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Factor IX inhibition and epitope localization of factor IX inhibitor antibodies in haemophilia B patients with anaphylactoid reactions
Author(s) -
YAMAMOTO M.,
KAMISUE S.,
SAWAMOTO Y.,
NAKAI H.,
TANAKA I.,
SHIMA M.,
TAKAMATSU J.,
OGUNI T.,
KINOSHITA S.,
GIDDINGS J. C.,
YOSHIOKA A.
Publication year - 1997
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1046/j.1365-2516.1997.00070.x
Subject(s) - antibody , haemophilia b , anaphylactoid reactions , immunoglobulin light chain , haemophilia , epitope , medicine , factor ix , haemophilia a , immunology , heavy chain , subclass , pathogenesis , anaphylaxis , allergy , pediatrics
Summary . We describe the results of immunological studies, reaction kinetics and epitope localization of six inhibitor antibodies to factor IX (FIX) developed in severe haemophilia B patients. Three of the six patients had suffered recent anaphylactoid reactions to FIX concentrates, two others had in the past and one had none. All six inhibitors rapidly inactivated FIX activity in vitro , and the prominent immunoglobulin (IgG) subclass of the antibody was IgG4 when analysed with ELISA. Interestingly, we found an additional IgG1 component in the antibody samples from the patients who had recently experienced anaphylactoid reactions to FIX. When analysed with Western blotting in these three patients, the IgG4 antibody bound with enhanced affinity to the heavy chain or the light chain of FIX, and in two of the three the IgG1 antibody also bound strongly to the FIX heavy chain. The results suggest that the heavy chain of FIX might play a more significant role than the light chain in the pathogenesis of anaphylactoid reactions in haemophilia B patients with FIX inhibitors.

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