CYTOKINE INHIBITORS - IN INTENSIVE-CARE
Citation
J. Villard et al., CYTOKINE INHIBITORS - IN INTENSIVE-CARE, Revue des maladies respiratoires, 12(4), 1995, pp. 335-342
Categorie Soggetti
Respiratory System
SICI code
0761-8425(1995)12:4<335:CI-II>2.0.ZU;2-7
Abstract
Objective. To examine three typical disease slates seen in intensive c
are, sepsis, Fulminant purpura and acute respiratory distress syndrome
(ARDS) to assess the implication of cytokines in their pathogenesis a
nd particularly in the clinical applications of possible cytokine inhi
bitors. Source of data. The data bank of MedLine and the Index Medicus
1985-1993 and the first part of 1994. These sources have enabled us t
o consult publications in French and English and to include informatio
n on both animals and humans. The publications issued from Intensive C
are Congresses have also been scrutinised; the Societe de Reanimation
de Langue Francaise, The American Thoracic Society and the 13th and 14
th International Symposium on Intensive Case and Emergency Medicine, B
russels. Selection of data. This review emphasizes certain areas of wo
rk including recognised work which has been published on the immunothe
rapy of sepsis in man, on those papers, which have been published as a
preliminary communication in the from of a summary and on certain pap
ers relating to animal work which are regularly cited in Intensive Car
e literature. Discussion. The relationship between cytokines and the t
hree selected disease states have been briefly described. The greater
part of those papers which have either been published or are in the pr
ocess of being published present pharmacotherapeutic data in phase 2 o
r phase 3 in relationship to anticytokines and sepsis. As for the trea
tment of Fulminant purpura and ARDS, using anticytokine antibodies in
1994 we are still in the stage of hypothesis and speculation. Conclusi
ons. Future clinical strategies designed to combat. Future clinical st
rategies designed to fight against the most critical diseases in inten
sive care medicine require some use of any kind of immunotherapy. In a
nimal studies, convincing data are available showing that immunotherap
y improves the prognosis of sepsis, whereas in humans, to date, the re
sults appear to be deceiving. Future research in this direction is man
datory, in sep sis and in other disease states, like ARDS, because no
other hope for treating these patients seems to appear in a near futur
e.