TY - JOUR T1 - Dendritic cell recruitment in lesions of human and experimental pulmonary hypertension JF - European Respiratory Journal JO - Eur Respir J SP - 462 LP - 468 DO - 10.1183/09031936.00094706 VL - 29 IS - 3 AU - F. Perros AU - P. Dorfmüller AU - R. Souza AU - I. Durand-Gasselin AU - S. Mussot AU - M. Mazmanian AU - P. Hervé AU - D. Emilie AU - G. Simonneau AU - M. Humbert Y1 - 2007/03/01 UR - http://erj.ersjournals.com/content/29/3/462.abstract N2 - In the present study, the hypothesis that dendritic cells (DCs), key players in immunity and tolerance, might be involved in the immunopathology of idiopathic pulmonary arterial hypertension (IPAH) was tested. The phenotype and localisation of DCs were characterised by immunohistochemistry and double-labelling immunofluorescence in lung samples from controls, human IPAH patients and an experimental pulmonary hypertension model (monocrotaline-exposed rats). As compared with controls, morphometric analysis demonstrated increased numbers of dendritic cell-specific intercellular adhesion molecule-grabbing nonintegrin (DC-SIGN)-positive cells in muscular pulmonary arteries in IPAH and OX-62-positive DCs in monocrotaline-induced pulmonary hypertension. In human samples, the mean±sem number of DC-SIGN-positive cells·artery−1 of 100–300 μm diameter was 1.4±0.4 in controls versus 26.4±2.7 in IPAH. In rats, the number of OX-62-positive cells·artery−1 of 50–150 μm diameter was 0.5±0.2 in controls, and 0.7±0.5, 3.1±0.5 and 8.4±0.6 at day 7, 14 and 28 after monocrotaline exposure, respectively. Human complex lesions of muscular pulmonary arteries showed transmural DC infiltration. Phenotyping revealed an immature DC profile in human and experimental pulmonary hypertension. The results support the concept that immature dendritic cells accumulate in remodelled pulmonary vessels and hence could be involved in the immunopathology of pulmonary hypertension. ER -