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

Pathological effects of SARS-CoV-2 on hematological and immunological cells: Alterations in count, morphology, and function

Ahmadi, E., Bagherpour, Z., Zarei, E., & Omidkhoda, A. (2022) · Pathology - Research and Practice · doi:10.1016/j.prp.2022.153782 · Cited by 29

Neutrophil Extracellular Traps in ANCA-Associated Vasculitis and Interstitial Lung Disease: A Scoping Review

d’Alessandro, M., Conticini, E., Bergantini, L., Cameli, P., Cantarini, L., Frediani, B., & Bargagli, E. (2022) · Life · doi:10.3390/life12020317 · Cited by 30

COVID‐19 as a trigger of Guillain‐Barré syndrome: A review of the molecular mechanism

Malekpour, M., Khanmohammadi, S., Meybodi, M. J. E., Shekouh, D., Rahmanian, M. R., Kardeh, S., & Azarpira, N. (2023) · Immunity Inflammation and Disease · doi:10.1002/iid3.875 · Cited by 29

Contribution of monocyte and macrophage extracellular traps to neutrophilic airway inflammation in severe asthma

Quoc, Q. L., Cao, T. B. T., Moon, J., Jang, J.-H., Shin, Y. S., Choi, Y., Ryu, M. S., & Park, H. (2023) · Allergology International · doi:10.1016/j.alit.2023.06.004 · Cited by 29

Anti-Ly6G binding and trafficking mediate positive neutrophil selection to unleash the anti-tumor efficacy of radiation therapy

Boivin, G., Ancey, P., de Silly, R. V., Kalambaden, P., Contat, C., Petit, B., Ollivier, J., Bourhis, J., Meylan, E., & Vozenin, M. (2021) · OncoImmunology · doi:10.1080/2162402x.2021.1876597 · Cited by 28

Metabolism: a potential regulator of neutrophil fate

Yipeng, Z., Chao, C., Li, R., Tingting, P., & Qu, H. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1500676 · Cited by 27

AGE/Non-AGE Glycation: An Important Event in Rheumatoid Arthritis Pathophysiology

Monu, M., Agnihotri, P., & Biswas, S. (2021) · Inflammation · doi:10.1007/s10753-021-01589-7 · Cited by 27

Role of Mitochondria in the Regulation of Effector Functions of Granulocytes

Vorobjeva, N. V., Chelombitko, M. A., Sud’ina, G. F., Zinovkin, R. A., & Chernyak, B. V. (2023) · Cells · doi:10.3390/cells12182210 · Cited by 28

Lenvatinib-activated NDUFA4L2/IL33/PADI4 pathway induces neutrophil extracellular traps that inhibit cuproptosis in hepatocellular carcinoma

Yi, N., Zhang, L., Huang, X., Ma, J., & Gao, J. J. (2024) · Cellular Oncology · doi:10.1007/s13402-024-01013-w · Cited by 26

CitH3, a Druggable Biomarker for Human Diseases Associated with Acute NETosis and Chronic Immune Dysfunction

Chen, Y., Tetz, Z., Zeng, X., Go, S. J., Ouyang, W., Lee, K. E., Dong, T., Li, Y., & Ma, J. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17070809 · Cited by 27

Presepsin production in monocyte/macrophage-mediated phagocytosis of neutrophil extracellular traps

Ikegame, A., Kondo, A., Kitaguchi, K., Sasa, K., & Miyoshi, M. (2022) · Scientific Reports · doi:10.1038/s41598-022-09926-y · Cited by 26

The molecular mechanism of neutrophil extracellular traps and its role in bone and joint disease

Xiang, M., Yin, M., Xie, S., Shi, L., Nie, W., Shi, B., & Yu, G. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e22920 · Cited by 25

Liquid biopsy in gynecological cancers: a translational framework from molecular insights to precision oncology and clinical practice

Martinelli, C. V., Ercoli, A., Vizzielli, G., Burk, S. R., Cuomo, M., Satasiya, V., Kacem, H., Braccia, S., Mazzarotti, G., Miriello, I., et al. (2025) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-025-03371-1 · Cited by 26

Senkyunolide I protect against lung injury via inhibiting formation of neutrophil extracellular trap in a murine model of cecal ligation and puncture

Zha, Y.-F., Xie, J., Ding, P., Zhu, C., Li, P., Zhao, Z., Li, Y., & Wang, J. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.107922 · Cited by 25

Long-Term Domiciliary High-Flow Nasal Therapy in Patients with Bronchiectasis: A Preliminary Retrospective Observational Case-Control Study

Crimi, C., Nolasco, S., Campisi, R., Nigro, M., Impellizzeri, P., Cortegiani, A., Noto, A., Gramegna, A., Vancheri, C., Blasi, F., et al. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm11247323 · Cited by 25

IDH1/MDH1 deacetylation promotes acute liver failure by regulating NETosis

Wang, Y., Shi, C., Guo, J., Zhang, D., Zhang, Y., Zhang, L., & Gong, Z. (2024) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-023-00529-7 · Cited by 25

Cyclic stretch enhances neutrophil extracellular trap formation

Khanmohammadi, M., Danish, H., Sekar, N. C., Suarez, S. A., Chheang, C., Peter, K., Khoshmanesh, K., & Baratchi, S. (2024) · BMC Biology · doi:10.1186/s12915-024-02009-6 · Cited by 24

Neutrophil Migration is a Crucial Factor in Wound Healing and the Pathogenesis of Diabetic Foot Ulcers: Insights into Pharmacological Interventions

Asunama, A. S. R., Nambi, N., Radhakrishnan, L., Prasad, M. K., & Ramkumar, K. M. (2024) · Current Vascular Pharmacology · doi:10.2174/0115701611308960241014155413 · Cited by 25

Neutrophil extracellular traps promote the activation of the NLRP3 inflammasome and PBMCs pyroptosis via the ROS-dependent signaling pathway in Kawasaki disease

Jin, J., Zhao, Y., Fang, Y., Pan, Y., Wang, P., Fan, Z., & Yu, H. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113783 · Cited by 24

Antioxidants as Modulators of NETosis: Mechanisms, Evidence, and Therapeutic Potential

Zambrano, F., Uribe, P., Schulz, M., Hermosilla, C. R., Taubert, A., & Sánchez, R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26115272 · Cited by 24

Role of nuclear receptors, lipid metabolism, and mitochondrial function in the pathogenesis of diabetic kidney disease

Hughes, E. P., Wang, X. X., Sabol, L., Barton, K., Hegde, S., Myakala, K., Krawczyk, E., Rosenberg, A. Z., & Levi, M. (2025) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00110.2025 · Cited by 27

Early ultrastructural lesions of anti‐neutrophil cytoplasmic antibody‐ versus complement‐associated vasculitis

Koike, H., Furukawa, S., Mouri, N., Fukami, Y., Iijima, M., & Katsuno, M. (2022) · Neuropathology · doi:10.1111/neup.12821 · Cited by 24

Prophylactic treatment of Glycyrrhiza glabra mitigates COVID-19 pathology through inhibition of pro-inflammatory cytokines in the hamster model and NETosis

Rizvi, Z. A., Babele, P., Sadhu, S., Madan, U., Tripathy, M. R., Goswami, S., Mani, S., Kumar, S., Awasthi, A., & Dikshit, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.945583 · Cited by 24

Pharmacological potential of Withania somnifera (L.) Dunal and Tinospora cordifolia (Willd.) Miers on the experimental models of COVID-19, T cell differentiation, and neutrophil functions

Rizvi, Z. A., Babele, P., Madan, U., Sadhu, S., Tripathy, M. R., Goswami, S., Mani, S., Dikshit, M., & Awasthi, A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1138215 · Cited by 24

How underappreciated autoinflammatory (innate immunity) mechanisms dominate disparate autoimmune disorders

Abacar, K., Macleod, T., Direskeneli, H., & McGonagle, D. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1439371 · Cited by 24

Liquid biopsy for gastric cancer: Techniques, applications, and future directions

del Arco, C. D., Fernández‐Aceñero, M. J., & Medina, L. O. (2024) · World Journal of Gastroenterology · doi:10.3748/wjg.v30.i12.1680 · Cited by 24

Targeting Neutrophil Extracellular Trap Formation: Exploring Promising Pharmacological Strategies for the Treatment of Preeclampsia

Hernandez‐Gonzalez, L., Mayoral, L. P.-C., Hernández‐Huerta, M. T., Andrade, G. M., Cruz, M. M., Ramos-Martínez, E. G., Mayoral, E. P., Hernández, V. C., García, I. A., Matias‐Cervantes, C. A., et al. (2024) · Pharmaceuticals · doi:10.3390/ph17050605 · Cited by 23

Role of Neutrophil Extracellular Traps in COVID-19 Progression: An Insight for Effective Treatment

Blanch‐Ruiz, M. A., Ortega‐Luna, R., Gómez-García, G., Martínez-Cuesta, M. Á., & Álvarez, Á. (2021) · Biomedicines · doi:10.3390/biomedicines10010031 · Cited by 24

Antioxidants as Therapeutic Agents in Acute Respiratory Distress Syndrome (ARDS) Treatment—From Mice to Men

von Knethen, A., Heinicke, U., Laux, V., Parnham, M. J., Steinbicker, A. U., & Zacharowski, K. D. (2022) · Biomedicines · doi:10.3390/biomedicines10010098 · Cited by 23

Neutrophil Extracellular Traps and Their Possible Implications in Ocular Herpes Infection

Kapoor, D., & Shukla, D. (2023) · Pathogens · doi:10.3390/pathogens12020209 · Cited by 23

NETosis in Parasitic Infections: A Puzzle That Remains Unsolved

Omar, M., & Abdelal, H. O. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24108975 · Cited by 24

The Evolving Role of Neutrophils and Neutrophil Extracellular Traps (NETs) in Obesity and Related Diseases: Recent Insights and Advances

Altamura, S., Lombardi, F., Palumbo, P., Cinque, B., Ferri, C., Pinto, R. D., & Pietropaoli, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413633 · Cited by 23

Neutrophil Extracellular Traps (NETs) in Sterile Inflammatory Diseases

Ji, Y., Li, T., Qin, Y., Xiao, S.-Y., Lv, Y., Dong, Y., Cui, X., & Hu, Y. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s526936 · Cited by 24

Mechanistic insights into PAMP and DAMP driven activation of NETosis in autoimmune disorders

Bhatia, N., George, B., Masih, D., Khan, M. M. U., & Malik, P. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115149 · Cited by 22

Effect of Vitamin D3 in combination with Omega‐3 Polyunsaturated Fatty Acids on NETosis in Type 2 Diabetes Mellitus Patients

Basyreva, L. Y., Vakhrusheva, T. V., Letkeman, Z. V., Maximov, D. I., Fedorova, E. A., Panasenko, O. M., Ostrovsky, E. M., & Гусев, С. А. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8089696 · Cited by 22

Rapid Screening of Urinary Tract Infection Using Microfluidic Inertial-Impedance Cytometry

Petchakup, C., Chen, Y. Y. C., Tay, H. M., Ong, H. B., Hon, P. Y., De, P. P., Yeo, T. W., Li, K. H. H., Vasoo, S. S., & Hou, H. W. (2023) · ACS Sensors · doi:10.1021/acssensors.3c00819 · Cited by 22

What fraction of cellular DNA turnover becomes cfDNA?

Sender, R., Noor, Ε., Milo, R., & Dor, Y. (2023) · eLife · doi:10.7554/elife.89321 · Cited by 22

Photoaging: UV radiation-induced cGAS-STING signaling promotes the aging process in skin by remodeling the immune network

Salminen, A., Kaarniranta, K., & Kauppinen, A. (2025) · Biogerontology · doi:10.1007/s10522-025-10268-1 · Cited by 21

miR‐3146 induces neutrophil extracellular traps to aggravate gout flare

Shan, L., Yang, D., Feng, F., Zhu, D., & Li, X. (2021) · Journal of Clinical Laboratory Analysis · doi:10.1002/jcla.24032 · Cited by 21

Inflammatory response to the ischaemia–reperfusion insult in the liver after major tissue trauma

Li, Y., Palmer, A., Lupu, L., & Huber-Lang, M. S. (2022) · European Journal of Trauma and Emergency Surgery · doi:10.1007/s00068-022-02026-6 · Cited by 21

Impact of CFTR Modulators on the Impaired Function of Phagocytes in Cystic Fibrosis Lung Disease

Meoli, A., Eickmeier, O., Pisi, G., Fainardi, V., Zielen, S., & Esposito, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012421 · Cited by 21

Transfusion support in hematopoietic stem cell transplantation

Jekarl, D. W., Kim, J. K., Han, J. H., Lee, H., Yoo, J., Lim, J., & Kim, Y. (2023) · Blood Research · doi:10.5045/br.2023.2023004 · Cited by 21

NET-(works) in arterial and venous thrombo-occlusive diseases

Zdanytė, M., Borst, O., & Münzer, P. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1155512 · Cited by 23

Molecular and functional changes in neutrophilic granulocytes induced by nicotine: a systematic review and critical evaluation

Brembach, T.-C., Sabat, R., Witte, K., Schwerdtle, T., & Wolk, K. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1281685 · Cited by 23

Immunoprotection Strategies in β‐Cell Replacement Therapy: A Closer Look at Porcine Islet Xenotransplantation

Grimus, S., Sarangova, V., Welzel, P. B., Ludwig, B., Seißler, J., Kemter, E., Wolf, E., & Ali, A. (2024) · Advanced Science · doi:10.1002/advs.202401385 · Cited by 22

Clinical complications in envenoming by Apis honeybee stings: insights into mechanisms, diagnosis, and pharmacological interventions

Cavalcante, J. S., Riciopo, P. M., Pereira, A. F. M., Jeronimo, B. C. [., Angstmam, D. G., Possas, F. C., Filho, A. D. A., Cerni, F. A., Pucca, M. B., & Ferreira, R. S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1437413 · Cited by 21

TLR4 Targeting: A Promising Therapeutic Approach Across Multiple Human Diseases

Kumar, S., Sharma, V., & Yadav, S. (2024) · Current Protein and Peptide Science · doi:10.2174/0113892037324425241018061548 · Cited by 21

Blood plasma proteome alteration after local tissue damage induced by Bothrops erythromelas snake venom in mice

Cavalcante, J. S., da Silva, W. R. G. B., de Oliveira, L. A., Brito, I. M. D. C., Muller, K. S., Vidal, I., dos Santos, L. D., Jorge, R. J. B., de Almeida, C. A. S., & Bicho, C. D. L. (2022) · Journal of Proteomics · doi:10.1016/j.jprot.2022.104742 · Cited by 20

Identification and validation of the molecular subtype and prognostic signature for clear cell renal cell carcinoma based on neutrophil extracellular traps

Quan, J., & Huang, B. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1021690 · Cited by 20

Rosavin inhibits neutrophil extracellular traps formation to ameliorate sepsis-induced lung injury by regulating the MAPK pathway

Gao, T., Li, J., Shi, L., & Hu, B. (2023) · Allergologia et Immunopathologia · doi:10.15586/aei.v51i4.879 · Cited by 20

Citrullination and the protein code: crosstalk between post-translational modifications in cancer

Harada, K., Carr, S. M., Shrestha, A., & Thangue, N. B. L. (2023) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2022.0243 · Cited by 20

Exploring the relations of NLR, hsCRP and MCP-1 with type 2 diabetic kidney disease: a cross-sectional study

Fang, Y., Wang, B., Pang, B., Zhou, Z., Xing, Y., Pang, P., Zheng, D., Zhang, G., & Yang, B. (2024) · Scientific Reports · doi:10.1038/s41598-024-53567-2 · Cited by 21

Dysregulated Neutrophil Phenotype and Function in Hospitalised Non-ICU COVID-19 Pneumonia

Belchamber, K. B. R., Thein, O. S., Hazeldine, J., Grudzinska, F. S., Faniyi, A. A., Hughes, M., Jasper, A. E., Yip, K. P., Crowley, L., Lugg, S. T., et al. (2022) · Cells · doi:10.3390/cells11182901 · Cited by 25

Epigallocatechin-3-Gallate and Genistein for Decreasing Gut Dysbiosis, Inhibiting Inflammasomes, and Aiding Autophagy in Alzheimer’s Disease

Muraleedharan, A., & Ray, S. K. (2024) · Brain Sciences · doi:10.3390/brainsci14010096 · Cited by 20

Involvement of regulated cell deaths in aging and age-related pathologies

Torre, L. D., Beato, A., Capone, V., Carannante, D., Verrilli, G., Favale, G., Gaudio, N. D., Megchelenbrink, W., Benedetti, R., Altucci, L., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102251 · Cited by 20

Type I Interferons in Systemic Autoimmune Rheumatic Diseases: Pathogenesis, Clinical Features and Treatment Options

Drougkas, K., Skarlis, C., & Mavragani, C. P. (2024) · Mediterranean Journal of Rheumatology · doi:10.31138/mjr.270324.tis · Cited by 19

Tamm-Horsfall protein augments neutrophil NETosis during urinary tract infection

Mercado-Evans, V., Branthoover, H., Chew, C., Serchejian, C., Saltzman, A. B., Mejia, M. E., Zulk, J. J., Cornax, I., Nizet, V., & Patras, K. A. (2024) · JCI Insight · doi:10.1172/jci.insight.180024 · Cited by 18

Reactive oxygen species in cell signaling and cell death: A redox perspective on metabolic and inflammatory disorders

Deepak, K., Shee, M., Roy, P., & Mandal, M. (2026) · Cell Death · doi:10.1016/j.celld.2026.100009 · Cited by 19

Autophagy-driven neutrophil extracellular traps: The dawn of sepsis

Huang, Z., Zhang, H., Fu, X., Han, L., Zhang, H., Zhang, L., Zhao, J., Xiao, D., Li, H., & Li, P. (2022) · Pathology - Research and Practice · doi:10.1016/j.prp.2022.153896 · Cited by 18

Morphology of Neutrophils during Their Activation and NETosis: Atomic Force Microscopy Study

Sergunova, V. A., Inozemtsev, V. A., Vorobjeva, N. V., Kozlova, E. K., Sherstyukova, E. A., Kandrashina, S., & Черныш, А. М. (2023) · Cells · doi:10.3390/cells12172199 · Cited by 18

Pathophysiological Role of Neutrophil Extracellular Traps in Diet-Induced Obesity and Metabolic Syndrome in Animal Models

Feješ, A., Šebeková, K., & Borbélyová, V. (2025) · Nutrients · doi:10.3390/nu17020241 · Cited by 17

Cadmium targeting MLKL-Drp1 axis to trigger mitochondrial oxidative stress contributes to necroinflammation in rat kidney

Lian, C.-Y., Xia, W.-H., Sun, M.-C., Wan, X., Zhou, X.-L., & Wang, Z. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.05.055 · Cited by 17

Role of damage-associated molecular patterns in the pathogenesis and therapeutics of traumatic brain injury

Sun, B., Zhang, J., Li, Z., Wang, J., Zhao, C., & Xu, X. (2025) · Burns & Trauma · doi:10.1093/burnst/tkaf043 · Cited by 18

Wip1 inhibits neutrophil extracellular traps to promote abscess formation in mice by directly dephosphorylating Coronin-1a

Chen, Y., Zhao, C., Guo, H., Zou, W., Zhang, Z., Dong, W., Lu, H., Zhang, L., & Zhao, Y. X. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01057-2 · Cited by 17

NADPH oxidase-dependent free radical generation and protein adduct formation in neutrophils

Manoharan, R. R., Zachová, K., Buzáš, M., Pospı́šil, P., Křupka, M., & Prasad, A. (2024) · RSC Advances · doi:10.1039/d4ra02739f · Cited by 17

New Insights on NETosis Induced by Entamoeba histolytica: Dependence on ROS from Amoebas and Extracellular MPO Activity

Díaz-Godínez, C., Jorge-Rosas, J. F., Néquiz, M., Martínez‐Calvillo, S., Laclette, J. P., Rosales, C., & Carrero, J. C. (2021) · Antioxidants · doi:10.3390/antiox10060974 · Cited by 17

How Cells Die in Psoriasis?

Chen, C.-H., Wu, N., & Tsai, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26083747 · Cited by 17

Neutrophil extracellular traps in tumor metastasis: mechanisms, and therapeutic implications

Li, N., Yin, C., & Tao, J. (2025) · Discover Oncology · doi:10.1007/s12672-025-03451-w · Cited by 17

NETosis in Long-Term Type 1 Diabetes Mellitus and Its Link to Coronary Artery Disease

Aukrust, S. G., Holte, K. B., Opstad, T. B., Seljeflot, I., Berg, T. J., & Helseth, R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.799539 · Cited by 18

Functional blood cell analysis by label-free biosensors and single-cell technologies

Szittner, Z., Péter, B., Kurunczi, S., Székács, I., & Horváth, R. (2022) · Advances in Colloid and Interface Science · doi:10.1016/j.cis.2022.102727 · Cited by 16

Immunity and Coagulation in COVID-19

Авдонин, П. П., Blinova, M. S., Serkova, A. A., Komleva, L. A., & Avdonin, P. V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252011267 · Cited by 17

The D-lactate enigma: exploring the inflammatory influence of D-lactate in cattle

Burgos, R. A., Manosalva, C., Alarcón, P., Navarro, M., Quiroga, J., Morán, G., Gallastegui, J., Brauchi, S., & Carretta, M. D. (2024) · Frontiers in Veterinary Science · doi:10.3389/fvets.2024.1509399 · Cited by 15

Immunomodulatory interactions between mesenchymal stromal/stem cells and immune cells in psoriasis: therapeutic potential and challenges

Dashti, M., Mohammadi, M., Dehnavi, S., & Sadeghi, M. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04375-6 · Cited by 16

Neutrophils and NETosis in Alzheimer’s disease: Unraveling pathogenic mechanisms and novel therapeutic targets

Chavoshinezhad, S., Beirami, E., & Izadpanah, E. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118568 · Cited by 15

Radiation from UV-A to Red Light Induces ROS-Dependent Release of Neutrophil Extracellular Traps

Arzumanyan, G., Маматкулов, К. З., Arynbek, Y., Zakrytnaya, D., Jevremović, A., & Vorobjeva, N. V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065770 · Cited by 15

Combined repetitive inhalant endotoxin and collagen-induced arthritis drive inflammatory lung disease and arthritis severity in a testosterone-dependent manner

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