The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.
Identification of Oxidative Stress and Toll-like Receptor 4 Signaling as a Key Pathway of Acute Lung Injury
Open accessAbstract
Multiple lung pathogens such as chemical agents, H5N1 avian flu, or SARS cause high lethality due to acute respiratory distress syndrome. Here we report that Toll-like receptor 4 (TLR4) mutant mice display natural resistance to acid-induced acute lung injury (ALI). We show that TLR4-TRIF-TRAF6 signaling is a key disease pathway that controls the severity of ALI. The oxidized phospholipid (OxPL) OxPAPC was identified to induce lung injury and cytokine production by lung macrophages via TLR4-TRIF. We observed OxPL production in the lungs of humans and animals infected with SARS, Anthrax, or H5N1. Pulmonary challenge with an inactivated H5N1 avian influenza virus rapidly induces ALI and OxPL formation in mice. Loss of TLR4 or TRIF expression protects mice from H5N1-induced ALI. Moreover, deletion of ncf1, which controls ROS production, improves the severity of H5N1-mediated ALI. Our data identify oxidative stress and innate immunity as key lung injury pathways that control the severity of ALI.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Macrophage activation via TLR4, a type of PRR, is also involved in gastric acid-induced ARDS and mouse ARDS models induced by SARS-CoV-1 or influenza virus H5N1 (355).”
From IL-6 in inflammation, autoimmunity and cancer (2021) · cites this paper as [355]
Experimental — accuracy not yet measuredIn the citing paper
“endogenous products such as oxidized phospholipids and matrix breakdown products also drive inflammation through TLR4 and probably other TLRs, providing a mechanism for perpetuating inflammation when microbial products are being cleared from the lungs (68,72).”
From Into the Eye of the Cytokine Storm (2012) · cites this paper as [68]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Pathogen Recognition and Innate Immunity
Akira, S., Uematsu, S., & Takeuchi, O. (2006) · Cell · doi:10.1016/j.cell.2006.02.015 · Cited by 12,401
Self-citationDefective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene
Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631
A Toll-like receptor recognizes bacterial DNA
Hemmi, H., Takeuchi, O., Kawai, T., Kaisho, T., Sato, S., Sanjo, H., Matsumoto, M., Hoshino, K., Wagner, H., Takeda, K., et al. (2000) · Nature · doi:10.1038/35047123 · Cited by 6,491 · cited 2×
“Lung pathology were not affected in tlr3 (Yamamoto et al., 2003) or tlr9 (Hemmi et al., 2000) mutant mice (Figures S2A and S2B).”
BackgroundSelf-citationThe Acute Respiratory Distress Syndrome
Matthay, M. A. (1996) · New England Journal of Medicine · doi:10.1056/nejm199605303342209 · Cited by 4,924
The Acute Respiratory Distress Syndrome
Ware, L. B., & Matthay, M. A. (2000) · New England Journal of Medicine · doi:10.1056/nejm200005043421806 · Cited by 4,666
Hoshino, K., Takeuchi, O., Kawai, T., Sanjo, H., Ogawa, T., Takeda, Y., Takeda, K., & Akira, S. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.7.3749 · Cited by 3,374
Self-citationRole of Adaptor TRIF in the MyD88-Independent Toll-Like Receptor Signaling Pathway
Yamamoto, M., Sato, S., Hemmi, H., Hoshino, K., Kaisho, T., Sanjo, H., Takeuchi, O., Sugiyama, M., Okabe, M., Takeda, K., et al. (2003) · Science · doi:10.1126/science.1087262 · Cited by 3,286
Self-citationAngiotensin-converting enzyme 2 protects from severe acute lung failure
Imai, Y., Kuba, K., Rao, S., Huan, Y., Guo, F., Guan, B., Yang, P., Sarao, R., Wada, T., Leong-Poi, H., et al. (2005) · Nature · doi:10.1038/nature03712 · Cited by 2,453
Self-citationTargeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function.
Adachi, O., Kawai, T., Takeda, K., Matsumoto, M., Tsutsui, H., Sakagami, M., Nakanishi, K., & Akira, S. (1998) · Immunity · doi:10.1016/s1074-7613(00)80596-8 · Cited by 2,358
Self-citationConditional gene targeting in macrophages and granulocytes using LysMcre mice
Clausen, B. E., Burkhardt, C., Reith, W., Renkawitz, R., & Förster, I. (1999) · Transgenic Research · doi:10.1023/a:1008942828960 · Cited by 2,098
Cited by
Sorted by citations
Items 101–200 of 1,000
Angiotensin-converting enzyme 2 inhibits lung injury induced by respiratory syncytial virus
Gu, H., Xie, Z., Li, T., Zhang, S., Lai, C., Zhu, P., Wang, K., Han, L., Duan, Y., Zhao, Z., et al. (2016) · Scientific Reports · doi:10.1038/srep19840 · Cited by 247
World Journal of Pharmaceutical Sciences
(2021) · World Journal of Pharmaceutical Sciences · doi:10.54037/wjps · Cited by 246
Evasion of Influenza A Viruses from Innate and Adaptive Immune Responses
van de Sandt, C. E., Kreijtz, J. H. C. M., & Rimmelzwaan, G. F. (2012) · Viruses · doi:10.3390/v4091438 · Cited by 267
Dai, J., Gu, L., Su, Y., Wang, Q., Zhao, Y., Chen, X.-X., Deng, H., Li, W., Wang, G., & Li, K. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.11.009 · Cited by 242
Inflammasomes and adaptive immune responses
Deets, K. A., & Vance, R. E. (2021) · Nature Immunology · doi:10.1038/s41590-021-00869-6 · Cited by 243
Inhibition of Nox2 Oxidase Activity Ameliorates Influenza A Virus-Induced Lung Inflammation
Vlahos, R., Stambas, J., Bozinovski, S., Broughton, B. R. S., Drummond, G. R., & Selemidis, S. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1001271 · Cited by 240
Olagnier, D. P., Peri, S., Steel, C., van Montfoort, N., Chiang, C., Beljanski, V., Slifker, M. J., He, Z., Nichols, C. N., Lin, R., et al. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004566 · Cited by 238
The Mechanism behind Influenza Virus Cytokine Storm
Gu, Y., Zuo, X., Zhang, S., Ouyang, Z., Jiang, S., Wang, F., & Wang, G. (2021) · Viruses · doi:10.3390/v13071362 · Cited by 241
Innate immune responses to influenza A H5N1: friend or foe?
Peiris, J. S. M., Cheung, C. Y., Leung, C. Y. H., & Nicholls, J. M. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.09.004 · Cited by 232
Self-citationABCA1 and ABCG1 Protect Against Oxidative Stress–Induced Macrophage Apoptosis During Efferocytosis
Yvan-Charvet, L., Pagler, T. A., Seimon, T. A., Thorp, E., Welch, C. L., Witztum, J. L., Tabas, I., & Tall, A. R. (2010) · Circulation Research · doi:10.1161/circresaha.110.217281 · Cited by 217
Zanoni, I., Tan, Y., Di Gioia, M., Springstead, J. R., & Kagan, J. C. (2017) · Immunity · doi:10.1016/j.immuni.2017.09.010 · Cited by 221
Cardiovascular Manifestations of COVID-19 Infection
Magadum, A., & Kishore, R. (2020) · Cells · doi:10.3390/cells9112508 · Cited by 230
Seki, H., Fukunaga, K., Arita, M., Arai, H., Nakanishi, H., Taguchi, R., Miyasho, T., Takamiya, R., Asano, K., Ishizaka, A., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901809 · Cited by 227
A Role for Neutrophils in Viral Respiratory Disease
Camp, J. V., & Jonsson, C. B. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00550 · Cited by 233
Schönrich, G., Raftery, M. J., & Samstag, Y. (2020) · Advances in Biological Regulation · doi:10.1016/j.jbior.2020.100741 · Cited by 226
Magro, G. (2020) · Cytokine X · doi:10.1016/j.cytox.2020.100029 · Cited by 214
Novel concepts of acute lung injury and alveolar-capillary barrier dysfunction
Herold, S., Gabrielli, N. M., & Vadász, I. (2013) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00232.2013 · Cited by 210
Biological role of Toll-like receptor-4 in the brain
Trotta, T., Porro, C., Calvello, R., & Panaro, M. A. (2014) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2014.01.014 · Cited by 209
Discovery of GSK2795039, a Novel Small Molecule NADPH Oxidase 2 Inhibitor
Hirano, K., Chen, W. S., Chueng, A. L. W., Dunne, A. A., Seredenina, T., Filippova, A., Ramachandran, S., Bridges, A., Chaudry, L., Pettman, G., et al. (2015) · Antioxidants & Redox Signaling · doi:10.1089/ars.2014.6202 · Cited by 205
Geiler, J., Michaelis, M., Naczk, P., Leutz, A., Langer, K., Doerr, H.-W., & Cinatl, J. J. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.08.025 · Cited by 205
Horan, K., Hansen, K., Jakobsen, M. R., Holm, C. K., Søby, S., Unterholzner, L., Thompson, M., West, J. A., Iversen, M. B., Rasmussen, S. B., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202749 · Cited by 212
Role of Phospholipid Oxidation Products in Atherosclerosis
Lee, S., Birukov, K. G., Romanoski, C. E., Springstead, J. R., Lusis, A. J., & Berliner, J. A. (2012) · Circulation Research · doi:10.1161/circresaha.111.256859 · Cited by 206
Neutralization of Oxidized Phospholipids Ameliorates Non-alcoholic Steatohepatitis
Sun, X., Seidman, J. S., Zhao, P., Troutman, T. D., Spann, N. J., Que, X., Zhou, F., Liao, Z., Pasillas, M. P., Yang, X., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.10.014 · Cited by 213
Shirey, K. A., Pletneva, L. M., Puche, A. C., Keegan, A. D., Prince, G. A., Blanco, J. C. G., & Vogel, S. N. (2010) · Mucosal Immunology · doi:10.1038/mi.2010.6 · Cited by 209
Pulmonary Surfactant: An Immunological Perspective
Chroneos, Z. C., Sever-Chroneos, Z., & Shepherd, V. L. (2009) · Cellular Physiology and Biochemistry · doi:10.1159/000272047 · Cited by 208
Toll-like receptor 4 in acute viral infection: Too much of a good thing
Olejnik, J., Hume, A. J., & Mühlberger, E. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007390 · Cited by 200
Hoetzenecker, W., Echtenacher, B., Guenova, E., Höetzenecker, K., Woelbing, F., Brück, J., Teske, A., Valtcheva, N., Fuchs, K., Kneilling, M., et al. (2011) · Nature Medicine · doi:10.1038/nm.2557 · Cited by 195
Roles of NF-κB in health and disease: mechanisms and therapeutic potential
Wong, E. T., & Tergaonkar, V. (2009) · Clinical Science · doi:10.1042/cs20080502 · Cited by 196
Memory CD4+ T cells induce innate responses independently of pathogen
Strutt, T. M., McKinstry, K. K., Dibble, J. P., Winchell, C. G., Kuang, Y., Curtis, J. D., Huston, G. E., Dutton, R. W., & Swain, S. L. (2010) · Nature Medicine · doi:10.1038/nm.2142 · Cited by 196
Wang, S., Le, T. Q., Kurihara, N., Chida, J., Cissé, Y., Yano, M., & Kido, H. (2010) · The Journal of Infectious Diseases · doi:10.1086/656044 · Cited by 195
Directing traffic: IL ‐17 and IL ‐22 coordinate pulmonary immune defense
McAleer, J. P., & Kolls, J. K. (2014) · Immunological Reviews · doi:10.1111/imr.12183 · Cited by 203
Chu, L. H., Indramohan, M., Ratsimandresy, R. A., Gangopadhyay, A., Morris, E. P., Monack, D. M., Dorfleutner, A., & Stehlik, C. (2018) · Nature Communications · doi:10.1038/s41467-018-03409-3 · Cited by 200
Modeling Host Genetic Regulation of Influenza Pathogenesis in the Collaborative Cross
Ferris, M. T., Aylor, D. L., Bottomly, D., Whitmore, A. C., Aicher, L. D., Bell, T. A., Bradel-Tretheway, B., Bryan, J. T., Buus, R. J., Gralinski, L. E., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003196 · Cited by 190
Tsai, S.-Y., Segovia, J. A., Chang, T.-H., Morris, I. R., Berton, M. T., Tessier, P. A., Tardif, M. R., Césaro, A., & Bose, S. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1003848 · Cited by 198
Tissue damage control in disease tolerance
Soares, M. P., Gozzelino, R., & Weis, S. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.08.001 · Cited by 187
Kong, X., Thimmulappa, R. K., Kombairaju, P., & Biswal, S. S. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0902315 · Cited by 195
Recognition of Streptococcus pneumoniae by the innate immune system
Koppe, U., Suttorp, N., & Opitz, B. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01746.x · Cited by 210
Effect of statins on toll-like receptors: a new insight to pleiotropic effects
Bahrami, A., Parsamanesh, N., Atkin, S. L., Banach, M., & Sahebkar, A. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.08.014 · Cited by 192
Askari, H., Rajani, S. F., Poorebrahim, M., Haghi‐Aminjan, H., Raeis-Abdollahi, E., & Abdollahi, M. R. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.01.012 · Cited by 191
Taleb, A., Witztum, J. L., & Tsimikas, S. (2011) · Biomarkers in Medicine · doi:10.2217/bmm.11.60 · Cited by 186
Innate Immune Evasion Strategies of Influenza Viruses
Hale, B. G., Albrecht, R. A., & García‐Sastre, A. (2009) · Future Microbiology · doi:10.2217/fmb.09.108 · Cited by 190
Can melatonin reduce the severity of COVID-19 pandemic?
Shneider, A., Kudriavtsev, A. V., & Vakhrusheva, A. (2020) · International Reviews of Immunology · doi:10.1080/08830185.2020.1756284 · Cited by 185
I mmunosenescence and Inflammaging: Risk Factors of Severe COVID-19 in Older People
Pietrobon, A. J., Teixeira, F. M. E., & Sato, M. N. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.579220 · Cited by 187
Ji, Y., Zhang, P., Zhang, X., Zhao, Y., Deng, K., Jiang, X., Wang, P., Huang, Z., & Li, H. (2016) · Nature Communications · doi:10.1038/ncomms11267 · Cited by 183
Regulation of redox balance in cancer and T cells
Kong, H., & Chandel, N. S. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.tm117.000257 · Cited by 182
Dong, Y., D’Mello, C., Pinsky, W., Lozinski, B. M., Kaushik, D. K., Ghorbani, S., Moezzi, D., Brown, D., Melo, F. C., Zandee, S., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00801-z · Cited by 181
COVID-19 and Respiratory System Disorders
Brosnahan, S. B., Jonkman, A. H., Kugler, M. C., Munger, J. S., & Kaufman, D. A. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.314515 · Cited by 182
The role of NADPH oxidases in infectious and inflammatory diseases
Taylor, J. P., & Tse, H. M. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102159 · Cited by 185
Haslund‐Vinding, J., McBean, G., Jaquet, V, & Vilhardt, F. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13425 · Cited by 169
Derivation and Diagnostic Accuracy of the Surgical Lung Injury Prediction Model
Kor, D. J., Warner, D. O., Alsara, A., Pérez, E. R. F., Malinchoc, M., Kashyap, R., Li, G., & Gajic, O. (2011) · Anesthesiology · doi:10.1097/aln.0b013e31821b5839 · Cited by 172
Models and mechanisms of acute lung injury caused by direct insults
Reiss, L. K., Uhlig, U., & Uhlig, S. (2012) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2011.11.004 · Cited by 178
Pathogenesis of emerging avian influenza viruses in mammals and the host innate immune response
Maines, T. R., Szretter, K. J., Perrone, L. A., Belser, J. A., Bright, R. A., Zeng, H., Tumpey, T. M., & Katz, J. M. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00690.x · Cited by 172
Function and Regulation of Noncanonical Caspase-4/5/11 Inflammasome
Matikainen, S., Nyman, T. A., & Cypryk, W. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000373 · Cited by 179
Endogenous oxidized phospholipids reprogram cellular metabolism and boost hyperinflammation
Gioia, M. D., Spreafico, R., Springstead, J. R., Mendelson, M., Joehanes, R., Levy, D. A., & Zanoni, I. (2019) · Nature Immunology · doi:10.1038/s41590-019-0539-2 · Cited by 176
The innate immune response to products of phospholipid peroxidation
Weismann, D., & Binder, C. J. (2012) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2012.01.018 · Cited by 174
Self-citationFunctional Role of Dietary Intervention to Improve the Outcome of COVID-19: A Hypothesis of Work
Messina, G., Polito, R., Monda, V., Cipolloni, L., Nunno, N. R. D., Mizio, G. D., Murabito, P., Carotenuto, M., Messina, A., Pisanelli, D., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093104 · Cited by 170
Wang, D., Lou, J., Ouyang, C., Chen, W., Liu, Y., Liu, X., Cao, X., Wang, J., & Lu, L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009428107 · Cited by 154
The SARS-Unique Domain (SUD) of SARS Coronavirus Contains Two Macrodomains That Bind G-Quadruplexes
Tan, J., Vonrhein, C., Smart, O. S., Bricogne, G., Bollati, M., Kusov, Y., Hansen, G., Mesters, J. R., Schmidt, C. L., & Hilgenfeld, R. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000428 · Cited by 174
A new era for the treatment of inflammatory autoimmune diseases by interleukin-6 blockade strategy
Tanaka, T., Narazaki, M., Ogata, A., & Kishimoto, T. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2014.01.009 · Cited by 166
Aberrant coagulation causes a hyper-inflammatory response in severe influenza pneumonia
Yang, Y., & Tang, H. (2016) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.1 · Cited by 165
Nová, Z., Škovierová, H., & Čalkovská, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040831 · Cited by 168
Sorokin, A. V., Karathanasis, S. K., Yang, Z., Freeman, L. A., Kotani, K., & Remaley, A. T. (2020) · The FASEB Journal · doi:10.1096/fj.202001451 · Cited by 170
Vergadi, E., Vaporidi, K., Theodorakis, E. E., Doxaki, C., Lagoudaki, E. D., Ieronymaki, E., Alexaki, V. I., Helms, M. W., Kondili, Ε., Sönnichsen, B., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300959 · Cited by 163
van den Brand, J. M. A., Haagmans, B. L., van Riel, D. A. J., Osterhaus, A. D. M. E., & Kuiken, T. (2014) · Journal of Comparative Pathology · doi:10.1016/j.jcpa.2014.01.004 · Cited by 161
Host response to influenza virus: protection versus immunopathology
Peiris, M. J. S., Hui, K. P. Y., & Yen, H. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.06.003 · Cited by 160
Treating influenza with statins and other immunomodulatory agents
Fedson, D. S. (2013) · Antiviral Research · doi:10.1016/j.antiviral.2013.06.018 · Cited by 162
Inhibition of Autophagy Ameliorates Acute Lung Injury Caused by Avian Influenza A H5N1 Infection
Sun, Y., Li, C., Shu, Y., Ju, X., Zou, Z., Wang, H., Rao, S., Guo, F., Liu, H., Nan, W., et al. (2012) · Science Signaling · doi:10.1126/scisignal.2001931 · Cited by 158
Self-citationToll-Like Receptor 4 Activation in Cancer Progression and Therapy
Oblak, A., & Jerala, R. (2011) · Clinical and Developmental Immunology · doi:10.1155/2011/609579 · Cited by 165
Mechanisms and Clinical Consequences of Acute Lung Injury
Fanelli, V., & Ranieri, V. M. (2015) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201407-340mg · Cited by 157
NOX Enzymes and Pulmonary Disease
Griffith, B. D., Pendyala, S., Hecker, L., Lee, P. J., Natarajan, V., & Thannickal, V. J. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2599 · Cited by 156
COVID 19: a clue from innate immunity
Birra, D., Benucci, M., Landolfi, L., Merchionda, A., Loi, G., Amato, P., Licata, G., Quartuccio, L., Triggiani, M., & Moscato, P. (2020) · Immunologic Research · doi:10.1007/s12026-020-09137-5 · Cited by 155
Yang, H.-Z., Wang, J.-P., Mi, S., Liu, H.-Z., Cui, B., Yan, H.-M., Yan, J., Li, Z., Liu, H., Hua, F., et al. (2012) · The American Journal of Pathology · doi:10.1016/j.ajpath.2011.09.019 · Cited by 155
Self-citationEndosomal nox2 oxidase exacerbates virus pathogenicity and is a target for antiviral therapy
To, E. E., Vlahos, R., Luong, R., Halls, M. L., Reading, P. C., King, P. T., Chan, C., Drummond, G. R., Sobey, C. G., Broughton, B. R. S., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00057-x · Cited by 154
Phenotypic modulation of macrophages in response to plaque lipids
Adamson, S., & Leitinger, N. (2011) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32834a97e4 · Cited by 154
Kuronuma, K., Mitsuzawa, H., Takeda, K., Nishitani, C., Chan, E. D., Kuroki, Y., Nakamura, M., & Voelker, D. R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.040832 · Cited by 154
Immune responses during COVID-19 infection
Melenotte, C., Silvin, A., Goubet, A., Lahmar, I., Dubuisson, A., Zumla, A. I., Raoult, D., Merad-Boudia, M., Gachot, B., Henon, C., et al. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1807836 · Cited by 167
Pathogenesis of Respiratory Viral and Fungal Coinfections
Salazar, F., Bignell, E., Brown, G. D., Cook, P. C., & Warris, A. (2021) · Clinical Microbiology Reviews · doi:10.1128/cmr.00094-21 · Cited by 164
Zhang, R., Ai, X., Duan, Y., Xue, M., He, W.-X., Wang, C.-L., Xu, T., Xu, M.-J., Liu, B., Li, C., et al. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.02.081 · Cited by 153
Self-citationZhao, J., Zhao, J., van Rooijen, N., & Perlman, S. M. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000636 · Cited by 151
Miura, K., Seki, E., Ohnishi, H., & Brenner, D. A. (2010) · Gastroenterology Research and Practice · doi:10.1155/2010/362847 · Cited by 152
Fessler, M. B., & Summer, R. S. (2016) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2016-0011ps · Cited by 151
Li, Y., Zeng, Z., Cao, Y., Liu, Y., Feng, P., Liang, M., Xue, Y., Xi, C., Zhou, M. S., & Jiang, W. (2016) · Scientific Reports · doi:10.1038/srep27911 · Cited by 150
Human Infection with Highly Pathogenic Avian Influenza A (H5N1) Virus: Review of Clinical Issues
Uyeki, T. M. (2009) · Clinical Infectious Diseases · doi:10.1086/600035 · Cited by 152
Gut mucosal DAMPs in IBD: from mechanisms to therapeutic implications
Boyapati, R. K., Rossi, A. G., Satsangi, J., & Ho, G. (2016) · Mucosal Immunology · doi:10.1038/mi.2016.14 · Cited by 150
Amatore, D., Sgarbanti, R., Aquilano, K., Baldelli, S., Limongi, D., Civitelli, L., Nencioni, L., Garaci, E., Ciriolo, M. R., & Palamara, A. T. (2014) · Cellular Microbiology · doi:10.1111/cmi.12343 · Cited by 150
Oxidized phospholipid-induced inflammation is mediated by Toll-like receptor 2
Kadl, A., Sharma, P. R., Chen, W., Agrawal, R., Meher, A. K., Rudraiah, S., Grubbs, N., Sharma, R., & Leitinger, N. (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.08.026 · Cited by 147
Inflammatory Caspases: Toward a Unified Model for Caspase Activation by Inflammasomes
Ross, C. M., Chan, A. H., von Pein, J. B., Maddugoda, M. P., Boucher, D., & Schroder, K. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101220-030653 · Cited by 157
Epidemiological and Experimental Links between Air Pollution and Type 2 Diabetes
Liu, C., Ying, Z., Harkema, J. R., Sun, Q., & Rajagopalan, S. (2012) · Toxicologic Pathology · doi:10.1177/0192623312464531 · Cited by 149
Covid-19: Perspectives on Innate Immune Evasion
Taefehshokr, N., Taefehshokr, S., Hemmat, N., & Heit, B. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.580641 · Cited by 152
Suppressing production of reactive oxygen species (ROS) for influenza A virus therapy
Vlahos, R., Stambas, J., & Selemidis, S. (2011) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2011.09.001 · Cited by 146
γ-Secretase Limits the Inflammatory Response Through the Processing of LRP1
Zurhove, K., Nakajima, C., Herz, J., Bock, H. H., & May, P. (2008) · Science Signaling · doi:10.1126/scisignal.1164263 · Cited by 151
The role of innate immunity in atherogenesis
Hartvigsen, K., Chou, M.-Y., Hansen, L. F., Shaw, P. X., Tsimikas, S., Binder, C. J., & Witztum, J. L. (2008) · Journal of Lipid Research · doi:10.1194/jlr.r800100-jlr200 · Cited by 143
Self-citationLee, C.-H. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6208067 · Cited by 142
The inflammatory response triggered by Influenza virus: a two edged sword
Tavares, L. P., Teixeira, M. M., & Garcia, C. C. (2016) · Inflammation Research · doi:10.1007/s00011-016-0996-0 · Cited by 148
Particulate Matter Air Pollution and Atherosclerosis
Brook, R. D., & Rajagopalan, S. (2010) · Current Atherosclerosis Reports · doi:10.1007/s11883-010-0122-7 · Cited by 138
Vijay, R., Hua, X., Meyerholz, D. K., Miki, Y., Yamamoto, K., Gelb, M. H., Murakami, M., & Perlman, S. M. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20150632 · Cited by 143
Role of the pulmonary epithelium and inflammatory signals in acute lung injury
Manicone, A. M. (2008) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.5.1.63 · Cited by 142
Context-Dependent Role of Oxidized Lipids and Lipoproteins in Inflammation
Miller, Y. I., & Shyy, J. Y.-J. (2016) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2016.11.002 · Cited by 141
Ling, L., Lu, Y., Zhang, Y., Zhu, H., Tu, P., Li, H., & Chen, D. (2019) · Phytomedicine · doi:10.1016/j.phymed.2019.153150 · Cited by 138
Regulation of innate immunity by NADPH oxidase
Segal, B. H., Grimm, M. J., Khan, A. N. H., Han, W., & Blackwell, T. S. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.04.022 · Cited by 140
Metadata
- Authors
- Imai, Y., Kuba, K., Neely, G. G., Yaghubian-Malhami, R., Perkmann, T., van Loo, G., Ermolaeva, M., Veldhuizen, R., Leung, Y. H. C., Wang, H., Liu, H., Sun, Y., Pasparakis, M., Kopf, M., Mech, C., Bavari, S., Peiris, J. S. M., Slutsky, A. S., Akira, S., Hultqvist, M., Holmdahl, R., Nicholls, J., Jiang, C., Binder, C. J., & Penninger, J. M.
- Affiliations
- Institute of Molecular Biotechnology (AT)
- Austrian Academy of Sciences (AT)
- University of Cologne (DE)
- Western University (CA)
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- United States Army Medical Research Institute of Infectious Diseases (US)
- St. Michael's Hospital (CA)
- Research Institute for Microbial Diseases, The University of Osaka (JP)
- Karolinska Institutet (SE)
- University of Hong Kong (HK)
- Corresponding author
- Imai, Yumiko
- Penninger, Josef M.
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2008-04
- Volume
- 133
- Issue
- 2
- Pages
- 235-249
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC7112336
- OpenAlex
- W2156613610
- Cited by
- 1,356
- References
- 60
- Citations by year
- 2026: 34 · 2025: 53 · 2024: 56 · 2023: 76 · 2022: 105 · 2021: 143 · 2020: 152 · 2019: 47 · 2018: 69 · 2017: 64 · 2016: 80 · 2015: 65 · 2014: 82 · 2013: 68 · 2012: 53
- FWCI
- 29.18
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1933 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- The HKU Scholars Hub (University of Hong Kong) (submittedVersion)
- Lund University Publications (Lund University) (submittedVersion)
- Funders
- University of Pittsburgh
- European Commission
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (100233)
- Defense Threat Reduction Agency
- Canadian Institutes of Health Research
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory Support and Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- acute lung injury, TLR4, TRIF, TRAF6, oxidized phospholipids, OxPAPC, oxidative stress, reactive oxygen species, NCF1, lung macrophages, H5N1 avian influenza, SARS, anthrax, innate immunity, respiratory distress syndrome
- MeSH terms
- Animals, Humans, Influenza, Human, Lung, Mice, Inbred C57BL, Orthomyxoviridae Infections, Phospholipids, Respiratory Distress Syndrome, Signal Transduction, Interleukin-6, NF-kappa B, Oxidative Stress, NADPH Oxidases, Adaptor Proteins, Vesicular Transport, Severe Acute Respiratory Syndrome, Toll-Like Receptor 4, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review