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J Pediatr Hematol Oncol ; 37(4): e220-2, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25411864

RESUMEN

We report an 11-month-old boy with severe hemophilia A who had regular exposure to factor VIII (FVIII) intended to reduce the risk of developing an inhibitor. He developed a high-titer inhibitor (peak titer 19 BU) that disappeared within 6 weeks of starting immune tolerance induction (ITI). Anti-FVIII IgG4 peaked briefly compared with anti-FVIII IgG1 and the Bethesda titer. Neither rapid resolution of an inhibitor after prophylaxis nor this behavior of anti-FVIII IgG4 has been previously reported. Transient anti-FVIII IgG4 may be a marker of an attenuated anti-FVIII response induced by prophylactic FVIII therapy.


Asunto(s)
Factor VIII/inmunología , Hemofilia A/inmunología , Tolerancia Inmunológica , Inmunoglobulina G/sangre , Factor VIII/antagonistas & inhibidores , Humanos
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