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The pathogenesis of immune thrombocytopaenic purpura Nichola Cooper and James Bussel Department of Pediatrics, Weill Medical College of Cornell University,

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Presentation on theme: "The pathogenesis of immune thrombocytopaenic purpura Nichola Cooper and James Bussel Department of Pediatrics, Weill Medical College of Cornell University,"— Presentation transcript:

1 The pathogenesis of immune thrombocytopaenic purpura Nichola Cooper and James Bussel Department of Pediatrics, Weill Medical College of Cornell University, New York, NY, USA British Journal of Haematology, 133, 364–374

2 The role of the spleen Kaznelson 1916  splenectomy normalizes platelet count  established crucial role of the spleen in ITP Doan et al 1960  sea blue (lipid laden) histiocytes in the spleen - the platelet ‘destroyer’

3 The antiplatelet factor Harrington et al 1951  infusion of plasma from patients with ITP induced thrombocytopenia in normal recipients Dixon and Rosse 1975  quantified platelet-associated IgG

4 The antiplatelet factor Leeuwen et al. 1982  Glanzman’s thrombasthenia : lack platelet GPIIb/IIIa Cines & Blanchette 2002  Epitope spreading : antibody to multiple glycoproteins  anti GPIIb/IIIa, anti GPIb/IX, anti GPIa/IIa

5 The antiplatelet factor Roark et al 2002  the extraordinarily high usage of the V H 3-30 heavy-chain gene in ITP patients Antiplatelet autoantibodies  clonally restricted  from a limited number of B cell clones T cell dependent antibody production

6 Immune tolerance Central thymic tolerance Peripheral tolerance  sequester from the circulation : lens, testes  co-stimulatory signals : deletion or anergy  T-regulatory cells check self-reactive T cells  B cell deletion in the bone marrow

7 Autoimmunity Co-stimulatory signals  CD40-CD40Ligand or CD28-CD28/86 Cross-reaction of antigens via molecular mimicry  H. pylori Platelets increase their expression of CD40L and other immune molecules  contribute to their immunological recognition

8 Th1 and Th2 responses Th1  IFN-γ, TNF-β, IL-2  cell-mediated inflammatory reactions  delayed hypersensitivity reactions Th2  IL-4, 5, 6, 9, 10, 13  regulation of strong antibody and allergic reactions

9 T-cell abnormalities

10 Th1 bias compared with Th2 in adults with chronic ITP Release of cytokines that interfere with megakaryocyte maturation and/or platelet release Direct toxic effect of T cells

11 T-cell abnormalities

12 Megakaryocytes and platelet production GPIIb–IIIa and GPIb–IX ITP plasma on control of megakaryocytopoiesis  suppression of in vitro production of megakaryocytes from cord blood cells by plasma from ITP patients with detectable antiplatelet antibodies. (Chang et al 2003)  ITP plasma also inhibited megakaryocyte maturation resulting in fewer 4N, 8N and 16N cells. (McMillan et al 2004)

13 Megakaryocytes and platelet production Electron microscopic studies  50–75% of ITP megakaryocytes had extensive damage with abnormalities of the membrane system (Stahl et al, 1986) Ultrastructural abnormalities  apoptosis have been described in around 78% of ITP megakaryocytes (Houwerzijl et al, 2004)

14 Fc receptors Destruction by MPS is primarily mediated by the Fc receptors Balance between activating and inhibitory receptors  FcγRIIA and FcγRIIIA  FcγRIIB Important for response to treatments  IV anti-D : FcRIIA  Rituximab : FcRIIIA

15 Genetic susceptibility increased incidence in patients with immunodeficiency diseases  common variable immunodeficiency (CVID)  secondary hypogammaglobulinaemia  selective IgA deficiency  autoimmune lymphoproliferative syndrome (ALPS)  CD40 ligand deficiency (hyper-IgM syndrome)

16 Genetic susceptibility SNP : TNF-β (+252) G/G  frequent in patients with ITP when compared with control (21% vs. 7%)  the frequency of circulating anti-GPIIb/IIIa antibody-producing B cells was significantly higher (Satoh et al, 2004)

17 Virus-associated ITP HIV  possibly via loss of T-cell regulation, and a wide variety of autoantibodies are reported in HIV patients HCV  this virus appears to generally increase the production of a number of autoantibodies (Pivetti et al, 1996) EBV  inducing lymphoproliferation and increased antibody formation

18 Bacteria-associated ITP H. pylori eradication and platelet increase  Gasbarrini et al 1998  Michel et al 2003, Franchi & Veneri 2004 Molecular mimicry  H.pylori CagA protein Change cytokine milieu

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