
The ASH abstract numbers are shown in parentheses. You can search on the number and read the complete abstract at: https://ashpublications.org/blood/issue/134/Supplement_1.
Abstracts 1 and 2 describe a novel mechanism to increase the platelet count in ITP that also might have application to other diseases. These two studies evaluate a novel method to treat ITP using molecules that target and bind to the so-called neonatal Fc receptor (FcRn). The drugs are designed to increase IgG clearance by blocking normal IgG recycling in the body. IgG antibodies normally may remain in the blood for thirty days but, when recycling is blocked, they may only last about five days. This is important because when you lower all IgG molecules, you also lower IgG antibodies to platelets. These IgG anti-platelet antibodies accelerate platelet clearance and destruction, and also interfere with proper platelet production. Therefore, it would be expected that lowering IgG levels will equally lower IgG anti-platelet antibody levels which will increase platelet count in patients with ITP.
CONTENTS:
CONTENTS:
CONTENTS:
CONTENTS: