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Updated: May 13, 2026

Flow Cytometry Analysis of Tissue Factor Expression in Human Platelets
Published on: November 22, 2024
Coordinated release of tissue factor and tissue factor pathway inhibitor in VLBW infants
Anniina Palojärvi1, Sture Andersson, Satu Långström
1Children's Hospital, University of Helsinki, and Helsinki University Central Hospital, Helsinki, Finland. anniina.palojarvi@gmail.com
Insights
In very low birthweight (VLBW) infants, plasma tissue factor (TF) does not correlate with thrombin generation. Despite TF pathway inhibitor (TFPI) release, a significant circulating TF pool persists, potentially causing inflammation.
Area of Science:
- Neonatal physiology
- Coagulation and inflammation
- Perinatal medicine
Background:
- Tissue factor (TF) is a key mediator linking coagulation and inflammation.
- TF is upregulated in the alveolar compartment and circulation of very low birthweight (VLBW) infants.
- The role of TF in systemic coagulation regulation in VLBW infants requires further investigation.
Purpose of the Study:
- To investigate the contribution of tissue factor (TF) to the systemic regulation of coagulation in very low birthweight (VLBW) infants.
- To assess the relationship between TF, thrombin generation markers, and TF pathway inhibitor (TFPI) in VLBW neonates.
Main Methods:
- Plasma samples from 51 VLBW infants were analyzed during the first week of life.
- Measurements included tissue factor (TF), total and free tissue factor pathway inhibitor (TFPIt, TFPIf), prothrombin fragment F1+2, and thrombin-antithrombin complexes (TAT).
Main Results:
- Prothrombin fragment F1+2 and TAT levels were high at birth and decreased significantly postnatally.
- Plasma TF levels increased postnatally, peaking on day 3, but did not correlate with F1+2 or TAT.
- TFPI levels increased postnatally and correlated with TF, suggesting a regulatory role, though a relative excess of TF over TFPIf was observed on day 3.
Conclusions:
- In VLBW infants, plasma TF does not directly associate with thrombin formation, partly due to TFPI release.
- Despite TFPI, VLBW infants possess a substantial circulating TF pool with potential proinflammatory effects.
- This highlights a complex interplay between coagulation and inflammation in VLBW neonates.
Aim:
Tissue factor (TF), a mediator between coagulation and inflammation, is upregulated in alveolar compartment and circulation in very low birthweight (VLBW) infants. We investigated the contribution of TF to systemic regulation of coagulation in VLBW infants.
Methods:
We measured TF, total and free tissue factor pathway inhibitor (TFPIt, TFPIf), prothrombin fragment (F1 + 2), and thrombin-antithrombin complexes (TAT) in plasma from 51 VLBW infants during their first week of life.
Results:
F1 + 2 in cord plasma was high (1385 pmol/mL) and decreased postnatally to 17% (p = 0.002). TAT decreased from a high cord concentration to 3% postnatally (p < 0.001). Plasma TF increased and peaked on day 3, showing no correlation with F1 + 2 or TAT. TFPIt and TFPIf increased postnatally, correlating with TF (day 1 TFPIf: R = 0.595, p < 0.001, day 3 TFPIf: R = 0.582, p < 0.001). Based on the TF/TFPIf ratio, a relative excess of plasma TF over TFPIf probably prevailed on day 3.
Conclusions:
In VLBW infants plasma TF fails to associate with thrombin formation. This is partly explained by release of TFPI. Despite TFPI, the newborn VLBW infant is subjected to a substantial circulating pool of TF with potential proinflammatory effects.
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