Cytokine profiling in patients with hepatic glycogen storage disease: Are there clues for unsolved aspects?

被引:2
作者
Colonetti, Karina [1 ,2 ]
Pinto e Vairo, Filippo [3 ,4 ]
Siebert, Marina [2 ,5 ,6 ]
Nalin, Tatiele [7 ]
Poloni, Soraia [2 ]
Roesch, Luiz Fernando Wurdig [8 ]
de Souza, Carolina Fischinger Moura [9 ,10 ]
Pinheiro, Franciele Cabral [1 ,2 ,11 ]
Schwartz, Ida Vanessa Doederlein [1 ,2 ,9 ,12 ]
机构
[1] Univ Fed Rio Grande do Sul, Postgrad Program Genet & Mol Biol, Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre, Lab Basic Res & Adv Invest Neurosci BRAIN, Porto Alegre, RS, Brazil
[3] Mayo Clin, Ctr Individualized Med, Rochester, MN USA
[4] Mayo Clin, Dept Clin Genom, Rochester, MN USA
[5] Univ Fed Rio Grande do Sul, Postgrad Program Sci Gastroenterol & Hepatol, Porto Alegre, RS, Brazil
[6] Hosp Clin Porto Alegre, Laboratorial Res Unit, Porto Alegre, RS, Brazil
[7] Ultragenyx Brasil Farmaceut Ltda, Sao Paulo, SP, Brazil
[8] Univ Florida, Inst Food & Agr Sci, Dept Microbiol & Cell Sci, Gainesville, FL USA
[9] Hosp Clin Porto Alegre, Med Genet Serv, Porto Alegre, RS, Brazil
[10] Univ Fed Rio Grande do Sul, Postgrad Program Child & Adolescent Hlth, Porto Alegre, RS, Brazil
[11] Univ Fed Pampa, Itaqui, RS, Brazil
[12] Univ Fed Rio Grande Sul UFRGS, Rua Ramiro Barcellos 2350-Bairro Santa Cecilia, BR-90035007 Porto Alegre, RS, Brazil
关键词
Cytokines; Glycogen storage disease; Chemokines; COLONY-STIMULATING FACTOR; HEPATOCELLULAR ADENOMAS; SIGNALING PATHWAY; CHEMOKINE; INFLAMMATION; DYSFUNCTION; MANAGEMENT; LIVER; IA; CHEMOATTRACTANT;
D O I
10.1016/j.cyto.2022.156088
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Hepatic Glycogen Storage Diseases (GSD) are rare genetic disorders in which the gluconeogenesis pathway is impaired. Cytokines control virtually every aspect of physiology and may help to elucidate some unsolved questions about phenotypes presented by GSD patients.Methods: This was an exploratory study in which 27 GSD patients on treatment (Ia = 16, Ib = 06, III = 02, IX alpha = 03) and 24 healthy age-and sex-matched subjects had plasma samples tested for a panel of 20 cytokines (G-CSF, GM-CSF, IL-1 alpha,IL-1 beta, IL-4, IL-6, IL-8, IL-10, IL-13, IL-17A, GRO, IP-10/CXCL10, MCP-1/CCL2, MIP-1 alpha/CCL3, MIP-1 beta/CCL4, MDC/CCL22, IFN-gamma, TNF-alpha, TNF-beta, VEGF) through a multiplex kit and analyzed in comparison to controls and among patients, regarding to clinical features as anemia, hepatic adenocarcinoma and triglyceride levels.Results: Patients (GSD-Ia/III/IX) presented reduced levels of IL-4 (p = 0.040), MIP-1 alpha/CCL3 (p = 0.003), MDC/ CCL22 (p < 0.001), TNF-beta (p = 0.045) and VEGF (p = 0.043) compared to controls. When different types of GSD were compared, G-CSF was higher in GSD-Ib than-Ia (p < 0.001) and than-III/IX (p = 0.033) patients; IL-10 was higher in GSD-Ib than in GSD-Ia patients (p = 0.019); and GSD-III/IX patients had increased levels of IP-10/ CXCL10 than GSD-Ib patients (p = 0.019). When GSD-I patients were gathered into the same group and compared with GSD-III/IX patients, IP10/CXCL10 and MCP-1 were higher in the latter group (p = 0.005 and p = 0.013, respectively). GSD-I patients with anemia presented higher levels of IL-4 and MIP-1 alpha in comparison with patients who had not. Triglyceride level was correlated with neutrophil count and MDC levels on GSD-Ia patients without HCA.Conclusion: Altogether, altered levels of cytokines in GSD-I patients reflect an imbalance in immunoregulation process. This study also indicates that neutrophils and some cytokines are affected by triglyceride levels, and future studies on the theme should consider this variable.
引用
收藏
页数:8
相关论文
共 56 条
[1]  
[Anonymous], R Project for Statistical Computing (Version 3.0.2)
[2]  
[Anonymous], 2013, DATABASE
[3]   Role of macrophage inflammatory protein (MIP)-1 alpha/CCL3 in leukemogenesis [J].
Baba, Tomohisa ;
Mukaida, Naofumi .
MOLECULAR & CELLULAR ONCOLOGY, 2014, 1 (01)
[4]   International Union of Pharmacology. LXXXIX. Update on the Extended Family of Chemokine Receptors and Introducing a New Nomenclature for Atypical Chemokine Receptors [J].
Bachelerie, Francoise ;
Ben-Baruch, Adit ;
Burkhardt, Amanda M. ;
Combadiere, Christophe ;
Farber, Joshua M. ;
Graham, Gerard J. ;
Horuk, Richard ;
Sparre-Ulrich, Alexander Hovard ;
Locati, Massimo ;
Luster, Andrew D. ;
Mantovani, Alberto ;
Matsushima, Kouji ;
Murphy, Philip M. ;
Nibbs, Robert ;
Nomiyama, Hisayuki ;
Power, Christine A. ;
Proudfoot, Amanda E. I. ;
Rosenkilde, Mette M. ;
Rot, Antal ;
Sozzani, Silvano ;
Thelen, Marcus ;
Yoshie, Osamu ;
Zlotnik, Albert .
PHARMACOLOGICAL REVIEWS, 2014, 66 (01) :1-79
[5]  
Beegle RD, 2015, JIMD REP, V18, P23, DOI 10.1007/8904_2014_344
[6]   Role of cytokines and chemokines in non-alcoholic fatty liver disease [J].
Braunersreuther, Vincent ;
Viviani, Giorgio Luciano ;
Mach, Francois ;
Montecucco, Fabrizio .
WORLD JOURNAL OF GASTROENTEROLOGY, 2012, 18 (08) :727-735
[7]   IL-10 Receptor Signaling Is Essential for TR1 Cell Function In Vivo [J].
Brockmann, Leonie ;
Gagliani, Nicola ;
Steglich, Babett ;
Giannou, Anastasios D. ;
Kempski, Jan ;
Pelczar, Penelope ;
Geffken, Maria ;
Mfarrej, Bechara ;
Huber, Francis ;
Herkel, Johannes ;
Wan, Yisong Y. ;
Esplugues, Enric ;
Battaglia, Manuela ;
Krebs, Christian F. ;
Flavell, Richard A. ;
Huber, Samuel .
JOURNAL OF IMMUNOLOGY, 2017, 198 (03) :1130-1141
[8]   Molecular characterization of hepatocellular adenomas developed in patients with glycogen storage disease type I [J].
Calderaro, Julien ;
Labrune, Philippe ;
Morcrette, Guillaume ;
Rebouissou, Sandra ;
Franco, Dominique ;
Prevot, Sophie ;
Quaglia, Alberto ;
Bedossa, Pierre ;
Libbrecht, Louis ;
Terracciano, Luigi ;
Smit, G. Peter A. ;
Bioulac-Sage, Paulette ;
Zucman-Rossi, Jessica .
JOURNAL OF HEPATOLOGY, 2013, 58 (02) :350-357
[9]   Regulated production of the interferon-gamma-inducible protein-10 (IP-10) chemokine by human neutrophils [J].
Cassatella, MA ;
Gasperini, S ;
Calzetti, F ;
Bertagnin, A ;
Luster, AD ;
McDonald, PP .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (01) :111-115
[10]   Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter [J].
Chen, LY ;
Shieh, JJ ;
Lin, BC ;
Pan, CJ ;
Gao, JL ;
Murphy, PM ;
Roe, TF ;
Moses, S ;
Ward, JM ;
Lee, EJ ;
Westphal, H ;
Mansfield, BC ;
Chou, JY .
HUMAN MOLECULAR GENETICS, 2003, 12 (19) :2547-2558