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      Therapeutic Targeting of Acute Lung Injury and ARDS

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          Abstract

          There is no FDA approved treatment for acute respiratory distress syndrome (ARDS), in spite of the relatively large number of patients with the diagnosis. In this report, we provide an overview of preclinical studies as well as a description of completed and future clinical trials in humans with ARDS. Preclinical studies dealing with acute lung injury (ALI) have suggested roles for complement and complement receptors, as well as the evolving role of histones, but details of these pathways are inadequately understood. Anti-inflammatory interventions have not been convincingly effective. Various cell growth factors are being considered for clinical study. Interventions to block complement activation or its products are under consideration. Stem cell therapies have shown efficacy in preclinical studies, which have motivated phase I/II trials in humans with ARDS.

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          Author and article information

          Journal
          101280339
          33033
          Transl Res
          Transl Res
          Translational research : the journal of laboratory and clinical medicine
          1931-5244
          1878-1810
          7 May 2015
          05 May 2015
          January 2016
          01 January 2017
          : 167
          : 1
          : 183-191
          Affiliations
          [1 ]Department of Internal Medicine, Pulmonary and Critical Care, University of Michigan Medical School, Ann Arbor, MI 48109
          [2 ]Department of Pathology, University of Michigan Medical School Ann Arbor, MI 48109
          Author notes
          [* ] Corresponding Author Peter A. Ward, M.D. The University of Michigan Medical School Department of Pathology 1301 Catherine Road Ann Arbor, MI 48109-5602 PH: 734-647-2921 FAX: 734-764-4308 pward@ 123456umich.edu
          Article
          PMC4635065 PMC4635065 4635065 nihpa687699
          10.1016/j.trsl.2015.04.015
          4635065
          26003524
          603edca8-03e5-4090-9bd5-abac4ca41d45
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