Measurement of tissue factor-positive extracellular vesicles in plasma: strengths and weaknesses of current methods

Purpose of review This review evaluates the different methods used to measure levels of tissue factor (TF) in plasma and on extracellular vesicles (EVs). Levels of TF-positive (TF+) EVs in blood are increased in a variety of diseases, such as cancer, sepsis, and viral infection, and are associated with thrombosis. Highly sensitive assays are required to measure the low levels of TF+ EVs in blood. Recent findings TF antigen levels in plasma have been measured using standard ELISAs, SimpleStep ELISA technology, and solid-phase proximity ligation assay. Some studies reported the detection of TF+ EVs in plasma by flow cytometry. In addition, TF+ EVs can be captured onto beads and chips using anti-TF antibodies. Several assays have been developed to measure TF activity in EVs isolated from plasma. Importantly, activity-based assays are more sensitive than antigen-based assays as a single TF/FVIIa complex can generate large amounts of FXa. We recommend isolating EVs from plasma and measuring TF activity using a functional assay in the presence and absence of an anti-TF antibody. We do not recommend using antigen-based assays as these are not sensitive enough to detect the low levels of TF in plasma.

Automated summary

This review evaluates different methods for measuring tissue factor (TF) levels in plasma and extracellular vesicles (EVs). TF+ EVs in blood are increased in various diseases and are associated with thrombosis. Sensitivity is crucial for detecting the low levels of TF+ EVs in blood. The results indicate that measuring TF activity in EVs isolated from plasma using functional assays is more sensitive than antigen-based assays.