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Clinical,Virological and Immunological Features from Patients Infected with Re-Emergent Avian-Origin Human H7N9 Influenza Disease of Varying Severity in Guangdong Province
Authors:Zi Feng Yang  Chris Ka Pun Mok  Xiao Qing Liu  Xiao Bo Li  Jian Feng He  Wen Da Guan  Yong Hao Xu  Wei Qi Pan  Li Yan Chen  Yong Ping Lin  Shi Guan Wu  Si Hua Pan  Ji Cheng Huang  Guo Yun Ding  Kui Zheng  Chang Wen Ke  Jin Yan Lin  Yong Hui Zhang  Horace Hok Yeung Lee  Wen Kuan Liu  Chun Guang Yang  Rong Zhou  Joseph Sriyal Malik Peiris  Yi Min Li  Rong Chang Chen  Ling Chen  Nan Shan Zhong
Abstract:BackgroundThe second wave of avian influenza H7N9 virus outbreak in humans spread to the Guangdong province of China by August of 2013 and this virus is now endemic in poultry in this region.MethodsFive patients with H7N9 virus infection admitted to our hospital during August 2013 to February 2014 were intensively investigated. Viral load in the respiratory tract was determined by quantitative polymerase chain reaction (Q-PCR) and cytokine levels were measured by bead-based flow cytometery.ResultsFour patients survived and one died. Viral load in different clinical specimens was correlated with cytokine levels in plasma and broncho-alveolar fluid (BALF), therapeutic modalities used and clinical outcome. Intravenous zanamivir appeared to be better than peramivir as salvage therapy in patients who failed to respond to oseltamivir. Higher and more prolonged viral load was found in the sputum or endotracheal aspirates compared to throat swabs. Upregulation of proinflammatory cytokines IP-10, MCP-1, MIG, MIP-1α/β, IL-1β and IL-8 was found in the plasma and BALF samples. The levels of cytokines in the plasma and viral load were correlated with disease severity. Reactivation of herpes simplex virus type 1(HSV-1) was found in three out of five patients (60%).ConclusionExpectorated sputum or endotracheal aspirate specimens are preferable to throat swabs for detecting and monitoring H7N9 virus. Severity of the disease was correlated to the viral load in the respiratory tract as well as the extents of cytokinemia. Reactivation of HSV-1 may contribute to clinical outcome.
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