Interleukin-8 and the chemokine family

Van Damme A.

Haine, M. M.-L., & Meeùs, N. (1986) · Cited by 3,464

Interleukin-8 and related chemotactic cytokines--CXC and CC chemokines.

Baggiolini, M., Dewald, B., & Moser, B. (1994) · PubMed · Cited by 2,232

lnterleukin-8 and Related Chemotactic Cytokines—CXC and CC Chemokines

Baggiolini, M., Dewald, B., & Moser, B. (1993) · Advances in immunology · doi:10.1016/s0065-2776(08)60509-x · Cited by 1,672

Structure and Functional Expression of a Human Interleukin-8 Receptor

Holmes, W. E., Lee, J., Kuang, W.-J., Rice, G. C., & Wood, W. I. (1991) · Science · doi:10.1126/science.1840701 · Cited by 1,088

The Neutrophil-Activating Protein (NAP-1) Is Also Chemotactic for T Lymphocytes

Grønhøj, C., Anderson, A. O., Appella, E., Oppenheim, J. J., & Matsushima, K. (1989) · Science · doi:10.1126/science.2648569 · Cited by 1,037

Purification of a human monocyte-derived neutrophil chemotactic factor that has peptide sequence similarity to other host defense cytokines.

Yoshimura, T., Matsushima, K., Tanaka, S., Robinson, E. A., Appella, E., Oppenheim, J. J., & Leonard, E. J. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.24.9233 · Cited by 984

Cloning of Complementary DNA Encoding a Functional Human Interleukin-8 Receptor

Murphy, P. M., & Tiffany, H. L. (1991) · Science · doi:10.1126/science.1891716 · Cited by 889

Purification and characterization of a novel monocyte chemotactic and activating factor produced by a human myelomonocytic cell line.

Matsushima, K., Larsen, C. G., DuBois, G. C., & Oppenheim, J. J. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.4.1485 · Cited by 756

Biology and biochemistry of the chemokines: a family of chemotactic and inflammatory cytokines.

Miller, M. D., & Krangel, M. S. (1992) · PubMed · Cited by 731

Preferential Migration of Activated CD4 + and CD8 + T Cells in Response to MIP-1α and MIP-1β

Taub, D. D., Conlon, K., Lloyd, A. R., Oppenheim, J. J., & Kelvin, D. J. (1993) · Science · doi:10.1126/science.7682337 · Cited by 730

Solution Structure of the Human CC Chemokine 2: A Monomeric Representative of the CC Chemokine Subtype ,

Sticht, H., Escher, S. E., Schweimer, K., Forssmann, W., ROSCH, P. J., & Adermann, K. (1999) · Biochemistry · doi:10.1021/bi990065i · Cited by 30

Interleukin-8 Synthesis, Regulation, and Steroidogenic Role in H295R Human Adrenocortical Cells

Romero, D. G., Vergara, G. R., Zhu, Z., Covington, G. S., Plonczynski, M. W., Yanes, L. L., Gómez-Sánchez, E. P., & Gómez-Sánchez, C. E. (2005) · Endocrinology · doi:10.1210/en.2005-0951 · Cited by 30

Activation of human fibroblast-like synoviocytes by uric acid crystals in rheumatoid arthritis

Chen, D. P., Wong, C. K., Tam, L., Li, E. K., & Lam, C. W. (2011) · Cellular and Molecular Immunology · doi:10.1038/cmi.2011.35 · Cited by 30

Immunomodulatory activity of shikimic acid and quercitin in comparison with oseltamivir (Tamiflu) in an “in vitro” model

Bertelli, A. A. E., Mannari, C., Santi, S., Filippi, C., MIGLIORI, M., & Giovannini, L. (2008) · Journal of Medical Virology · doi:10.1002/jmv.21072 · Cited by 28

Expression of the inflammatory chemokines CCL2, CCL5 and CXCL2 and the receptors CCR1–3 and CXCR2 in T lymphocytes from mammary tumor-bearing mice

Owen, J. L., Criscitiello, M. F., Libreros, S., Garcia‐Areas, R., Guthrie, K. M., Torroella‐Kouri, M., & Iragavarapu‐Charyulu, V. (2011) · Cellular Immunology · doi:10.1016/j.cellimm.2011.05.004 · Cited by 28

The dual role of CXCL8 in human CNS stem cell function: Multipotent neural stem cell death and oligodendrocyte progenitor cell chemotaxis

Kelland, E. E., Gilmore, W., Weiner, L. P., & Lund, B. T. (2011) · Glia · doi:10.1002/glia.21230 · Cited by 27

Platelet‐activating factor and distinct chemokines are elevated in mucosal biopsies of erosive compared with non‐erosive reflux disease patients and controls

Altomare, A., Ma, J., Guarino, M. P. L., Cheng, L., Rieder, F., Ribolsi, M., Fiocchi, C., Biancani, P., Harnett, K. M., & Cicala, M. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01963.x · Cited by 26

Interleukin-8 gene and protein expression are up-regulated by interleukin-1β in normal human ovarian cells and a granulosa tumor cell line

Fujii, A., Harada, T., Yamauchi, N., Iwabe, T., Nishi, Y., Yanase, T., Nawata, H., & Terakawa, N. (2003) · Fertility and Sterility · doi:10.1016/s0015-0282(02)04408-4 · Cited by 26

Elevated plasma levels of interleukin 8 in patients with acute anterior ischaemic optic neuropathy

Goldenberg-Cohen, N., Kramer, M., Bahar, I., Monselise, Y., & Weinberger, D. (2004) · British Journal of Ophthalmology · doi:10.1136/bjo.2004.046524 · Cited by 31

Molecular characterization and gene expression analysis of the pro-inflammatory cytokines IL-1β and IL-8 in the South American fish Piaractus mesopotamicus challenged with Aeromonas dhakensis

Carriero, M. M., Henrique‐Silva, F., Meira, C. M., Gato, I. M. Q., Caetano, A. R., Lobo, F. P., Alves, A. L., Varela, E. S., & Maia, A. A. M. (2020) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2020-0006 · Cited by 25

Suppressive Effect of an Isoflavone Fraction on Tumor Necrosis Factor-α-Induced Interleukin-8 Production in Human Intestinal Epithelial Caco-2 Cells

Satsu, H., Hyun, J. S., Shin, H. S., & Shimizu, M. (2009) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.55.442 · Cited by 25

Tetrahydropalmatine Inhibits Pro-Inflammatory Mediators in Lipopolysaccharide-Stimulated THP-1 Cells

Oh, Y.-C., Choi, J., Lee, Y., Brice, O.-O., Lee, S.-C., Kwak, H.-S., Byun, Y.-H., Kang, O., Rho, J., Shin, D.-W., et al. (2010) · Journal of Medicinal Food · doi:10.1089/jmf.2009.1388 · Cited by 25

Mucosal Concentrations of Proinflammatory Cytokines and Chemokines at Gastric Cardia: Implication of Helicobacter pylori Infection and Gastroesophageal Reflux

Isomoto, H., Nishi, Y., Wang, A., Takeshima, F., Omagari, K., Mizuta, Y., Shikuwa, S., Murata, I., & Kohno, S. (2004) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2004.30847.x · Cited by 25

Direct Activation of Human Peritoneal Mesothelial Cells by Heat-killed Microorganisms

Kinnaert, P., Wilde, J.-P. D., Bournonville, B., Husson, C. P., & Salmon, I. J. (1996) · Annals of Surgery · doi:10.1097/00000658-199612000-00010 · Cited by 25

Pirfenidone regulates LPS mediated activation of neutrophils

Evani, S. J., Karna, S. L. R., Seshu, J., & Leung, K. P. (2020) · Scientific Reports · doi:10.1038/s41598-020-76271-3 · Cited by 25

Description of the Follicular Fluid Cytokine and Hormone Profiles in Human Physiological Natural Cycles

Piccinni, M., Vicenti, R., Logiodice, F., Fabbri, R., Kullolli, O., Pallecchi, M., Paradisi, R., Danza, G., Macciocca, M., Lombardelli, L., et al. (2020) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaa880 · Cited by 24

Chemokine Regulation in Temporomandibular Joint Disease: A Comprehensive Review

Qiao, Y., Li, J., Yuh, C., Ko, F. C., Mercuri, L. G., Alkhudari, J., Pourzal, R., & Oh, C. (2023) · Genes · doi:10.3390/genes14020408 · Cited by 24

Sleep Apnea Determines Soluble TNF-α Receptor 2 Response to Massive Weight Loss

Pallayová, M., Steele, K. E., Magnuson, T. H., Schweitzer, M., Smith, P. L., Patil, S. P., Bevans‐Fonti, S., Polotsky, V. Y., & Schwartz, A. R. (2011) · Obesity Surgery · doi:10.1007/s11695-011-0359-4 · Cited by 24

N-Methyl-D-Aspartate and σ-Ligands Change the Production of Interleukins 8 and 10 in Lymphocytes through Modulation of the NMDA Glutamate Receptor

Kvaratskhelia, E., Maisuradze, E., Dabrundashvili, N., Natsvlishvili, N., Zhuravliova, E., & Mikeladze, D. (2009) · NeuroImmunoModulation · doi:10.1159/000204234 · Cited by 24

Cytokine modulation in acute pancreatitis

Yamauchi, J.-I., Shibuya, K., Sunamura, M., Arai, K., Shimamura, H., Motoi, F., Takeda, K., & Matsuno, S. (2001) · Journal of Hepato-Biliary-Pancreatic Surgery · doi:10.1007/s005340170016 · Cited by 24

Cell-Associated Interleukin-8 in Cord Blood of Term and Preterm Infants

Dembinski, J., Behrendt, D., Heep, A., Dorn, C., REINSBERG, J., & Bartmann, P. (2002) · Clinical and Vaccine Immunology · doi:10.1128/cdli.9.2.320-323.2002 · Cited by 24

Interleukins and Inflammatory Markers in In-Stent Restenosis after Femoral Percutaneous Transluminal Angioplasty

Araújo, P. V., Ribeiro, M. S., Dalio, M. B., Rocha, L. A., Viaro, F., Dellalibera-Joviliano, R., Piccinato, C. E., Évora, P. R. B., & Joviliano, E. É. (2015) · Annals of Vascular Surgery · doi:10.1016/j.avsg.2014.12.006 · Cited by 23

The Hyper-IgE Syndromes: Lessons in Nature, From Bench to Bedside

Rael, E. L., Marshall, R. T., & McClain, J. J. (2012) · World Allergy Organization Journal · doi:10.1097/wox.0b013e31825a73b2 · Cited by 23

Receptor-binding conformation of the ?ELR? motif of IL-8: X-ray structure of the L5C/H33C variant at 2.35 ? resolution

Gerber, N. C., Lowman, H. B., Artis, D. R., & Eigenbrot, C. W. (2000) · Proteins Structure Function and Bioinformatics · doi:10.1002/(sici)1097-0134(20000301)38:4 · Cited by 23

Functionalized optical fiber ball-shaped biosensor for label-free, low-limit detection of IL-8 protein

Rashidova, G., Tilegen, M., Pham, T. T., Bekmurzayeva, A., & Tosi, D. (2023) · Biomedical Optics Express · doi:10.1364/boe.504780 · Cited by 22

Effect of a phytotherapeutic agent, Eviprostat®, on prostatic and urinary cytokines/chemokines in a rat model of nonbacterial prostatitis

Sugimoto, M., Oka, M., Tsunemori, H., Yamashita, M., & Kakehi, Y. (2010) · The Prostate · doi:10.1002/pros.21299 · Cited by 22

Relationship of Cytokines and Age Products in Diabetic and Non-Diabetic Patients with Cataract

Hamid, S., Gul, A., & Hamid, Q. (2016) · International Journal of Health Sciences · doi:10.12816/0048891 · Cited by 22

SQSTM1/p62 regulates the production of IL-8 and MCP-1 in IL-1β-stimulated human retinal pigment epithelial cells

Korhonen, E., Piippo, N., Hytti, M., Hyttinen, J. M. T., Kaarniranta, K., & Kauppinen, A. (2019) · Cytokine · doi:10.1016/j.cyto.2018.12.015 · Cited by 21

Differences in Potency of CXC Chemokine Ligand 8-, CC Chemokine Ligand 11-, and C5a-Induced Modulation of Integrin Function on Human Eosinophils

Ulfman, L. H., Alblas, J., van Aalst, C. W., Zwaginga, J. J., & Koenderman, L. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.9.6092 · Cited by 22

Harnessing functional food strategies for the health challenges of space travel—Fermented soy for astronaut nutrition

Buckley, N. D., Champagne, C. P., Masotti, A. I., Wagar, L. E., Tompkins, T. A., & Green-Johnson, J. M. (2010) · Acta Astronautica · doi:10.1016/j.actaastro.2010.08.023 · Cited by 22

Monocyte chemoattractant protein‐1 is generated via TGF‐β by myofibroblasts in gastric intestinal metaplasia and carcinoma without H. pylori infection

Mutoh, H., Sashikawa, M., Hayakawa, H., & Sugano, K. (2010) · Cancer Science · doi:10.1111/j.1349-7006.2010.01609.x · Cited by 22

Parenteral Administration of Medium- but Not Long-Chain Lipid Emulsions May Increase the Risk for Infections byCandida albicans

Wanten, G. J. A., Netea, M. G., Naber, A. H. J., Curfs, J. H. A. J., Jacobs, L., Verver-Jansen, T. J. G., & Kullberg, B. J. (2002) · Infection and Immunity · doi:10.1128/iai.70.11.6471-6474.2002 · Cited by 22

The effects of prebiotics on growth performance and in vitro immune biomarkers in weaned pigs1

Andres, J. V. S., Mastromano, G., Li, Y., Tran, H., Bundy, J. W., Miller, P. S., & Burkey, T. E. (2019) · Translational Animal Science · doi:10.1093/tas/txz129 · Cited by 21

The strange connection between epidermal growth factor receptor tyrosine kinase inhibitors and dapsone: from rash mitigation to the increase in anti-tumor activity

Boccellino, M., Quagliuolo, L., Alaia, C., Grimaldi, A., Addeo, R., Nicoletti, G. F., Kast, R. E., & Caraglia, M. (2016) · Current Medical Research and Opinion · doi:10.1080/03007995.2016.1211522 · Cited by 21

Functional characterisation of bovine interleukin 8 promoter haplotypes in vitro

Meade, K. G., O’Gorman, G. M., Narciandi, F., MacHugh, D. E., & O’Farrelly, C. (2012) · Molecular Immunology · doi:10.1016/j.molimm.2011.12.011 · Cited by 21

Interruption of G Protein-Coupling in CXCR2 Does Not Alter Ligand Binding, but Eliminates Ligand-Activation of GTPγ35S Binding, Calcium Mobilization, and Chemotaxis

Yang, W., Schraw, W. P., Mueller, S. G., & Richmond, A. J. (1997) · Biochemistry · doi:10.1021/bi971594u · Cited by 21

Involvement of tumor necrosis factor‐α and interleukin‐8 in antigen‐induced arthritis of the rabbit temporomandibular joint

Sukedai, M., Tominaga, K., Habu, M., Matsukawa, A., Nishihara, T., & Fukuda, J. (2004) · Journal of Oral Pathology and Medicine · doi:10.1111/j.1600-0714.2004.00008.x · Cited by 21

Variables affecting production of monocyte chemotactic factor 1 from human leukocytes stimulated with Cryptococcus neoformans

Levitz, S. M., North, E. A., Jiang, Y., Nong, S., Kornfeld, H., & Harrison, T. S. (1997) · Infection and Immunity · doi:10.1128/iai.65.3.903-908.1997 · Cited by 21

Simvastatin down-regulates the production of Interleukin-8 by neutrophil leukocytes from dyslipidemic patients

Marino, F., Maresca, A. M., Castiglioni, L., Cosentino, M., Maio, R. C., Schembri, L., Klersy, C., Mongiardi, C., Test, L. R., Grandi, A. M., et al. (2014) · BMC Cardiovascular Disorders · doi:10.1186/1471-2261-14-37 · Cited by 20

CagA+ H.pylori Induces Akt1 Phosphorylation and Inhibits Transcription of p21WAF1/CIP1 and p27KIP1 via PI3K/Akt1 Pathway

Li, S., Chen, X., Sun, A., Zhao, J., & Yan, J. (2010) · Biomedical and Environmental Sciences · doi:10.1016/s0895-3988(10)60063-3 · Cited by 20

Secretion of inflammatory factors from chondrocytes by layilin signaling

Asano, K., Arito, M., Kurokawa, M. S., Omoteyama, K., Okamoto, K., Suematsu, N., Yudoh, K., Nakamura, H., Beppu, M., & Kato, T. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.08.053 · Cited by 20

Nitric oxide-induced IL-8 expression is mediated by NF-kappaB and AP-1 in gastric epithelial AGS cells.

Jy, S., Jh, Y., Jw, L., Mukaida, N., & Kim, H. (2009) · PubMed · Cited by 20

High dose of intravenously given glucocorticosteroids decrease IL-8 production by monocytes in multiple sclerosis patients treated during relapse.

Mirowska-Guzel, D., Kurowska, K., Skierski, J., Koronkiewicz, M., Wicha, W., Kruszewska, J., Członkowski, A., & Członkowska, A. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.03.024 · Cited by 17

Recombinant Attenuated Edwardsiella piscicida Vaccine Displaying Regulated Lysis to Confer Biological Containment and Protect Catfish against Edwardsiellosis

Swain, B., Campodonico, V. A., & Curtiss, R. (2023) · Vaccines · doi:10.3390/vaccines11091470 · Cited by 19

Proton pump inhibitors as also inhibitors of atrial fibrillation

Lin, K., Chen, X., Zhang, L., Wang, Y., & Shan, Z. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.07.043 · Cited by 19

Serum concentrations of interleukin-8 in relation to different levels of alcohol consumption

González‐Quintela, A., Franco, J. C., Gudé, F., Perez, L., & Tomé, S. (2007) · Cytokine · doi:10.1016/j.cyto.2007.05.006 · Cited by 19

Candida Soluble Cell Wall β-D-Glucan Induces Lung Inflammation in Mice

Inoue, K., Takano, H., Oda, T., Yanagisawa, R., Tamura, H., Ohno, N., Adachi, Y., Ishibashi, K., & Yoshikawa, T. (2007) · International Journal of Immunopathology and Pharmacology · doi:10.1177/039463200702000308 · Cited by 18

Bivalent hemagglutinin and neuraminidase influenza replicon particle vaccines protect pigs against influenza a virus without causing vaccine associated enhanced respiratory disease

Brand, M. W., Anderson, T. K., Kitikoon, P., Kimble, J. B., Otis, N., Gauger, P. C., Souza, C. K., Kaplan, B. S., Mogler, M. A., Strait, E. L., et al. (2022) · Vaccine · doi:10.1016/j.vaccine.2022.07.042 · Cited by 18

Influence of the delivery modus on subpopulations and replication of lymphocytes in mothers and newborns

Almanzar, G., Schönlaub, J., Hammerer‐Lercher, A., Koppelstaetter, C., Bernhard, D., & Prelog, M. (2015) · Early Human Development · doi:10.1016/j.earlhumdev.2015.09.010 · Cited by 18

A model of insulin fibrils derived from the x-ray crystal structure of a monomeric insulin (despentapeptide insulin)

Brange, J., Dodson, G. G., Edwards, D. J., Holden, P., & Whittingham, J. L. (1997) · Proteins Structure Function and Bioinformatics · doi:10.1002/(sici)1097-0134(199704)27:4 · Cited by 78

RANTES in onchocerciasis: changes with ivermectin treatment

Cooper, P. J., Guderian, R. H., Prakash, D., Remick, D. G., Espinel, I., Nutman, T. B., Taylor, D. W., & Griffin, G. E. (1996) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.1996.d01-868.x · Cited by 18

Identification of a Novel Apoptosis-Inducing Factor Derived from Leukemic Cells: Endothelial Interleukin-8, but Not Monocyte-Derived, Induces Apoptosis in Leukemic Cells

Terui, Y., Ikeda, M., Tomizuka, H., Kasahara, T., Ohtsuki, T., Uwai, M., Mori, M., Itoh, T., Tanaka, M., Yamada, M., et al. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8103 · Cited by 18

Erlotinib augmentation with dapsone for rash mitigation and increased anti-cancer effectiveness

Kast, R. E. (2015) · SpringerPlus · doi:10.1186/s40064-015-1441-5 · Cited by 17

Endometriosis pain and epithelial neutrophil activating peptide-78 levels

Gardella, B., Dominoni, M., Gritti, A., Arrigo, A., Antonucci, S., Carletti, G. V., Musacchi, V., & Pietrocola, G. (2022) · Scientific Reports · doi:10.1038/s41598-022-07349-3 · Cited by 17

Chemokines: structure, receptors and functions. A new target for inflammation and asthma therapy?

van Acker, F. A. A., Voss, H., & Timmerman, H. (1996) · Mediators of Inflammation · doi:10.1155/s0962935196000567 · Cited by 17

Effect of Hydrogen Peroxide on Interleukin-8 Synthesis and Death of Caco-2 Cells

Németh, E., Halász, A., Baráth, Á., Domokos, M., & Gálfi, P. (2007) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923970701513443 · Cited by 17

Interferon Gamma Expression in Human Nasal Polyps

Dellacono, F. R., Eisma, R. J., Lafreniere, D. C., Leonard, G., & Kreutzer, D. L. (1997) · The Laryngoscope · doi:10.1097/00005537-199705000-00013 · Cited by 17

STAPHYLOCOCCAL SUPERANTIGENS INDUCE LYMPHOTACTIN PRODUCTION BY HUMAN CD4+ AND CD8+ T CELLS

Tikhonov, I., Kitabwalla, M., Wallace, M., Malkovský, M., Volkman, B. F., & Pauza, C. D. (2001) · Cytokine · doi:10.1006/cyto.2001.0944 · Cited by 16

Interleukin 8 (IL-8) Induces the Expression of Kinin B1Receptor in Human Lung Fibroblasts

Bastian, S., Paquet, J. L., Robert, C., Cremers, B., Loillier, B., Larrivée, J.-F., Bachvarov, D. R., Marceau, F., & Pruneau, D. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9848 · Cited by 16

Interference ofSalmonella enteritidis andLactobacillus spp. with IL-8 levels and transepithelial electrical resistance of enterocyte-like caco-2 cells

Fajdiga, S., Koninkx, J. F. J. G., Tooten, P. C. J., & Marinšek-Logar, R. (2006) · Folia Microbiologica · doi:10.1007/bf02931810 · Cited by 16

Interaction of PDE4 Inhibitors with Enzymes and Cell Functions

Dent, G., & Giembycz, M. A. (1996) · Elsevier eBooks · doi:10.1016/b978-012210720-7/50009-5 · Cited by 16

Bacteriocin BacSp222 and Its Succinylated Forms Exhibit Proinflammatory Activities Toward Innate Immune Cells

Śmiałek, J., Bzowska, M., Hinz, A., Mężyk-Kopeć, R., Sołtys, K., & Mak, P. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s362066 · Cited by 18

ERK/Egr-1 signaling pathway is involved in CysLT2 receptor-mediated IL-8 production in HEK293 cells

Lin, K.-N., Fang, S., Cai, B., Huang, X., Zhang, X., Lu, Y., Zhang, W., & Wei, E.-Q. (2014) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2014.05.001 · Cited by 15

Rapamycin Enhances TNF-α-Induced Secretion of IL-6 and IL-8 through Suppressing PDCD4 Degradation in Orbital Fibroblasts

Lee, W.-M., Paik, J., Cho, W., Oh, E., Lee, S., & Yang, S.-W. (2013) · Current Eye Research · doi:10.3109/02713683.2012.750368 · Cited by 15

Reduced expression of chemoattractant receptors by polymorphonuclear leukocytes in Hyper IgE Syndrome patients

Mintz, R. C., Garty, B. Z., Meshel, T., Marcus, N., Katanov, C., Cohen-Hillel, E., & Ben‐Baruch, A. (2009) · Immunology Letters · doi:10.1016/j.imlet.2009.12.006 · Cited by 15

Cerebrospinal fluid IL-8 levels reflect symptoms of alexithymia in patients with non-inflammatory neurological disorders

Uher, T., & Bob, P. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.02.006 · Cited by 14

The Role of Interleukins and Inflammatory Markers in the Early Restenosis of Covered Stents in the Femoropopliteal Arterial Segment

Guimaraes, T. S., Rocha, L. A., Becari, C., Piccinato, C. E., Dellalibera-Joviliano, R., Ribeiro, M. S., & Joviliano, E. É. (2018) · Annals of Vascular Surgery · doi:10.1016/j.avsg.2017.11.064 · Cited by 14

Stress decreases, while central nucleus amygdala lesions increase, IL-8 and MIP-1α gene expression during tissue healing in non-human primates

Kalin, N. H., Shelton, S. E., Engeland, C. G., Haraldsson, H. M., & Marucha, P. T. (2006) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2006.01.003 · Cited by 14

Cytokines, Chemokines and Growth Factors in the Pathogenesis and Treatment of Inflammatory Bowel Disease

O′Neil, D. A., & Steidler, L. (2003) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0171-8_15 · Cited by 14

Analysis of the cytokine interaction among interleukin-1β, interleukin-8, and interleukin-1 receptor antagonist in the rabbit ovulatory process

Ujioka, T., Matsukawa, A., Tanaka, N., Matsuura, K., Yoshinaga, M., & Okamura, H. (1998) · Fertility and Sterility · doi:10.1016/s0015-0282(98)00267-2 · Cited by 14

A biologically active peptide mimetic of N-acetylgalactosamine/galactose

Eggink, L. L., & Hoober, J. K. (2009) · BMC Research Notes · doi:10.1186/1756-0500-2-23 · Cited by 13

AEOL 10150 Alleviates Radiation-induced Innate Immune Responses in Non-human Primate Lung Tissue

Cui, W., Zhang, P., Hankey, K. G., Xiao, M., Farese, A. M., & MacVittie, T. J. (2021) · Health Physics · doi:10.1097/hp.0000000000001443 · Cited by 13

IL-8 is involved in homologous TNFα-, but not in IL-1β-induced neutrophil infiltration in rabbits

Miyamoto, K., Matsukawa, A., Ohkawara, S., Takagi, K., & Yoshinaga, M. (1997) · Inflammation Research · doi:10.1007/s000110050227 · Cited by 13

Change in cytokine levels after administration ofsaikokaryuukotsuboreitoor testosterone in patients with symptoms of late-onset hypogonadism

Tsujimura, A., Miyagawa, Y., Okuda, H., Yamamoto, K., Fukuhara, S., Nakayama, J., Takao, T., Nonomura, N., & Okuyama, Ä. (2010) · The Aging Male · doi:10.3109/13685538.2010.502268 · Cited by 13

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Lee, J., Paik, J., Yun, M., Lee, S., & Yang, S.-W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148645 · Cited by 12

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Brigaud, I., Garabédian, C., Bricout, N., Pieuchot, L., Ponche, A., Deltombe, R., Delille, R., Atlan, M., Bigerelle, M., & Anselme, K. (2019) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000006606 · Cited by 12

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ALMOUSA, L. A., Salter, A. M., Castellanos, M., May, S. T., & Langley‐Evans, S. C. (2022) · Nutrients · doi:10.3390/nu14173586 · Cited by 12

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Laureano, R. S., Vanmeerbeek, I., Sprooten, J., Govaerts, J., Naulaerts, S., & Garg, A. D. (2023) · Immunological Reviews · doi:10.1111/imr.13287 · Cited by 13

αPix interacts withHelicobacter pyloriCagA to induce IL-8 expression in gastric epithelial cells

Lim, J. W., Kim, K. H., & Kim, H. (2009) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365520903144398 · Cited by 12

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Noël, L., Fransolet, M., Jacobs, N., Foidart, J., Nisolle, M., & Munaut, C. (2020) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-020-01692-y · Cited by 12

Keratinocyte chemoattractant (interleukin‐8) regulation of sinonasal cilia function in a murine model

Shen, J. C., Chen, B., & Cohen, N. A. (2011) · International Forum of Allergy & Rhinology · doi:10.1002/alr.20087 · Cited by 12

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Fragão-Marques, M., Francisca-Marques, M., Rocha-Neves, J. P., & Özben, T. (2025) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2025.2512472 · Cited by 12

Cytokine expression by neutrophils of adult horses stimulated with virulent and avirulent Rhodococcus equi in vitro

Nerren, J. R., Payne, S., Halbert, N. D., Martens, R. J., & Cohen, N. D. (2008) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2008.10.003 · Cited by 11

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Wiedemann, T., Hofbaur, S., Loell, E., & Rieder, G. (2016) · European Journal of Microbiology and Immunology · doi:10.1556/1886.2016.00020 · Cited by 11

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Stojkovic, B., Mullen, M. P., Donofrío, G., McLoughlin, R. M., & Meade, K. G. (2016) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2016.12.006 · Cited by 11

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Matiašková, K., Kavanová, L., Kulich, P., Gebauer, J., Nedbalcová, K., Kudláčková, H., Tesařı́k, R., & Faldyna, M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.635097 · Cited by 11

Cloning and characterization of guinea pig interleukin-8 receptor

Catusse, J., Faye, P., Loillier, B., Cremers, B., Franck, R., Luccarini, J., Pruneau, D., & Paquet, J. (2003) · Biochemical Pharmacology · doi:10.1016/s0006-2952(03)00459-3 · Cited by 11

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Cohen, M. (1999) · Toxicological Sciences · doi:10.1093/toxsci/48.2.163 · Cited by 11

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Suzuki, N., Purba, F. Y., Nii, T., & Isobe, N. (2022) · Animal Science Journal · doi:10.1111/asj.13773 · Cited by 10

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Du, Y., Zong, M., Guan, Q., Huang, Z., Zhou, L., Cai, J., da Roza, G., Wang, H., Qi, H., Lu, Y., et al. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02473-9 · Cited by 11

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Tran, T., Tran, Q.-H., Nguyen, Q., Le, M.-T., Trinh, D.-T. T., Tran, V. H., & Thai, K. (2022) · SAR and QSAR in environmental research · doi:10.1080/1062936x.2022.2132536 · Cited by 10

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Sanacora, S., Urdinez, J., Chang, T., & Vancurova, I. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.03.041 · Cited by 10

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Oh, M., Bathige, S. D. N. K., Kim, Y., Lee, S., Yang, H., Kim, M., & Lee, J. (2017) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2017.05.050 · Cited by 10

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Moghimi, M., Dastgheib, S. A., Heiranizadeh, N., Zare, M. H., Sheikhpour, E., & Neámatzadeh, H. (2020) · Arquivos de Gastroenterologia · doi:10.1590/s0004-2803.202000000-16 · Cited by 10

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Ghazarian, A., Garner, W. L., & Ehrlich, H. P. (2000) · Experimental and Molecular Pathology · doi:10.1006/exmp.2000.2329 · Cited by 10

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Isbir, C. S., Doǧan, R., Demircin, M., Yaylim, I., & Paşaoǧlu, I. (2001) · Cardiovascular Surgery · doi:10.1016/s0967-2109(01)00011-4 · Cited by 10

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Reddy, A. S., Patel, J. R., Vogler, C. A., Klein, R. S., & Sands, M. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064647 · Cited by 9

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Avraham-Lubin, B.-C. R., Dotan, G., Hasanreisoğlu, M., Kramer, M., Monselise, Y., Cohen, Y., Weinberger, D., & Goldenberg‐Cohen, N. (2008) · Current Eye Research · doi:10.1080/02713680801932891 · Cited by 9

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Cagliani, R., Gatto, F., Cibecchini, G., Marotta, R., Catalano, F., Sánchez‐Moreno, P., Pompa, P. P., & Bardi, G. (2019) · Cells · doi:10.3390/cells9010056 · Cited by 9

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Baggiolini, M., Moser, B., & Clark‐Lewis, I. (1994) · CHEST Journal · doi:10.1378/chest.105.3_supplement.95s · Cited by 200

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Groves, D., & Jiang, Y. (1995) · Critical Reviews in Oral Biology & Medicine · doi:10.1177/10454411950060020101 · Cited by 219

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Haelens, A., Wuyts, A., Proost, P., Struyf, S., Opdenakker, G., & Damme, J. V. (1996) · Immunobiology · doi:10.1016/s0171-2985(96)80019-2 · Cited by 70

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Mukaida, N., Harada, A., & Matsushima, K. (1998) · Cytokine & Growth Factor Reviews · doi:10.1016/s1359-6101(97)00022-1 · Cited by 401

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Palomino, D. C. T., & Marti, L. C. (2015) · Einstein (São Paulo) · doi:10.1590/s1679-45082015rb3438 · Cited by 411