1. Academic Validation
  2. PG490-88, a derivative of triptolide, attenuates obliterative airway disease in a mouse heterotopic tracheal allograft model

PG490-88, a derivative of triptolide, attenuates obliterative airway disease in a mouse heterotopic tracheal allograft model

  • J Heart Lung Transplant. 2002 Dec;21(12):1314-8. doi: 10.1016/s1053-2498(02)00449-7.
Colm T Leonard 1 Paola M Soccal Gerald J Berry Ramona L Doyle James Theodore Steven R Duncan Glenn D Rosen
Affiliations

Affiliation

  • 1 Division of Pulmonary and Critical Care Medicine, Department of Histopathology, Stanford University Medical Center, Stanford, California, USA. [email protected]
Abstract

The current treatment of obliterative bronchiolitis in lung transplant recipients is sub-optimal. Triptolide is a novel immunosuppressant that has a mechanism of action distinct from currently available immunosuppressants, including induction of T-cell Apoptosis, blockade of fibroblast proliferation/maturation and inhibition of transforming growth factor-beta (TGF-beta) mRNA production. We hypothesized that triptolide may be helpful in blocking obliterative airway disease in lung transplant recipients. We investigated the effect of PG490-88, a water-soluble derivative of triptolide, in a mouse heterotopic tracheal allograft model of obliterative airway disease. We show that PG490-88 attenuates airway obliteration in this model and inhibits accumulation of inflammatory cells, and therefore may have preventive or therapeutic benefits for patients with obliterative airway disease (OAD) following lung transplantation.

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