Rhesus Theta-Defensin Prevents Death in a Mouse Model of Severe Acute Respiratory Syndrome Coronavirus Pulmonary Disease

被引:95
作者
Wohlford-Lenane, Christine L. [1 ]
Meyerholz, David K. [2 ]
Perlman, Stanley [4 ]
Zhou, Haixia [4 ]
Tran, Dat [5 ]
Selsted, Michael E. [5 ]
McCray, Paul B., Jr. [1 ,3 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Pediat, Iowa City, IA 52242 USA
[2] Univ Iowa, Carver Coll Med, Dept Pathol, Iowa City, IA 52242 USA
[3] Univ Iowa, Carver Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[4] Univ Iowa, Carver Coll Med, Dept Microbiol, Iowa City, IA 52242 USA
[5] Univ Calif Irvine, Dept Pathol & Lab Med, Irvine, CA 92697 USA
关键词
SARS-CORONAVIRUS; HUMAN INTERFERONS; IMMUNE-RESPONSES; ALPHA-DEFENSINS; LUNG PATHOLOGY; INFECTION; MICE; REPLICATION; CHEMOKINES; LEUKOCYTES;
D O I
10.1128/JVI.01363-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We evaluated the efficacy of rhesus theta-defensin 1 (RTD-1), a novel cyclic antimicrobial peptide, as a prophylactic antiviral in a mouse model of severe acute respiratory syndrome (SARS) coronavirus (CoV) lung disease. BALB/c mice exposed to a mouse-adapted strain of SARS-CoV demonstrated 100% survival and modest reductions in lung pathology without reductions in virus titer when treated with two intranasal doses of RTD-1, while mortality in untreated mice was similar to 75%. RTD-1-treated, SARS-CoV-infected mice displayed altered lung tissue cytokine responses 2 and 4 days postinfection compared to those of untreated animals, suggesting that one possible mechanism of action for RTD-1 is immunomodulatory.
引用
收藏
页码:11385 / 11390
页数:6
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