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Systemic inflammatory response syndrome in nonhuman primates culminating in multiple organ failure, acute lung injury, and disseminated intravascular coagulation.

TitleSystemic inflammatory response syndrome in nonhuman primates culminating in multiple organ failure, acute lung injury, and disseminated intravascular coagulation.
Publication TypeJournal Article
Year of Publication2009
AuthorsHukkanen, RR, H Liggitt, D, Murnane, RD, Frevert, CW
JournalToxicol Pathol
Volume37
Issue6
Pagination799-804
Date Published2009 Oct
ISSN1533-1601
KeywordsAcute Lung Injury, Animals, Cytokines, Disseminated Intravascular Coagulation, Female, Macaca nemestrina, Male, Multiple Organ Failure, Papio anubis, Risk Factors, Systemic Inflammatory Response Syndrome
Abstract

The systemic inflammatory response syndrome (SIRS) is a clinicopathological manifestation of overexuberant acute-phase inflammation caused by infectious or noninfectious etiologies. The systemic release of pro-inflammatory cytokines, chemokines, and lipid and vasoactive mediators induces endothelial damage and microvascular thrombosis, potentially culminating in disseminated intravascular coagulation (DIC), acute respiratory distress syndrome (ARDS), and multiple organ dysfunction (MOD) or failure (MOF). We present five cases in the pig-tailed macaque and olive baboon where SIRS resulted in MOF, ARDS, DIC, and the Waterhouse-Friderichsen syndrome; each with gross and histological elements manifested as edema, deposition of fibrin, hemorrhage, and thrombosis. In the described cases, SIRS was the end-common pathway for multiple risk factors that parallel those documented in humans: major surgery, obstetric complications, and infection. The diagnosis of SIRS should be considered when evaluating nonhuman primate (NHP) cases of MOF manifesting with histological evidence of vascular leakage. Experimental manipulation of NHP models may be complicated by SIRS and accompanying rapid clinical decompensation. Such adverse events may compromise toxicological studies and should be avoided when possible.

DOI10.1177/0192623309343778
Alternate JournalToxicol Pathol
PubMed ID19773593
Grant ListP51 RR000166 / RR / NCRR NIH HHS / United States
R21 RR030249-02 / RR / NCRR NIH HHS / United States