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Ponatinib Protects Mice From Lethal Influenza Infection by Suppressing Cytokine Storm.


ABSTRACT: Excessive inflammation associated with the uncontrolled release of pro-inflammatory cytokines is the main cause of death from influenza virus infection. Previous studies have indicated that inhibition of interferon gamma-induced protein 10 (IP-10), interleukin-8 (IL-8), monocyte chemoattractant protein 1 (MCP-1), or their cognate receptors has beneficial effects. Here, by using monocytic U937 cells that capable of secreting the three important cytokines during influenza A virus infection, we measured the inhibitory activities on the production of three cytokines of six anti-inflammatory compounds reported in other models of inflammation. We found that ponatinib had a highly inhibitory effect on the production of all three cytokines. We tested ponatinib in a mouse influenza model to assess its therapeutic effects with different doses and administration times and found that the delayed administration of ponatinib was protective against lethal influenza A virus infection without reducing virus titers. Therefore, we suggest that ponatinib may serve as a new immunomodulator in the treatment of influenza.

SUBMITTER: Chen S 

PROVIDER: S-EPMC6598400 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Ponatinib Protects Mice From Lethal Influenza Infection by Suppressing Cytokine Storm.

Chen Si S   Liu Ge G   Chen Jungang J   Hu Ao A   Zhang Li L   Sun Wenyu W   Tang Wei W   Liu Chunlan C   Zhang Haiwei H   Ke Chang C   Wu Jianguo J   Chen Xulin X  

Frontiers in immunology 20190621


Excessive inflammation associated with the uncontrolled release of pro-inflammatory cytokines is the main cause of death from influenza virus infection. Previous studies have indicated that inhibition of interferon gamma-induced protein 10 (IP-10), interleukin-8 (IL-8), monocyte chemoattractant protein 1 (MCP-1), or their cognate receptors has beneficial effects. Here, by using monocytic U937 cells that capable of secreting the three important cytokines during influenza A virus infection, we mea  ...[more]

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