Revisiting caspases in sepsis
Open accessAbstract
Sepsis is a life-threatening illness that occurs due to an abnormal host immune network which extends through the initial widespread and overwhelming inflammation, and culminates at the late stage of immunosupression. Recently, interest has been shifted toward therapies aimed at reversing the accompanying periods of immune suppression. Studies in experimental animals and critically ill patients have demonstrated that increased apoptosis of lymphoid organs and some parenchymal tissues contributes to this immune suppression, anergy and organ dysfunction. Immediate to the discoveries of the intracellular proteases, caspases for the induction of apoptosis and inflammation, and their striking roles in sepsis have been focused elaborately in a number of original and review articles. Here we revisited the different aspects of caspases in terms of apoptosis, pyroptosis, necroptosis and inflammation and focused their links in sepsis by reviewing several recent findings. In addition, we have documented striking perspectives which not only rewrite the pathophysiology, but also modernize our understanding for developing novel therapeutics against sepsis.
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Pyroptosis is etiologically involved in pathological conditions such as lethal septic shock at least as induced by LPS.
“(4) is etiologically involved in pathological conditions such as lethal septic shock (at least as induced by LPS) [610, 611].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [610]
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Angus, D. C., Linde-Zwirble, W. T., Lidicker, J., Clermont, G., Carcillo, J., & Pinsky, M. R. (2001) · Critical Care Medicine · doi:10.1097/00003246-200107000-00002 · Cited by 8,503 · see citing works
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
Bootman, M. D., Missiaen, L., Parys, J. B., SMEDT, H. D., & Casteels, R. (1995) · Biochemical Journal · doi:10.1042/bj3060445 · Cited by 5,120 · see citing works
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837 · see citing works
Caspase-12 mediates endoplasmic-reticulum-specific apoptosis and cytotoxicity by amyloid-β
Nakagawa, T., Zhu, H., Morishima, N., Li, E., Xu, J., Yankner, B. A., & Yuan, J. (2000) · Nature · doi:10.1038/47513 · Cited by 3,262 · see citing works
A novel heterodimeric cysteine protease is required for interleukin-1βprocessing in monocytes
Thornberry, N., Bull, H., Calaycay, J., Chapman, K., Howard, A., Kostura, M., Miller, D. K., Molineaux, S., Weidner, J., Auniņš, J., et al. (1992) · Nature · doi:10.1038/356768a0 · Cited by 2,725 · see citing works
Caspase Functions in Cell Death and DiseasePreprint
McIlwain, D. R., Berger, T., & Mak, T. W. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008656 · Cited by 2,607 · see citing works
Non-canonical inflammasome activation targets caspase-11
Kayagaki, N., Warming, S., Lamkanfi, M., Walle, L. V., Louie, S., Dong, J., Newton, K., Qu, Y., Liu, J., Heldens, S., et al. (2011) · Nature · doi:10.1038/nature10558 · Cited by 2,530 · see citing works
Ji, Y. (1993) · Cell · doi:10.1016/0092-8674(93)90485-9 · Cited by 2,497 · see citing works
In Vivo Protein Transduction: Delivery of a Biologically Active Protein into the Mouse
Schwarze, S. R., Ho, A. L., Vocero-Akbani, A. M., & Dowdy, S. F. (1999) · Science · doi:10.1126/science.285.5433.1569 · Cited by 2,418 · see citing works
Molecular mechanisms of necroptosis: an ordered cellular explosion
Vandenabeele, P., Galluzzi, L., Vanden Berghe, T., & Kroemer, G. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2970 · Cited by 2,382 · see citing works
Human ICE/CED-3 Protease Nomenclature
Alnemri, E. S., Livingston, D. J., Nicholson, D. W., Salvesen, G. S., Thornberry, N. A., Wong, W. W., & Yuan, J. (1996) · Cell · doi:10.1016/s0092-8674(00)81334-3 · Cited by 2,371 · see citing works
Molecular mechanisms of caspase regulation during apoptosis
Riedl, S. J., & Shi, Y. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1496 · Cited by 1,893 · see citing works
Noncanonical Inflammasome Activation by Intracellular LPS Independent of TLR4
Kayagaki, N., Wong, M. T., Stowe, I. B., Ramani, S. R., Gonzalez, L. C., Akashi‐Takamura, S., Miyake, K., Zhang, J., Lee, W. P., Muszyński, A., et al. (2013) · Science · doi:10.1126/science.1240248 · Cited by 1,545 · see citing works
Necroptosis: The Release of Damage-Associated Molecular Patterns and Its Physiological Relevance
Kaczmarek, A., Vandenabeele, P., & Krysko, D. V. (2013) · Immunity · doi:10.1016/j.immuni.2013.02.003 · Cited by 1,411 · see citing works
Mechanisms of caspase activation
Boatright, K. M., & Salvesen, G. S. (2003) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2003.10.009 · Cited by 1,374 · see citing works
Apoptotic cell death in patients with sepsis, shock, and multiple organ dysfunction
Hotchkiss, R. S., Swanson, P. E., Freeman, B. D., Tinsley, K. W., Cobb, J. P., Matuschak, G. M., Buchman, T. G., & Karl, I. E. (1999) · Critical Care Medicine · doi:10.1097/00003246-199907000-00002 · Cited by 1,341 · see citing works
Plasma membrane translocation of trimerized MLKL protein is required for TNF-induced necroptosis
Cai, Z., Jitkaew, S., Zhao, J., Chiang, H.-C., Choksi, S., Liu, J., Ward, Y., Wu, L.-G., & Liu, Z.-G. (2014) · Nature Cell Biology · doi:10.1038/ncb2883 · Cited by 1,322 · see citing works
Catalytic activity of the caspase-8–FLIPL complex inhibits RIPK3-dependent necrosis
Oberst, A., Dillon, C. P., Weinlich, R., McCormick, L. L., Fitzgerald, P., Pop, C., Hakem, R., Salvesen, G. S., & Green, D. R. (2011) · Nature · doi:10.1038/nature09852 · Cited by 1,278 · see citing works
Cytoplasmic LPS Activates Caspase-11: Implications in TLR4-Independent Endotoxic Shock
Hagar, J. A., Powell, D. A., Aachoui, Y., Ernst, R. K., & Miao, E. A. (2013) · Science · doi:10.1126/science.1240988 · Cited by 1,261 · see citing works
Molecular Cloning of the Interleukin-1β Converting Enzyme
Cerretti, D. P., Kozlosky, C. J., Mosley, B., Nelson, N. C., Ness, K. V., Greenstreet, T. A., March, C. J., Kronheim, S. R., Druck, T., Cannizzaro, L. A., et al. (1992) · Science · doi:10.1126/science.1373520 · Cited by 1,147 · see citing works
Caspase‐1‐induced pyroptotic cell death
Miao, E. A., Rajan, J. V., & Aderem, A. A. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01044.x · Cited by 1,139 · see citing works
Muller, A. J., DuHadaway, J. B., Donover, P. S., Sutanto-Ward, E., & Prendergast, G. C. (2005) · Nature Medicine · doi:10.1038/nm1196 · Cited by 1,064 · see citing works
RIP3 mediates the embryonic lethality of caspase-8-deficient mice
Kaiser, W. J., Upton, J. W., Long, A. B., Livingston-Rosanoff, D., Daley-Bauer, L. P., Hakem, R., Caspary, T., & Mocarski, E. S. (2011) · Nature · doi:10.1038/nature09857 · Cited by 1,057 · see citing works
Sir Isaac Newton, sepsis, SIRS, and CARS
Bone, R. C. (1996) · Critical Care Medicine · doi:10.1097/00003246-199607000-00010 · Cited by 995 · see citing works
Sepsis-Induced Apoptosis Causes Progressive Profound Depletion of B and CD4+ T Lymphocytes in Humans
Hotchkiss, R. S., Tinsley, K. W., Swanson, P. E., Schmieg, R. E., Hui, J. J., Chang, K. C., Osborne, D. F., Freeman, B. D., Cobb, J. P., Buchman, T. G., et al. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.11.6952 · Cited by 939 · see citing works
The protein structures that shape caspase activity, specificity, activation and inhibition
Fuentes‐Prior, P., & Salvesen, G. S. (2004) · Biochemical Journal · doi:10.1042/bj20041142 · Cited by 877 · see citing works
Inflammatory caspases and inflammasomes: master switches of inflammation
Martinon, F., & Tschopp, J. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402038 · Cited by 821 · see citing works
Apoptosis and caspases regulate death and inflammation in sepsis
Hotchkiss, R. S., & Nicholson, D. W. (2006) · Nature reviews. Immunology · doi:10.1038/nri1943 · Cited by 796 · see citing works
Caspase-independent cell death
Kroemer, G., & Martin, S. J. (2005) · Nature Medicine · doi:10.1038/nm1263 · Cited by 719 · see citing works
Chun, H. J., Zheng, L., Ahmad, M., Wang, J., Speirs, C. K., Siegel, R. M., Dale, J. K., Puck, J. M., Davis, J., Hall, C. G., et al. (2002) · Nature · doi:10.1038/nature01063 · Cited by 706 · see citing works
RIP Kinase-Dependent Necrosis Drives Lethal Systemic Inflammatory Response Syndrome
Duprez, L., Takahashi, N., Hauwermeiren, F. V., Vandendriessche, B., Goossens, V., Berghe, T. V., Declercq, W., Libert, C., Cauwels, A., & Vandenabeele, P. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.020 · Cited by 591 · see citing works
Caspases in cell survival, proliferation and differentiation
Lamkanfi, M., Festjens, N., Declercq, W., Berghe, T. V., & Vandenabeele, P. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402047 · Cited by 564 · see citing works
Caspase inhibitors improve survival in sepsis: a critical role of the lymphocyte
Hotchkiss, R. S., Chang, K., Swanson, P. E., Tinsley, K. W., Hui, J. J., Klender, P. M., Xanthoudakis, S., Roy, S., Black, C. A., Grimm, E. L., et al. (2000) · Nature Immunology · doi:10.1038/82741 · Cited by 526 · see citing works
Essential role for caspase 8 in T-cell homeostasis and T-cell-mediated immunity.Preprint
Salmena, L., Lemmers, B., Hakem, A., Matysiak-Zablocki, E., Murakami, K., Au, P. Y. B., Berry, D., Tamblyn, L., Shehabeldin, A., Migon, E., et al. (2003) · Genes & Development · doi:10.1101/gad.1063703 · Cited by 517 · see citing works
Inflammasome-Dependent Release of the Alarmin HMGB1 in Endotoxemia
Lamkanfi, M., Sarkar, A., Walle, L. V., Vitari, A. C., Amer, A. O., Wewers, M. D., Tracey, K. J., Kanneganti, T., & Dixit, V. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000803 · Cited by 468 · see citing works
Takahashi, N., Duprez, L., Grootjans, S., Cauwels, A., Nerinckx, W., DuHadaway, J. B., Goossens, V, Roelandt, R., Van Hauwermeiren, F., Libert, C., et al. (2012) · Cell Death & Disease · doi:10.1038/cddis.2012.176 · Cited by 465 · see citing works
Prevention of lymphocyte cell death in sepsis improves survival in mice
Hotchkiss, R. S., Tinsley, K. W., Swanson, P. E., Chang, K. C., Cobb, J. P., Buchman, T. G., Korsmeyer, S. J., & Karl, I. E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.25.14541 · Cited by 454 · see citing works
Mlkl knockout mice demonstrate the indispensable role of Mlkl in necroptosis
Wu, J., Huang, Z., Ren, J., Zhang, Z., He, P., Li, Y., Ma, J., Chen, W., Zhang, Y., Zhou, X., et al. (2013) · Cell Research · doi:10.1038/cr.2013.91 · Cited by 452 · see citing works
Requirement for Caspase-8 in NF-κB Activation by Antigen Receptor
Su, H. C., Bidère, N., Zheng, L., Cubre, A., Sakai, K., Dale, J. K., Salmena, L., Hakem, R., Straus, S. E., & Lenardo, M. J. (2005) · Science · doi:10.1126/science.1104765 · Cited by 427 · see citing works
Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms
Saleh, M., Vaillancourt, J. P., Graham, R. K., Huyck, M., Srinivasula, S. M., Alnemri, E. S., Steinberg, M. H., Nolan, V., Baldwin, C. T., Hotchkiss, R. S., et al. (2004) · Nature · doi:10.1038/nature02451 · Cited by 423 · see citing works
Recognition of Bacteria by Inflammasomes
von Moltke, J., Ayres, J. S., Kofoed, E. M., Chavarría‐Smith, J., & Vance, R. E. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095944 · Cited by 414 · see citing works
Many stimuli pull the necrotic trigger, an overview
Vanlangenakker, N., Berghe, T. V., & Vandenabeele, P. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.164 · Cited by 407 · see citing works
Overexpression of Bcl-2 in Transgenic Mice Decreases Apoptosis and Improves Survival in Sepsis
Hotchkiss, R. S., Swanson, P. E., Knudson, C. M., Chang, K. C., Cobb, J. P., Osborne, D. F., Zollner, K., Buchman, T. G., Korsmeyer, S. J., & Karl, I. E. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.7.4148 · Cited by 381 · see citing works
Coeshott, C. M., Ohnemus, C., Pilyavskaya, A., Ross, S., Wieczorek, M., Kroona, H., Leimer, A. H., & Cheronis, J. C. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6261 · Cited by 365 · see citing works
Accelerated Lymphocyte Death in Sepsis Occurs by both the Death Receptor and Mitochondrial Pathways
Hotchkiss, R. S., Osmon, S., Chang, K. C., Wagner, T. H., Coopersmith, C. M., & Karl, I. E. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.8.5110 · Cited by 343 · see citing works
Enhanced bacterial clearance and sepsis resistance in caspase-12-deficient mice
Saleh, M., Mathison, J. C., Wolinski, M. K., Bensinger, S. J., Fitzgerald, P., Droin, N. M., Ulevitch, R. J., Green, D. R., & Nicholson, D. W. (2006) · Nature · doi:10.1038/nature04656 · Cited by 323 · see citing works
Shao, W., Yeretssian, G., Doiron, K., Hussain, S. N. A., & Saleh, M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m708182200 · Cited by 321 · see citing works
Specific involvement of caspases in the differentiation of monocytes into macrophages
Sordet, O., Rébé, C., Plenchette, S., Zermati, Y., Hermine, O., Vainchenker, W., Garrido, C., Solary, É., & Dubrez, L. (2002) · Blood · doi:10.1182/blood-2002-06-1778 · Cited by 313 · see citing works
IL-7 Promotes T Cell Viability, Trafficking, and Functionality and Improves Survival in Sepsis
Unsinger, J., McGlynn, M., Kasten, K. R., Hoekzema, A. S., Watanabe, E., Muenzer, J. T., McDonough, J. S., Tschöp, J., Ferguson, T. A., McDunn, J. E., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903151 · Cited by 313 · see citing works
Current trends in inflammatory and immunomodulatory mediators in sepsis
Aziz, M., Jacob, A., Yang, W.-L., Matsuda, A., & Wang, P. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0912437 · Cited by 309 · see citing works
Self-citationViral infection and the evolution of caspase 8-regulated apoptotic and necrotic death pathways
Mocarski, E. S., Upton, J. W., & Kaiser, W. J. (2011) · Nature reviews. Immunology · doi:10.1038/nri3131 · Cited by 300 · see citing works
Inflammasome-mediated pyroptotic and apoptotic cell death, and defense against infection
Aachoui, Y., Sagulenko, V., Miao, E. A., & Stacey, K. J. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.04.004 · Cited by 296 · see citing works
Joosten, L. A. B., Netea, M. G., Fantuzzi, G., Koenders, M. I., Helsen, M. M. A., Sparrer, H., Pham, C. T. N., van der Meer, J. W. M., Dinarello, C. A., & van den Berg, W. B. (2009) · Arthritis & Rheumatism · doi:10.1002/art.25006 · Cited by 296 · see citing works
Neuroprotection by a caspase inhibitor in acute bacterial meningitis
Braun, J., Novak, R., Herzog, K., Bodner, S. M., Cleveland, J. L., & TUOMANEN, E. I. (1999) · Nature Medicine · doi:10.1038/6514 · Cited by 262 · see citing works
Raupach, B., Peuschel, S.-K., Monack, D. M., & Zychlinsky, A. (2006) · Infection and Immunity · doi:10.1128/iai.00417-06 · Cited by 255 · see citing works
The new normal: immunomodulatory agents against sepsis immune suppression
Hutchins, N. A., Unsinger, J., Hotchkiss, R. S., & Ayala, A. (2014) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2014.01.002 · Cited by 240 · see citing works
Inoue, S., Unsinger, J., Davis, C. G., Muenzer, J. T., Ferguson, T. A., Chang, K. C., Osborne, D. F., Clark, A. T., Coopersmith, C. M., McDunn, J. E., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0902307 · Cited by 229 · see citing works
Cauwels, A., Janssen, B. J., Waeytens, A., Cuvelier, C. A., & Brouckaert, P. (2003) · Nature Immunology · doi:10.1038/ni914 · Cited by 217 · see citing works
Activity and specificity of necrostatin-1, small-molecule inhibitor of RIP1 kinase
Degterev, A., Maki, J. L., & Yuan, J. (2012) · Cell Death and Differentiation · doi:10.1038/cdd.2012.133 · Cited by 214 · see citing works
Remijsen, Q., Goossens, V., Grootjans, S., den Haute, C. V., Vanlangenakker, N., Dondelinger, Y., Roelandt, R., Bruggeman, I., Gonçalves, A. C., Bertrand, M. J. M., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2013.531 · Cited by 203 · see citing works
Inhibitor of Apoptosis Protein cIAP2 Is Essential for Lipopolysaccharide-Induced Macrophage Survival
Conte, D., Holčı́k, M., Lefebvre, C. A., LaCasse, E. C., Picketts, D. J., Wright, K. E., & Korneluk, R. G. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.26.2.699-708.2006 · Cited by 192 · see citing works
Cutting Edge: Innate Immunity Conferred by B Cells Is Regulated by Caspase-8
Beisner, D. R., Ch’en, I. L., Kolla, R. V., Hoffmann, A., & Hedrick, S. Μ. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.6.3469 · Cited by 181 · see citing works
Syncytial fusion of human trophoblast depends on caspase 8
Black, S., Kadyrov, M., Kaufmann, P., Ugele, B., Emans, N., & Huppertz, B. (2003) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401307 · Cited by 178 · see citing works
In vivo delivery of caspase-8 or Fas siRNA improves the survival of septic mice
Szollosi, D. E., Chung, C., Lomas‐Neira, J., Doughty, L., Gregory, S. H., & Ayala, A. (2005) · Blood · doi:10.1182/blood-2004-10-4086 · Cited by 177 · see citing works
Caspase-3 regulates cell cycle in B cells: a consequence of substrate specificity
Woo, M., Hakem, R., Furlonger, C. L., Hakem, A., Duncan, G. S., Sasaki, T., Bouchard, D., Lu, L., Wu, G. E., Paige, C. J., et al. (2003) · Nature Immunology · doi:10.1038/ni976 · Cited by 176 · see citing works
Berghe, T. V., Demon, D., Bogaert, P., Vandendriessche, B., Goethals, A., Depuydt, B., Vuylsteke, M., Roelandt, R., Van Wonterghem, E., Vandenbroecke, J., et al. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201308-1535oc · Cited by 173 · see citing works
Intravenous TAT–Bcl‐Xl is protective after middle cerebral artery occlusion in mice
Kılıç, E., Dietz, G. P. H., Hermann, D. M., & Bähr, M. (2002) · Annals of Neurology · doi:10.1002/ana.10356 · Cited by 166 · see citing works
Sarkar, A., Hall, M. W., Exline, M. C., Hart, J., Knatz, N. L., Gatson, N. T., & Wewers, M. D. (2006) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200604-546oc · Cited by 149 · see citing works
Chung, C., Song, G. Y., Lomas, J. L., Simms, H. H., Chaudry, I. H., & Ayala, A. (2003) · Journal of Leukocyte Biology · doi:10.1189/jlb.0102006 · Cited by 143 · see citing works
Hu, Z.-S., Murakami, T., Suzuki, K., Tamura, H., Kuwahara-Arai, K., Iba, T., & Nagaoka, I. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085765 · Cited by 141 · see citing works
Akt Decreases Lymphocyte Apoptosis and Improves Survival in Sepsis
Bommhardt, U., Chang, K. C., Swanson, P. E., Wagner, T. H., Tinsley, K. W., Karl, I. E., & Hotchkiss, R. S. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.12.7583 · Cited by 131 · see citing works
TAT-BH4 and TAT-Bcl-xL Peptides Protect against Sepsis-Induced Lymphocyte Apoptosis In Vivo
Hotchkiss, R. S., McConnell, K. W., Bullok, K. E., Davis, C. G., Chang, K. C., Schwulst, S. J., Dunne, J. C., Dietz, G. P. H., Bähr, M., McDunn, J. E., et al. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.9.5471 · Cited by 113 · see citing works
Cheyuo, C., Jacob, A., Wu, R., Zhou, M., Lei, Q., Dong, W., Ji, Y., Chaung, W. W., Wang, H., Nicastro, J. M., et al. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.09.018 · Cited by 99 · see citing works
Self-citationAziz, M., Matsuda, A., Yang, W.-L., Jacob, A., & Wang, P. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200262 · Cited by 82 · see citing works
Self-citationOver-Expression of Bcl-2 Provides Protection in Septic Mice by a trans Effect
Iwata, A., Stevenson, V. M., Minard, A., Tasch, M., Tupper, J. C., Lagasse, E., Weissman, I. L., Harlan, J. M., & Winn, R. K. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.6.3136 · Cited by 77 · see citing works
Improved survival in experimental sepsis with an orally administered inhibitor of apoptosis
Weaver, J., Rouse, M. S., Steckelberg, J. M., & Badley, A. D. (2004) · The FASEB Journal · doi:10.1096/fj.03-1230com · Cited by 76 · see citing works
Inhibition of caspase-1 activation in gram-negative sepsis and experimental endotoxemia
Giamarellos‐Bourboulis, E. J., van de Veerdonk, F. L., Mouktaroudi, M., Raftogiannis, M., Antonopoulou, A., Joosten, L. A. B., Pickkers, P., Savva, A., Georgitsi, M., van der Meer, J. W. M., et al. (2011) · Critical Care · doi:10.1186/cc9974 · Cited by 74 · see citing works
Novel Therapeutic Targets for Sepsis: Regulation of Exaggerated Inflammatory Responses
Matsuda, A., Jacob, A., Wu, R., Aziz, M., Yang, W.-L., Matsutani, T., Suzuki, H., Furukawa, K., Uchida, E., & Wang, P. (2012) · Journal of Nippon Medical School · doi:10.1272/jnms.79.4 · Cited by 72 · see citing works
Self-citationAyala, A., CHUNG, Xu, Evans, Redmond, & Chaudry (1999) · Immunology · doi:10.1046/j.1365-2567.1999.00765.x · Cited by 71 · see citing works
Caspase Activity Is Required for Stimulated B Lymphocytes to Enter the Cell Cycle
Olson, N. E., Graves, J. D., Shu, G. L., Ryan, E. J., & Clark, E. A. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.12.6065 · Cited by 66 · see citing works
Caspase-7 deficiency protects from endotoxin-induced lymphocyte apoptosis and improves survival
Lamkanfi, M., Moreira, L. O., Makena, P. S., Spierings, D. C. J., Boyd, K. L., Murray, P. J., Green, D. R., & Kanneganti, T. (2009) · Blood · doi:10.1182/blood-2008-09-178038 · Cited by 65 · see citing works
Power, C. P., Wang, J. H., Manning, B. J., Kell, M., Aherne, N. F., Wu, Q. D., & Redmond, H. P. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.8.5229 · Cited by 61 · see citing works
Matsuda, N., Takano, Y., Kageyama, S., HATAKEYAMA, N., Shakunaga, K., Kitajima, I., YAMAZAKI, M., & Hattori, Y. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.05.024 · Cited by 60 · see citing works
Inhibition of Fas signaling prevents hepatic injury and improves organ blood flow during sepsis
Chung, C., Yang, S., Song, G. Y., Lomas, J. L., Wang, P., Simms, H. H., Chaudry, I. H., & Ayala, A. (2001) · Surgery · doi:10.1067/msy.2001.116540 · Cited by 57 · see citing works
Self-citationCoeshott, C. M., Pilyavskaya, A., Ross, S., Wieczorek, M., Kroona, H., Leimer, A. H., & Cheronis, J. C. (1999) · Cited by 57 · see citing works
Kenneth, N. S., Younger, J. M., Hughes, E. D., Marcotte, D., Barker, P. A., Saunders, T. L., & Duckett, C. S. (2012) · Biochemical Journal · doi:10.1042/bj20120249 · Cited by 56 · see citing works
Méthot, N., Huang, J., Coulombe, N., Vaillancourt, J. P., Rasper, D., Tam, J., Han, Y., Colucci, J. T., Zamboni, R. J., Xanthoudakis, S., et al. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031791 · Cited by 55 · see citing works
VX-166: a novel potent small molecule caspase inhibitor as a potential therapy for sepsis
Weber, P., Wang, P., Maddens, S., Wang, P. S., Wu, R., Miksa, M., Dong, W., Mortimore, M., Golec, J. M. C., & Charlton, P. (2009) · Critical Care · doi:10.1186/cc8041 · Cited by 48 · see citing works
Self-citationMicrovesicular Caspase-1 Mediates Lymphocyte Apoptosis in Sepsis
Exline, M. C., Justiniano, S. E., Hollyfield, J. L., Berhe, F., Besecker, B. Y., Das, S., Wewers, M. D., & Sarkar, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090968 · Cited by 47 · see citing works
Endotoxin reduces CD95-induced neutrophil apoptosis by cIAP-2-mediated caspase-3 degradation
Mica, L., Härter, L., Trentz, O., & Keel, M. (2004) · Journal of the American College of Surgeons · doi:10.1016/j.jamcollsurg.2004.05.272 · Cited by 40 · see citing works
Chung, C., Venet, F., Chen, Y., Jones, L. N., Wilson, D. C., Ayala, C. A., & Ayala, A. (2010) · Shock · doi:10.1097/shk.0b013e3181cf70fb · Cited by 29 · see citing works
Immune Functions of Proteinase 3
Sugawara, S. (2005) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.v25.i5.10 · Cited by 20 · see citing works
An Inactivating Caspase-11 Passenger Mutation Muddles Sepsis Research
Berghe, T. V., Goethals, A., Demon, D., Bogaert, P., Mak, T. W., Cauwels, A., & Vandenabeele, P. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201210-1775le · Cited by 19 · see citing works
Demeyere, K., Remijsen, Q., Demon, D., Breyne, K., Notebaert, S., Boyen, F., Guérin, C. J., Vandenabeele, P., & Meyer, E. (2013) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2013.02.003 · Cited by 15 · see citing works
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Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680 · see citing works
Pyroptosis: Mechanisms and Diseases
Yu, P., Zhang, X., Liu, N., Tang, L., Peng, C., & Chen, X. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-021-00507-5 · Cited by 2,353 · see citing works
Mechanisms and treatment of organ failure in sepsis
Lelubre, C., & Vincent, J. (2018) · Nature Reviews Nephrology · doi:10.1038/s41581-018-0005-7 · Cited by 860 · see citing works
Han, X., Xu, T., Fang, Q., Zhang, H., Yue, L., Hu, G., & Sun, L. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102010 · Cited by 554 · see citing works
Recent Insights into the Molecular Mechanisms Underlying Pyroptosis and Gasdermin Family Functions
Aglietti, R. A., & Dueber, E. C. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.01.003 · Cited by 409 · see citing works
Ceria–Zirconia Nanoparticles as an Enhanced Multi‐Antioxidant for Sepsis Treatment
Soh, M., Kang, D., Jeong, H., Kim, D., Kim, D. Y., Yang, W., Song, C., Baik, S., Choi, I., Ki, S., et al. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201704904 · Cited by 371 · see citing works
Mechanism and regulation of pyroptosis-mediated in cancer cell death
Ruan, J., Wang, S., & Wang, J. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109052 · Cited by 274 · see citing works
Mechanism of membrane pore formation by human gasdermin‐D
Mulvihill, E., Sborgi, L., Mari, S. A., Pfreundschuh, M., Hiller, S., & Müller, D. J. (2018) · The EMBO Journal · doi:10.15252/embj.201798321 · Cited by 263 · see citing works
The Role and Mechanism of Pyroptosis and Potential Therapeutic Targets in Sepsis: A Review
Zheng, X., Chen, W., Gong, F., Chen, Y., & Chen, E. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.711939 · Cited by 222 · see citing works
Necroptosis Promotes Staphylococcus aureus Clearance by Inhibiting Excessive Inflammatory Signaling
Kitur, K., Wachtel, S., Brown, A. O., Wickersham, M., Paulino, F. E., Peñaloza, H. F., Soong, G., Bueno, S. M., Parker, D., & Prince, A. S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.039 · Cited by 180 · see citing works
A Mechanistic Understanding of Pyroptosis: The Fiery Death Triggered by Invasive Infection
Liu, X., & Lieberman, J. (2017) · Advances in immunology · doi:10.1016/bs.ai.2017.02.002 · Cited by 164 · see citing works
Sun, Y., Zhao, H., Mu, D.-L., Zhang, W., Jiang, C., Wu, L., Alam, A., Wang, D., & Ma, D. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1416-5 · Cited by 168 · see citing works
Wei, Z., Wang, L., Tang, C., Chen, S., Wang, Z., Wang, Y., Bao, J., Xie, Y., Zhao, W., Su, B., et al. (2020) · Advanced Functional Materials · doi:10.1002/adfm.202002234 · Cited by 161 · see citing works
B-1a cells protect mice from sepsis-induced acute lung injury
Aziz, M., Ode, Y., Zhou, M., Ochani, M., Holodick, N. E., Rothstein, T. L., & Wang, P. (2018) · Molecular Medicine · doi:10.1186/s10020-018-0029-2 · Cited by 143 · see citing works
Self-citationENDOPLASMIC RETICULUM STRESS IN SEPSIS
Khan, M. M., Yang, W.-L., & Wang, P. (2015) · Shock · doi:10.1097/shk.0000000000000425 · Cited by 142 · see citing works
Self-citationZhao, S., Chen, F., Yin, Q., Wang, D., Han, W., & Zhang, Y. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.571810 · Cited by 141 · see citing works
Gabarin, R., Li, M., Zimmel, P. A., Marshall, J. C., Li, Y., & Zhang, H. (2021) · Journal of Innate Immunity · doi:10.1159/000515740 · Cited by 139 · see citing works
Intracellular Lipopolysaccharide Sensing as a Potential Therapeutic Target for Sepsis
Pfalzgraff, A., & Weindl, G. (2019) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2019.01.001 · Cited by 139 · see citing works
Wu, D., Pan, P., Liu, B., Su, X., Zhang, L., Tan, H., Cao, Z., Zhou, Z.-R., Li, H.-T., Li, H., et al. (2015) · Chinese Medical Journal · doi:10.4103/0366-6999.166039 · Cited by 106 · see citing works
Apoptosis induced by Staphylococcus aureus toxins
Zhang, X., Hu, X., & Rao, X. (2017) · Microbiological Research · doi:10.1016/j.micres.2017.08.006 · Cited by 103 · see citing works
Heme Oxygenase-1 Reduces Sepsis-Induced Endoplasmic Reticulum Stress and Acute Lung Injury
Chen, X., Wang, Y., Xie, X., Chen, H., Zhu, Q., Ge, Z., Wei, H., Deng, J., Xia, Z., & Lian, Q. (2018) · Mediators of Inflammation · doi:10.1155/2018/9413876 · Cited by 89 · see citing works
The role of glycine in regulated cell death
Weinberg, J. M., Bienholz, A., & Venkatachalam, M. A. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2201-6 · Cited by 84 · see citing works
Irmscher, S., Brix, S. R., Zipfel, S. L. H., Halder, L. D., Mutlutürk, S., Wulf, S., Girdauskas, E., Reichenspurner, H. C., Stahl, R. A. K., Jungnickel, B., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10766-0 · Cited by 72 · see citing works
Wang, X., Xia, Z., Wang, H., Wang, D., Sun, T., Hossain, E., Pang, X., & Liu, Y. (2023) · Theranostics · doi:10.7150/thno.81520 · Cited by 72 · see citing works
The Role of Cell-Free Plasma DNA in Critically Ill Patients with Sepsis
Clementi, A., Virzì, G. M., Brocca, A., Pastori, S., de Cal, M., Marcante, S., Granata, A. R. M., & Ronco, C. (2015) · Blood Purification · doi:10.1159/000440975 · Cited by 69 · see citing works
Bolívar, B. E., Vogel, T. P., & Bouchier‐Hayes, L. (2019) · FEBS Journal · doi:10.1111/febs.14926 · Cited by 67 · see citing works
Kombucha ameliorates LPS-induced sepsis in a mouse model
Wang, P., Feng, Z., Sang, X., Chen, W., Zhang, X., Xiao, J., Chen, Y., Chen, Q., Min-he, Y., & Su, J. (2021) · Food & Function · doi:10.1039/d1fo01839f · Cited by 70 · see citing works
Self-citationWang, Y.-C., Liu, Q., Liu, T., Xie, X., Gao, W., Bai, X., & Li, Z. (2018) · Medicine · doi:10.1097/md.0000000000009859 · Cited by 66 · see citing works
PPAR‐γ Activation Prevents Septic Cardiac Dysfunction via Inhibition of Apoptosis and Necroptosis
Peng, S., Xu, J., Ruan, W., Li, S., & Xiao, F. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/8326749 · Cited by 65 · see citing works
Pei, F., Wang, H., Chen, Z., & Zhang, L. (2016) · Cell Death and Disease · doi:10.1038/cddis.2015.397 · Cited by 61 · see citing works
Neuroblastoma: oncogenic mechanisms and therapeutic exploitation of necroptosis
Nicolai, S., Pieraccioli, M., Peschiaroli, A., Melino, G., & Raschellà, G. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.354 · Cited by 59 · see citing works
Ceria–Zirconia Nanoparticles as an Enhanced Multi‐Antioxidant for Sepsis Treatment
Soh, M., Kang, D., Jeong, H., Kim, D., Kim, D. Y., Yang, W., Song, C., Baik, S., Choi, I., Ki, S., et al. (2017) · Angewandte Chemie · doi:10.1002/ange.201704904 · Cited by 57 · see citing works
Liang, Y., Bai, W.-J., Li, C.-G., Xu, L., Wei, H., Pan, H., He, X., & Ouyang, D. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2016.00390 · Cited by 54 · see citing works
The “Self-Sacrifice” of ImmuneCells in Sepsis
Wen, X., Xie, B., Yuan, S., & Zhang, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.833479 · Cited by 50 · see citing works
Angiotensin-(1–7) attenuates organ injury and mortality in rats with polymicrobial sepsis
Tsai, H.-J., Liao, M., Shih, C.-C., Ka, S., Tsao, C., & Wu, C.-C. (2018) · Critical Care · doi:10.1186/s13054-018-2210-y · Cited by 47 · see citing works
Li, Q., Zhang, M., Zhao, Y., & Dong, M. (2021) · Shock · doi:10.1097/shk.0000000000001775 · Cited by 45 · see citing works
Jung, S.-Y., Kim, H., Park, S., Jhee, J. H., Yun, H., Kim, H., Kee, Y. K., Yoon, C.-Y., Oh, H. J., Chang, T. I., et al. (2016) · Medicine · doi:10.1097/md.0000000000004542 · Cited by 43 · see citing works
Aly, A. A., Sayed, S. M., Abdelhafez, E. M. N., Hafez, S. M. N. A., Abdelzaher, W. Y., Raslan, M. A.-E., Ahmed, A. E., Thabet, K., El‐Reedy, A. A. M., Brown, A. B., et al. (2019) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2019.103348 · Cited by 42 · see citing works
Wang, Y.-C., Liu, Y., Liu, Q., Zheng, Q., Dong, X., Liu, X., Gao, W., Bai, X., & Li, Z. (2020) · BioMed Research International · doi:10.1155/2020/9152140 · Cited by 41 · see citing works
Jakka, P., Namani, S., Murugan, S., Rai, N., & Radhakrishnan, G. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.815878 · Cited by 39 · see citing works
Proteases: Pivot Points in Functional Proteomics
Verhamme, I. M., Leonard, S. E., & Perkins, R. C. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8814-3_20 · Cited by 39 · see citing works
Extracellular CIRP Induces Macrophage Extracellular Trap Formation Via Gasdermin D Activation
Lee, Y., Reilly, B., Tan, C., Wang, P., & Aziz, M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.780210 · Cited by 37 · see citing works
Self-citationLi, X., Xiao, G.-Y., Guo, T., Song, Y., & Li, Q. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.986565 · Cited by 37 · see citing works
Cen, C., Aziz, M., Yang, W.-L., Nicastro, J. M., Coppa, G. F., & Wang, P. (2016) · Shock · doi:10.1097/shk.0000000000000721 · Cited by 36 · see citing works
Self-citationDying to protect: cell death and the control of T‐cell homeostasis
Li, K., Shanmuganad, S., Carroll, K. R., Katz, J. D., Jordan, M. B., & Hildeman, D. A. (2017) · Immunological Reviews · doi:10.1111/imr.12538 · Cited by 34 · see citing works
Tosi, M., Coloretti, I., Meschiari, M., Biasi, S. D., Girardis, M., & Busani, S. (2024) · Antibiotics · doi:10.3390/antibiotics13050406 · Cited by 32 · see citing works
Role of Thymoquinone in Cardiac Damage Caused by Sepsis from BALB/c Mice
Liu, H., Sun, Y. K., Zhang, Y., Yang, G., Guo, L., Zhao, Y., & Pei, Z. (2018) · Inflammation · doi:10.1007/s10753-018-0909-1 · Cited by 30 · see citing works
Ringel-Scaia, V. M., McDaniel, D. K., & Allen, I. C. (2016) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2017019158 · Cited by 29 · see citing works
Therapeutic Potential of B-1a Cells in COVID-19
Aziz, M., Brenner, M., & Wang, P. (2020) · Shock · doi:10.1097/shk.0000000000001610 · Cited by 30 · see citing works
Self-citationSurvivin and caspases serum protein levels and survivin variants mRNA expression in sepsis
Miliaraki, M., Briassoulis, P., Ilia, S., Polonifi, A., Mantzourani, M., Briassouli, E., Vardas, K., Nanas, S., Pistiki, A. C., Θεοδωρακοπούλου, Μ., et al. (2021) · Scientific Reports · doi:10.1038/s41598-020-78208-2 · Cited by 29 · see citing works
Vrentas, C. E., Schaut, R. G., Boggiatto, P. M., Olsen, S. C., Sutterwala, F. S., & Moayeri, M. (2018) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2018.05.008 · Cited by 29 · see citing works
Wu, Y. C., Li, D., Wang, H., & Wan, X. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.887949 · Cited by 28 · see citing works
Non-Canonical Inflammasome Pathway: The Role of Cell Death and Inflammation in Ehrlichiosis
Sharma, A. K., & Ismail, N. (2023) · Cells · doi:10.3390/cells12222597 · Cited by 27 · see citing works
Current insight on the mechanisms of programmed cell death in sepsis-induced myocardial dysfunction
Liu, A.-B., Li, S.-J., Yu, Y., Zhang, J., & Ma, L. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1309719 · Cited by 27 · see citing works
Cell death signaling and immune regulation: new perspectives on targeted therapy for sepsis
Wu, H., Cui, J., Huang, J., Feng, Y., Zhao, J., Zhu, Y., Deng, X., Li, X., Zhang, W., & Wang, C. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00784-w · Cited by 29 · see citing works
da Costa, L. H. A., dos Santos, N. N., Catalão, C., Sharshar, T., Chrétien, F., & da Rocha, M. J. A. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0094-x · Cited by 27 · see citing works
Chapela, S. P., Simancas‐Racines, D., Montalván, M., Frías-Toral, E., Simancas-Racines, A., Muscogiuri, G., Barrea, L., Sarno, G., Martinez, P. I., Reberendo, M. J., et al. (2023) · Nutrients · doi:10.3390/nu15051071 · Cited by 28 · see citing works
El‐Sheref, E. M., Aly, A. A., Alshammari, M. B., Brown, A. B., Hafez, S. M. N. A., Abdelzaher, W. Y., Bräse, S., & Abdelhafez, E. M. N. (2020) · Molecules · doi:10.3390/molecules25215057 · Cited by 25 · see citing works
Role of pyroptosis in hemostasis activation in sepsis
Zhu, C., Liang, Y., Luo, Y., & Ma, X. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1114917 · Cited by 25 · see citing works
Metabolic Inflammatory Complex in Sepsis: Septic Cachexia as a Novel Potential Therapeutic Target
Kaneki, M. (2017) · Shock · doi:10.1097/shk.0000000000000906 · Cited by 24 · see citing works
Xu, X., Zhang, Q., Lv, Z., Cheng, C., Zha, J., Shu, H., Xiao, H., & Pan, S. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1551138 · Cited by 24 · see citing works
Zhan, L., Song, Y., Yuan, P., Guo, W., Hu, X., Xing, W., Ao, L., Tan, Y. H., Wu, X., Ao, X., et al. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.05.014 · Cited by 24 · see citing works
No Time to Die: How Kidney Cancer Evades Cell Death
Ganini, C., Montanaro, M., Scimeca, M., Palmieri, G., Anemona, L., Concetti, L., Melino, G., Bove, P., Amelio, I., Candi, E., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23116198 · Cited by 24 · see citing works
Protective effects of rapamycin induced autophagy on CLP septic mice
Wang, Z., Li, Y., Yang, X., Zhang, L., Shen, H., Xu, W., & Yuan, C. (2019) · Comparative Immunology Microbiology and Infectious Diseases · doi:10.1016/j.cimid.2019.01.009 · Cited by 24 · see citing works
Dysregulated IL-1β Secretion in Autoinflammatory Diseases: A Matter of Stress?
Carta, S., Semino, C., Sitia, R., & Rubartelli, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00345 · Cited by 22 · see citing works
Necroptosis-Mediated eCIRP Release in Sepsis
Reilly, B., Tan, C., Murao, A., Nofi, C. P., Jha, A., Aziz, M., & Wang, P. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s370615 · Cited by 23 · see citing works
Self-citationLiu, Y., Wang, K., Feng, Q., Zhang, Y., Wang, C., Liu, Q., Liu, X., Wang, X., Gao, W., Bai, X., et al. (2021) · Journal of Immunology Research · doi:10.1155/2021/9998517 · Cited by 20 · see citing works
Resta, S. C., Guerra, F., Talà, A., Bucci, C., & Alifano, P. (2024) · Cells · doi:10.3390/cells13211758 · Cited by 19 · see citing works
Distinct cell death markers identified in critical care patient survivors diagnosed with sepsis
Mallarpu, C. S., Ponnana, M., Prasad, S., Singarapu, M., Kim, J., Haririparsa, N., Bratic, N., Brar, H., Chelluri, L. K., & Madiraju, C. (2021) · Immunology Letters · doi:10.1016/j.imlet.2020.12.009 · Cited by 18 · see citing works
Zhou, J., Lu, X., Tan, T. Z., & Chng, W. J. (2017) · Molecular Oncology · doi:10.1002/1878-0261.12146 · Cited by 17 · see citing works
Wang, X., Wang, T., Sun, L., Zhang, H., Liu, C., Zhang, C. M., & Yu, L. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.115146 · Cited by 17 · see citing works
Rooney, M. D., Duduskar, S. N., Ghait, M., Reißing, J., Stengel, S., Reuken, P. A., Quickert, S., Zipprich, A., Bauer, M. W., Russo, A. J., et al. (2024) · Journal of Hepatology · doi:10.1016/j.jhep.2024.06.019 · Cited by 16 · see citing works
The necroptotic cell death pathway operates in megakaryocytes, but not in platelet synthesis
Moujalled, D., Gangatirkar, P., Kauppi, M., Corbin, J., Lebois, M., Murphy, J. M., Lalaoui, N., Hildebrand, J., Silke, J., Alexander, W., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03418-z · Cited by 13 · see citing works
Schindler, K., Bondeva, T., Schindler, C., Claus, R. A., Franke, S., & Wolf, G. (2016) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfv442 · Cited by 15 · see citing works
Positive Feedback Cycle of TNFα Promotes Staphylococcal Enterotoxin B-Induced THP-1 Cell Apoptosis
Zhang, X., Shang, W., Yuan, J., Hu, Z., Peng, H., Zhu, J., Hu, Q., Yang, Y., Liu, H., Jiang, B., et al. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00109 · Cited by 15 · see citing works
Inhibition of regulated cell death by cell-penetrating peptides
Krautwald, S., Dewitz, C., Fändrich, F., & Kunzendorf, U. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2200-7 · Cited by 14 · see citing works
Milk fat globule-epidermal growth factor-factor VIII attenuates sepsis-induced acute kidney injury
Cen, C., Aziz, M., Yang, W.-L., Zhou, M., Nicastro, J. M., Coppa, G. F., & Wang, P. (2017) · Journal of Surgical Research · doi:10.1016/j.jss.2017.02.024 · Cited by 13 · see citing works
Self-citationKoch, A. H., Yagmur, E., Linka, J., Schumacher, F., Bruensing, J., Buendgens, L., Herbers, U., Koek, G. H., Weiskirchen, R., Trautwein, C., et al. (2018) · Disease Markers · doi:10.1155/2018/8583121 · Cited by 15 · see citing works
Potential of piperine for neuroprotection in sepsis-associated encephalopathy
Ferreira, F. M., Gomes, S. V., Carvalho, L. C. F., de Alcântara, A. C., Castro, M. L. D. C., Perucci, L. O., Pio, S., Talvani, A., Vieira, P. M. D. A., Calsavara, A. J. C., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122353 · Cited by 13 · see citing works
The protective role of human ghrelin in sepsis: Restoration of CD4 T cell proliferation
Zhou, M., Aziz, M., Ochani, M., Yang, W.-L., Sharma, A., & Wang, P. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201139 · Cited by 13 · see citing works
Self-citationZhou, M., Aziz, M., Ochani, M., & Wang, P. (2020) · Molecular Medicine · doi:10.1186/s10020-020-00195-x · Cited by 13 · see citing works
Self-citationProtease-activated Nanomaterials for Targeted Cancer Theranostics
Chan, Y., & Hsiao, M. (2017) · Nanomedicine · doi:10.2217/nnm-2017-0068 · Cited by 12 · see citing works
Ji, X., Guo, Y., Zhou, G., Wang, Y., Zhang, J., Wang, Z., & Wang, Q. (2019) · Cell Biology International · doi:10.1002/cbin.11140 · Cited by 11 · see citing works
Pyocyanin induces NK92 cell apoptosis via mitochondrial damage and elevated intracellular Ca 2+
Li, T., Huang, X., Yuan, Z., Wang, L., Chen, M., Su, F., Ling, X.-J., & Piao, Z.-H. (2018) · Innate Immunity · doi:10.1177/1753425918809860 · Cited by 11 · see citing works
Cueno, M. E., Saito, Y., & Ochiai, K. (2015) · Microbial Pathogenesis · doi:10.1016/j.micpath.2015.10.021 · Cited by 11 · see citing works
Andreu‐Ballester, J. C., Arribas, M. A., Rico, M. Á., García‐Ballesteros, C., Galindo-Regal, L., Serra, R. S., Albert, L., Navarro, A., López-Chuliá, F., Peydro, F., et al. (2022) · Clinical Immunology · doi:10.1016/j.clim.2022.108956 · Cited by 10 · see citing works
Pyroptosis in sepsis induced organ dysfunction
Song, R., He, S., Wu, Y., & Tan, S. (2023) · Current Research in Translational Medicine · doi:10.1016/j.retram.2023.103419 · Cited by 9 · see citing works
Bryant, C. E. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20202413 · Cited by 9 · see citing works
Serum reactive oxygen species and apoptosis markers in septic patients
Chapela, S. P., Burgos, I., Schiel, A., Alonso, M., & Stella, C. A. (2021) · Anaesthesiology Intensive Therapy · doi:10.5114/ait.2021.104360 · Cited by 9 · see citing works
Teymournejad, O., Sharma, A. K., Abdelwahed, M. S., Kader, M., Ahmed, I., Elkafas, H., & Ismail, N. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1212167 · Cited by 7 · see citing works
Armandeh, M., Bameri, B., Samadi, M., Heidari, S., Foroumadi, R., & Abdollahi, M. R. (2022) · Current Pharmaceutical Design · doi:10.2174/1381612828666220513125312 · Cited by 7 · see citing works
Richendrfer, H. A., Levy, M. M., Elsaid, K. A., Schmidt, T. A., Zhang, L., Cabezas, R., & Jay, G. D. (2020) · Critical Care Explorations · doi:10.1097/cce.0000000000000126 · Cited by 7 · see citing works
Role of non-canonical pyroptosis in sepsis and other inflammatory diseases.
Liang, H., Huang, Y., & Gao, Q. F. (2021) · PubMed Central · doi:10.11817/j.issn.1672-7347.2021.210174 · Cited by 8 · see citing works
Yan, L., Liang, J., Zhou, Y., Huang, J., Zhang, T., Wang, X., & Yin, H. H. (2020) · Advanced Biosystems · doi:10.1002/adbi.202000037 · Cited by 6 · see citing works
Stressing the endoplasmic reticulum response as a diagnostic tool for sepsis
Yousof, T. R., Sharma, H., Austin, R. C., & Fox‐Robichaud, A. (2022) · Annals of Translational Medicine · doi:10.21037/atm-22-3120 · Cited by 6 · see citing works
Role of MFG-E8 in Neonatal Inflammation
Aziz, M., Hansen, L. W., Prince, J. M., & Wang, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809868-4.00002-9 · Cited by 4 · see citing works
Self-citationMostafa, S. M., Aly, A. A., Bräse, S., Nieger, M., Hafez, S. M. N. A., Abdelzaher, W. Y., & Abdelhafez, E. M. N. (2022) · Molecules · doi:10.3390/molecules27072266 · Cited by 4 · see citing works
Manipulating Cell Death in Cancer
Al-Janabi, I. I. (2025) · Al-Rafidain Journal of Medical Sciences · doi:10.54133/ajms.v9i1.2131 · Cited by 3 · see citing works
Hyperactivity of the non-canonical inflammasome in SPG11 and SPG48
Afzal, M. A., Ghait, M., Hussain, A., Siegmund, A., Tuchscherr, L. P. N., Babic, P., Press, A. T., Hardt, R., Winter, D., Rödiger, A., et al. (2025) · EBioMedicine · doi:10.1016/j.ebiom.2025.105985 · Cited by 3 · see citing works
Research progress on the role of mesenchymal stem cells in pyroptosis in sepsis
Xu, X., An, J., Yang, T., Li, B., & Dou, Z. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04837-x · Cited by 3 · see citing works
- Authors
- Aziz, M., Jacob, A., & Wang, P.
- Affiliations
- Feinstein Institute for Medical Research (US)
- Corresponding author
- Wang, P
- Venue
- Cell Death & Disease
- Published
- 2014-11-20
- Volume
- 5
- Issue
- 11
- Pages
- e1526-e1526
- ISSN
- 2041-4889 (ISSN-L)
- PMC
- PMC4260746
- OpenAlex
- W2048204476
- Cited by
- 125
- References
- 94
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 4 · 2023: 12 · 2022: 13 · 2021: 15 · 2020: 14 · 2019: 8 · 2018: 16 · 2017: 15 · 2016: 12 · 2015: 7
- FWCI
- 1.07
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Cell Death and Disease (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Vertex Pharmaceuticals
- National Institutes of Health
- National Institute of General Medical Sciences (R01GM053008, R01GM057468)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Epidemiology › Sepsis Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Keywords
- caspases, sepsis, apoptosis, pyroptosis, necroptosis, inflammation, immunosuppression, organ dysfunction, anergy, host immune response
- MeSH terms
- Animals, Anti-Bacterial Agents, Gene Expression Regulation, Humans, Immunologic Factors, Signal Transduction, Cytokines, Apoptosis, Sepsis, Caspases, Tumor Necrosis Factor Receptor-Associated Peptides and Proteins, Mice, Inflammasomes
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