Lijun18ORCID,Esmon Charles T.8,Han Yue156,Wu Depei156,Xu Jun4ORCID

Affiliation:

1. 1Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases, NHC Key Laboratory of Thrombosis and Hemostasis, The First Affiliated Hospital of Soochow University, Suzhou, China

2. 2Department of Cardiology, Dushu Lake Hospital Affiliated to Soochow University, Medical Center of Soochow University, Suzhou, China

3. 3Department of Hematology, The First Affiliated Hospital of Wannan Medical College, Wuhu, China

4. 4Shanghai RAAS Blood Products Co, Ltd, Shanghai, China

5. 5Collaborative Innovation Center of Hematology, Soochow University, Suzhou, China

6. 6State Key Laboratory of Radiation Medicine and Protection, Soochow University, Suzhou, China

7. 7Shanghai ChemPartner Co, Ltd, Shanghai, China

8. 8Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK

Abstract

Abstract Rebalance of coagulation and anticoagulation to achieve a hemostatic effect has recently gained attention as an alternative therapeutic strategy for hemophilia. We engineered a humanized chimeric antibody, SR604, based on a previously published murine antibody, HAPC1573, which selectively blocks the anticoagulant activity of human activated protein C (APC). SR604 effectively blocked the anticoagulation activities of APC in human plasma deficient in various coagulation factors in vitro with affinities ∼60 times greater than that of HAPC1573. SR604 exhibited prophylactic and therapeutic efficacy in the tail-bleeding and knee-injury models of hemophilia A and B mice expressing human APC (humanized hemophilic mice). SR604 did not interfere with the cytoprotection and endothelial barrier function of APC, nor were there obvious toxicity effects in humanized hemophilic mice. Pharmacokinetic study showed a high bioavailability (106%) of subcutaneously injected SR604 in cynomolgus monkeys. These results demonstrate that SR604 is expected to be a safe and effective therapeutic and/or prophylactic agent with a prolonged half-life for patients with congenital factor deficiencies including hemophilia A and B.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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