Circulating levels of miR-150 are associated with poorer outcomes of A/H1N1 infection

被引:31
|
作者
Moran, Juan [1 ]
Ramirez-Martinez, Gustavo [1 ]
Jimenez-Alvarez, Luis [1 ]
Cruz, Alfredo [1 ]
Perez-Patrigeon, Santiago [2 ]
Hidalgo, Alfredo [3 ]
Orozco, Lorena [3 ]
Martinez, Angelica [3 ]
Padilla-Noriega, Luis [4 ]
Avila-Moreno, Federico [5 ]
Cabello, Carlos [1 ]
Granados, Julio [6 ]
Ortiz-Quintero, Blanca [1 ]
Ramirez-Venegas, Alejandra [1 ]
Ruiz-Palacios, Guillermo M. [2 ]
Zlotnik, Albert [7 ]
Merino, Enrique [8 ]
Zuniga, Joaquin [1 ]
机构
[1] Inst Nacl Enfermedades Resp Ismael Cosio Villegas, Mexico City 14080, DF, Mexico
[2] Inst Natl Ciencias Med & Nutr Salvador Zubiran, Dept Infect Dis, Ciudad De Mexico, DF, Mexico
[3] Inst Natl Med Genom, Mexico City, DF, Mexico
[4] Univ Nacl Autonoma Mexico, Posgrad Ciencias Biol, Fac Med, Dept Microbiol & Parasitol, Mexico City 04510, DF, Mexico
[5] Univ Nacl Autonoma Mexico, UBIMED, Unidad Biomed, FES Iztacala, Mexico City 04510, DF, Mexico
[6] Inst Natl Ciencias Med & Nutr Salvador Zubiran, Dept Transplantat, Mexico City, DF, Mexico
[7] Univ Calif Irvine, Dept Physiol & Biophys, Irvine, CA 92717 USA
[8] Univ Nacl Autonoma Mexico, Inst Biotecnol, Cuernavaca 62191, Morelos, Mexico
关键词
miRNAs; Pandemic influenza A/H1N1; Critically ill patients; Circulating microRNAs; miR-150; Influenza; INFLUENZA-A H1N1; RESPIRATORY-DISTRESS-SYNDROME; PANDEMIC INFLUENZA; VIRUS-INFECTION; POTENTIAL BIOMARKERS; MICRORNA EXPRESSION; NEGATIVE REGULATION; INTERFERON-GAMMA; IN-VITRO; CELLS;
D O I
10.1016/j.yexmp.2015.07.001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Overproduction of pro-inflammatory cytokines and chemokines is frequently associated with severe clinical manifestations in patients infected with influenza A/H1N1 virus. Micro-RNAs (miRNAs) are highly conserved small non-coding RNA molecules that post-transcriptionally regulate gene expression and are potential biomarkers and therapeutic targets in different inflammatory conditions. Methods: We studied the circulating and miRNA profiles in critically ill A/H1N1 patients, A/H1N1 patients with milder disease, asymptomatic housemates and healthy controls. Cytokine, chemokine and growth factors that were potential targets of differentially expressed miRNAs were assessed. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment and interactome analysis of these miRNAs were also performed. Results: Critically ill patients exhibited a significant over-expression of circulating miR-150 (p<0.005) when compared to patients with milder disease. miR-29c, miR-145 and miR-22 were differentially expressed in patients with severe A/H1N1 disease whereas miR-210, miR-126 and miR-222 were downregulated in individuals exposed to the A/H1N1 virus. Significant correlations (p<0.05) between circulating levels of miR-150 with IL-1ra, IL-2, IL-6, CXCL8, IFN-gamma, CXCL10 and G-CSF were detected, particularly in critically ill patients. Conclusion: The up-regulation of miR-150 is associated with poorer outcomes of A/H1N1 infection. The differential expression of miRNAs related with immune processes in severe A/H1N1 disease supports the potential role of these miRNAs as biomarkers of disease progression. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:253 / 261
页数:9
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