Background. Blood clotting activation is an important component of the inflammatory response; the outbursts of unstable angina are usually associated with increased thrombin formation and coronary mural thrombosis. Methods and Results. To investigate 1) whether monocyte activation is responsible for the enhanced thrombin formation during bursts of unstable angina and 2) what mechanism(s) might be responsible for monocyte activation, we studied patients with unstable angina (n=31), stable effort angina (n=23), left endoventricular thrombosis (n=8), and control subjects (n=44), measuring plasma fibrinopeptide A (FPA) levels and the capacity of monocytes to express procoagulant activity (PCA) and of lymphocytes to modulate this expression. Patients with unstable angina and patients with endoventricular thrombosis had significantly (p<0.0001) higher FPA plasma levels than patients with effort angina and control subjects. However, only monocytes from unstable angina patients expressed significantly increased PCA characterized as tissue factor-like activity (units/105 monocytes, median and range; 120, 1.1-463.2 versus 10.8, 0.8-39.1 in control subjects; p<0.0001 versus the other groups). When 14 patients with unstable angina were restudied 8-12 weeks later, they showed neither elevated plasma FPA levels nor monocyte PCA. In unstable angina patients, there was a correlation between FPA and PCA (r=0.56,p<0.001). For expression of PCA by monocytes, both an incubation of at least 2 hours with lymphocytes and direct monocyte-lymphocyte contact were needed. In reconstitution and cross-mixing experiments, only lymphocytes from patients with active unstable angina induced the expression ofPCA by monocytes from both control and patient groups. Conclsions. The results demonstrate that the increased thrombin formation in unstable angina patients is due to the expression of tissue factor-like activity by activated monocytes. The monocyte activation appears to be a part of a lymphocytic cell-instructed response intermittently triggered by unknown factors. (Circulation 1992;86:790-797)

Transient intermittent lymphocyte activation is responsible for the instability of angina / GG.SERNERI; R.ABBATE; AM.GORI; M.ATTANASIO; F.MARTINI; B.GIUSTI; P.DABIZZI; L.POGGESI; PA.MODESTI; F.TROTTA; C.ROSTAGNO; M.BODDI; GF.GENSINI. - In: CIRCULATION. - ISSN 0009-7322. - STAMPA. - 86:(1992), pp. 790-797.

Transient intermittent lymphocyte activation is responsible for the instability of angina.

NERI SERNERI, GIAN GASTONE;ABBATE, ROSANNA;GORI, ANNA MARIA;ATTANASIO, MONICA;GIUSTI, BETTI;DABIZZI, ROBERTO PIERO;POGGESI, LOREDANA;MODESTI, PIETRO AMEDEO;ROSTAGNO, CARLO;BODDI, MARIA;GENSINI, GIAN FRANCO
1992

Abstract

Background. Blood clotting activation is an important component of the inflammatory response; the outbursts of unstable angina are usually associated with increased thrombin formation and coronary mural thrombosis. Methods and Results. To investigate 1) whether monocyte activation is responsible for the enhanced thrombin formation during bursts of unstable angina and 2) what mechanism(s) might be responsible for monocyte activation, we studied patients with unstable angina (n=31), stable effort angina (n=23), left endoventricular thrombosis (n=8), and control subjects (n=44), measuring plasma fibrinopeptide A (FPA) levels and the capacity of monocytes to express procoagulant activity (PCA) and of lymphocytes to modulate this expression. Patients with unstable angina and patients with endoventricular thrombosis had significantly (p<0.0001) higher FPA plasma levels than patients with effort angina and control subjects. However, only monocytes from unstable angina patients expressed significantly increased PCA characterized as tissue factor-like activity (units/105 monocytes, median and range; 120, 1.1-463.2 versus 10.8, 0.8-39.1 in control subjects; p<0.0001 versus the other groups). When 14 patients with unstable angina were restudied 8-12 weeks later, they showed neither elevated plasma FPA levels nor monocyte PCA. In unstable angina patients, there was a correlation between FPA and PCA (r=0.56,p<0.001). For expression of PCA by monocytes, both an incubation of at least 2 hours with lymphocytes and direct monocyte-lymphocyte contact were needed. In reconstitution and cross-mixing experiments, only lymphocytes from patients with active unstable angina induced the expression ofPCA by monocytes from both control and patient groups. Conclsions. The results demonstrate that the increased thrombin formation in unstable angina patients is due to the expression of tissue factor-like activity by activated monocytes. The monocyte activation appears to be a part of a lymphocytic cell-instructed response intermittently triggered by unknown factors. (Circulation 1992;86:790-797)
1992
86
790
797
GG.SERNERI; R.ABBATE; AM.GORI; M.ATTANASIO; F.MARTINI; B.GIUSTI; P.DABIZZI; L.POGGESI; PA.MODESTI; F.TROTTA; C.ROSTAGNO; M.BODDI; GF.GENSINI
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/256943
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