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Twenty-seven patients with chronic plaque-type psoriasis and 7 patients with acute psoriatic lesions were given topical dithranol on an area of the body. The areas of active psoriatic lesions cleared rapidly in most of the patients. The clearance rate was significantly faster in the patients with chronic plaque-type psoriasis than in those with acute psoriatic lesions.The procoagulant activity of recombinant human VWF involves surface binding of dimeric proteins: evidence for divalent interactions between a potentiating glycoprotein, GPIb, and the A1 domain of VWF.
In vitro, we previously found that the procoagulant activity of recombinant human von Willebrand factor (rHu VWF) increased approximately 100-fold by divalent interactions between dimerized proteins [H. Yeh, K.K. Tu, J.L. Borghi, A. Knuiman, I.D. Seeger, R.H.O. Koopman, J.D. Dunn and C.J. Michael, Blood 96:1809-1816, (2000)]. We have now investigated the conditions for this potentiation, with a view to detecting a potential role for divalent interactions in in vivo situations such as myocardial infarction (MI). We found that, in a dose-dependent fashion, the titer of prothrombinase activity of rHu VWF was increased (3-fold at 80 pM), when rHu VWF was pretreated with VWF-A1 prior to adding factor (F)Xa and phospholipids to form the enzyme complex. The titer of rHu VWF-dependent factor X activation was similarly increased. The titer of factor Xa generation by rHu VWF, but not of its activation, was potently potentiated (3-fold at 80 pM) by mAb 17-44, a potentiated polyclonal antibody to the A1 domain of VWF
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