Tumor Necrosis Factor Alpha Exerts Powerful Anti-Influenza Virus Effects in Lung Epithelial Cells

An endotoxin-induced serum factor that causes necrosis of tumors

Carswell, E. A., Old, L. J., Kassel, R. L., Green, S., Fiore, N., & Williamson, B. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.9.3666 · Cited by 4,532

Cellular and Molecular Immunology

Abbas, A. K., Lichtman, A. H., & Pillai, S. S. (1994) · Cited by 3,571

Tumor necrosis factor alpha and interleukin 1 stimulate the human immunodeficiency virus enhancer by activation of the nuclear factor kappa B.

Osborn, L., Kunkel, S. L., & Nabel, G. J. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.7.2336 · Cited by 1,583

Influenza A Virus Lacking the NS1 Gene Replicates in Interferon-Deficient Systems

García‐Sastre, A., Egorov, A., Matassov, D., Brandt, S., Levy, D. E., Durbin, J. E., Palese, P., & Muster, T. (1998) · Virology · doi:10.1006/viro.1998.9508 · Cited by 1,000

Tumor necrosis factor alpha activates human immunodeficiency virus type 1 through induction of nuclear factor binding to the NF-kappa B sites in the long terminal repeat.

Duh, E. J., Maury, W. J., Folks, T. M., Fauci, A. S., & Rabson, A. B. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.15.5974 · Cited by 767

Tumour necrosis factors α and β inhibit virus replication and synergize with interferons

Wong, G. H., & Goeddel, D. V. (1986) · Nature · doi:10.1038/323819a0 · Cited by 707

Tumor necrosis factor alpha induces expression of human immunodeficiency virus in a chronically infected T-cell clone.

Folks, T. M., Clouse, K. A., Justement, J. S., Rabson, A. B., Duh, E. J., Kehrl, J. H., & Fauci, A. S. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.7.2365 · Cited by 701

Local and systemic cytokine responses during experimental human influenza A virus infection. Relation to symptom formation and host defense.

Hayden, F. G., Fritz, R., Lobo, M. C., Alvord, W. G., Strober, W., & Straus, S. E. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1355 · Cited by 680

Mx protein: Constitutive expression in 3T3 cells transformed with cloned Mx cDNA confers selective resistance to influenza virus

Staeheli, P., Haller, O., Boll, W., Lindenmann, J.-M., & Weissmann, C. (1986) · Cell · doi:10.1016/0092-8674(86)90493-9 · Cited by 488

Antiviral effects of recombinant tumour necrosis factor in vitro

Mestan, J., Digel, W., Mittnacht, S., Hillen, H., Blohm, D. H., Möller, A., Jacobsen, H., & Kirchner, H. (1986) · Nature · doi:10.1038/323816a0 · Cited by 379

Chronic exposure to arsenite enhances influenza virus infection in cultured cells

Amouzougan, E. A., Lira, R., & Klimecki, W. T. (2020) · Journal of Applied Toxicology · doi:10.1002/jat.3918 · Cited by 5

Evaluation of the added value of viral genomic information for predicting severity of influenza infection

Goethem, N. V., Robert, A. R., Bossuyt, N., Poelvoorde, L. A. E. V., Quoilin, S., Keersmaecker, S. C. J. D., Devleesschauwer, B., Thomas, I., Vanneste, K., Roosens, N. H. C., et al. (2021) · BMC Infectious Diseases · doi:10.1186/s12879-021-06510-z · Cited by 5

Severe Acute Respiratory Syndrome Coronavirus 2 and the Use of Biologics in Patients With Psoriasis

Ladda, M. A., Lynde, C. W., & Fleming, P. (2020) · Journal of Cutaneous Medicine and Surgery · doi:10.1177/1203475420945234 · Cited by 5

Transfection of influenza A virus nuclear export protein induces the expression of tumor necrosis factor alpha

Lara-Sampablo, A., Flores-Alonso, J. C., Jesús-Ortega, N. D., Santos‐López, G., Vallejo‐Ruiz, V., Rosas-Murrieta, N. H., Reyes-Carmona, S. R., Camacho, I. H., & Reyes‐Leyva, J. (2014) · Virus Research · doi:10.1016/j.virusres.2014.03.011 · Cited by 5

Piperazine inhibits Anatid herpesvirus-1 infection by possible modulation of host cytokines

Bhattacharya, S., & Kumar, S. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107786 · Cited by 4

Host cell and viral protease targets of human SERPINs identified by in silico docking

Galvan, J. R., de Vries, M., Belblidia, S., Fisher, A., Prescott, R. A., Crosse, K. M., Hearing, P., Mangel, W. F., Duerr, R., & Dittmann, M. (2025) · The EMBO Journal · doi:10.1038/s44318-025-00546-6 · Cited by 4

PENGARUH KONSUMSI MINUMAN BEROKSIGEN TERHADAP INFLAMASI DAN KAPASITAS ANTIOKSIDAN PENDERITA PENYAKIT-PARU-OBSTRUKTIF-KRONIK (PPOK)

Departemen Ilmu dan Teknologi Pangan, F. T. P., Zakaria, F. R., Azni, I. N., Program Studi Ilmu Pangan, F. T. P., Syamsir, E., Program Studi Ilmu Pangan, F. T. P., Amalia, K. M., Klinik dr. Katili, J. R. D., Yamani, C., & Klinik dr. Katili, J. R. D. (2014) · Jurnal Teknologi dan Industri Pangan · doi:10.6066/jtip.2014.25.1.31 · Cited by 4

Gripe aviar: lo que un intensivista debe conocer

Casillas, S., Fernández, S. H., & Varón, J. (2008) · Medicina Intensiva · doi:10.1016/s0210-5691(08)70936-7 · Cited by 4

Systemic immunobiological, immunosuppressant, and oncologic agents for the treatment of dermatologic diseases during the SARS‐CoV ‐2 ( COVID‐19 ) pandemic emergency: A quick review for a quick consultation

Paolino, G., Mercuri, S. R., Bearzi, P., & Mattozzi, C. (2020) · Dermatologic Therapy · doi:10.1111/dth.13537 · Cited by 4

The Immune Response to Influenza A Viruses

Mintern, J. D., Guillonneau, C., Turner, S. J., & Doherty, P. C. (2010) · Springer eBooks · doi:10.1007/978-3-0346-0279-2_8 · Cited by 4

Reconstructing signaling pathways using regular language constrained paths

Wagner, M. J., Pratapa, A., & Murali, T. M. (2019) · Bioinformatics · doi:10.1093/bioinformatics/btz360 · Cited by 4

Viral Defense Mechanisms against Interferon

Bose, S., & Banerjee, A. K. (2006) · Wiley eBooks · doi:10.1002/3527608206.ch9 · Cited by 4

The immune receptors TLR4 and SLAMF1 regulate TNF release by human metapneumovirus in human macrophages

Bye, K. S., Rian, K., Ryan, L., Espevik, T., Anthonsen, M. W., & Yurchenko, M. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1697494 · Cited by 3

Organoids in COVID-19: can we break the glass ceiling?

Chau, C. W., & Sugimura, R. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiad098 · Cited by 3

Salmonella-Delivered COBRA-HA1 Antigen Derived from H1N1 Hemagglutinin Sequences Elicits Broad-Spectrum Protection Against Influenza A Subtypes

Aganja, R. P., Senevirathne, A., Sivasankar, C., & Lee, J. H. (2023) · Engineering · doi:10.1016/j.eng.2023.08.001 · Cited by 3

Identifying Conserved DR1501-Restricted CD4 + T-Cell Epitopes in Avian H5N1 Hemagglutinin Proteins

Wang, S., Yao, L., Liu, S., Chong, P. C.-S., Liu, W.-T., Chen, Y. A., & Huang, J. C. (2010) · Viral Immunology · doi:10.1089/vim.2010.0058 · Cited by 3

Lung Cytokine Gene Expression is Correlated with Increased Severity of Disease in a Novel H4N8 Influenza Virus Isolated from Shorebirds

Arai, Y., Bui, V. N., Takeda, Y., Trinh, D. Q., Nibuno, S., Runstadler, J. A., Ogawa, H. K., & Imai, K. (2013) · Journal of Veterinary Medical Science · doi:10.1292/jvms.13-0201 · Cited by 3

Regulation of the chikungunya-virus-induced innate inflammatory response by protein tyrosine phosphatase non-receptor 6 in muscle cells

Thanapati, S., Sudeep, A. B., Kulkarni, S. P., & Tripathy, A. S. (2017) · Archives of Virology · doi:10.1007/s00705-017-3615-7 · Cited by 3

Human complement Factor H and Properdin act as soluble pattern recognition receptors and differentially modulate SARS-CoV-2 InfectionPreprint

Beirag, N., Varghese, P. M., Kumar, C., Idicula‐Thomas, S., Neto, M. M., Khan, H. A., Sim, R. B., Madan, T., Temperton, N. J., & Kishore, U. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.07.548083 · Cited by 3

Micro-transcriptome analysis reveals miRNA-mediated survival strategies between megalocytivirus RBIV-C1 and Scophthalmus maximus

Zhang, J., Sun, X., Zhang, S., & Li, X. (2024) · Aquaculture · doi:10.1016/j.aquaculture.2024.740762 · Cited by 2

Differential modulation of SARS-CoV-2 infection by complement factor H and properdin

Kishore, U., Varghese, P. M., Kumar, C., Idicula‐Thomas, S., Neto, M. M., Tsolaki, A. G., Ponnachan, P., Masmoudi, K., al-Ramadi, B. K., Vatish, M., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1620229 · Cited by 2

Modulation of CD8+T cells, NK cells and Th1cytokines by metabolic milieu in decline of HBV-viremia in pregnant women treated with tenofovir-disoproxil from second trimester of pregnancy

Pahwa, P., Vyas, A. K., Sevak, J. K., Singh, R., Maras, J. S., Patra, S., Sarin, S. K., & Trehanpati, N. (2024) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2024.104208 · Cited by 2

Immune checkpoints are suppressed during pregnancy following influenza A virus infection

Vanders, R. L., Gomez, H. M., Daly, K., Wark, P. A. B., Horvat, J. C., & Hansbro, P. M. (2024) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00391.2023 · Cited by 2

Avian Influenza Viruses and Pandemic Influenza

de Jong, M. D. (2006) · Springer eBooks · doi:10.1007/978-0-387-32830-0_9 · Cited by 2

Invited commentary on David Fedson’s article

Clark, I. A., & Alleva, L. M. (2009) · Influenza and Other Respiratory Viruses · doi:10.1111/j.1750-2659.2009.00098.x · Cited by 2

The mRNA and Proteins Expression Levels Analysis of TC-1 Cells Immune Response to H9N2 Avian Influenza Virus

Liu, J., Li, N., Meng, D., Hao, M., Wei, L., & Chai, T. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01039 · Cited by 2

Impact of patient characteristics on innate immune responses and inflammasome activation in ex vivo human lung tissues infected with influenza A virus

Huang, C., Wu, Y.-C., Hsieh, M., Lin, Y.-J., Hsieh, T.-H., Huang, P.-W. D., Yang, S.-L., Tsao, K., Shih, S., & Lee, L. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1269329 · Cited by 2

Strategies of NF-κB signaling modulation by ectromelia virus in BALB/3T3 murine fibroblasts

Struzik, J., Szulc‐Dąbrowska, L., Winnicka, A., & Niemiałtowski, M. (2015) · Microbial Pathogenesis · doi:10.1016/j.micpath.2015.07.017 · Cited by 2

Assessment of In Vitro Models of the Human Buccal Mucosa for Vaccine and Adjuvant Development

Davis, M. M., Bajrovic, I., & Croyle, M. A. (2025) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.4c01186 · Cited by 1

Changes in cytokine profile of M1 macrophages with administration of Swarna vachadi yoga - An observation

Rawat, H., Bhatia, K., Gupta, V. K., Upadhyay, S. K., & Ojha, N. K. (2025) · International Journal of Ayurveda Research · doi:10.4103/ijar.ijar_161_24 · Cited by 1

Let-7f-5p Inhibits PRRSV Replication by Regulating Lipid Metabolic Reprogramming in Infected Cells

Jiang, D., Huang, J., Wang, X., Zhao, G., Li, C., Yang, L., Meng, X., & Xu, Q. (2025) · Veterinary Sciences · doi:10.3390/vetsci12121176 · Cited by 1

Антивирусные и противовоспалительные мишени апротинина: перспективы нового использования

Жирнов, О. П., Poyarkov, S. V., & Малышев, Н. А. (2009) · PULMONOLOGIYA · doi:10.18093/0869-0189-2009-3-109-118 · Cited by 1

Gene expression ranking change based single sample pre-disease state detection

Bao, Z., Li, X., Xu, P., & Zan, X. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2024.1509769 · Cited by 1

Diet composition affects bat viral shedding with potential consequences for pathogen spillover

Vanalli, C., Falvo, C., Crowley, D. E., Schwarz, B. H., Plowright, R. K., Hudson, P. J., Rynda‐Apple, A., & Cattadori, I. M. (2025) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2025.0547 · Cited by 1

Genetic characterization and pathogenicity in a mouse model of newly isolated bat-originated mammalian orthoreovirus in South Korea

Do, H.-Q., Yeom, M., Moon, S., Lee, H., Chung, C., Chung, H., Park, J. W., Na, W., & Song, D. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.01762-23 · Cited by 1

Cytokine Expression at Different Stages of Influenza A(H1N1)pdm09 Virus Infection in the Porcine Lung, Using Laser Capture Microdissection

Hicks, D. J., Kelly, M., Brookes, S. M., Löndt, B. Z., Peláez, A., Orłowska, A., Brown, I. H., Spencer, Y. I., & Núñez, A. (2014) · Transboundary and Emerging Diseases · doi:10.1111/tbed.12232 · Cited by 1

Induction profiles of mRNA of toll like receptors and cytokines in chickens pre-exposed to low pathogenic avian influenza H9N2 virus followed by challenge with highly pathogenic avian influenza H5N1 virus

Dash, S. K., Kumar, M., Kataria, J. M., Nagarajan, S., Tosh, C., Murugkar, H. V., Rajukumar, K., Kalaiyarasu, S., Kumar, D. S., & Kulkarni, D. D. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.02.041 · Cited by 1

COVID-19 Cytokine Storm, Co-Infections, and Secondary Infections: Recent Information and Clinical Implications

Shahzaib, A., Raza, T., & Areej, A. (2023) · Hosts and Viruses · doi:10.17582/journal.hv/2023/10.1.13 · Cited by 1

Natural killer cell activation, trafficking, and contribution to immune responses to viral pathogens

Carlin, L. E. (2013) · doi:10.17077/etd.mj5sjj3n · Cited by 1

Exploring Cell Tropism as a Possible Contributor to Influenza Infection Severity

Beauchemin, C. A. A., Dobrovolny, H. M., Baron, M. J., Gieschke, R., Davies, B. E., & Jumbe, N. L. ‘. (2021) · doi:10.32920/14639763.v1 · Cited by 1

In-silico docking platform with serine protease inhibitor (SERPIN) structures identifies host cysteine protease targets with significance for SARS-CoV-2Preprint

Galvan, J. R., de Vries, M., Belblidia, S., Fisher, A., Prescott, R. A., Crosse, K. M., Mangel, W. F., Duerr, R., & Dittmann, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.18.517133 · Cited by 1

FLUAV RAM-IGIP: A modified live influenza virus vaccine that enhances humoral and mucosal responses against influenzaPreprint

Cáceres, C. J., Gay, L. C., Jain, A., Mejías, T. D., Cárdenas, M., Seibert, B., Faccin, F. C., Cowan, B., Geiger, G., Baker, A. L. V., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.23.576908 · Cited by 1

Crucial role for iron metabolism in mediating influenza A virus infection and associated diseasePreprint

Pillar, A. L., Daly, K., Gomez, H. M., Essilfie, A., Tan, K. S., Liu, J., Andiappan, A. K., Brown, A. C., Kim, R., Nichol, K., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.20.644262 · Cited by 1

Comparison of the CD4+ T cell and antibody responses to different Influenza vaccination regimens and to infection in naive and pre-exposed mice

Ronconi, V. (2010) · Padua Research Archive (University of Padova)

Influenza-specific B cell responses in HLA-DR1 transgenic mice

Huan, L. (2010)

Early host response and immune signaling to 2009 pandemic influenza A (H1N1) viruses in primary cell culture models.

Gerlach, R. L. (2015) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2078

Traitement anti-TNFα et vaccination de l'adulte

Duchet-Niedziolka, P., Coutsinos, Z., Hanslik, T., & Launay, O. (2007) · Revue du Rhumatisme · doi:10.1016/j.rhum.2007.08.001

Simian varicella virus and varicella-zoster virus immune evasion of NFkB activation

Whitmer, T. (2015) · doi:10.6083/m4k07374

Effect of influenza A virus and bacterial lipopolysaccharide on proliferation and expression of cytokines and other cellular factors in the endothelial cell line ECV-304

Смирнова, С. С., Pisareva, M., Smirnova, T. D., Plotnikova, M. A., Сивак, К. В., & Vorobiev, K. V. (2017) · Cell and Tissue Biology · doi:10.1134/s1990519x17020055

Viral and bacterial sepsis: identification and characterization of cytokine profiles and cell death pathways

Paul, M. (2016) · Lu Zone Ul (Laurentian University)

The effects of Tumour necrosis factor-alpha and Interleukin-1-beta on intracellular calcium handling and contractility in sheep ventricular myocytes

Hadgraft, N. (2019) · University of Salford Institutional Repository (University of Salford)

The Effect of COPD on the Immune Response to Influenza Virus Vaccination

Rossitch, E. G. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/t5cg-9460

The immune response to influenza A viruses

Mintern, J. D., Guillonneau, C., Turner, S. J., & Doherty, P. C. (2008) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-8371-8_6

A Spatial Model For The Spread Of Influenza Within The Human Respiratory Tract

Younis, N. P. (2021) · doi:10.32920/ryerson.14661615.v1

Kinetics of influenza A virus infections in a heterogeneous cell population

Baron, M. J. (2021) · doi:10.32920/ryerson.14656902

A Spatial Model For The Spread Of Influenza Within The Human Respiratory Tract

Younis, N. P. (2021) · doi:10.32920/ryerson.14661615

Kinetics of influenza A virus infections in a heterogeneous cell population

Baron, M. J. (2021) · doi:10.32920/ryerson.14656902.v1

Human placental hematopoietic stem cell-derived natural killer cells (CYNK) recognize and eliminate influenza A virus-infected cells

Gunasekaran, M., DiFiglia, A., Fitzgerald, J., HARIRI, R. J., van der Touw, W., & Mahlakõiv, T. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.900624

Induction of interleukin-1 receptor antagonist (IL-1Ra) by porcine reproductive and respiratory syndrome virus (PRRSV)

Nedumpun, T. (2017) · doi:10.58837/chula.the.2017.356

The role of cytokine response in influenza virus pathogenesis in humans

Gouri, V., Singh, S. R., Khan, A., Sharma, A., & Samant, M. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-15283-2.00013-0

Evaluation of the immunomodulatory and antiviral effects of small interfering RNAs Nup98.1 and Nup205.1 in an in vivo influenza model

Pashkov, E. A., Файзулоев, Е. Б., Milchakov, D., Lushnikov, R., Bogdanova, E. A., Rozhkova, L. S., Свитич, О. А., & Zverev, V. V. (2024) · Cytokines and inflammation · doi:10.17816/ci636513

Differential expression of cytokine genes during natural course of lumpy skin disease virus infection in cattle with varied clinical presentation of the disease

Poloju, D., Gulzar, S., Lodugu, P., Sharma, G. K., Nandi, S., Mahendran, K., Sankar, M., Balaji, K. S., Mahajan, S., Mishra, R., et al. (2025) · International Journal of Advanced Biochemistry Research · doi:10.33545/26174693.2025.v9.i8sc.5104

Additional file 1 of Evaluation of the added value of viral genomic information for predicting severity of influenza infection

Goethem, N. V., Robert, A. R., Bossuyt, N., Poelvoorde, L. A. E. V., Quoilin, S., Keersmaecker, S. C. J. D., Devleesschauwer, B., Thomas, I., Vanneste, K., Roosens, N. H. C., et al. (2021) · Figshare · doi:10.6084/m9.figshare.15145872

Additional file 1 of Sinensetin suppresses influenza a virus-triggered inflammation through inhibition of NF-κB and MAPKs signalings

Li, J., Jie, X., Liang, X., Chen, Z., Xie, P., 潘锡平, Zhou, B., & Li, J. (2020) · Figshare · doi:10.6084/m9.figshare.12258008

Pentameric M2e influenza vaccine candidate generates strong immunity with limited survival benefit

Kumar, V., Vishwakarma, P., Raj, S., Saxena, S., Rizvi, Z. A., Kumar, A., Awasthi, A., & Samal, S. (2026) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2025.2610073

The adult nasal mucosa is defined by distinct immune profiles that modulate in-vitro SARS-CoV-2 infection

Gowanlock, S. N., Lam, V. H. K., Tepe, Z. G., Park, D. E., Tai, V., Salazar, J. E., Pham, T., Khan, Y. N., Nelson, S., Horn, C., et al. (2026) · Respiratory Research · doi:10.1186/s12931-026-03697-0

α-Galactosylceramide-expanded virtual memory CD8+ T cells confer protection against a broad range of pathogens

Xie, J.-X., Li, D., Lai, M.-C., Su, Y.-L., Tai, C., Wang, C.-C., & Lin, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1799271

A functional genomics-pharmacotranscriptomics framework identifies host-directed anti-influenza agents

Qiu, J., Xing, X., Wang, J., Yuan, W., Li, X., Wu, A., Gu, Z., Zhou, Z., & Wang, J. (2026) · iScience · doi:10.1016/j.isci.2026.116899

Endogenous Expression of an RNA-Hydrolyzing Minibody Enhances the Therapeutic Effects Against Influenza a Virus Compared to Therapeutically Intranasal Administration

Luong, Q. X. T., Lee, Y., Lin, C., Akram, M. S., Ho, P. T., Hoang, P. T., Ayun, R. Q., Thuỷ, V. T. B., Lee, T., & Lee, S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27177850

Red Pitahaya Betacyanins Selectively Upregulate Proinflammatory Cytokines In Vitro During Influenza A Virus Infection

Lim, C., Isa, N. M., Omar, A. R., & Choo, W. S. (2026) · International Journal of Microbiology · doi:10.1155/ijm/4807321

Integrated mechanistic and serological analyses reveal determinants of antibody-dependent enhancement in respiratory coronaviruses

Tingting, X., Jiang, Y., Li, C., Chen, H., Zhang, Z., Zhang, H., Qiu, Y., & Zhou, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1967945

The immune response in Influenza A-S. pneumoniae coinfection

Ellis, G. T. (2014) · UCL Discovery (University College London)

Tumor necrosis factor as a mediator of inflammation in influenza A viral pneumonia

Peper, R. L., & Campen, H. V. (1995) · Microbial Pathogenesis · doi:10.1006/mpat.1995.0056 · Cited by 137

Tumor Necrosis Factor Alpha Enhances Influenza A Virus-Induced Expression of Antiviral Cytokines by Activating RIG-I Gene Expression

Matikainen, S., Sirén, J., Tissari, J., Veckman, V., Pirhonen, J., Severa, M., Sun, Q., Lin, R., Meri, S., Uzé, G., et al. (2006) · Journal of Virology · doi:10.1128/jvi.80.7.3515-3522.2006 · Cited by 152

Antiviral Effect of TNF-α and IFN-γ Secreted from a CD8 + Influenza Virus-Specific CTL Clone

Kuwano, K., Kawashima, T., & Arai, S. (1993) · Viral Immunology · doi:10.1089/vim.1993.6.1 · Cited by 27

Influenza A virus replication is inhibited by tumor necrosis factor-α in vitro

Campen, H. V. (1994) · Archives of Virology · doi:10.1007/bf01321073 · Cited by 26

TNF-α and IFN-α enhance influenza-A-virus-induced chemokine gene expression in human A549 lung epithelial cells

Veckman, V., Österlund, P., Fagerlund, R., Melén, K., Matikainen, S., & Julkunen, I. (2005) · Virology · doi:10.1016/j.virol.2005.09.043 · Cited by 111