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

Colm Leonard, Colm T. Leonard, Paola M. Soccal, Gerald J. Berry, Ramona L. Doyle, James Theodore, Steven R. Duncan, Glenn D. Rosen

    Research output: Contribution to journalArticlepeer-review

    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-β (TGF-β) 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.
    Original languageEnglish
    Pages (from-to)1314-1318
    Number of pages4
    JournalJournal of Heart and Lung Transplantation
    Volume21
    Issue number12
    Publication statusPublished - 1 Dec 2002

    Keywords

    • Animal
    • etiology: Bronchiolitis Obliterans
    • Comparative Study
    • Disease Models, Animal
    • pharmacology: Diterpenes
    • Graft Rejection
    • Graft Survival
    • Immunohistochemistry
    • adverse effects: Lung Transplantation
    • Male
    • Mice
    • Mice, Inbred C57BL
    • Reference Values
    • Sensitivity and Specificity
    • pathology: Trachea
    • Transplantation, Heterotopic
    • Treatment Outcome

    Fingerprint

    Dive into the research topics of 'PG490-88, a derivative of triptolide, attenuates obliterative airway disease in a mouse heterotopic tracheal allograft model'. Together they form a unique fingerprint.

    Cite this