Failure of Immunosuppression in a Severe Haemophilia B Patient with Specific Antibody

Jean-Pierre Allain; Dominique Frommel

doi:10.1055/s-0038-1648012

Thrombosis and Haemostasis, Inhaltsverzeichnis

Thromb Haemost 1976; 36(01): 086-089
DOI: 10.1055/s-0038-1648012

Original Article

Schattauer GmbH

Failure of Immunosuppression in a Severe Haemophilia B Patient with Specific Antibody

Jean-Pierre Allain

¹Centre pour Enfants hémophiles, Croix-Rouge Française, F 78940 La Queue-les-Yvelines and the Unité 56 de l’I.N.S.E.R.M., Hôpital d’Enfants, F 94270 Bicêtre.

,

Dominique Frommel

¹Centre pour Enfants hémophiles, Croix-Rouge Française, F 78940 La Queue-les-Yvelines and the Unité 56 de l’I.N.S.E.R.M., Hôpital d’Enfants, F 94270 Bicêtre.

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Abstract

Summary

Prevention of a secondary response to factor IX by cyclophosphamide was attempted in an 11 year old patient with severe Christmas disease. An antibody to factor IX had been present for 4 years before immunosuppressive therapy was tried. Despite profound lymphopenia, synthesis of factor IX antibody was not depressed. The difficulties of modifying the anamnestic response to factor IX by chemical immunosuppression may be as real as has been reported for factor VIII in classical haemophilia.

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Referenzen

References
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