2010, Number 4
<< Back Next >>
Rev Med Inst Mex Seguro Soc 2010; 48 (4)
CXCL5 into the upper airways of children with influenza A virus infection
Duemmler A, Montes-Vizuet AR, Cruz JS, Terán LM
Language: English
References: 27
Page: 393-398
PDF size: 45.50 Kb.
ABSTRACT
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.
REFERENCES
Williams BG, Gouws E, Boschi-Pinto C, Bryce J, Dye C. Estimates of worldwide 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: electronmicroscopy 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, Tapia- Díaz 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