Annexin A1 and glucocorticoids as effectors of the resolution of inflammation

How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions

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Antiinflammatory Action of Glucocorticoids — New Mechanisms for Old Drugs

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Resolution of inflammation: the beginning programs the end

Serhan, C. N., & Savill, J. (2005) · Nature Immunology · doi:10.1038/ni1276 · Cited by 2,552

Annexins: linking Ca2+ signalling to membrane dynamics

Gerke, V., Creutz, C. E., & Moss, S. E. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1661 · Cited by 1,412

Resolution of in flammation: state of the art, definitions and terms

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Promotion of Tissue Inflammation by the Immune Receptor Tim-3 Expressed on Innate Immune Cells

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Histone deacetylase 2–mediated deacetylation of the glucocorticoid receptor enables NF-κB suppression

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Glucocorticoids and the Th1/Th2 Balance

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Glucocorticoids promote a TH2 cytokine response by CD4+ T cells in vitro

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The Lipoxin Receptor ALX: Potent Ligand-Specific and Stereoselective Actions in Vivo

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A Physiological Function of Inflammation-Associated SerpinB2 Is Regulation of Adaptive Immunity

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Annexin A1 localization and its relevance to cancer

Boudhraa, Z., Bouchon, B., Viallard, C., D'Incan, M., & Degoul, F. (2016) · Clinical Science · doi:10.1042/cs20150415 · Cited by 138

Macrophage activation and polarization modify P2X7 receptor secretome influencing the inflammatory process

de Torre‐Minguela, C., Barberà-Cremades, M., Gómez, A. I., Martín‐Sánchez, F., & Pelegrı́n, P. (2016) · Scientific Reports · doi:10.1038/srep22586 · Cited by 135

Anti-Inflammatory Mechanisms of the Annexin A1 Protein and Its Mimetic Peptide Ac2-26 in Models of Ocular Inflammation In Vivo and In Vitro

Girol, A. P., Mimura, K. K. O., Drewes, C. C., Bolonheis, S. M., Solito, E., Farsky, S. H. P., Gil, C. D., & Oliani, S. M. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202030 · Cited by 128

Annexin-A1 enhances breast cancer growth and migration by promoting alternative macrophage polarization in the tumour microenvironment

Moraes, L. A., Kar, S., Foo, S. L., Gu, T., Toh, Y. Q., Ampomah, P. B., Sachaphibulkij, K., Yap, G. L. R., Zharkova, O., Lukman, H. M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-17622-5 · Cited by 133

Targeting Neutrophils for Promoting the Resolution of Inflammation

Filep, J. G. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.866747 · Cited by 131

Immune resolution mechanisms in inflammatory arthritis

Perretti, M., Cooper, D., Dalli, J., & Norling, L. V. (2017) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2016.193 · Cited by 133

Lipoxin A4 impairment of apoptotic signaling in macrophages: implication of the PI3K/Akt and the ERK/Nrf-2 defense pathways

Prieto, P., Cuenca, J., Través, P. G., Fernández‐Velasco, M., Martín‐Sanz, P., & Boscá, L. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2009.220 · Cited by 123

Self-Limited versus Delayed Resolution of Acute Inflammation: Temporal Regulation of Pro-Resolving Mediators and MicroRNA

Fredman, G., Li, Y., Dalli, J., Chiang, N., & Serhan, C. N. (2012) · Scientific Reports · doi:10.1038/srep00639 · Cited by 122

Characterization of ZK 245186, a novel, selective glucocorticoid receptor agonist for the topical treatment of inflammatory skin diseases

Schäcke, H., Zollner, T., Döcke, W., Rehwinkel, H., Jaroch, S., Skuballa, W., Neuhaus, R., May, E., Zügel, U., & Asadullah, K. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00238.x · Cited by 121

Potential Role of Anxa1 in Cancer

Guo, C., Liu, S., & Sun, M. (2013) · Future Oncology · doi:10.2217/fon.13.114 · Cited by 121

Modulation of Neutrophil Apoptosis and the Resolution of Inflammation through β2 Integrins

Kebir, D. E., & Filep, J. G. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00060 · Cited by 130

The role of peripheral inflammatory insults in Alzheimer’s disease: a review and research roadmap

Walker, K. A., Page, L. M. L., Terrando, N., Duggan, M. R., Heneka, M. T., & Bettcher, B. M. (2023) · Molecular Neurodegeneration · doi:10.1186/s13024-023-00627-2 · Cited by 121

Therapeutic anti-inflammatory potential of formyl-peptide receptor agonists

Dufton, N., & Perretti, M. (2010) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2010.04.010 · Cited by 118

Annexin A1 restores Aβ1‐42‐induced blood–brain barrier disruption through the inhibition of RhoA‐ ROCK signaling pathway

Park, J., Baik, S. H., Han, S., Cho, H. J., Choi, H., Kim, H. J., Choi, H., Lee, W., Kim, D. K., & Mook‐Jung, I. (2016) · Aging Cell · doi:10.1111/acel.12530 · Cited by 115

Resolution of Cochlear Inflammation: Novel Target for Preventing or Ameliorating Drug-, Noise- and Age-related Hearing Loss

Kalinec, G. M., Lomberk, G. A., Urrutia, R. A., & Kalinec, F. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00192 · Cited by 117

Annexin A1 as a Regulator of Immune Response in Cancer

Araújo, T. G., Mota, S. T. S., Ferreira, H. S. V., Ribeiro, M. A., Goulart, L. R., & Vecchi, L. (2021) · Cells · doi:10.3390/cells10092245 · Cited by 116

15-Epi-LXA 4 and 17-epi-RvD1 restore TLR9-mediated impaired neutrophil phagocytosis and accelerate resolution of lung inflammation

Sekheri, M., Kebir, D. E., Edner, N. M., & Filep, J. G. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1920193117 · Cited by 114

Structure of formylpeptide receptor 2-Gi complex reveals insights into ligand recognition and signaling

Zhuang, Y., Liu, H., Zhou, X. E., Verma, R. K., de Waal, P. W., Jang, W., Xu, T.-H., Wang, L., Meng, X. M., Zhao, G., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14728-9 · Cited by 112

Towards targeting resolution pathways of airway inflammation in asthma

Barnig, C., Frossard, N., & Levy, B. D. (2018) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2018.01.004 · Cited by 115

Formyl peptide receptors at the interface of inflammation, angiogenesis and tumor growth

Prevete, N., Liotti, F., Marone, G., Melillo, R. M., & de Paulis, A. (2015) · Pharmacological Research · doi:10.1016/j.phrs.2015.09.017 · Cited by 112

Evaluation of Intracellular Signaling Downstream Chimeric Antigen Receptors

Karlsson, H., Svensson, E., Gigg, C., Jarvius, M., Olsson‐Strömberg, U., Savoldo, B., Dotti, G., & Loskog, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144787 · Cited by 115

Exercise reprograms the inflammatory landscape of multiple stem cell compartments during mammalian aging

Liu, L. A., Kim, S., Buckley, M. T., Reyes, J. M., Kang, J., Tian, L., Wang, M., Lieu, A. C., Mao, M., Rodríguez-Mateo, C., et al. (2023) · Cell stem cell · doi:10.1016/j.stem.2023.03.016 · Cited by 115

Targeting ANXA1 abrogates Treg-mediated immune suppression in triple-negative breast cancer

Bai, F., Zhang, P., Fu, Y., Chen, H., Zhang, M., Huang, Q., Li, D., Li, B., & Wu, K. (2020) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2019-000169 · Cited by 109

Annexin-A1: Therapeutic Potential in Microvascular Disease

Purvis, G. S. D., Solito, E., & Thiemermann, C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00938 · Cited by 107

Annexin A1 is associated with gastric cancer survival and promotes gastric cancer cell invasiveness through the formyl peptide receptor/extracellular signal‐regulated kinase/integrin beta‐1‐binding protein 1 pathway

Cheng, T., Wu, M., Lin, J., Lin, M., Shun, C., Huang, H., Hua, K., & Kuo, M. (2012) · Cancer · doi:10.1002/cncr.27565 · Cited by 107

Anti-annexins autoantibodies: Their role as biomarkers of autoimmune diseases

Iaccarino, L., Ghirardello, A., Canova, M., Zen, M., Bettio, S., Nalotto, L., Punzi, L., & Doria, A. (2011) · Autoimmunity Reviews · doi:10.1016/j.autrev.2011.04.007 · Cited by 106

Endogenous annexin A1 is a novel protective determinant in nonalcoholic steatohepatitis in mice

Locatelli, I., Sutti, S., Jindal, A., Vacchiano, M., Bozzola, C., Reutelingsperger, C. P. M., Kusters, D. H. M., Bena, S., Parola, M., Paternostro, C., et al. (2014) · Hepatology · doi:10.1002/hep.27141 · Cited by 106

The anti-inflammatory Annexin A1 induces the clearance and degradation of the amyloid-β peptide

Ries, M., Loiola, R. A., Shah, U. N., Gentleman, S., Solito, E., & Sastre, M. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0692-6 · Cited by 106

Genetic approaches to hypothalamic-pituitary-adrenal axis regulation

Arnett, M. G., Muglia, L. M., Laryea, G., & Muglia, L. J. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.215 · Cited by 105

Glucocorticoids promote survival of anti-inflammatory macrophages via stimulation of adenosine receptor A3

Barczyk, K., Ehrchen, J. M., Tenbrock, K., Ahlmann, M., Kneidl, J., Viemann, D., & Roth, J. (2010) · Blood · doi:10.1182/blood-2009-10-247106 · Cited by 106

Proresolving and Tissue-Protective Actions of Annexin A1–Based Cleavage-Resistant Peptides Are Mediated by Formyl Peptide Receptor 2/Lipoxin A4 Receptor

Dalli, J., Consalvo, A. P., Ray, V., Filippo, C. D., D’Amico, M., Mehta, N., & Perretti, M. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203000 · Cited by 105

Anti-inflammatory glucocorticoids: Changing concepts

Newton, R. C. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.05.035 · Cited by 104

Defining the role of glucocorticoids in inflammation

Ronchetti, S., Migliorati, G., Bruscoli, S., & Riccardi, C. (2018) · Clinical Science · doi:10.1042/cs20171505 · Cited by 104

Butyrate Modulates Inflammation in Chondrocytes via GPR43 Receptor

Pirozzi, C., Francisco, V., Guida, F., Gómez, R., Lago, F., Pino, J., Meli, R., & Gualillo, O. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000495203 · Cited by 104

Glucocorticoids Shape Macrophage Phenotype for Tissue Repair

Desgeorges, T., Caratti, G., Mounier, R., Tuckermann, J. P., & Chazaud, B. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01591 · Cited by 109

The Local and Peripheral Immune Responses to Stroke: Implications for Therapeutic Development

Zera, K. A., & Buckwalter, M. S. (2020) · Neurotherapeutics · doi:10.1007/s13311-020-00844-3 · Cited by 103

Triple-Negative Breast Cancer with High Levels of Annexin A1 Expression Is Associated with Mast Cell Infiltration, Inflammation, and Angiogenesis

Okano, M., Oshi, M., Butash, A. L., Katsuta, E., Tachibana, K., Saito, K., Okayama, H., Peng, X., Yan, L., Kono, K., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174197 · Cited by 101

Role of Neutrophil Apoptosis in the Resolution of Inflammation

Kebir, D. E., & Filep, J. G. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.169 · Cited by 103

Compartmentalized regulation of lipid signaling in oxidative stress and inflammation: Plasmalogens, oxidized lipids and ferroptosis as new paradigms of bioactive lipid research

Astudillo, A. M., Balboa, M. A., & Balsinde, J. (2022) · Progress in Lipid Research · doi:10.1016/j.plipres.2022.101207 · Cited by 102

The Role and Effects of Glucocorticoid-Induced Leucine Zipper in the Context of Inflammation Resolution

Vago, J. P., Tavares, L. P., Garcia, C. C., Lima, K. M., Perucci, L. O., Vieira, É. L. M., Nogueira, C. R. C., Soriani, F. M., Martins, J. O., Silva, P., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1401722 · Cited by 100

Activation of Resolution Pathways to Prevent and Fight Chronic Inflammation: Lessons From Asthma and Inflammatory Bowel Disease

Barnig, C., Bezema, T., Calder, P. C., Charloux, A., Frossard, N., Garssen, J., Haworth, O., Dilevskaya, K., Levi‐Schaffer, F., Lonsdorfer‐Wolf, E., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01699 · Cited by 104

Annexin A1: potential for glucocorticoid sparing in RA

Yang, Y. H., Morand, E. F., & Leech, M. T. (2013) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2013.126 · Cited by 99

Regulation of immune responses by neutrophils

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Tailored Protection against Plasmalemmal Injury by Annexins with Different Ca2+ Sensitivities

Potez, S., Luginbühl, M., Monastyrskaya, K., Hostettler, A., Draeger, A., & Babiychuk, E. B. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.187625 · Cited by 98

Muscle membrane repair and inflammatory attack in dysferlinopathy

Han, R. (2011) · Skeletal Muscle · doi:10.1186/2044-5040-1-10 · Cited by 96

Nanomedicine-based strategies for treatment of atherosclerosis

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Dysregulation of Anti-Inflammatory Annexin A1 Expression in Progressive Crohns Disease

Sena, A. A. S., Grishina, I., Thai, A., Goulart, L., Macal, M., Fenton, A. N., Li, J., Prindiville, T. P., Oliani, S. M., Dandekar, S., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076969 · Cited by 94

Multidimensional degradomics identifies systemic autoantigens and intracellular matrix proteins as novel gelatinase B/MMP-9 substrates

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Multi-component clobetasol-loaded monolithic lipid-polymer hybrid nanoparticles ameliorate imiquimod-induced psoriasis-like skin inflammation in Swiss albino mice

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Annexin A1 regulates neutrophil clearance by macrophages in the mouse bone marrow

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Exosomes from Human Dental Pulp Stem Cells Suppress Carrageenan-Induced Acute Inflammation in Mice

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Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection

Tzelepis, F., Verway, M. J., Daoud, J., Gillard, J., Hassani‐Ardakani, K., Dunn, J. L., Downey, J., Gentile, M., Jaworska, J., Sanchez, A. M. J., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci77014 · Cited by 95

Role of intracellular and extracellular annexin A1 in migration and invasion of human pancreatic carcinoma cells

Belvedere, R., Bizzarro, V., Popolo, A., Piaz, F. D., Vasaturo, M., Picardi, P., Parente, L., & Petrella, A. (2014) · BMC Cancer · doi:10.1186/1471-2407-14-961 · Cited by 92

2016 Russell Ross Memorial Lecture in Vascular Biology

Tabas, I. A. (2016) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.116.308036 · Cited by 92

Cleavage of Annexin A1 by ADAM10 during Secondary Necrosis Generates a Monocytic “Find-Me” Signal

Blume, K., Soeroes, S., Keppeler, H., Stevanović, S., Kretschmer, D., Rautenberg, M., Wesselborg, S., & Lauber, K. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004073 · Cited by 92

Hanging in the balance: endogenous anti‐inflammatory mechanisms in tissue repair and fibrosis

Ariel, A., & Zeituni-Timor, O. (2012) · The Journal of Pathology · doi:10.1002/path.4108 · Cited by 92

Resolution-associated molecular patterns (RAMP): RAMParts defending immunological homeostasis?

Shields, A. M., Panayi, G. S., & Corrigall, V. M. (2011) · Clinical and Experimental Immunology · doi:10.1111/j.1365-2249.2011.04433.x · Cited by 90

Annexins – insights from knockout mice

Grewal, T., Wason, S. J., Enrich, C., & Rentero, C. (2016) · Biological Chemistry · doi:10.1515/hsz-2016-0168 · Cited by 90

Neutrophil apoptosis: A target for enhancing the resolution of inflammation

Filep, J. G., & Kebir, D. E. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22351 · Cited by 91

Targeting Neutrophil Apoptosis for Enhancing the Resolution of Inflammation

Kebir, D. E., & Filep, J. G. (2013) · Cells · doi:10.3390/cells2020330 · Cited by 91

Anti-inflammatory glucocorticoid drugs: reflections after 60 years

Whitehouse, M. W. (2010) · Inflammopharmacology · doi:10.1007/s10787-010-0056-2 · Cited by 88

Inflammation and Cancer: Role of Annexin A1 and FPR2/ALX in Proliferation and Metastasis in Human Laryngeal Squamous Cell Carcinoma

Bizotto, T. S. G., da Cunha, B. R., Raposo, L. S., Maníglia, J. V., Cury, P. M., Rodrigues‐Lisoni, F. C., Tajara, E. H., & Oliani, S. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111317 · Cited by 89

Molecular Mechanisms Mediating the Effect of Mono-(2-Ethylhexyl) Phthalate on Hormone-Stimulated Steroidogenesis in MA-10 Mouse Tumor Leydig Cells

Fan, J., Traore, K., Li, W., Amri, H., Huang, H., Wu, C. H., Chen, H., Zirkin, B. R., & Papadopoulos, V. (2010) · Endocrinology · doi:10.1210/en.2010-0010 · Cited by 88

HPA axis activity in multiple sclerosis correlates with disease severity, lesion type and gene expression in normal-appearing white matter

Melief, J., de Wit, S. J., van Eden, C. G., Teunissen, C. E., Hamann, J., Uitdehaag, B. M. J., Swaab, D. F., & Huitinga, I. (2013) · Acta Neuropathologica · doi:10.1007/s00401-013-1140-7 · Cited by 89

Resolution metabolomes activated by hypoxic environment

Norris, P. C., Libreros, S., & Serhan, C. N. (2019) · Science Advances · doi:10.1126/sciadv.aax4895 · Cited by 87

Anti‐inflammatory and antiviral roles of hydrogen sulfide: Rationale for considering H2S donors in COVID‐19 therapy

Citi, V., Martelli, A., Brancaleone, V., Brogi, S., Gojon, G., Montanaro, R., Morales, G. A., Testai, L., & Calderone, V. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15230 · Cited by 85

Changes in the Inflammatory Response to Injury and Its Resolution during the Loss of Regenerative Capacity in Developing Xenopus Limbs

Mescher, A. L., Neff, A. W., & King, M. W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080477 · Cited by 85

Annexin A2 binds to endosomes and negatively regulates TLR4-triggered inflammatory responses via the TRAM-TRIF pathway

Zhang, S., Yu, M., Guo, Q., Li, R., Li, G., Tan, S., Li, X., Wei, Y., & Wu, M. (2015) · Scientific Reports · doi:10.1038/srep15859 · Cited by 85

Immunogenic cell death: The cornerstone of oncolytic viro-immunotherapy

Palanivelu, L., Liu, C., & Lin, L. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1038226 · Cited by 86

The impact of endogenous annexin A1 on glucocorticoid control of inflammatory arthritis

Patel, H., Kornerup, K. N., Sampaio, A. L. F., D’Acquisto, F., Seed, M. P., Girol, A. P., Gray, M., Pitzalis, C., Oliani, S. M., & Perretti, M. (2012) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2011-201180 · Cited by 84

Pharmacomimetics of Exercise: Novel Approaches for Hippocampally- Targeted Neuroprotective Agents

Stranahan, A. M., Zhou, Y., Martin, B., & Maudsley, S. R. (2009) · Current Medicinal Chemistry · doi:10.2174/092986709789878292 · Cited by 84

Corticosteroids for COVID-19 Therapy: Potential Implications on Tuberculosis

Gopalaswamy, R., & Subbian, S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073773 · Cited by 82

FPR1 is the plague receptor on host immune cells

Osei‐Owusu, P., Charlton, T. M., Kim, H. K., Missiakas, D. M., & Schneewind, O. (2019) · Nature · doi:10.1038/s41586-019-1570-z · Cited by 80

From NSAIDs to Glucocorticoids and Beyond

Sinniah, A., Yazid, S., & Flower, R. (2021) · Cells · doi:10.3390/cells10123524 · Cited by 82

Annexins in Translational Research: Hidden Treasures to Be Found

Schloer, S., Pajonczyk, D., & Rescher, U. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061781 · Cited by 80

Local drug delivery systems for inflammatory diseases: Status quo, challenges, and opportunities

Chen, Y.-C., Gad, S. F., Chobisa, D., Li, Y., & Yeo, Y. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.12.025 · Cited by 80

Anxa1 in smooth muscle cells protects against acute aortic dissection

Zhou, C., Lin, Z., Cao, H., Chen, Y., Li, J., Zhuang, X., Ma, D., Liang, J., Li, W., Xu, S., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab109 · Cited by 79

Cardioprotective potential of annexin-A1 mimetics in myocardial infarction

Qin, C. X., Yang, Y. H., May, L. T., Gao, X., Stewart, A. G., Tu, Y., Woodman, O. L., & Ritchie, R. H. (2014) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2014.11.012 · Cited by 79

Anti-inflammatory and Cytoprotective Properties of Hydrogen Sulfide

Gemici, B., & Wallace, J. L. (2015) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2014.11.034 · Cited by 79

New insights into the novel anti-inflammatory mode of action of glucocorticoids

Ingawale, D. K., & Mandlik, S. K. (2020) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2020.1728765 · Cited by 78

Quantitative milk proteomics – Host responses to lipopolysaccharide‐mediated inflammation of bovine mammary gland

Danielsen, M., Codrea, M. C., Ingvartsen, K. L., Friggens, N. C., Bendixen, E., & Røntved, C. M. (2010) · PROTEOMICS · doi:10.1002/pmic.200900771 · Cited by 78

General Adaptation in Critical Illness: Glucocorticoid Receptor-alpha Master Regulator of Homeostatic Corrections

Meduri, G. U., & Chrousos, G. P. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00161 · Cited by 80

Oncolytic Virotherapy: A New Paradigm in Cancer Immunotherapy

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Multi-antibody composition in lupus nephritis: Isotype and antigen specificity make the difference

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Differentially expressed proteins in gill and skin mucus of Atlantic salmon (Salmo salar) affected by amoebic gill disease

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Cell Surface Externalization of Annexin A1 as a Failsafe Mechanism Preventing Inflammatory Responses during Secondary Necrosis

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Definition of a Novel Pathway Centered on Lysophosphatidic Acid To Recruit Monocytes during the Resolution Phase of Tissue Inflammation

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Investigational Analysis Reveals a Potential Role for Neutrophils in Giant-Cell Arteritis Disease Progression

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Activation of the Annexin A1 Pathway Underlies the Protective Effects Exerted by Estrogen in Polymorphonuclear Leukocytes

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The Pattern of Signatures in Gastric Cancer Prognosis

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Neutrophil heterogeneity and fate in inflamed tissues: implications for the resolution of inflammation

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Annexin A1: shifting the balance towards resolution and repair

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Macrophage proliferation and apoptosis in atherosclerosis

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Milk fat globule-EGF factor 8 mediates the enhancement of apoptotic cell clearance by glucocorticoids

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Wielding the double-edged sword: Redox drug delivery systems for inflammatory bowel disease

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The interplay between obesity, immunosenescence, and insulin resistance

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Eosinophils in the Lung – Modulating Apoptosis and Efferocytosis in Airway Inflammation

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Annexin A1 promotes timely resolution of inflammation in murine gout

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Annexin A6—A multifunctional scaffold in cell motility

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Annexin‐A1: a pivotal regulator of the innate and adaptive immune systems

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[Annexin-1: 2nd messanger of the anti-inflammatory actions of glucocorticoids].

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Overview of the Role of Annexin 1 in the Innate and Adaptive Immune Response

D’Acquisto, F., & Perretti, M. (2008) · Immunology Endocrine & Metabolic Agents - Medicinal Chemistry · doi:10.2174/187152208785748313

Annexin-1 regulates inflammatory response via glucocorticoid-induced genes

Yang, Y. H., Rao, Z., Aeberli, D., Liu, J., Leech, M. T., Dacumos, A., Xue, J., & Morand, E. F. (2009)

The annexin-1 knockout mouse: what it tells us about the inflammatory response.

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