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Anti-HK antibody inhibits the plasma contact system by blocking prekallikrein and factor XI activation in vivo.
Chen, Zu-Lin; Singh, Pradeep K; Horn, Katharina; Calvano, Marissa R; Kaneki, Shigeru; McCrae, Keith R; Strickland, Sidney; Norris, Erin H.
Affiliation
  • Chen ZL; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
  • Singh PK; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
  • Horn K; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
  • Calvano MR; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
  • Kaneki S; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
  • McCrae KR; Taussig Cancer Institute and Department of Cardiovascular and Metabolic Sciences, Cleveland Clinic, Cleveland, OH.
  • Strickland S; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
  • Norris EH; The Rockefeller University, Patricia and John Rosenwald Laboratory of Neurobiology and Genetics, New York, NY.
Blood Adv ; 7(7): 1156-1167, 2023 04 11.
Article in En | MEDLINE | ID: mdl-36409609
ABSTRACT
A dysregulated plasma contact system is involved in various pathological conditions, such as hereditary angioedema, Alzheimer disease, and sepsis. We previously showed that the 3E8 anti-high molecular weight kininogen (anti-HK) antibody blocks HK cleavage and bradykinin generation in human plasma ex vivo. Here, we show that 3E8 prevented not only HK cleavage but also factor XI (FXI) and prekallikrein (PK) activation by blocking their binding to HK in mouse plasma in vivo. 3E8 also inhibited contact system-induced bradykinin generation in vivo. Interestingly, FXII activation was also inhibited, likely because of the ability of 3E8 to block the positive feedback activation of FXII by kallikrein (PKa). In human plasma, 3E8 also blocked PK and FXI binding to HK and inhibited both thrombotic (FXI activation) and inflammatory pathways (PK activation and HK cleavage) of the plasma contact system activation ex vivo. Moreover, 3E8 blocked PKa binding to HK and dose-dependently inhibited PKa cleavage of HK. Our results reveal a novel strategy to inhibit contact system activation in vivo, which may provide an effective method to treat human diseases involving contact system dysregulation.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Prekallikrein Limits: Animals / Humans Language: En Journal: Blood Adv Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Prekallikrein Limits: Animals / Humans Language: En Journal: Blood Adv Year: 2023 Document type: Article