Literature DB >> 8403981

Tumor necrosis factor and the therapeutic potential of anti-tumor necrosis factor antibodies.

J C Wherry1, J E Pennington, R P Wenzel.   

Abstract

OBJECTIVE: To review the relationship of tumor necrosis factor (TNF) to clinical sepsis and the clinical potential of anti-TNF therapy in decreasing morbidity and mortality rates due to sepsis. DATA SOURCES: The international English language literature was reviewed, including animal studies and human clinical trials regarding TNF, anticytokine therapy, and sepsis. STUDY SELECTION: Studies which characterized the immunopharmacologic interactions between TNF and sepsis were emphasized. DATA EXTRACTION: This study specifically focused on experiments and clinical trials that directly involve the activity of TNF or anti-TNF antibodies, particularly but not limited to data derived from septic patients. DATA SYNTHESIS: The relationship between TNF and sepsis is described. Clinical aspects of anti-TNF therapy (timing, empiric use) are discussed. Phase I, II, and III trail of anti-TNF antibodies in clinical trials are reviewed.
CONCLUSIONS: Current clinical strategies for sepsis therapy are only partially effective. Recent immunopharmacologic advancements have resulted in the identification of TNF as a pivotal proinflammatory cytokine mediator of sepsis. Animal studies demonstrate that anti-TNF therapy protects animals from the morbidity and mortality of sepsis. Phase I clinical studies of anti-TNF antibodies demonstrate the safety of monoclonal antibody therapy. The therapeutic application of anti-TNF antibodies in sepsis trials is ongoing.

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Year:  1993        PMID: 8403981     DOI: 10.1097/00003246-199310001-00004

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  6 in total

Review 1.  Advanced and controlled drug delivery systems in clinical disease management.

Authors:  J R Brouwers
Journal:  Pharm World Sci       Date:  1996-10

Review 2.  New strategies for treatment of pulmonary fibrosis.

Authors:  S H Phan
Journal:  Thorax       Date:  1995-04       Impact factor: 9.139

3.  Attenuation of shock-induced inflammation in the rat liver depends on the time of TNF-alpha inhibition.

Authors:  C Bauer; W Roth; S Bahrami; I Marzi
Journal:  J Mol Med (Berl)       Date:  1996-01       Impact factor: 4.599

4.  Acute ethanol consumption synergizes with trauma to increase monocyte tumor necrosis factor alpha production late postinjury.

Authors:  G Szabo; P Mandrekar; B Verma; A Isaac; D Catalano
Journal:  J Clin Immunol       Date:  1994-11       Impact factor: 8.317

5.  Inhibition of TNFalpha in vivo prevents hyperoxia-mediated activation of caspase 3 in type II cells.

Authors:  Florian Guthmann; Heide Wissel; Christian Schachtrup; Angelika Tölle; Mario Rüdiger; Friedrich Spener; Bernd Rüstow
Journal:  Respir Res       Date:  2005-01-21

6.  Erythropoietin attenuates hyperoxia-induced lung injury by down-modulating inflammation in neonatal rats.

Authors:  Jang Hoon Lee; Dong Kyung Sung; Soo Hyun Koo; Bong Kyung Shin; Young Sook Hong; Chang Sung Son; Joo Won Lee; Yun Sil Chang; Won Soon Park
Journal:  J Korean Med Sci       Date:  2007-12       Impact factor: 2.153

  6 in total

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