NETosis: Molecular Mechanisms, Role in Physiology and Pathology

Neutrophil Extracellular Traps Kill Bacteria

Brinkmann, V., Reichard, U., Goosmann, C., Fauler, B., Uhlemann, Y., Weiss, D. S., Weinrauch, Y., & Zychlinsky, A. (2004) · Science · doi:10.1126/science.1092385 · Cited by 10,268

COVID-19: consider cytokine storm syndromes and immunosuppression

Mehta, P., McAuley, D. F., Brown, M., Sanchez, E., Tattersall, R. S., & Manson, J. J. (2020) · The Lancet · doi:10.1016/s0140-6736(20)30628-0 · Cited by 9,664

Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018.

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

Novel cell death program leads to neutrophil extracellular traps

Fuchs, T. A., Abed, U., Goosmann, C., Hurwitz, R., Schulze, I., Wahn, V., Weinrauch, Y., Brinkmann, V., & Zychlinsky, A. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200606027 · Cited by 3,197

Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood

Clark, S. R., Ma, A. C., Tavener, S. A., McDonald, B., Goodarzi, Z., Kelly, M. M., Patel, K. D., Chakrabarti, S., McAvoy, E., Sinclair, G. D., et al. (2007) · Nature Medicine · doi:10.1038/nm1565 · Cited by 2,309

Neutrophil elastase and myeloperoxidase regulate the formation of neutrophil extracellular traps

Papayannopoulos, V., Metzler, K. D., Hakkim, A., & Zychlinsky, A. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201006052 · Cited by 2,103

THE MITOCHONDRIAL DEATH/LIFE REGULATOR IN APOPTOSIS AND NECROSIS

Kroemer, G., Dallaporta, B., & Resche-Rigon, M. (1998) · Annual Review of Physiology · doi:10.1146/annurev.physiol.60.1.619 · Cited by 1,975

Neutrophil extracellular traps in COVID-19

Zuo, Y., Yalavarthi, S., Shi, H., Gockman, K., Zuo, M., Madison, J. A., Blair, C., Weber, A. G., Barnes, B. J., Egeblad, M., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.138999 · Cited by 1,598

Neutrophil extracellular traps enriched in oxidized mitochondrial DNA are interferogenic and contribute to lupus-like disease

Lood, C., Blanco, L. P., Purmalek, M. M., Carmona-Rivera, C., De Ravin, S. S., Smith, C. K., Malech, H. L., Ledbetter, J. A., Elkon, K. B., & Kaplan, M. J. (2016) · Nature Medicine · doi:10.1038/nm.4027 · Cited by 1,570

Cleavage of DFNA5 by caspase-3 during apoptosis mediates progression to secondary necrotic/pyroptotic cell death

Rogers, C., Fernandes-Alnemri, T., Mayes, L., Alnemri, D., Cingolani, G., & Alnemri, E. S. (2017) · Nature Communications · doi:10.1038/ncomms14128 · Cited by 1,510

Sepsis: Immunopathology, Immunotherapies, and Future Perspectives

Tavacı, T., & Akgun, N. (2023) · Eurasian Journal of Medicine · doi:10.5152/eurasianjmed.2022.22314 · Cited by 6

Saxitoxin induces the release of human neutrophil extracellular traps

Zhou, E., Yu, H., Wu, Z., Li, P., Xie, Y., Jiang, M., Wang, J., & Yang, Z. (2023) · Toxicon · doi:10.1016/j.toxicon.2023.107163 · Cited by 6

Neutrophils are atypical antigen-presenting cells

Vorobjeva, N. V. (2023) · Vestnik Moskovskogo universiteta Seria 16 Biologia · doi:10.55959/msu0137-0952-16-78-2-8 · Cited by 6

Exhaustive Exercise Increases Spontaneous but Not fMLP-Induced Production of Reactive Oxygen Species by Circulating Phagocytes in Amateur Sportsmen

Chmielecki, A., Bortnik, K., Gałczyński, S., Padula, G., Jerczyńska, H., Stawski, R. S., & Nowak, D. (2022) · Biology · doi:10.3390/biology11010103 · Cited by 6

Lights and Shadows on the Role of Rhg-CSF in Cancer Patients During the COVID-19 Pandemic and Future Perspectives of Research

Lasagna, A., Muzzana, M., & Pedrazzoli, P. (2021) · Immunotherapy · doi:10.2217/imt-2021-0219 · Cited by 6

Characterization of a predictive signature for tumor microenvironment and immunotherapy response in hepatocellular carcinoma involving neutrophil extracellular traps

Yuan, Z., Yang, X., Hu, Z., Gao, Y., Yan, P., Zheng, F., Guo, Y., Wang, X., & Zhou, J. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e30827 · Cited by 5

Construction of a NETosis-related gene signature for predicting the prognostic status of sepsis patients

Wu, J., Cao, X., Huang, L., & Quan, Y. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e36831 · Cited by 5

High-mobility group protein B1 derived mutant peptide mB Box-97 inhibits the formation of neutrophil extracellular traps

More, K. R., Devaraj, A., Robledo-Avila, F. H., Partida‐Sánchez, S., Bakaletz, L. O., & Goodman, S. D. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1565252 · Cited by 5

NOX1-ROS axis regulates the MAPK signaling pathway and activates caspase-1 to resist Edwardsiella piscicida infection

Wu, X. M., & Chang, M. X. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2025.742784 · Cited by 5

NETosis-based prognostic model reveals immune modulation in clear cell renal cell carcinoma using single-cell and bulk RNA sequencing

Yu, Z., Xu, Z., Zhang, X., Shao, W., Zhong, D., Yan, X., Jiang, T., Wang, Y., & Song, N. (2025) · Scientific Reports · doi:10.1038/s41598-025-11095-7 · Cited by 5

Mitochondrial dysfunction and its impact on pyroptosis and ferroptosis cross talk in glioma cells

Guo, Y., Liu, H., Gao, Z., Zhou, Z., Zhao, Y., Wang, M., Li, S., Xiang, W., Liao, J., & Zhou, J. (2025) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlaf099 · Cited by 5

The relationship between NETosis findings and disease activity in Behçet disease: an exploratory study

Bektaş, E., Deniz, R., Emrence, Z., Ekmekçi, S. S., Abacı, N., Amikishiyev, S., Yalçınkaya, Y., Artım-Esen, B., İnanç, M., & Gül, A. (2025) · Clinical and Experimental Rheumatology · doi:10.55563/clinexprheumatol/4thkqz · Cited by 5

The Unseen Enemies: Harnessing the Role of Neutrophil Extracellular Traps in Breast Cancer Progression, Immune Evasion, and Treatment Resistance

Moradpanah, S., Forouzin, S., Nasab, F. S., Amirlatifi, S., Shirkosh, P., Marashi, S. M., & Khodakarim, N. (2025) · Clinical Breast Cancer · doi:10.1016/j.clbc.2025.09.003 · Cited by 5

Neutrophil extracellular trap inhibition revitalizes PDAC immunotherapy responsiveness via reduced fibrosis and TCF1 + CD8 + progenitor T-cell expansion

Niemann, B. R., Ivey, A. D., Hopen, Q., Dakhlallah, D. A., Brundage, K. M., Mihalik, N. E., Eubank, T. D., & Boone, B. A. (2025) · OncoImmunology · doi:10.1080/2162402x.2025.2601394 · Cited by 5

Multimodal characterization of flow-induced thrombus initiation and growth in extracorporeal membrane oxygenation

Nilsson, F., Sochor, B., Henriksson, S., Roth, S. V., Broman, L. M., & Wittberg, L. P. (2026) · Scientific Reports · doi:10.1038/s41598-026-40177-3 · Cited by 5

Neutrophil-derived reactive oxygen species and bystander tissue damage in inflammatory bowel disease

Kim, J. Y., Colgan, S. P., & Cartwright, I. M. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.04.146 · Cited by 5

Beyond the horizon: Neutrophils leading the way in the evolution of immunotherapy

Rajgopal, S., Nakano, K., & Cook, L. M. (2023) · Cancer Medicine · doi:10.1002/cam4.6761 · Cited by 5

The impact of NETosis on hematological malignancies as a promising therapeutic target

Aydemir, D. (2024) · Frontiers in Hematology · doi:10.3389/frhem.2024.1377806 · Cited by 5

Neutrophil extracellular traps ( NETs ) and NETosis in alcohol‐associated diseases: A systematic review

Khan, M. A. S., Song, B., Wang, X., Iqbal, S. I., Szabó, G., & Chang, S. L. (2025) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.70019 · Cited by 5

Synergistic inhibition of CitH3 and S100A8/A9: A novel therapeutic strategy for mitigating sepsis-induced inflammation and lung injury

Dong, T., Ouyang, W., Yu, X., Zhao, T., Shao, L.-J.-Z., Quan, C., Wang, S. H., Ma, J., & Li, Y. (2025) · International Journal of Immunopathology and Pharmacology · doi:10.1177/03946320251338661 · Cited by 5

IL-1beta expressing neutrophil extracellular traps in Legionella pneumophila infection

Koutantou, M., Konstantinidis, T. G., Chochlakis, D., Xingi, E., Psaroulaki, A., Tsiotis, G., Kambas, K., & Angelakis, E. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1573151 · Cited by 5

Indications of platelet indices in coronary artery disease (CAD): more insights into their diagnostic and prognostic importance

Hosseini, E., Pezeshki, S. M. S., Ghasemzadeh, A., & Ghasemzadeh, M. (2025) · Journal of Thrombosis and Thrombolysis · doi:10.1007/s11239-025-03121-2 · Cited by 5

The Role of Neutrophil Extracellular Traps (NETs) in the Pathogenesis of Ovarian Cancer: New Insight and Future Perspectives

Lorestani, K., Ghorbanzade, S., Rahimi, S., Fazeli, R., Khdakarim, N., Hasanvand, A., & Hazari, V. (2025) · Molecular Biotechnology · doi:10.1007/s12033-025-01473-x · Cited by 5

Highlighting the versatility of the citrullination process

Sarnik, J., & Makowska, J. S. (2022) · Immunobiology · doi:10.1016/j.imbio.2022.152233 · Cited by 5

Neutrophils extracellular traps myeloperoxidase and elastase predict cerebral vasospasms after aneurysmal subarachnoid hemorrhage

Sajjad, S., Hewera, M., Rana, M., Gliem, M., Fischer, I., & Khan, D. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e40562 · Cited by 5

Correlation between REDOX enzymes and NET markers expression during the development of periapical lesions in mice

Silva, C. M. P. C., Massoni, V. V., Araújo, L. D. C., Lima, R. B., Filho, A. E. D. F. M., Pucinelli, C. M., Lucisano, M. P., Nelson‐Filho, P., Consolaro, A. G., da Silva, R. A. B., et al. (2025) · Clinical Oral Investigations · doi:10.1007/s00784-025-06246-z · Cited by 5

Impact of peptidylarginine deiminase 4 (PAD4) deficiency in a fecal-induced peritonitis model of sepsis

Cani, E., Dwivedi, D. J., Carlin, S., Sharma, N., Chen, A., & Liaw, P. C. (2025) · Journal of Thrombosis and Haemostasis · doi:10.1016/j.jtha.2025.03.025 · Cited by 5

Neutrophil extracellular traps as markers of thromboinflammation in the pathogenesis of female genital tract and breast malignant neoplasms

Викторовна, С. Е., Bitsadze, V. O., Солопова, А. Г., Khizroeva, J. K., Gris, J., Elalamy, I., & Makatsariya, A. D. (2022) · Obstetrics Gynecology and Reproduction · doi:10.17749/2313-7347/ob.gyn.rep.2022.335 · Cited by 5

Trichomonas vaginalis induces extracellular trap release in mouse neutrophils in vitro

Gao, Y., Li, X., Zhang, N., Zhao, P., Li, S., Tai, L., Li, X., Li, L., Li, J., Zhang, X., et al. (2021) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmab139 · Cited by 5

Neutrophils enhance the clearance of systemic amyloid deposits in a murine amyloidoma model

Hancock, T. J., Vlasyuk, M., Foster, J. S., Macy, S. D., Wooliver, D. C., Balachandran, M., Williams, A. D., Martin, E. B., Kennel, S. J., Heidel, E. R., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1487250 · Cited by 4

The role and application of Coronin family in human tumorigenesis and immunomodulation

Gao, H., Sun, F., Zhang, X., Qiao, X., & Guo, Y. (2025) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2025.189304 · Cited by 4

Hijacking the autophagy-apoptosis crosstalk: African swine fever virus orchestrates immune evasion via host remodeling for viral pathogenesis

Zhang, S., Zhang, T., Cao, Z., Yang, Y., & Lü, P. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107609 · Cited by 4

Fh15 Reduces Colonic Inflammation and Leukocyte Infiltration in a Dextran Sulfate Sodium-Induced Ulcerative Colitis Mouse Model

Figueroa-Gispert, M. D. M., Ramos-Lugo, C. M., Ocasio‐Malavé, C., Scott, R. P., Ahrendsen, J. T., Gómez-Samblás, M., Osuna, A., Dorta-Estremera, S. M., & Espino, A. M. (2025) · Cells · doi:10.3390/cells14110799 · Cited by 4

Plant flavonoid effects on the non-apoptotic mechanisms of regulated cell death

Białek, W., Czechowicz, P., Grzyb, J., Sławski, J., Collawn, J. F., & Bartoszewski, R. (2025) · Phytochemistry Reviews · doi:10.1007/s11101-025-10140-7 · Cited by 4

Aryl hydrocarbon receptor impairs HK2-controlled flux of the hexosamine biosynthesis pathway to suppress NETosis in an N-glycosylation-dependent manner

Li, S., Zhu, J., Song, J., Yang, L., Gong, Y., Dai, Y., & Wei, Z. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.06.078 · Cited by 4

Engineered Dual‐Function Antibody‐Like Proteins to Combat SARS‐CoV‐2‐Induced Immune Dysregulation and Inflammation

Wang, Y., Bai, C., Hou, K., Zhang, Z., Guo, M. S., Wang, X., Yang, F., & Liu, X. (2025) · Advanced Science · doi:10.1002/advs.202504690 · Cited by 4

The role of epigenetic regulation in cuproptosis, ferroptosis and NETosis in the pathogenesis of autoimmune diseases

Zhao, W., Wang, L., Jia, H., Shan, J., Zhang, Y., Gu, H., Xu, Y., Ma, X., Li, P., & Wu, J. (2025) · APOPTOSIS · doi:10.1007/s10495-025-02158-1 · Cited by 4

Urban dust nanoparticles drive inflammatory activation of human neutrophils and macrophages in vitro

Pavlyuchenkova, A. N., Vorobjeva, N. V., Ivaneev, A. I., Ermolin, M. S., Fedotov, P. S., Zinovkin, R. A., Chelombitko, M. A., & Chernyak, B. V. (2025) · Environmental Science and Pollution Research · doi:10.1007/s11356-025-37172-y · Cited by 4

Adjunctive GM-CSF therapy enhances host defense against systemic Candida auris infection in immunosuppressed mice

Mattos, E. C., Gupta, K. D., Quintanilla, D., Hautau, H., Ibrahim, A. S., & Singh, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1731315 · Cited by 4

Elevation of Myeloperoxidase Correlates with Disease Severity in Patients with Hantaan Virus Infection

Li, P., Zhang, C., Wang, M., Zhang, X., Zhang, Y., Tang, K., Hu, H., Jia, X., Zhuang, R., Jin, B., et al. (2022) · Viral Immunology · doi:10.1089/vim.2022.0007 · Cited by 4

Whole transcriptome analysis of Mycoplasma bovis-host interactions under in vitro and in vivo conditions

Gelgie, A. E., Gelalcha, B. D., Freeman, T., Ault-Seay, T. B., Beever, J. E., & Dego, O. K. (2025) · Veterinary Microbiology · doi:10.1016/j.vetmic.2025.110426 · Cited by 4

Circulating Nucleosomes and Histones in the Development of Lung Injury and Sepsis

Dutta, S., Dutta, S., Somanath, P. R., Narayanan, S. P., Wang, X., & Zhang, D. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47020133 · Cited by 5

Neutrophil extracellular traps in the sinus mucosa in patients with chronic rhinosinusitis without polyps

Свистушкин, В. М., Николаевна, Н. Г., Сергеевич, Д. А., Dagil, Y. A., Vtorova, Y. A., Guseva, N. B., Vorobjeva, N. V., & Pinegin, B. V. (2024) · Immunologiya · doi:10.33029/1816-2134-2024-45-6-731-741 · Cited by 4

Bidirectional roles of neutrophil extracellular traps in oral microbiota carcinogenesis: A systematic review

Shen, J. M., Lin, H., Mo, K., Liang, Z., Zhang, Y., Quan, H., Wang, X., Zhang, C., & Chen, C. (2025) · Translational Oncology · doi:10.1016/j.tranon.2025.102361 · Cited by 5

Murine gut microbiota dysbiosis via enteric infection modulates the foreign body response to a distal biomaterial implant

Yang, B., Rutkowski, N., Ruta, A., Gray-Gaillard, E. F., Maestas, D. R., Kelly, S. H., Krishnan, K., Wu, X., Wu, S., Chen, A. R., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2422169122 · Cited by 4

Characterization of the B-Cell Epitopes of Echinococcus granulosus Histones H4 and H2A Recognized by Sera From Patients With Liver Cysts

Maglioco, A., Agüero, F. A., Valacco, P., Valdez, A., Paulino, M., & Fuchs, A. G. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.901994 · Cited by 4

The role of platelets and neutrophil extracellular traps (NETs) in sepsis: A comprehensive literature review

Vélez-Páez, J. L., Barragán, F. E. R., Dueñas-Andrade, S., Rodriguez-Morales, A. J., & Kyriakidis, N. C. (2023) · Microbes Infection and Chemotherapy · doi:10.54034/mic.e1595 · Cited by 4

Innate Immune Mechanism of Neutrophil Extracellular Trap Formation is Impaired in at-Risk Term Low Birth Weight Newborns

Das, D., Singh, V. V., Chauhan, S. K., Rai, R., Kumar, A., Jain, M., & Rai, G. (2023) · Pediatric Hematology and Oncology · doi:10.1080/08880018.2023.2218409 · Cited by 4

Cell Death Mechanisms Elicited by Multifactorial Stress Inducers- A Minireview

Girigoswami, A., & Girigoswami, K. (2023) · Coronaviruses · doi:10.2174/0126667975259454230920150008 · Cited by 4

Tamoxifen triggers the in vitro release of neutrophil extracellular traps in healthy horses

Salinas, C., Barriga, K., Albornoz, A., Alarcón, P., Quiroga, J., Uberti, B., Sarmiento, J., Henríquez, C., Ehrenfeld, P., Burgos, R. A., et al. (2023) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.1025249 · Cited by 4

Role of Platelet Activation in the Development and Metastasis of Solid Tumors

Sveshnikova, A. N., Tesakov, I. P., Kuznetsova, S. A., & Shamova, Е. М. (2024) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093024010150 · Cited by 4

Pro-inflammatory interactions of streptolysin O toxin with human neutrophils in vitro

Joseph, D., Theron, A. J., Feldman, C. H., Anderson, R., & Tintinger, G. R. (2024) · Journal of Immunotoxicology · doi:10.1080/1547691x.2024.2345152 · Cited by 3

Identification of Renal Ischemia-Reperfusion Injury Subtypes and Predictive Model for Graft Loss after Kidney Transplantation Based on Programmed Cell Death-Related Genes

Ji, J., Ma, Y., Liu, X., Zhou, Q., Zheng, X., Chen, Y., Li, Z., & Yang, L. (2024) · Kidney Diseases · doi:10.1159/000540158 · Cited by 3

Bio-responsive polymers for dual 31P/19F-magnetic resonance to detect reactive oxygen species in vivo

Ziółkowska, N., Sulková, K., Kracíková, L., Androvič, L., Havlíček, D., Laga, R., & Jirák, D. (2024) · Communications Materials · doi:10.1038/s43246-024-00623-z · Cited by 3

Targeting the HDAC6/Hint2/MICU1 axis to ameliorate acute liver failure via inhibiting NETosis

Guo, J., Shi, C., Wang, Y., Zhang, D., Zhang, Q., Zhang, X., Wang, L., & Gong, Z. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123498 · Cited by 3

From current landscape to future horizon in stem cell therapy for tissue regeneration and wound healing: bridging the gap

Morakhia, K. R., Shah, A. C., Patel, M. P., Shah, J., Patel, R., & Chorawala, M. R. (2025) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2025-0020 · Cited by 3

Neutrophil-Mediated Effects on Hemostasis and Thrombosis: Unraveling Their Complex Interaction in Thrombotic Events

Hassani, S., Fazeli, A., Dorgalaleh, A., Tabibian, S., Lomei, J., Alipour, M., Zadeh, M. K., & Shams, M. (2025) · Seminars in Thrombosis and Hemostasis · doi:10.1055/a-2605-8019 · Cited by 3

Next-Generation Regenerative Therapies for Alpha-1 Antitrypsin Deficiency: Molecular Pathogenesis to Clinical Translation

Se-Ran, Y., & Kim, H. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178504 · Cited by 3

Role of NETosis in the Pathogenesis of Respiratory Diseases: Molecular Mechanisms and Emerging Insights

KIM, S., & Kim, G. (2025) · Biocell · doi:10.32604/biocell.2025.073781 · Cited by 3

SodA promotes immune evasion of Streptococcus suis by suppressing ROS accumulation and GSDMD-mediated mitochondrial disruption in neutrophils

Xie, H., Li, Y., Fang, Q., Xie, H., Huang, J., Wu, Z., Deng, Z., Sun, Q., Huang, Y., Liao, J., et al. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.01901-25 · Cited by 3

NETs in ovarian cancer progression: innovative nanoparticle-based therapeutic strategies

Moradpanah, S., Aghaei, Z. H., Eslamnik, P., Goldiani, N. K., Sargolzaei, Z., Doosty, F., Barsam, M., Feli, M., & Zarifi, N. (2025) · European journal of medical research · doi:10.1186/s40001-025-03475-6 · Cited by 3

A Developmental Roadmap Toward Abdominal Adhesions Prevention Technologies

Christensen, R. R., Wright, K. E., Ives, J. K., Minnick, C. E., Chen, Q., Girgis, M. D., Ko, C., Gibbons, M. M., Russell, T. A., Huy, T. C., et al. (2025) · Annals of Surgery Open · doi:10.1097/as9.0000000000000637 · Cited by 3

Sepsis-induced coagulopathy: recent insights on the role and clinical application of neutrophil extracellular trap formation

Zaiema, S. E. G. E., Shalaby, N. A., Mohamed, T. E., Bayoumy, A. A. M., & Galal, R. E. S. A. M. (2025) · Scientific Reports · doi:10.1038/s41598-025-31771-y · Cited by 3

Neutrophil extracellular traps (NETosis) in gynecologic cancers: from pathogenesis to therapeutic opportunities: a narrative review

Kumar, N. (2026) · Clinical & Translational Oncology · doi:10.1007/s12094-025-04149-9 · Cited by 3

Mitochondrial metabolism in neutrophils: emerging roles in inflammatory skin diseases

Zhao, F., Gao, L., Guo, Y., Jiao, Y., Zou, W., Li, W., Li, W., Qi, R., & Wan, W. (2026) · British Journal of Dermatology · doi:10.1093/bjd/ljag060 · Cited by 3

Regulation of histones in thromboinflammation

Mohiuddin, N., Shah, Y., & Subramaniam, S. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1791619 · Cited by 4

Toxic Alpha-Synuclein and the Opening of the Gate: Blood–Brain Barrier Damage and Stepwise Leukocyte Infiltration

Wójcik, P., Culmsee, C., & Adamczyk, A. (2026) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-026-01733-7 · Cited by 3

WKYMVm Works by Targeting Immune Cells

Yang, Y., Zhao, J., Jiang, C., Zhang, Y., Han, M., & Liu, H. (2023) · Journal of Inflammation Research · doi:10.2147/jir.s390394 · Cited by 3

Programmed cell death-index (PCDi) as a prognostic biomarker and predictor of drug sensitivity in cervical cancer: a machine learning-based analysis of mRNA signatures

Wang, W., Chen, P., & Yuan, S. (2024) · Journal of Cancer · doi:10.7150/jca.91798 · Cited by 3

Induction of Netosis by 2,2,4,4‐Tetrabromodiphenyl Ether ( BDE ‐47) in Cyprinus Carpio

Gao, Z., Yu, J., Huang, Y., Jiang, Y., Cai, J., & Zhang, Z. (2025) · Environmental Toxicology · doi:10.1002/tox.24529 · Cited by 3

Idiopathic Inflammatory Myopathy—Molecular Mechanisms Underlying Its Pathogenesis and Physical Therapy Effects

Markowska, A., & Tarnacka, B. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26178369 · Cited by 3

COVID-19 Infection, Drugs, and Liver Injury

Qiu, D., Cao, W., Zhang, Y., Hao, H., Wei, X. C., Yao, L., Wang, S., Gao, Z., Xie, Y., & Li, M. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14207228 · Cited by 3

The Role of Neutrophil Extracellular Traps in the Outcome of Malignant Epitheliomas: Significance of CA215 Involvement

Himcinschi, M., Uscătescu, V., Gherghe, G., Stoian, I. A.-M., Vlad, A., Popa, D. C., Coriu, D., & Anghel, A. (2024) · Diagnostics · doi:10.3390/diagnostics14030328 · Cited by 4

Multiple Sclerosis. Some Features of Pathology and Prospects for Therapy. Part 1

Константиновна, Ф. Е., Vorobjeva, N. V., & Muntyan, M. S. (2024) · Advances in Gerontology · doi:10.1134/s2079057024600630 · Cited by 3

Neutrophil extracellular traps and reactive oxygen species: Predictors of prognosis in bladder cancer

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