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. 2022 Aug 9;13:918775. doi: 10.3389/fimmu.2022.918775

Table 1.

Table of Abbreviations.

ADAMTS13 a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13
aHUS atypical hemolytic uremic syndrome
AP alternative pathway
APAS antiphospholipid antibody syndrome
aPL anionic phospholipid (e.g., phosphatidyl serine)
AT anti-thrombin
BK bradykinin
C1-INH C1 inhibitor
C3aR, C5aR, C5aL2 receptors for C3a and C5a
CP classical pathway
CPB2 carboxypeptidase B2
CS contact system
CsA chondroitin sulfate A
DAMP damage/danger associated molecular pattern
FB factor B
FD factor D
FH factor H
HITT heparin induced thrombocytopenia and thrombosis
HK high molecular weight kininogen
LP lectin pathway
MAC membrane attack complex (C5b-9)
MASP MBL-associated serine protease
MBL mannose binding lectin
MMP matrix metalloprotease
NETs neutrophil extracellular traps
PAI-1 plasminogen activator inhibitor-1
PAMP pathogen associated molecular pattern
PAR protease activated receptor
PC, APC protein C, activated PC
PF4 platelet factor 4
Pg plasminogen
PGI prostacyclin
PK, PKa plasma prekallikrein, plasma kallikrein
PNH paroxysmal nocturnal hemoglobinuria
PRM pathogen recognition molecule
prothrombinase Factor Va/Factor Xa (FVa/FXa) enzymatic complex
PSGL-1 P-selectin glycoprotein 1
SUSD4 sushi domain-containing protein 4
TAFI thrombin activatable fibrinolysis inhibitor, activated TAFI
tenase TF/Factor VIIa (TF/FVIIa) enzymatic complex
TF tissue factor
TFPI tissue factor pathway inhibitor
tPA tissue type plasminogen activator
ULIC ultra large immune complexes
VWF, ULVWF von Willebrand Factor, ultra large multimeric VWF