1. Moschowitz ‘ Disease Galila Zaher MRCPath

2. Case Presentation  20 years old Saudi patient  Easy fatigability  Easy bruising  Afebrile  Systemic examination normal  Anaemia & thrombocytopenia  Blood film  High urea & creatinin

3. Clinical course  Abdominal US  Auto-immune profile  Seizures  Plasma pharesis  Normal platelets count  Renal dialysis  Relapse

4. Thrombotic Thrombocytopenic Purpura  Thrombotic thrombocytopenic purpura (TTP) is characterized by  Microangiopathic hemolytic anemia  Thrombocytopenia  Microvascular thrombosis causes variable degrees of tissue ischemia and infarction

5. VWF Biochemistry  VWF monomers synthesized in EC  Monomers linked into multimers  Multimers constructed in megacaryocytes & EC  Stored in alpha granules & weibel-palade bodies  ULVWF entangled to sub-endothelial collagen  Bind to platelets GP1b-IX –V and activated plt GPIIb-IIIa  adhesion and aggregation Moake et al 1982

6. VWF Biochemistry  Activation, immobilization and spreading  Recruit more VWF and more platelets  A disintegrin and metalloprotease with eight thrombospondin -1-like domain ADAMTS  Metalloprotease cleaves ULVWF in A2 domain  Impaired degradation of VWF by deficiency of metalloprotease Tsai 1996  Characterization of ADAMTS and elicidation of its cDNA and gene structure 2001

8. ADAMTS 13  Encoded on chromosome 9q34  Produced mainly in liver  Activator : Zn and Ca requiring protein  Inhibitors : metal chelators & EDTA  Substrate : VWF  Plasma activity 50-178%  Half-life 2-3 days

9. Patho-physiology TTP favored by conditions that combine  Increased VWF level (late pregnancy)  Decreased ADAMTS13 activity  Two-hit model could explain substantial variation in age at which patients with inherited TTP develop symptoms.

10. Platelet-rich Microvascular Thrombi  Wide spread of intravascular thrombosis  Organ ischemia :Renal, Cerebral  Blood flows through turbulent area of partially occluded by platelet aggergates  Schistocytes  High LDH correlates with severity of ischemia

11. Clinical Presentation Pentad  Thrombocytopenia (increased marrow megakaryocytes)  Microangiopathic hemolytic anemia (MAHA)  Renal failure (50%)  Neurologic abnormality (25%)  Fever  Thrombocytopenia, schistocytes & elevated LDH  Nonspecific symptoms: weakness, abdominal pain, nausea, vomiting, and diarrhea  Median duration of symptoms prior to diagnosis was 6 days Oklahoma TTP-HUS Registry

12. Types Of TTP  Congenital TTP  Acquired idiopathic TTP  Secondary TTP

13. Congenital Familial TTP  Moschowitz ‘ Disease  Rare : Autosomal recessive  Homozygous mutations in both ADAMTS13 alleles  Both parents showing 50% of activity  Infancy or childhood  Severe ischemic brain lesions by MRI  ADAMTS13 < 5% of normal plasma  Almost always have ULVWF multimers  Response to FFP infusion is rapid :Prophylactic FFP q2- 3 weeks avoid relapses

14. Conditions Associated  Bone marrow transplantation  Pregnancy & Postpartum  Drugs  Autoimmune disorders  TBI  Kidney, liver, heart, or lung transplant

15. Drug-associated TTP  Acute immune-mediated or dose-related toxic  Most common cause of immune-mediated TTP  Quinine ( isolated thrombocytopenia)  Ticlopidine (TTP and HUS)  Clopidogrel (TTP and HUS)  Mitomycin C- Cyclosporine  Tacrolimus (FK506)  Discontinuation or dose adjustment is sufficient  Trial of plasma exchange :efficacy is uncertain

16. Acquired idiopathic  Adults and older children  Sever ADAMTS 13 deficiency :acute episodes  IgG autoantibody produced transiently  Return to normal upon recovery  Mortality rate 13%  Worse prognosis :Prolonged courses & more frequent complications

17. HUS  Children, usually >5 years old  Bloody diarrhea  E.coli O157:H7  Shiga toxin  Acute renal failure  Thrombocytopenia and MAHA  Mortality is 3-5%  Normal plasma ADAMTS13 activity  Plasma exchange treatment is rarely considered

18. Laboratory Tests  Anemia  Thrombocytopenia  Blood film : (Schistocytes > 1% of total RBCs)  High LDH (hemolysis and leakage from ischemic tissue)  High bilirubin  DCT negative  High urea and ceriatnin  PT, APTT, fibrinogen & D-dimers :normal

20. Diagnosis  No “gold standard” for diagnosis  ADAMTS13 activity  Auto-antibodies against ADAMTS13

21. Clinical Applications  Diagnosis  Discrimination of TTP from HUS  Discrimination of congenital and acquired  Estimating risk of relapse  Monitoring therapeutic efficacy of plasma exchange or plasma infusion.

22. Furlan  NP VWF as substrate  Test plasma is activated by barium chloride  Mix over night in presence of 1.5M urea  Separated by SDS agarose gel electophoresis  Followed by immunoblotting.  Excellent resolution leader  Very sensitive  Reproducible  Requires several days

23. Bohm et al  Test plasma is incubated with recombinant substrate  Separated by SDS polyacrelamide gel  Quantitate residual VWF using RIPA  Short incubation

24. Immunoassay Assay  Residual VWF binding to collagen after its degradation  ELISA simple  Fast few hours  Less sensitive and less precise  Problems with reproducibility

25. Low Levels Of ADAMTS  PLiver disease  DIC  Chronic metabolic conditions & inflammatory conditions  Uremia  HIT  Pregnancy third trimesters  Newborn  Healthy controls :levels 20-50% and none < 10%

26. Management  Untreated almost always fatal (90%)  FFP Byrnes and Khurana 1977  Cryo-supernatant contain ADAMTS Tsai 1998  Solvent/detergent-treated plasma contain ADAMTS Tsai and Lian and Furlan 1998

27. Plasma pheresis  Plasma exchange reduced MR from 90%- 25%  Remove circulating ULVWF multimer-platelet strings  Remove circulating auto-antibodies against ADAMTS13  Infusion of FFP or cryosupernatant, SD or methylene blue/light-treated plasma  Response rate 80%–90%  T1/2 of infused ADAMTS13 activity is 2 days  Prompt and complete response : no further therapy

28. Risk For Relapse  Severe ADAMTS13 deficiency  Idiopathic TTP auto-Abs  Non following SCT  No relapse following drug toxicity  No relapse who had a prodrome of bloody diarrhea Oklahoma TTP-HUS Registry

29. Management Of Relapse  Most relapses occur within the first year  Suboptimal response or relapse :steroids  Sever neurologic defect :immunosuppressive treatment  Spleenectomy: eliminates autoantibody- producing B cells

30. Acquired idiopathic TTP  Lower titers better responses  High titer inhibitor wore prognosis  Inconsistent response to steroids and other immunosuppressive agents  Rituximab or cyclophosphamide  Removal of autoantibody-producing cells by splenectomy.

31. Pregnancy And TTP  During pregnancy,postpartum 70% around time of delivery  Pre-eclampsia/HELLP :3 rd trimester or following delivery, HT, protinurea & Spontaneous postpartum recovery  Observation for several days after delivery  Acute, severe multi-organ failure :prompt plasma exchange

32. TTP Following BMT  Post allogeneic : 2-76%  Post autologous : 0-27%  Mortality rate : 0-93%  DD : Renal and neurotoxicities of GVHD  Cyclosporine and Tacrolimus  Clinically suspected TTP: efforts to diagnose & treat GVHD and sepsis & delay a decision for plasma exchange  ADAMTS13 activity :normal  No response to plasma exchange

33. HIV  Typical TTP  Acquired autoantibody to ADAMTS13  Rapidly fatal course  Plasma exchange :one plasma volume once daily  Glucocorticoids auto-antibodies to ADAMTS13

34. Thank you

35. Central Venous Catheter Insertion  Deaths  Cardiac arrest with near-death  Hemorrhage  Pneumothrax  Pericardial tamponade  Allergic reactions  Severe hypotension and hypoxia  Fatal sepsis

36. ADAMTS13 Absent Clinical Presentation Familial TTP; chronic relapsing TTPADAMTS13 mutations i. Presentation in infancy/childhood ii. Disease presentation delayed Acquired idiopathic TTP Single episode Recurrent (intermittent) TTP Ticlopidine/clopidogrel-TTP Autoantibodies against ADAMTS13 i. Transient ii. Recurrent iii. Thienopyridine-associated Acquired idiopathic TTP (?)ADAMTS13 transient production or survival (?) defect Pregnancy-associated TTPPregnancy

37.  Tsai  Plasma samples incubated with guanidine HCl-treated VWF X1hr  Products separated by SDS–polyacrylamide gel electrophoresis  Immunoblotting  Obert et al  Plasma samples incubated with recombinant VWF overnight  Degraded VWF fragments detected by two-site immunoradiometric assay  Performed in hospital laboratory  High-throughput method  Gerritsen et al Functional assay  Preferential binding of HMWt forms of VWF to collagen.  Plasma treated with EDTA to abolishes the VWF-cleaving activity.  Dialyzed against the buffer and used as substrate.

38.  Recombinant protein as ADAMTS13 substrate E coli culture  Direct assay for measuring ADAMTS13 product generation  More accurate  Protease-free VWF.  Substrate tagged with two different molecules makes it easy to modify the detection of product.  One potential disadvantage : GST-VWF73-H is not a natural substrate

39. Sensitivity And Specificity  Specificity: Severe deficiency (<5% ) is specific  Sensitivity remains questionable 66%- 100% Tsai and Lian.  Levy et al identified 12 gene mutations

40. ParameterFindingPoints Neurologic findingsNone0 Confusion, lethargy, behavioral changes1 Focal neurologic deficits, convulsions, stupor, coma2 Renal function impairmentNone0 BUN > 30 and 2 g per day and/or hematuria 1 BUN >= 70 mg/dL and/or creatinine >= 2.5 mg/dL and/or dialysis2 Platelet count at presentation> 100,000 per L0 20,000 – 100,000 per L1 < 20,000 per L2 Hemoglobin level at presentation> 12 g/dL0 9-12 g/dL1 < 9 g/dL2

41. Thrombotic thrombocytopenic purpura (TTP) Immune thrombocytopenia purpura (ITP) Autoimmune hemolytic anemia Hemolytic uremic syndrome (HUS) Pregnancy, eclampsia Disseminated intravascular coagulation (DIC) Septicemia with DIC Systemic lupus erythematosus (SLE) Scleroderma Paroxysmal nocturnal hemoglobinuria (PNH) Differential Diagnosis

42. FeatureTTPHUS AgePeak incidence at 40 yearsChildhood GenderFemaleEqual EpidemicNoYes Re-occurrenceCommonRare Link to E. coli 0157:H7OccasionalYes Renal failureUncommonCommon NeurologicCommonUncommon ThrombocytopeniaSevereModerate to severe Organ involvementMultipleLimited to kidney Comparison of the features of TTP and hemolytic uremic syndrome (HUS)