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Inhibition of Reactive Oxygen Species Production Ameliorates Inflammation Induced by Influenza A Viruses via Upregulation of SOCS1 and SOCS3

Ye, S., Lowther, S., & Stambas, J. (2014) · Journal of Virology · doi:10.1128/jvi.03529-14 · Cited by 77 · see citing works

Influenza A virus and TLR7 activation potentiate NOX2 oxidase-dependent ROS production in macrophages

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NADPH Oxidases as Novel Pharmacologic Targets against Influenza A Virus Infection

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Innate Immunity and Influenza A Virus Pathogenesis: Lessons for COVID-19

Hartshorn, K. L. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.563850 · Cited by 44 · see citing works

1918 pandemic influenza virus and Streptococcus pneumoniae co‐infection results in activation of coagulation and widespread pulmonary thrombosis in mice and humans

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Apoptosis induction and release of inflammatory cytokines in the oviduct of egg-laying hens experimentally infected with H9N2 avian influenza virus

Wang, J., Tang, C., Wang, Q., Li, R., Chen, Z., Han, X., Wang, J., & Xu, X. (2015) · Veterinary Microbiology · doi:10.1016/j.vetmic.2015.04.005 · Cited by 44 · see citing works

Immunostimulants in respiratory diseases: focus on Pidotimod

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Making Universal Influenza Vaccines: Lessons From the 1918 Pandemic

Morens, D. M., & Taubenberger, J. K. (2019) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiy728 · Cited by 42 · see citing works

Pleiotropic Effects of Levofloxacin, Fluoroquinolone Antibiotics, against Influenza Virus-Induced Lung Injury

Enoki, Y., Ishima, Y., Tanaka, R., Sato, K., Kimachi, K., Shirai, T., Watanabe, H., Chuang, V. T. G., Fujiwara, Y., Takeya, M., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0130248 · Cited by 41 · see citing works

Capillary leakage provides nutrients and antioxidants for rapid pneumococcal proliferation in influenza-infected lower airways

Sender, V., Hentrich, K., Pathak, A. K., Tan, A. Q. L., Embaie, B. T., Lundström, S. L., Gaetani, M., Bergstrand, J., Nakamoto, R., Sham, L., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2012265117 · Cited by 36 · see citing works

Anti-inflammatory effects of rosmarinic acid-4-O-β-D-glucoside in reducing acute lung injury in mice infected with influenza virus

Liu, J.-X., Zhang, Y., Hu, Q., Li, J., Liu, Y., Wu, Q., Wu, J., Lai, X., Zhang, Z., Li, X., et al. (2017) · Antiviral Research · doi:10.1016/j.antiviral.2017.04.010 · Cited by 34 · see citing works

Contemporary Avian Influenza A Virus Subtype H1, H6, H7, H10, and H15 Hemagglutinin Genes Encode a Mammalian Virulence Factor Similar to the 1918 Pandemic Virus H1 Hemagglutinin

Qi, L., Pujanauski, L. M., Davis, A. S., Schwartzman, L. M., Chertow, D. S., Baxter, D. H., Scherler, K., Hartshorn, K. L., Slemons, R. D., Walters, K., et al. (2014) · mBio · doi:10.1128/mbio.02116-14 · Cited by 34 · see citing works

An inactivated multivalent influenza A virus vaccine is broadly protective in mice and ferrets

Park, J.-K., Legaspi, S. L. F., Schwartzman, L. M., Gygli, S. M., Sheng, Z.-M., Freeman, A. D., Matthews, L., Xiao, Y., Ramuta, M. D., Batchenkova, N. A., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abo2167 · Cited by 31 · see citing works

PA-X-associated early alleviation of the acute lung injury contributes to the attenuation of a highly pathogenic H5N1 avian influenza virus in mice

Hu, J., Mo, Y., Gao, Z., Wang, X., Gu, M., Liang, Y., Cheng, X., Hu, S., Liu, W., Liu, H., et al. (2016) · Medical Microbiology and Immunology · doi:10.1007/s00430-016-0461-2 · Cited by 30 · see citing works

Histone H4 potentiates neutrophil inflammatory responses to influenza A virus: Down-modulation by H4 binding to C-reactive protein and Surfactant protein D

Hsieh, I.-N., White, M. R., Hoeksema, M., Deluna, X., & Hartshorn, K. L. (2021) · PLoS ONE · doi:10.1371/journal.pone.0247605 · Cited by 24 · see citing works

Pursuing the Elixir of Life: In Vivo Antioxidative Effects of Manganosalen Complexes

Rouco, L., Noya, A. M. G., Pedrido, R. M., & Maneiro, M. (2020) · Antioxidants · doi:10.3390/antiox9080727 · Cited by 22 · see citing works

Salen‑manganese complexes for controlling ROS damage: Neuroprotective effects, antioxidant activity and kinetic studies

Rouco, L., Liberato, A., Fernández‐Trujillo, M. J., Máñez, Á., Basallote, M. G., Alvariño, R., Alfonso, A., Botana, L. M., & Maneiro, M. (2019) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2019.110918 · Cited by 18 · see citing works

Pyrrolidine dithiocarbamate inhibits enterovirus 71 replication by down-regulating ubiquitin–proteasome system

Lin, L., Qin, Y., Wu, H., Chen, Y., Wu, S., Si, X., Wang, H., Wang, T., Zhong, X., Zhai, X., et al. (2014) · Virus Research · doi:10.1016/j.virusres.2014.10.012 · Cited by 16 · see citing works

Pitfalls in the ABTS Peroxidase Activity Test: Interference of Photochemical Processes

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Differential Ability of Pandemic and Seasonal H1N1 Influenza A Viruses To Alter the Function of Human Neutrophils

Małachowa, N., Freedman, B. A., Sturdevant, D. E., Kobayashi, S. D., Nair, V., Feldmann, F., Starr, T., Steele‐Mortimer, O., Kash, J. C., Taubenberger, J. K., et al. (2018) · mSphere · doi:10.1128/mspheredirect.00567-17 · Cited by 11 · see citing works

Novel neuroendocrine role of γ-aminobutyric acid and gastrin-releasing peptide in the host response to influenza infection

Shirey, K. A., Lai, W., Sunday, M. E., Cuttitta, F. F., Blanco, J. C. G., & Vogel, S. N. (2023) · Mucosal Immunology · doi:10.1016/j.mucimm.2023.03.004 · Cited by 11 · see citing works

Interpretation of the anti-influenza active ingredients and potential mechanisms of Ge Gen Decoction based on spectrum-effect relationships and network analysis

Liu, X., Ke, S., Wang, X., Li, Y., Lyu, J., Liu, Y., & Geng, Z. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.117290 · Cited by 11 · see citing works

iTRAQ-based quantitative proteomics reveals important host factors involved in the high pathogenicity of the H5N1 avian influenza virus in mice

Hu, J., Gao, Z., Wang, X., Gu, M., Liang, Y., Liu, X., Hu, S., Liu, W., Liu, W., Chen, S., et al. (2016) · Medical Microbiology and Immunology · doi:10.1007/s00430-016-0489-3 · Cited by 11 · see citing works

Effect of pandemic influenza A virus PB1 genes of avian origin on viral RNA polymerase activity and pathogenicity

Williams, S. L., Qi, L., Sheng, Z.-M., Xiao, Y., Freeman, A. D., Matthews, L., Legaspi, S. L. F., Fodor, E., & Taubenberger, J. K. (2024) · Science Advances · doi:10.1126/sciadv.ads5735 · Cited by 10 · see citing works

Salen Manganese Complexes Mitigate Radiation Injury in Normal Tissues Through Modulation of Tissue Environment, Including Through Redox Mechanisms

Doctrow, S. R., Fish, B. L., Huffman, K. D., Lazarova, Z., Medhora, M. M., Williams, J. P., & Moulder, J. E. (2016) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-30705-3_11 · Cited by 8 · see citing works

Searching for a Lifeline: Transcriptome Profiling Studies of Influenza Susceptibility and Resistance

Kobzik, L. (2017) · Journal of Innate Immunity · doi:10.1159/000457902 · Cited by 5 · see citing works

Anti-influenza virus activity of a salcomine derivative mediated by inhibition of viral RNA synthesis

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Possibilities of using multidirectional immunomodulators for acute and recurrent infectious and inflammatory diseases of the upper respiratory tract

Вячеславовна, М. С., & Валерьевна, С. Л. (2021) · Meditsinskiy sovet = Medical Council · doi:10.21518/2079-701x-2021-4-89-95 · Cited by 1 · see citing works

The role of ADAMTS enzymes in influenza virus immunity

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Clinical Utility of Viral Loads in Influenza Virus Infections

Granados, A. (2018) · TSpace (University of Toronto)

Vanin-1 deficiency enhances host tolerance to influenza infection by modulating cellular redox status

Joo, J. S., Pasman, L., Yu, S., Homer, R., Naquet, P., Medzhitov, R. M., & Hong, J. Y. (2026) · PNAS Nexus · doi:10.1093/pnasnexus/pgag222

Genomic analysis of increased host immune and cell death responses induced by 1918 influenza virus

Kash, J. C., Tumpey, T. M., Proll, S. C., Carter, V., Perwitasari, O., Thomas, M. J., Basler, C. F., Palese, P., Taubenberger, J. K., García-Sastre, A., et al. (2006) · Nature · doi:10.1038/nature05181 · Cited by 551 · see citing works

An absence of reactive oxygen species improves the resolution of lung influenza infection

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Therapeutic Effect of Recombinant Human Catalase on H1N1 Influenza-induced Pneumonia in Mice

Shi, X., Shi, Z., Huang, H. Y., Zhu, H., Zhou, P., & Ju, D. (2009) · Inflammation · doi:10.1007/s10753-009-9170-y · Cited by 33 · see citing works

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(2006) · Lab Animal · doi:10.1038/laban1106-9

Pathogenicity of Influenza Viruses with Genes from the 1918 Pandemic Virus: Functional Roles of Alveolar Macrophages and Neutrophils in Limiting Virus Replication and Mortality in Mice

Tumpey, T. M., García‐Sastre, A., Taubenberger, J. K., Palese, P., Swayne, D. E., Pantin‐Jackwood, M. J., Schultz‐Cherry, S., Solórzano, A., van Rooijen, N., Katz, J. M., et al. (2005) · Journal of Virology · doi:10.1128/jvi.79.23.14933-14944.2005 · Cited by 504 · see citing works