A novel recombinant fibrinogenase of Agkistrodon acutus venom protects against hyperacute rejection via degradation of complements

• Published in: Biochemical pharmacology Vol. 85; no. 6; pp. 772 - 779
• Main Authors: Lin, Xi, Qi, Jie-zhen, Chen, Ming-hui, Qiu, Bi-tao, Huang, Zhen-hua, Qiu, Peng-xin, Chen, Jia-shu, Yan, Guang-mei
• Format: Journal Article
• Language: English
• Published: England Elsevier Inc 15.03.2013
• Subjects: Agkistrodon; Agkistrodon acutus; Animals; blood serum; Complement; Complement System Proteins - metabolism; Crotalid Venoms - enzymology; Crotalid Venoms - pharmacology; fluorescence microscopy; Graft Rejection - prevention & control; Guinea Pigs; heart; Heart Transplantation; heat; Hemolysis; humans; Hyperacute rejection; Immunohistochemistry; Metalloendopeptidases - pharmacology; Microscopy, Fluorescence; pharmacology; Proteolysis; Rats; Recombinant Proteins - pharmacology; thrombin; transgenic animals; venoms; Xenotransplantation; rFII; XNAs; Xenotransplantation; SCR1; HR; Complement; ADP; ATII; IgM; MAC; CVF; LSCM; Hyperacute rejection; LVDP; HAR; HUVEC; CH50
• ISSN: 0006-2952; 1873-2968
• DOI: 10.1016/j.bcp.2012.11.012

Hyperacute rejection (HAR) is a main barrier in xenotransplantation, which is mediated by the combination of natural antibody to the xenograft and complement activation. Current therapies have focus on the inhibition of complement by development of complement inhibitor and transgenic animal organ. Here, we investigated the effects of rFII, a recombinant fibrinogenase from Agkistrodon acutus venom, on complement and HAR. The degradation effect of rFII on complement was tested by SDS-PAGE, CH50 examination, ELISA Kit and cofocal immunofluorescence microscopy in vitro and in vivo. An ex-vivo rat-to-human perfusion model and a vivo guinea-pig-to-rat heat HAR model were used to determine the protection of rFII against HAR. Our investigation indicated that rFII could significantly degrade human C5, C6, and C9, decrease the activity of complement, and inhibit the MAC deposition on HUVECs membrane in vitro. In addition, serum levels of C1q, C3 and C4 in rat were gradually reduced after infusion of rFII. Importantly, in an ex vivo rat-to-human perfusion model, the survival of rat hearts perfused with human serum treated with rFII (83.36±16.63min) were significantly longer than that of hearts perfused with fresh human serum(15.94±4.75min). At the time of 15minutes after perfusion, functions of hearts added with 50ug/ml rFII sustained well with heart rates at 283±65.32 beats/minute and LVDP at 13.70±5.45Kpa, while that of hearts perfused with fresh human serum were severely damaged by HAR with heart rates at 107.77±40.31 beats/minute and LVDP at 1.01±0.83Kpa. We also found that rFII significantly decreased the levels of C1q, C3 and C4 in human fresh serum perfusate. In a vivo guinea-pig-to-rat heat HAR model, the survival of rat hearts treated with rFII were significantly longer than that of hearts perfused with normal saline; and relieved heart damage by complete activation. Our finding demonstrates the anti-complement property of rFII and its protection against HAR, indicating that rFII might be as a potential therapeutic agent for xenotransplantation.