The Clinical Core of this Acute Lung Injury SCOR is designed as a key support unit to promote the overall scientific objectives of the SCOR effort. This Core will be responsible for obtained and recording all clinical-physiologic-laboratory data relating to other samples from patients needed by SCOR investigators; and for the appropriate handling, storage/transport of such samples. In addition, the Clinical Core will collaborate with the Clinical Cores within other SCORs to standardize the collection and management of patient data and analysis of such pooled data. Of particular interest to other Acute Lung Injury SCORs may be access to samples from the UCSD patient population of individuals undergoing pulmonary art6ery thromboendarterectomy (PT-E). Of these patients, approximately two thirds develop acute lung injury. Because of the predictable nature of the injury, it is possible to collect serial samples of plasma and lavage fluid prior to injury, during the acute phase of injury, and during resolution. Such samples may be of interest of investigators in other SCORs, and, together with correlative physiologic and clinical data are available through the UCSD Clinical Core. Therefore, specific aims of this Clinical Core reflect these overall objectives; namely, 91) collection, organization and entry of clinical- physiologic-laboratory data from all patients studied within the SCOR in a specially-designed computer-software system which facilitates retrieval and analysis; (2) coordination with all SCOR investigators in the acquisition and appropriate handling of tissue and other samples required by SCOR investigators; (3) identification of patients with, or at risk, or ARDS and such with other SCOR Clinical Cores in an effort to standardize the collection and management of patients data and analyze such pooled data.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL023584-22
Application #
6302126
Study Section
Project Start
1999-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
22
Fiscal Year
2000
Total Cost
$148,366
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Kerr, Kim M; Auger, William R; Marsh, James J et al. (2012) Efficacy of methylprednisolone in preventing lung injury following pulmonary thromboendarterectomy. Chest 141:27-35
Dunzendorfer, Stefan; Lee, Hyun-Ku; Soldau, Katrin et al. (2004) Toll-like receptor 4 functions intracellularly in human coronary artery endothelial cells: roles of LBP and sCD14 in mediating LPS responses. FASEB J 18:1117-9
Lee, Hyun-Ku; Dunzendorfer, Stefan; Tobias, Peter S (2004) Cytoplasmic domain-mediated dimerizations of toll-like receptor 4 observed by beta-lactamase enzyme fragment complementation. J Biol Chem 279:10564-74
Spragg, Roger G; Ponganis, Paul J; Marsh, James J et al. (2004) Surfactant from diving aquatic mammals. J Appl Physiol 96:1626-32
Dunzendorfer, Stefan; Lee, Hyun-Ku; Soldau, Katrin et al. (2004) TLR4 is the signaling but not the lipopolysaccharide uptake receptor. J Immunol 173:1166-70
Spragg, Roger G; Lewis, James F; Wurst, Wilhelm et al. (2003) Treatment of acute respiratory distress syndrome with recombinant surfactant protein C surfactant. Am J Respir Crit Care Med 167:1562-6
Thompson, Patricia A; Tobias, Peter S; Viriyakosol, Suganya et al. (2003) Lipopolysaccharide (LPS)-binding protein inhibits responses to cell-bound LPS. J Biol Chem 278:28367-71
Tapping, Richard I; Tobias, Peter S (2003) Mycobacterial lipoarabinomannan mediates physical interactions between TLR1 and TLR2 to induce signaling. J Endotoxin Res 9:264-8
Bussolati, Benedetta; David, Salvatore; Cambi, Vincenzo et al. (2002) Urinary soluble CD14 mediates human proximal tubular epithelial cell injury induced by LPS. Int J Mol Med 10:441-9
Li, Jiali; Marsh, James J; Spragg, Roger G (2002) Effect of CTP:phosphocholine cytidylyltransferase overexpression on the mouse lung surfactant system. Am J Respir Cell Mol Biol 26:709-15

Showing the most recent 10 out of 107 publications