Comparative Analysis of Epidemiology, Clinical Features, and Cytokine Response of Respiratory Syncytial and Human Metapneumovirus Infected Children with Acute Lower Respiratory Infections

被引:2
|
作者
Sarkar, Subhabrata [1 ]
Ratho, Radha Kanta [1 ]
Singh, Meenu [2 ]
Singh, Mini Pritam [1 ]
Singh, Amarjeet [3 ]
Sharma, Megha [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Virol, Chandigarh, India
[2] Postgrad Inst Med Educ & Res, Adv Pediat Ctr, Dept Pediat Pulmonol, Chandigarh, India
[3] Postgrad Inst Med Educ & Res, Sch & Publ Hlth, Chandigarh, India
关键词
VIRUS; BRONCHIOLITIS; SEASONALITY; PREVALENCE; SEVERITY;
D O I
10.7883/yoken.JJID.2021.151
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Both human respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) cause immune-mediated under-five acute respiratory infections (ARIs), but differences in their disease pathogenesis, if any, are not well-known. This study was undertaken to analyze the epidemiological and immunological features of RSV and hMPV infections. Nasopharyngeal aspirates from children (aged 2 months to 5 years) with ARI, presenting to our tertiary care center between December 2013 and March 2016, were subjected to real-time polymerase chain reaction for the detection of RSV and hMPV. Positive samples were analyzed for co-infection and cytokine levels. Of the 349 nasopharyngeal aspirates, RSV was detected in 40.68% (142/349), hMPV in 6.59% (23/349), and both in 1.4% (5/349). Co-infections were common, with rhinovirus being the most common co-offender. The demographic and clinical parameters of RSV- and hMPV-infected children were comparable. The MMP-9/TIMP-1 ratio was significantly higher in RSV-mediated ARI and IFN-gamma in hMPV-mediated ARI. Both RSV and hMPV are common among North Indian children with ARI, and coinfections are common. Their clinical features are non-discriminatory, and molecular diagnosis should be utilized to ascertain their individual epidemiology. The differences in their immune-pathogenesis (MMP-9/TIMP-1 ratio in RSV and IFN-gamma in hMPV) could serve as useful tools for developing newer drugs.
引用
收藏
页码:56 / 62
页数:7
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