Proinflammatory cytokines.

STUDY OBJECTIVES To review the concept of proinflammatory cytokines. DESIGN Review of published literature. SETTING Academic (university hospital). RESULTS Cytokines are regulators of host responses to infection, immune responses, inflammation, and trauma. Some cytokines act to make disease worse (proinflammatory), whereas others serve to reduce inflammation and promote healing (anti-inflammatory). Attention also has focused on blocking cytokines, which are harmful to the host, particularly during overwhelming infection. Interleukin (IL)-1 and tumor necrosis factor (TNF) are proinflammatory cytokines, and when they are administered to humans, they produce fever, inflammation, tissue destruction, and, in some cases, shock and death. Reducing the biological activities of IL-1 and TNF is accomplished by several different, but highly specific, strategies, which involve neutralizing antibodies, soluble receptors, receptor antagonist, and inhibitors of proteases that convert inactive precursors to active, mature molecules. Blocking IL-1 or TNF has been highly successful in patients with rheumatoid arthritis, inflammatory bowel disease, or graft-vs-host disease but distinctly has not been successful in humans with sepsis. Agents such as TNF-neutralizing antibodies, soluble TNF receptors, and IL-1 receptor antagonist have been infused into > 10,000 patients in double-blind, placebo-controlled trials. Although there has been a highly consistent small increase (2 to 3%) in 28-day survival rates with anticytokine therapy, the effect has not been statistically significant. CONCLUSIONS Anticytokine therapy should be able to "rescue" the patient whose condition continues to deteriorate in the face of considerable support efforts. Unfortunately, it remains difficult to identify those patients who would benefit from anticytokine therapy for septic shock.

[1]  J. Bray,et al.  Mapping receptor binding sites in interleukin (IL)-1 receptor antagonist and IL-1 beta by site-directed mutagenesis. Identification of a single site in IL-1ra and two sites in IL-1 beta , 1995, The Journal of Biological Chemistry.

[2]  S. Dower,et al.  The two interleukin-1 receptors play different roles in IL-1 actions. , 1994, Clinical immunology and immunopathology.

[3]  M. Gelb,et al.  Interleukin 1 alpha causes rapid activation of cytosolic phospholipase A2 by phosphorylation in rat mesangial cells. , 1994, The Journal of clinical investigation.

[4]  Klaus Resch,et al.  The Interleukin-1 Receptor Accessory Protein (IL-1RAcP) Is Essential for IL-1-induced Activation of Interleukin-1 Receptor-associated Kinase (IRAK) and Stress-activated Protein Kinases (SAP Kinases)* , 1997, The Journal of Biological Chemistry.

[5]  M. Kester,et al.  Interleukin-1 generates transmembrane signals from phospholipids through novel pathways in cultured rat mesangial cells. , 1989, The Journal of clinical investigation.

[6]  J. Pfeilschifter,et al.  Interleukin‐1 stimulates de novo synthesis of mitogen‐activated protein kinase in glomerular mesangial cells , 1994, FEBS letters.

[7]  B. Roe,et al.  Genetic and physical mapping of the Lps locus: identification of the toll-4 receptor as a candidate gene in the critical region. , 1998, Blood cells, molecules & diseases.

[8]  J. Camonis,et al.  A Novel Protein That Interacts with the Death Domain of Fas/APO1 Contains a Sequence Motif Related to the Death Domain (*) , 1995, The Journal of Biological Chemistry.

[9]  J. Nerup,et al.  Interleukin 1β induces diabetes and fever in normal rats by nitric oxide via induction of different nitric oxide synthases , 1994 .

[10]  S. Mizel Cyclic AMP and interleukin 1 signal transduction , 1990 .

[11]  R. Kolesnick,et al.  The sphingomyelin pathway in tumor necrosis factor and interleukin-1 signaling , 1994, Cell.

[12]  C. Dinarello IL-18: A TH1-inducing, proinflammatory cytokine and new member of the IL-1 family. , 1999, The Journal of allergy and clinical immunology.

[13]  M. Karin,et al.  Interleukin-1 costimulatory activity on the interleukin-2 promoter via AP-1. , 1989, Science.

[14]  R. Kastelein,et al.  Comparison of the effects of interleukin‐1α, interleukin‐lβ and interferon‐γ‐inducing factor on the production of interferon‐γ by natural killer , 1997 .

[15]  A. Mantovani,et al.  Interleukin-1 type II receptor: a decoy target for IL-1 that is regulated by IL-4. , 1993, Science.

[16]  L A O'Neill,et al.  Towards an understanding of the signal transduction pathways for interleukin 1. , 1995, Biochimica et biophysica acta.

[17]  J. Sims,et al.  Genomic organization of the type I and type II IL-1 receptors. , 1995, Cytokine.

[18]  I. Orlow,et al.  Activation of the sphingomyelin signaling pathway in intact EL4 cells and in a cell-free system by IL-1 beta. , 1993, Science.

[19]  N. Gay,et al.  Drosophila Toll and IL-1 receptor , 1991, Nature.

[20]  M. Kracht,et al.  Interleukin 1 alpha activates two forms of p54 alpha mitogen-activated protein kinase in rabbit liver , 1994, The Journal of experimental medicine.

[21]  M. Labow,et al.  Molecular Cloning and Characterization of a Second Subunit of the Interleukin 1 Receptor Complex (*) , 1995, The Journal of Biological Chemistry.

[22]  P. Herrlich,et al.  Interleukin 1 induction of the c-jun promoter. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Ronald W. Barrett,et al.  A new cytokine-receptor binding mode revealed by the crystal structure of the IL-1 receptor with an antagonist , 1997, Nature.

[24]  B. Brandhuber,et al.  Crystal structure of the type-I interleukin-1 receptor complexed with interleukin-1β , 1997, Nature.

[25]  J. Hsuan,et al.  Interleukin-1 activates a novel protein kinase cascade that results in the phosphorylation of hsp27 , 1994, Cell.

[26]  C. Dinarello,et al.  Interleukin-1 stimulates diacylglycerol production in T lymphocytes by a novel mechanism , 1988, Cell.