Pharmacological Inhibitors of the NLRP3 Inflammasome
Open accessAbstract
Inflammasomes play a crucial role in innate immunity by serving as signaling platforms which deal with a plethora of pathogenic products and cellular products associated with stress and damage. By far, the best studied and most characterized inflammasome is NLRP3 inflammasome, which consists of NLRP3 (nucleotide-binding domain leucine-rich repeat (NLR) and pyrin domain containing receptor 3), ASC (apoptosis-associated speck-like protein containing a caspase recruitment domain), and procaspase-1. Activation of NLRP3 inflammasome is mediated by highly diverse stimuli. Upon activation, NLRP3 protein recruits the adapter ASC protein, which recruits the procaspase-1 resulting in its cleavage and activation, inducing the maturation and secretion of inflammatory cytokines and pyroptosis. However, aberrant activation of the NLRP3 inflammasome is implicated in various diseases including diabetes, atherosclerosis, metabolic syndrome, cardiovascular and neurodegenerative diseases; raising a tremendous clinical interest in exploring the potential inhibitors of NLRP3 inflammasome. Recent investigations have disclosed various inhibitors of the NLRP3 inflammasome pathway which were validated through in vitro studies and in vivo experiments in animal models of NLRP3-associated disorders. Some of these inhibitors directly target the NLRP3 protein whereas some are aimed at other components and products of the inflammasome. Direct targeting of NLRP3 protein can be a better choice because it can prevent off target immunosuppressive effects, thus restrain tissue destruction. This paper will review the various pharmacological inhibitors of the NLRP3 inflammasome and will also discuss their mechanism of action.
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The NLRP3 inflammasome is a key regulator of SASP induction, widely involved in disease and for which drug development is active.
“the NLRP3 inflammasome is a key regulator of SASP induction, widely involved in disease and for which drug development is active (Zahid et al. 2019).”
From Senescence and the SASP: many therapeutic avenues (2020) · cites this paper as Zahid et al. 2019
The “NLRP3 Inflammasome Associated Diseases” section links NLRP3 activation to numerous diseases, and “Pharmacological Inhibition of NLRP3 Inflammasome” describes active investigation of inhibitors. The paper describes NLRP3-driven inflammatory cytokine release, but the passages do not identify it as a key regulator of SASP induction (searched: SASP, senescence, secretory phenotype). (LLM, conf=0.87)
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Cites
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Senescence and the SASP: many therapeutic avenues
Birch, J., & Gil, J. (2020) · Genes & Development · doi:10.1101/gad.343129.120 · Cited by 1,177 · see citing works
“Similarly, the NLRP3 inflammasome is a key regulator of SASP induction, widely involved in disease and for which drug development is active (Zahid et al. 2019).”
BackgroundHyperuricemia and its related diseases: mechanisms and advances in therapy
Du, L., Yao, Z., Li, H., Wang, Q., Xie, L., Yang, B., Pang, Y., Zhang, C., Zhong, Z., & Gao, J. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01916-y · Cited by 719 · see citing works
Blevins, H. M., Xu, Y., Biby, S., & Zhang, S. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.879021 · Cited by 587 · see citing works
Metabolic syndrome and cardiovascular diseases: Going beyond traditional risk factors
Rossi, J. L. S., Barbalho, S. M., de Araújo, R. R., Bechara, M. D., Sloan, K. P., & Sloan, L. A. (2021) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.3502 · Cited by 606 · see citing works
“Triggering: in response to the second contact of a PRR with DAMPs or PAMPs, there is the oligomerisation of NLRP3 complexes and consequent activation of caspase‐1, the enzyme responsible for the conversion of pro‐IL‐1β and pro‐IL‐18 precursors into their respective effector molecules.(50)”
BackgroundAdamu, A., Li, S., Gao, F., & Xue, G. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1347987 · Cited by 564 · see citing works
NLRP3 inflammasome in endothelial dysfunction
Bai, B., Yang, Y., Wang, Q., Li, M., Tian, C., Liu, Y., Aung, L. H. H., Li, P., Yu, T., & Chu, X. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02985-x · Cited by 492 · see citing works
Therapeutic application of quercetin in aging-related diseases: SIRT1 as a potential mechanism
Cui, Z., Zhao, X., Amevor, F. K., Du, X., Wang, Y., Li, D., Shu, G., Tian, Y., & Zhao, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.943321 · Cited by 400 · see citing works
NLRP3 Inflammasome and Inflammatory Diseases
Wang, Z., Zhang, S., Xiao, Y., Zhang, W., Wu, S., Qin, T., Yue, Y., Qian, W., & Li, L. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/4063562 · Cited by 315 · see citing works
“Compared to blocking IL-1β, specific targeting with NLRP3 inhibitors may be a good choice for related diseases [133].”
BackgroundNLRP3 inflammasome in neuroinflammation and central nervous system diseases
Xu, W. R., Huang, Y., & Zhou, R. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01275-w · Cited by 309 · see citing works
Interconnections between Inflammageing and Immunosenescence during Ageing
Teissier, T., Boulanger, É., & Cox, L. S. (2022) · Cells · doi:10.3390/cells11030359 · Cited by 310 · see citing works
“NLRP3 is looking to be a very interesting target for drug inhibition to reduce inflammation without unwanted off-target effects on the wider immune system (reviewed in [429]).”
BackgroundInflammasomes and Pyroptosis as Therapeutic Targets for COVID-19
Yap, J. K. Y., Moriyama, M., & Iwasaki, A. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000513 · Cited by 245 · see citing works
“Various dedicated inhibitors of NLRP3 have existed mostly in the form of clinically unproven experimental compounds, both of natural and synthetic origins (60).”
BackgroundThe Role of Microglia and the Nlrp3 Inflammasome in Alzheimer's Disease
Hanslik, K. L., & Ulland, T. K. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.570711 · Cited by 236 · see citing works
“Likewise, inhibitors focused on reducing cytokine secretion alone does not address Nlrp3-induced pyroptosis, which may contribute to additional pathology (72).”
BackgroundDobrev, D., Heijman, J., Hiram, R., Li, N., & Nattel, S. (2022) · Nature Reviews Cardiology · doi:10.1038/s41569-022-00759-w · Cited by 274 · see citing works
Role of the NLRP3 inflammasome in autoimmune diseases
Li, Z., Guo, J., & Bi, L. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110542 · Cited by 268 · see citing works
Ma, Q. (2023) · Pharmacological Reviews · doi:10.1124/pharmrev.122.000629 · Cited by 256 · see citing works
Emerging Microglia Biology Defines Novel Therapeutic Approaches for Alzheimer’s Disease
Lewcock, J. W., Schlepckow, K., Di Paolo, G., Tahirovic, S., Monroe, K. M., & Haass, C. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.029 · Cited by 221 · see citing works
Role of pyroptosis in spinal cord injury and its therapeutic implications
Mamun, A. A., Wu, Y., Monalisa, I., Jia, C., Zhou, K., Munir, F., & Xiao, J. (2020) · Journal of Advanced Research · doi:10.1016/j.jare.2020.08.004 · Cited by 230 · see citing works
McElwain, C. J., Tuboly, E., McCarthy, F. P., & McCarthy, C. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00655 · Cited by 224 · see citing works
“A similar sulfonylurea compound, MCC950, is considered one of the most selective and potent NLRP3 inhibitors (212).”
BackgroundNLRP3 Inflammasome Activation in Cancer: A Double-Edged Sword
Hamarsheh, S., & Zeiser, R. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01444 · Cited by 227 · see citing works
“A number of small-molecule compounds were proposed to show specific inhibitory effects on NLRP3 activation [reviewed further in detail elsewhere (130, 131)].”
BackgroundAnti-inflammatory potential of Quercetin in COVID-19 treatment
Saeedi‐Boroujeni, A., & Mahmoudian‐Sani, M. (2021) · Journal of Inflammation · doi:10.1186/s12950-021-00268-6 · Cited by 235 · see citing works
Inhibition of the NLRP3 inflammasome prevents ovarian aging
Navarro-Pando, J., Alcocer-Gómez, E., Castejón-Vega, B., Navarro-Villarán, E., Condés-Hervás, M., Mundi-Roldan, M., Muntané, J., Pérez-Pulido, A., Bullón, P., Wang, C., et al. (2020) · Science Advances · doi:10.1101/2020.04.26.062646 · Cited by 181
Higashikuni, Y., Liu, W., Numata, G., Tanaka, K., Fukuda, D., Tanaka, Y., Hirata, Y., Imamura, T., Takimoto, E., Komuro, I., et al. (2022) · Circulation · doi:10.1161/circulationaha.122.060860 · Cited by 229 · see citing works
NLRP3 inflammasome as a key driver of vascular disease
Takahashi, M. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab010 · Cited by 188 · see citing works
The World Goes Bats: Living Longer and Tolerating Viruses
Gorbunova, V., Seluanov, A., & Kennedy, B. K. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.06.013 · Cited by 162 · see citing works
NLRP3 inflammasome-mediated cytokine production and pyroptosis cell death in breast cancer
Faria, S. S., Costantini, S., de Lima, V. C. C., Andrade, V. P., Rialland, M., Rébé, C., Budillon, A., & Magalhães, K. G. (2021) · Journal of Biomedical Science · doi:10.1186/s12929-021-00724-8 · Cited by 189 · see citing works
“Some of these inhibitors directly target the NLRP3 protein whereas others target components and products of the inflammasome [116].”
BackgroundCan melatonin reduce the severity of COVID-19 pandemic?
Shneider, A. M., Kudriavtsev, A., & Vakhrusheva, A. (2020) · International Reviews of Immunology · doi:10.20944/preprints202004.0122.v1 · Cited by 171
“inhibition have been studied [38], and melatonin reported as NLRP3 inflammasome inhibitor [39].”
BackgroundGSDMD is critical for autoinflammatory pathology in a mouse model of Familial Mediterranean Fever
Kanneganti, A., Malireddi, R. K. S., Saavedra, P. H. V., Walle, L. V., Gorp, H. V., Kambara, H., Sheppard, H., Vogel, P., Luo, H. R., Xavier, R. J., et al. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20172060 · Cited by 180 · see citing works
Corcoran, S. E., Halai, R., & Cooper, M. A. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000171 · Cited by 179 · see citing works
“An extensive list of covalent and noncovalent inhibitors is reviewed elsewhere (Mangan et al., 2018; Zahid et al., 2019).”
BackgroundMultiple roles of caspase-8 in cell death, inflammation, and innate immunity
Ørning, P., & Lien, E. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mr0420-305r · Cited by 199 · see citing works
The NLRP3 inflammasome in depression: Potential mechanisms and therapies
Xia, C., Guo, Y., Lian, W., Yan, Y., Ma, B.-Z., Cheng, Y., Xu, J., He, J., & Zhang, W. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106625 · Cited by 184 · see citing works
Unmet medical needs in chronic, non-communicable inflammatory skin diseases
Ujiie, H., Rosmarin, D., Schön, M. P., Ständer, S., Boch, K., Metz, M., Maurer, M., Thaci, D., Schmidt, E., Cole, C., et al. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.875492 · Cited by 158 · see citing works
Targeted Immunotherapy for Autoimmune Disease
Jung, S. M., & Kim, W. (2022) · Immune Network · doi:10.4110/in.2022.22.e9 · Cited by 175 · see citing works
“As a new therapeutic approach to inhibit IL-1 signaling, oral NLRP3 inhibitors, including dapansutrile (OLT177), are under investigation (51).”
BackgroundPyroptosis is a critical immune-inflammatory response involved in atherosclerosis.
He, X., Fan, X.-H., Bai, B., Lu, N., Zhang, S., & Zhang, L.-M. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105447 · Cited by 153 · see citing works
New Insights into Pathomechanisms and Treatment Possibilities for Lung Silicosis
Adamčáková, J., & Mokrá, D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084162 · Cited by 179 · see citing works
Structural basis for the oligomerization-mediated regulation of NLRP3 inflammasome activation
Ohto, U., Kamitsukasa, Y., Ishida, H., Zhang, Z., Murakami, K., Hirama, C., Maekawa, S., & Shimizu, T. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2121353119 · Cited by 147 · see citing works
Zeller, M. V., Dias, D., Sebastião, A. M., & Valente, C. A. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-210268 · Cited by 173 · see citing works
“Pharmacological approaches to 1256 inhibit the NLRP3 inflammasome, either directly 1257 or indirectly, were exhaustedly reviewed by Zahid 1258 and coworkers [171], such as blocking the expres1259 sion of NLRP3, ASC, caspase-1, and neutralizing 1260”
MethodNew Dawn for Atherosclerosis: Vascular Endothelial Cell Senescence and Death
Bu, L.-L., Yuan, H., Xie, L., Guo, M.-H., Liao, D., & Zheng, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242015160 · Cited by 129 · see citing works
Yu, L., Hong, W., Lu, S., Li, Y., Guan, Y., Weng, X., & Feng, Z. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.780496 · Cited by 122 · see citing works
“Given the complexity of NLRP3 inflammasome signaling cascades, activation of various target proteins can be suppressed in many ways, including blockade of upstream signals, inhibition of inflammasome assembly, suppression of caspase-1 activation, prevention of GSDMD cleavage, and arrest of inflammatory cytokines produ…”
BackgroundPyroptosis and Its Role in Autoimmune Disease: A Potential Therapeutic Target
You, R., He, X., Zeng, Z., Zhan, Y., Xiao, Y., & Xiao, R. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.841732 · Cited by 147 · see citing works
NLRP inflammasomes in health and disease
Xu, Z., Kombe, A. J. K., Deng, S., Zhang, H., Wu, S., Ruan, J., Zhou, Y. Y., & Jin, T. (2024) · Molecular Biomedicine · doi:10.1186/s43556-024-00179-x · Cited by 120 · see citing works
“Parthenolide* CASP-1 activation; NLRP3 ATPase activity [345] Bay 11–708 NF-κB pathway [317, 345] CPG 15d-PGJ2 CASP-1 activation [346] RKIP CASP-1 activation and IL-1β secretion Gouty arthritis and T2D [347] IVIg** Ischemic stroke [348] ADS032 IL-1β and TNF-α Pulmonary inflammation [349] Arsenic…”
BackgroundInfluentialSelf-citationPathway network of pyroptosis and its potential inhibitors in acute kidney injury
Li, N., Wang, Y., Wang, X., Sun, N., & Gong, Y.-H. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.106033 · Cited by 123 · see citing works
Guo, H.-H., Zhu, L.-L., Tang, P.-F., Chen, D., Li, Y.-C., Li, J.-B., & Bao, C. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.4885 · Cited by 115
“The NLR family pyrin domain containing 3 (NLRP3) inflammasome, which consists of NLRP3, apoptosis‑associ‑ ated speck‑like protein (ASC) and caspase‑1, is an important component of the innate immune system (5).”
Chronic low‐grade inflammation in heart failure with preserved ejection fraction
Mesquita, T., Lin, Y., & Ibrahim, A. G.-E. (2021) · Aging Cell · doi:10.1111/acel.13453 · Cited by 117 · see citing works
“Inhibiting the NLRP3 inflammasome activation with MCC950 ameliorates diabetic encephalopathy in db/db mice.”
BackgroundInfluentialLee, A.-H., Shin, H.-Y., Park, J.-H., Koo, S. Y., Kim, S. M., & Yang, S. (2021) · Scientific Reports · doi:10.1038/s41598-020-80748-6 · Cited by 102 · see citing works
Diabetes Mellitus Promotes the Development of Atherosclerosis: The Role of NLRP3
Ye, J., Li, L., Wang, M., Ma, Q., Tian, Y., Zhang, Q., Liu, J., Li, B., Zhang, B., Liu, H., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.900254 · Cited by 100 · see citing works
“Examples include 16673-34-0, JC124, and FC11A-2 (132).”
Self-citationRole of Caspase-1 in the Pathogenesis of Inflammatory-Associated Chronic Noncommunicable Diseases
Molla, M. D., Akalu, Y., Geto, Z., Dagnew, B., Ayelign, B., & Shibabaw, T. (2020) · Journal of Inflammation Research · doi:10.2147/jir.s277457 · Cited by 110 · see citing works
Que, R., Zheng, J., Chang, Z., Zhang, W., Li, H., Xie, Z., Huang, Z., Wang, H., Xu, J., Jin, D., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.794770 · Cited by 111 · see citing works
“Studies have suggested that increased intracellular ROS accumulation can promote NLRP3:ASC:pro-caspase-1 complex assembly and enhance microglia activation, while using antioxidant to reduce ROS production can suppress NLRP3 inflammasome and microglia activation, and finally alleviate microglia mediated neurotoxicity (…”
BackgroundJin, M., Fang, J. C., Wang, J., Shao, X., Xu, S., Liu, P., Ye, W., & Liu, Z. (2023) · Acta Pharmacologica Sinica · doi:10.1038/s41401-023-01123-5 · Cited by 102 · see citing works
Jin, X., Fu, W., Zhou, J., Shuai, N., Yang, Y., & Wang, B. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.5020 · Cited by 90 · see citing works
“, interleukin (IL)‐1β and IL‐18], a process referred to as NLRP3 inflammasome activation‐mediated pyroptosis (5‐7), which has been reported as an important event in endothelial injury (8,9) and the pathophysiological process of atherosclerosis (10,11).”
BackgroundIL-1 Superfamily Members and Periodontal Diseases
Papathanasiou, E., Conti, P., Carinci, F., Lauritano, D., & Theoharides, T. (2020) · Journal of dentistry research · doi:10.1177/0022034520945209 · Cited by 86 · see citing works
“members of the IL-1 family, such as IL-18 (Zahid et al. 2019).”
BackgroundCell-to-cell and organ-to-organ crosstalk in the pathogenesis of alcohol-associated liver disease
Gao, H., Jiang, Y., Zeng, G., Huda, N., Thoudam, T., Yang, Z.-H., Liangpunsakul, S., & Ma, J. (2024) · eGastroenterology · doi:10.1136/egastro-2024-100104 · Cited by 85 · see citing works
The role of the microbiome and the NLRP3 inflammasome in the gut and lung
Donovan, C., Liu, G., Shen, S., Marshall, J. E., Kim, R., Alemao, C. A., Budden, K. F., Choi, J. P., Kohonen‐Corish, M. R. J., El-Omar, E. M., et al. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3mr0720-472rr · Cited by 94 · see citing works
Yaqinuddin, A., & Kashir, J. (2020) · Medical Hypotheses · doi:10.1016/j.mehy.2020.109906 · Cited by 86 · see citing works
“A potential alternative is 16673-34-0, an intermediate substrate of glyburide with no hypoglycaemic activity [27].”
BackgroundBakhshi, S., & Shamsi, S. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108595 · Cited by 85 · see citing works
Litwiniuk, A., Bik, W., Kalisz, M., & Baranowska-Bik, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115603 · Cited by 82 · see citing works
“, inhibition of NLRP3 inflammasome activation and formation, suppression of upstream signals, inhibition of caspase-1 activation, blockage of gasdermin D pore-forming protein (GSDMD) cleavage, and neutralization of IL-1β and IL-18 production [145].”
BackgroundThe NLRP3 Inflammasome: Role and Therapeutic Potential in Pain Treatment
Starobova, H., Nadar, E. I., & Vetter, I. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.01016 · Cited by 85 · see citing works
NLRP3 Inflammasome-Mediated Inflammation in Acute Pancreatitis
Ferrero-Andrés, A., Rosello, A. P., Roselló‐Catafau, J., & Folch‐Puy, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155386 · Cited by 91 · see citing works
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NLRP3 inflammasome and IL-1β pathway in type 2 diabetes and atherosclerosis: Friend or foe?
Chen, X., Zhang, D., Li, Y., Wang, W., Bei, W., & Guo, J. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105885 · Cited by 84 · see citing works
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From Innate Immunity to Metabolic Disorder: A Review of the NLRP3 Inflammasome in Diabetes Mellitus
Nițulescu, I. M., Ciulei, G., Cozma, A., Procopciuc, L. M., & Orasan, O. H. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12186022 · Cited by 83 · see citing works
“While glyburide has shown inhibitory effects both in vitro and in vivo against NLRP3 activation, its high doses in vivo can lead to hypoglycemia, limiting its use for T2D treatment [88].”
BackgroundRecent insights into the regulatory networks of NLRP3 inflammasome activation
Weber, A. N. R., Bittner, Z., Shankar, S., Liu, X., Chang, T.-H., Jin, T., & Tapia‐Abellán, A. (2020) · Journal of Cell Science · doi:10.1242/jcs.248344 · Cited by 81 · see citing works
“directly interact with NLRP3 have been reported (Zahid et al., 2019).”
BackgroundSelf-citationThe role of interleukin-1 family members in hyperuricemia and gout.
Klück, V., Liu, R., & Joosten, L. (2020) · Joint Bone Spine · doi:10.1016/j.jbspin.2020.105092 · Cited by 75 · see citing works
ATP-Binding and Hydrolysis in Inflammasome Activation
Sandall, C. F., Ziehr, B. K., & MacDonald, J. A. (2020) · Molecules · doi:10.3390/molecules25194572 · Cited by 74 · see citing works
Soriano, A., Soriano, M., Espinosa, G., Manna, R., Emmi, G., Cantarini, L., & Hernández-Rodríguez, J. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00865 · Cited by 75
Elmadbouh, I. S., & Singla, D. K. (2021) · Cells · doi:10.3390/cells10102640 · Cited by 81 · see citing works
“However, these treatments for diabetic cardiomyopathy are limited in use due to their cost and side effects, including dyslipidemia, neutropenia, infection, muscle aches and myalgia, poor solubility, and hepatoxicity [40,42,44,45].”
BackgroundResultPang, Y., Zhang, P., Lu, R., Li, H., Li, J., Fu, H., Cao, Y., Fang, G., Liu, B., Wu, J., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.541426 · Cited by 81 · see citing works
“Active caspase-1 has a specific structure of heterotetramers that mediate proteolytic processes of inflammatory and inflammatory cytokines, including interleukin-1b (IL-1b) and IL-18 (Vanaja et al., 2015).”
BackgroundPaniri, A., & Akhavan‐Niaki, H. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118114 · Cited by 81 · see citing works
“Therefore, designing and administration of potential drugs to target the wide spectrum molecules involved in IL-6 and inflammasome-associated epigenetic mechanisms along with IL-6 and inflammasome blockers may improve the efficacy of SARS-CoV-2s' treatment [12,13].”
Boron-Containing heterocycles as promising pharmacological agents
Das, B. C., Shareef, M. A., Das, S., Nandwana, N. K., Das, Y., Saito, M., & Weiss, L. M. (2022) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2022.116748 · Cited by 100 · see citing works
Gut-liver axis: Recent concepts in pathophysiology in alcohol-associated liver disease
Raya Tonetti, F., Eguileor, A., Mrdjen, M., Pathak, V., Travers, J., Nagy, L. E., & Llorente, C. (2024) · Hepatology · doi:10.1097/hep.0000000000000924 · Cited by 78 · see citing works
Targeting NLRP3 Inflammasome With Nrf2 Inducers in Central Nervous System Disorders
Tastan, B., Arioz, B. I., & Genç, Ş. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.865772 · Cited by 86 · see citing works
“These inhibitors could indirectly inhibit NLRP3 inflammasome activation via distinct mechanisms like obstruction of K efflux (Glyburide, BHB), hampering oligomerization, or binding of ASC (16673-34-0, BHB), and preventing auto-cleavage of procaspase-1 (FC11A-2) (68).”
BackgroundInfluentialSaber, S., & El-Kader, E. M. A. (2020) · Inflammopharmacology · doi:10.1007/s10787-020-00730-6 · Cited by 74 · see citing works
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Targeting NLRP3 Inflammasome Reduces Age-Related Experimental Alveolar Bone Loss
Zang, Y., Song, J. H., Oh, S., Kim, J. W., Lee, M. N., Piao, X., Yang, J.-W., Kim, O. S., Kim, T. S., Kim, S. H., et al. (2020) · Journal of Dental Research · doi:10.1177/0022034520933533 · Cited by 81 · see citing works
“MCC950 was recently discovered as a selective and small molecule inhibitor of NLRP3 inflammasome and has been experimentally shown to have beneficial effects on controlling inflammatory and metabolic diseases (Coll et al. 2015; Zahid et al. 2019).”
BackgroundThe innate immune system and cell death in autoinflammatory and autoimmune disease
Place, D. E., & Kanneganti, T. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.10.013 · Cited by 80 · see citing works
The role of dopamine in NLRP3 inflammasome inhibition: Implications for neurodegenerative diseases
Possemato, E., Barbera, L. L., Nobili, A., Krashia, P., & D’Amelio, M. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101907 · Cited by 75 · see citing works
Cellular Models and Assays to Study NLRP3 Inflammasome Biology
Zito, G., Buscetta, M., Cimino, M., Dino, P., Bucchieri, F., & Cipollina, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21124294 · Cited by 77 · see citing works
“In recent years, a wide range of molecules has been developed as NLRP3 inhibitors (reviewed in [46]).”
BackgroundGatlik, E., Mehes, B., Voltz, E., Sommer, U., Tritto, E., Lestini, G., Liu, X., Pal, P., Velinova, M., Denney, W. S., et al. (2024) · Clinical and Translational Science · doi:10.1111/cts.13789 · Cited by 65 · see citing works
Targeting the NLRP3 Inflammasome in Glaucoma
Coyle, S., Khan, M. N., Chemaly, M., Callaghan, B., Doyle, C., Willoughby, C. E., Atkinson, S. D., Gregory-Ksander, M. S., & McGilligan, V. (2021) · Biomolecules · doi:10.3390/biom11081239 · Cited by 68 · see citing works
Posttranslational and Therapeutic Control of Gasdermin-Mediated Pyroptosis and Inflammation
Fischer, F. A., Chen, K. W., & Bezbradica, J. S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.661162 · Cited by 68 · see citing works
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Quagliariello, V., Passariello, M., Rea, D., Barbieri, A., Iovine, M., Bonelli, A., Caronna, A., Botti, G., Lorenzo, C. D., & Maurea, N. (2020) · Journal of Personalized Medicine · doi:10.3390/jpm10040179 · Cited by 67 · see citing works
“Based on the pathophysiology of myocardial damage during the treatment with Ipilimumab described here, new inhibitors could be considered: first, NLRP3 or MyD88 inhibitors [71]; second, cytokine inhibitors like IL-6 blocking agents (Tocilizumab or Sarilumab, both clinically used for the treatment of rheumatoid arthrit…”
BackgroundNLRP3 inflammasome in hepatic diseases: A pharmacological target
Ramos‐Tovar, E., & Muriel, P. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115861 · Cited by 63 · see citing works
The NLRP3 inflammasome: role in the pathobiology of chronic pain
Chen, C., & Smith, M. T. (2023) · Inflammopharmacology · doi:10.1007/s10787-023-01235-8 · Cited by 63 · see citing works
Zhou, Y., Zeng, L., Cai, L., Wang, Z., Liu, X., Xiao, Y., Jin, X., Bai, Y., Lai, M., Li, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56456-y · Cited by 52 · see citing works
Oxidative Stress and the NLRP3 Inflammasome: Focus on Female Fertility and Reproductive Health
Moustakli, E., Stavros, S., Katopodis, P., Skentou, C., Potiris, A., Panagopoulos, P., Domali, E., Arkoulis, I., Karampitsakos, T., Sarafi, E., et al. (2025) · Cells · doi:10.3390/cells14010036 · Cited by 64 · see citing works
“Because they can lower inflammasome activity, these substances may help with inflammatory IVF failures [64].”
Nunes, P. R., Viana-Mattioli, S., & Sandrim, V. C. (2021) · Cells · doi:10.3390/cells10112828 · Cited by 73 · see citing works
“Bay 11-7082 [87,99] No No Prevents the organization of ASC pyroptosome”
BackgroundThe NLRP3 inflammasome in fibrosis and aging: The known unknowns
Liu, Y., Xu, X., Lei, W., Hou, Y., Zhang, Y., Tang, R., Yang, Z. P., Tian, Y., Zhu, Y., Wang, C., et al. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101638 · Cited by 62 · see citing works
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Holtmann, T. M., Inzaugarat, M. E., Knorr, J., Geisler, L. J., Schulz, M., Bieghs, V., Frissen, M., Feldstein, A. E., Tacke, F., Trautwein, C., et al. (2021) · Cells · doi:10.3390/cells10102618 · Cited by 60 · see citing works
“Several of these drugs directly target the NLRP3 protein, whereas others block other components or downstream effectors [49].”
BackgroundNLRP3 inflammasome in cognitive impairment and pharmacological properties of its inhibitors
Xu, Y., Yang, Y., Chen, X., Jiang, D., Zhang, F., Guo, Y., Hu, B., Xu, G., Peng, S., Wu, L., et al. (2023) · Translational Neurodegeneration · doi:10.1186/s40035-023-00381-x · Cited by 62 · see citing works
“In neurodegenerative diseases such as AD, persistent accumulation of misfolded protein aggregates or mitochondrial dysfunction can trigger and maintain inflammasome activation, thereby driving CNS inflammation and neuropathology that aggravate cognitive impairment [162, 165].”
BackgroundMoltrasio, C., Romagnuolo, M., & Marzano, A. V. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1007705 · Cited by 67 · see citing works
NEK7: a potential therapy target for NLRP3-related diseases
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“(92-93) However, these inhibitors just disturb the signaling pathways of NLRP3 Inflammasome activation rather than directly regulate NLRP3 to abolish the inflammation response.”
BackgroundZhang, P., Wu, P., Khan, U. Z., Zhou, Z., Sui, X., Li, C., Dong, K., Liu, Y.-J., Qing, L., & Tang, J. (2023) · Journal of Nanobiotechnology · doi:10.1186/s12951-023-02087-8 · Cited by 58 · see citing works
“…which is an intracellular multimeric protein signaling complex, can activate potent inflammatory responses and has been associated with many inflammatory and autoimmune diseases, including diabetes, atherosclerosis, asthma, systemic lupus ery-thematosus and rheumatoid arthritis [22, 23, 45].”
BackgroundInflammasome activation in traumatic brain injury and Alzheimer's disease
Johnson, N. H., Vaccari, J. P. D. R., Bramlett, H. M., Keane, R. W., & Dietrich, W. D. (2022) · Translational research · doi:10.1016/j.trsl.2022.08.014 · Cited by 73 · see citing works
Dysfunctions, molecular mechanisms, and therapeutic strategies of pancreatic β-cells in diabetes
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“The inhibition of NLRP3 inflammasome action through the genetic knockout of the NLRP3 gene has been demonstrated to improve renal cell function in diabetic nephropathy by enhancing the survival of beta cells [132].”
BackgroundCharan, H. V., Dwivedi, D. K., Khan, S., & Jena, G. (2022) · Genes & Diseases · doi:10.1016/j.gendis.2021.12.006 · Cited by 55 · see citing works
“reduced IL-1b/18 secretions.(129,137) Reduced hepatic lipid accumulation and fibrosis, and alcohol and age associated liver damage.”
BackgroundInfluentialPeli1 facilitates NLRP3 inflammasome activation by mediating ASC ubiquitination
Zhang, L., Ko, C., Li, Y., Jie, Z., Zhu, L., Zhou, X., Xie, X., Gao, T., Liu, T., Cheng, X., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109904 · Cited by 68 · see citing works
Role of Microgliosis and NLRP3 Inflammasome in Parkinson’s Disease Pathogenesis and Therapy
de Araújo, F. M., Cuenca‐Bermejo, L., Fernández‐Villalba, E., Costa, S. L., da Silva, V. D. A., & Herrero, M. T. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-01027-6 · Cited by 61 · see citing works
- Authors
- Zahid, A., Li, B., Kombe, A. J. K., Jin, T., & Tao, J.
- Affiliations
- University of Science and Technology of China (CN)
- Corresponding author
- Jin, Tengchuan
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2019-10-25
- Volume
- 10
- Pages
- 2538-2538
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC6842943
- OpenAlex
- W2982061867
- Cited by
- 671
- References
- 123
- Citations by year
- 2026: 49 · 2025: 94 · 2024: 107 · 2023: 101 · 2022: 129 · 2021: 122 · 2020: 69
- FWCI
- 7.09
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (201904a07020103, 81771774)
- Natural Science Foundation of Anhui Province (1708085MH191)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Hematology › Autoimmune and Inflammatory Disorders Research
- Keywords
- NLRP3 inflammasome, inflammasome inhibitors, NLRP3, ASC, pyroptosis, inflammatory cytokines, innate immunity, diabetes mellitus, atherosclerosis, metabolic syndrome, neurodegenerative diseases, cardiovascular disease, mechanism of action
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Dipeptides, Glyburide, Humans, Nitriles, Sulfones, Inflammasomes, para-Aminobenzoates, ortho-Aminobenzoates
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