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Complex immune dysregulation contributes to significant clinical and QoL burdens of which: 

Accelerated PLT destruction in ITP and hemolysis in wAIHA lead to thrombocytopenia and increased bleeding risk in ITP and anemia in wAIHA1,2
Across, ITP, wAIHA, and SCD, immune dysregulation and inflammation may influence fatigue2−4
In SCD, chronic inflammation and a hyperactive innate immune system help sustain the vicious cycle of VOCs6
Thrombo-inflammation—marked by endothelial dysfunction, complement/coagulation dysregulation, and platelet/leukocyte activation—is increasingly recognized in ITP, wAIHA, and SCD1,5,6
Pain has a major impact on the QoL of individuals with SCD. Both acute and chronic pain have an inflammatory component, and can lead to eventual sensitization4,7

Abbreviations:

ITP, immune thrombocytopenia; PLT, platelet; QoL, quality of life; SCD, sickle cell disease; wAIHA, warm autoimmune hemolytic anemia; VOC, vaso-occlusive crisis.

MAT-KW-2600102-V1-Mar-2026