Prevention and treatment of blood coagulation-related disases

Abstract

Provided herein is an animal having a persistent hypercoagulable state by implanting a cell, for example a tumor cell, in which the gene of human tissue factor is implanted to an experimental animal such as a mouse and then growing the cell, thereby persistently supplying human tissue factor to the experimental animal. This animal model is useful for research and development of therapeutic agents for diseases having a persistent hypercoagulable state. Also provided are preventive or therapeutic agents for diseases having a persistent hypercoagulable state, a hypercoagulable state resulting from infections, venous thrombosis, arterial thrombosis, and diseases resulting from the hypertrophy of vascular media, the agent comprising an antibody against human tissue factor (human TF) as an active ingredient.

Description

FIELD OF THE INVENTION[0001]The present invention relates to a method of generating an animal model having a persistently hypercoagulable state, preventive or therapeutic agents for diseases having a persistent hypercoagulable state, preventive or therapeutic agents for a hypercoagulable state resulting from infections, preventive or therapeutic agents for venous or arterial thrombosis, and preventive or therapeutic agents for diseases resulting from the hypertrophy of vascular media.BACKGROUND ART[0002]Blood coagulation is a reaction in which serine protease precursors are successively activated by activated-form proteases, which finally generate thrombin thereby leading to fibrin formation. Thrombosis arises as a consequence of an excessively enhanced blood coagulation reaction that was caused by changes in the plasma coagulation and fibrinolytic system, and in the functions of platelets, leucocytes and vascular endothelial cells associated with the progression of various disease ...

AI Technical Summary

Benefits of technology

[0020]After intensive and extensive research to resolve the above first problem, the inventors of the present invention have found out that by implanting, into an experimental animal, an animal cell capable of constantly expressing human tissue factor by introducing therein the gene of a human tissue factor (TF) and thereby increasing the concentration of human tissue factor in the animal, the hypercoagulable state of said animal can be maintained for a long period of time, and thereby have completed the present invention.

[0025]After intensive and extensive research to resolve the above second problem, the inventors of the present invention have found out that an antibody (anti-human TF antibody, or sometimes referred to as anti-TF antibody) against human tissue factor can prevent the persistence of a hypercoagulable state.

[0028]After intensive and extensive research to resolve the above third problem, the inventors of the present invention have found out that an antibody (anti-human TF antibody, or sometimes referred to as anti-TF antibody) against human tissue factor can prevent or treat a hypercoagulable state resulting from infections.

[0031]After intensive and extensive research to resolve the above fourth problem, the inventors of the present invention have found out that an antibody (anti-human TF antibody, or sometimes referred to as anti-TF antibody) against human tissue factor can prevent or treat venous thrombosis.

[0034]After intensive and extensive research to resolve the above fifth problem, the inventors of the present invention have found out that an antibody (anti-human TF antibody, or sometimes referred to as anti-TF antibody) against human tissue factor can prevent or treat arterial thrombosis.

[0037]After intensive and extensive research to resolve the above sixth problem, the inventors of the present invention have found out that an antibody (anti-human TF antibody, or sometimes referred to as anti-TF antibody) against human tissue factor can prevent or treat diseases caused by the hypertrophy of vascular media.

Problems solved by technology

Once tissue factor comes into contact with the blood, the blood coagulation reaction proceeds in a very short period of time and leads to the formation of blood clots.

Once TF comes into contact with the blood, the blood coagulation reaction proceeds in a very short period of time leading to the formation of blood clots.

As a result, microthrombi occur systemically, which elicits circulatory failures in the organs leading to multiple organ failure.

In particular, invasive events such as surgery, childbirth and trauma induce physical injuries to the vascular wall and abnormalities in the coagulation and fibrinolysis system, and decubitus after surgery induces a renous stasis.

Not only the resulting blood clots in the vein induce circulatory failure in the limbs but the clots themselves enter into the blood circulation and flows into the pulmonary artery leading to fatal pulmonary embolism.

In arterial thrombosis, blood clots occur in the blood vessel having an advanced sclerosis, and the onset of the disease in the important organs such as the brain and the heart would be fatal in most cases.

In particular, acute coronary syndromes such as unstable angina and acute myocardial infarction are believed to be dangerous disease states that could easily cause sudden death.

But restenosis that occurs several months after the operation hinders the effectiveness of the treating method and thus is posing a problem.

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