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Inducible nitric oxide synthase protection against coxsackievirus pancreatitis.
Zaragoza, C; Ocampo, C J; Saura, M; Bao, C; Leppo, M; Lafond-Walker, A; Thiemann, D R; Hruban, R; Lowenstein, C J.
Affiliation
  • Zaragoza C; Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
J Immunol ; 163(10): 5497-504, 1999 Nov 15.
Article in En | MEDLINE | ID: mdl-10553076
Coxsackievirus infection causes myocarditis and pancreatitis in humans. In certain strains of mice, Coxsackievirus causes a severe pancreatitis. We explored the role of NO in the host immune response to viral pancreatitis. Coxsackievirus replicates to higher titers in mice lacking NO synthase 2 (NOS2) than in wild-type mice, with particularly high viral titers and viral RNA levels in the pancreas. Mice lacking NOS have a severe, necrotizing pancreatitis, with elevated pancreatic enzymes in the blood and necrotic acinar cells. Lack of NOS2 leads to a rapid increase in the mortality of infected mice. Thus, NOS2 is a critical component in the immune response to Coxsackievirus infection.
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Collection: 01-internacional Database: MEDLINE Main subject: Pancreatitis / Nitric Oxide Synthase / Coxsackievirus Infections Type of study: Etiology_studies Limits: Animals Language: En Journal: J Immunol Year: 1999 Document type: Article Affiliation country: United States Country of publication: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Pancreatitis / Nitric Oxide Synthase / Coxsackievirus Infections Type of study: Etiology_studies Limits: Animals Language: En Journal: J Immunol Year: 1999 Document type: Article Affiliation country: United States Country of publication: United States