ISSN: 0443-511
e-ISSN: 2448-5667
Usuario/a
Idioma
Herramientas del artículo
Envíe este artículo por correo electrónico (Inicie sesión)
Enviar un correo electrónico al autor/a (Inicie sesión)
Tamaño de fuente

Open Journal Systems

CXCL5 into the upper airways of children with influenza A virus infection

Annett Duemmler, Aurea Rosalía Montes-Vizuet, Julio Santiago Cruz, Luis Manuel Terán

Resumen


Background: neutrophil infiltration is a major feature in the pathogenesis of influenza infection. The factors regulating the neutrophil influx are not fully understood. The chemokine CXCL5/ENA-78 is a potent neutrophil chemoattractant, that has been implicated in several inflammatory diseases. Our objectives was to study the release of CXCL5 in children with natural acquired influenza.

Methods: CXCL5 concentration was investigated by immunoenzyme assay in nasal aspirates of children (n = 18) in whom respiratory symptoms were precipitated predominantly by influenza A virus.

Results: there were increased CXCL5 levels in nasal aspirates when children were symptomatic as compared with samples from the same children when they had been asymptomatic for four weeks (medians 1850 pg/mL vs. 30 pg/mL, p < 0.005). We purified CXCL5 from these samples, and demonstrated biological neutrophil chemotactic activity.

Conclusions: it is the first in vivo data that suggest an important role for CXCL5 in neutrophil influx in proven upper respiratory influenza infection. We suggest that CXCL5 might provide a target for therapeutic intervention in influenza induced respiratory diseases.


Palabras clave


Influenza, human; Influenza A virus, H1N1 subtypes; Neutrophils; Chemokines

Texto completo:

PDF

Referencias


Williams BG, Gouws E, Boschi-Pinto C, Bryce J, Dye C. Estimates of world-wide distribution of child deaths from acute respiratory infections. Lancet Infect Dis 2002;2(1):25-32. 

 

Morens D. Influenza-related mortality: considerations for practice and public health. JAMA 2003;289(2):227-229

 

Wold Health Organization. Pandemic (H1N1) 2009-update 74[Internet];2009. Available at http://www.who.int/csr/don/2009_11_27a/en/index.html 

 

Douglas RG Jr, Alford RH, Cate TR, Couch RB. The leukocyte response during viral respiratory illness in man. Ann Intern Med 1966;64(3):521-530.

 

Wang SZ, Forsyth KD. The interaction of neutrophils with respiratory epithelial cells in viral infection. Respirology 2000;5(1):1-10.

 

Tate MD, Brooks AG, Reading PC. The role of neutrophils in the upper and lower respiratory tract during influenza virus infection in mice. Respir Res 2008;9:57. Available at http://www.ncbi.nlm.nih. gov/pmc/articles/PMC252 6083/pdf/1465-9921-9-57.pdf 

 

Yamamoto K, Suzuki K, Suzuki K, Mizuno S. Phagocytosis and ingestion of influenza virus by human polymorphonuclear leukocytes in vitro: electron-microscopy studies. J Med Microbiol 1989;28(3):191-198. Available at http://jmm.sgmjournals.org/cgi/reprint/28/3/191 

 

Perrone LA, Plowden JK, García-Sastre A, Katz JM, Tumpey T. H5N1 and 1918 pandemic influenza virus infection results in early and excessive infiltration of macrophages and neutrophils in the lungs of mice. PLoS Pathog 2008; 4(8):e1000115. Available at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2483250/pdf/ppat.1000115.pdf 

 

Tumpey TM, García-Sastre A, Taubenberger JK, Palese P, Swayne DE, Pantin-Jackwood MJ, et al. Pathogenicity of influenza viruses with genes from the 1918 pandemic virus: functional roles of alveolar macrophages and neutrophils in limiting virus repli-cation and mortality in mice. J Virol 2005;79(23):14933-14944. 

 

Fujisawa H. Inhibitory role of neutrophils on influenza virus multiplication in the lung of mice. Microbiol Immunol 2001;45(10):679-688.

 

Fujisawa H. Neutrophils play an essential role in cooperation with antibody in both protection against and recovery from pulmonary infection with influenza virus in mice. J Virol 2008;82(6):2772-2783. Available at http://www.ncbi.nlm. nih.gov/pmc/articles/PMC2258992/pdf/1210-07.pdf 

 

Ratcliffe D, Nolin SL, Cramer EB. Neutrophil interaction with influenza-infected epithelial cells. Blood. 1988;72(1):142-149. Available at http://bloodjournal. hematologylibrary.org/cgi/reprint/72/1/142 

 

Zlotnik A, Yoshie O. Chemokines: a new classification system and their role in immunity. Immunity 2000;1282):121-127

 

Walz A, Burgener R, Car B, Baggiolini M, Kunkel SL, Strieter RM. Structure and neutrophil-activating properties of a novel inflammatory peptide (ENA-78) with homology to interleukin-8. J Exp Med. 1991;174(6):1355-1362. Available at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119025/pdf/je17461355. pdf 

 

Walz A, Schmutz P, Mueller C, Schnyder-Candrian S. Regulation and function of the CXC chemokine ENA-78 in monocytes and its role in disease. J Leukoc Biol 1997;62(5):604-611. Available at http://www.jleukbio.org/cgi/reprint/62/5/604 

 

Pauksens K, Fjaertoft G, Douhan-Hakansson L, Venge P. Neutrophil and monocyte receptor expression in uncomplicated and complicated influenza A infection with pneumonia. Scand J Infect Dis 2008;40(4):326-337

 

Pizzichini MM, Pizzichini E, Efthimiadis A, Chauhan AJ, Johnston SL, Hussack P, et al. Asthma and natural colds. Inflammatory indices in induced sputum: a feasibility study. Am J. Respir Crit Care Med 1998;158(4):1178-1184. Available at http://ajrccm.atsjournals.org/cgi/content/full/158/4/1178 

 

Teran, LM, Johnston SL, Schröder J, Church MK, Holgate ST. Role of nasal interleukin8 in neutrophil recruitment and activation in children with virus induced asthma. Am J Respir Crit Care Med 1997;155(4):1362-1366.

 

Wuytz A, Proost P, Lenaerts JP, Ben-Baruch A, Van Damme J, Wang JM. Differential usage of the CXC chemokine receptors 1 and 2 by interleukin-8, granulocyte chemotactic protein-2 and epithelial-cell derived neutrophil attractant-78. Eur J Biochem 1998;255(1):67-73. Available at http://onlinelibrary.wiley.com/doi/10.1046/j.1432- 1327.1998.2550067.x/pdf

 

Wareing MD, Shea AL, Inglis CA, Dias PB, Sarawar SR. CXCR2 is required for neutrophil recruitment to the lung during influenza virus infection, but is not essential for viral clearance. Viral Immunol 2007;20(3):369-378.

Gern JE, Martin MS, Anklam KA, Shen K, Roberg KA, Carlson-Dakes KT, et al. Relationship among specific viral pathogens, virus induced interleukin- 8, and respiratory symptoms in infancy. Pediatr Allergy Immunol 2002;13(6):386-393.

 

Hayden FG, Fritz RS, Lobo M, Alvord G, Strober W, Straus SE. Local and systemic cytokine responses during experimental human Influenza A virus infection. J Clin Invest 1998;101(3):643-649.

 

Williams BG, Gouws E, Boschi-Pinto C, Bryce J, Dye C. Estimates of world-wide distribution of child deaths from acute respiratory infections. Lancet Infect Dis 2002;2(1):25-32.

 

Ghildyal R, Dagher H, Donninger H, de Silva D, Li X, Freezer NJ, et al Rhinovirus infects primary human airway fibroblasts and induces a neutrophil chemokine and permeability factor. J Med Virol. 2005;75(4):608-615.

 

Santiago J, Hernández-Cruz JL, Manjarrez-Zavala ME, Montes-Vizuet R, Rosete-Olvera DP, TapiaDíaz AM, et al. Role of monocyte chemotactic protein-3 and -4 in children with virus exacerbation of asthma. Eur Respir J 2008;32 (5):1243-1249. Available at http://erj. ersjournals.com/content/32/ 5/1243.full.pdf+html

 

Donninger H, Glashoff R, Haitchi HM, Syce J, Ghildyal R, van Rensburg E, et al. Rhinovirus induction of the CXC chemokine epithelial activating peptide-78 in bronchial epithelium. J Infect Dis 2003;187(11):1809-1817.

 

Tecle T, White MR, Gantz D, Crouch EC, Hartshorn KL. Human neutrophil defensins increase neutrophl uptake of influenza A virus and bacteria and modify virus-induced respiratory burst responses. J Immunol 2007;178(12):8046-8052. Available at http://www.jimmunol.org/cgi/content/full/178/12/ 8046.


Enlaces refback

  • No hay ningún enlace refback.