Figure 1.
Pathophysiology of ITP and key therapeutic targets. AMR, Ashwell-Morell receptor; BAFF, B-cell activating factor; BCR, B-cell receptor; BLyS, B lymphocyte stimulator; BTK, Bruton's tyrosine kinase; FCR, Fc receptor; FcRn, neonatal Fc receptor; IgG, immunoglobulin; mTOR, mammalian target of rapamycin; Tc, cytotoxic T cell; Th, helper T cell. Drugs in light orange boxes are FDA approved for ITP and not discussed in this article but are shown for completeness; they include fostamatinib and TPO-RAs, thrombopoietin receptor agonists. Rituximab is shown and has sufficient literature to support its use, although it does not have FDA or other regulatory indication for use in ITP.

Pathophysiology of ITP and key therapeutic targets. AMR, Ashwell-Morell receptor; BAFF, B-cell activating factor; BCR, B-cell receptor; BLyS, B lymphocyte stimulator; BTK, Bruton's tyrosine kinase; FCR, Fc receptor; FcRn, neonatal Fc receptor; IgG, immunoglobulin; mTOR, mammalian target of rapamycin; Tc, cytotoxic T cell; Th, helper T cell. Drugs in light orange boxes are FDA approved for ITP and not discussed in this article but are shown for completeness; they include fostamatinib and TPO-RAs, thrombopoietin receptor agonists. Rituximab is shown and has sufficient literature to support its use, although it does not have FDA or other regulatory indication for use in ITP.

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