Respiratory Syncytial Virus (RSV) RNA loads in peripheral blood correlates with disease severity in mice

被引:26
|
作者
Torres, Juan Pablo [1 ]
Gomez, Ana M. [2 ,3 ]
Khokhar, Shama [1 ]
Bhoj, Vijay G. [4 ]
Tagliabue, Claudia [1 ]
Chang, Michael L. [1 ]
Kiener, Peter A. [5 ]
Revell, Paula A. [2 ,3 ]
Ramilo, Octavio [6 ,7 ]
Mejias, Asuncion [1 ,6 ,7 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Div Infect Dis, Dept Pediat, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[3] Childrens Med Ctr Dallas, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[5] Medimmune Inc, Gaithersburg, MD 20878 USA
[6] Ohio State Univ, Dept Pediat, Div Infect Dis, Columbus, OH 43205 USA
[7] Ohio State Univ, Nationwide Childrens Hosp, Res Inst, Ctr Vaccines & Immun, Columbus, OH 43205 USA
关键词
AIRWAY-OBSTRUCTION; CYTOKINE RESPONSES; INFLUENZA-VIRUS; CHILDREN; INFLAMMATION; INFECTION; CELLS; TIME; PERSISTENCE; LEUKOCYTES;
D O I
10.1186/1465-9921-11-125
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Respiratory Syncytial Virus (RSV) infection is usually restricted to the respiratory epithelium. Few studies have documented the presence of RSV in the systemic circulation, however there is no consistent information whether virus detection in the blood correlates with disease severity. Methods: Balb/c mice were inoculated with live RSV, heat-inactivated RSV or medium. A subset of RSV-infected mice was treated with anti-RSV antibody 72 h post-inoculation. RSV RNA loads were measured by PCR in peripheral blood from day 1-21 post-inoculation and were correlated with upper and lower respiratory tract viral loads, the systemic cytokine response, lung inflammation and pulmonary function. Immunohistochemical staining was used to define the localization of RSV antigens in the respiratory tract and peripheral blood. Results: RSV RNA loads were detected in peripheral blood from day 1 to 14 post-inoculation, peaked on day 5 and significantly correlated with nasal and lung RSV loads, airway obstruction, and blood CCL2 and CXCL1 expression. Treatment with anti-RSV antibody reduced blood RSV RNA loads and improved airway obstruction. Immunostaining identified RSV antigens in alveolar macrophages and peripheral blood monocytes. Conclusions: RSV RNA was detected in peripheral blood upon infection with live RSV, followed a time-course parallel to viral loads assessed in the respiratory tract and was significantly correlated with RSV-induced airway disease.
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页数:11
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