View Item 

Show simple item record

Dual role of interleukin‐10 in the regulation of respiratory syncitial virus ( RSV )‐induced lung inflammation

dc.contributor.authorSun, L.en_US
dc.contributor.authorCornell, T. T.en_US
dc.contributor.authorLeVine, A.en_US
dc.contributor.authorBerlin, A. A.en_US
dc.contributor.authorHinkovska‐galcheva, V.en_US
dc.contributor.authorFleszar, A. J.en_US
dc.contributor.authorLukacs, N. W.en_US
dc.contributor.authorShanley, T. P.en_US
dc.date.accessioned2013-05-02T19:35:17Z
dc.date.available2014-07-01T15:53:32Zen_US
dc.date.issued2013-05en_US
dc.identifier.citationSun, L.; Cornell, T. T.; LeVine, A.; Berlin, A. A.; Hinkovska‐galcheva, V. ; Fleszar, A. J.; Lukacs, N. W.; Shanley, T. P. (2013). "Dual role of interleukinâ 10 in the regulation of respiratory syncitial virus ( RSV )â induced lung inflammation." Clinical & Experimental Immunology (2): 263-279. <http://hdl.handle.net/2027.42/97500>en_US
dc.identifier.issn0009-9104en_US
dc.identifier.issn1365-2249en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/97500
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherChemokinesen_US
dc.subject.otherRSVen_US
dc.subject.otherT H1en_US
dc.subject.otherT H2 Cytokinesen_US
dc.subject.otherPulmonary Inflammationen_US
dc.titleDual role of interleukin‐10 in the regulation of respiratory syncitial virus ( RSV )‐induced lung inflammationen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.identifier.pmid23574323en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/97500/1/cei12059.pdf
dc.identifier.doi10.1111/cei.12059en_US
dc.identifier.sourceClinical & Experimental Immunologyen_US
dc.identifier.citedreferenceHogan SP, Foster PS. Cellular and molecular mechanisms involved in the regulation of eosinophil trafficking in vivo. Med Res Rev 1996; 16: 407 – 432.en_US
dc.identifier.citedreferenceDolgachev V, Petersen BC, Budelsky AL, Berlin AA, Lukacs NW. Pulmonary IL‐17E (IL‐25) production and IL‐17RB+ myeloid cell‐derived Th2 cytokine production are dependent upon stem cell factor‐induced responses during chronic allergic pulmonary disease. J Immunol 2009; 183: 5705 – 5715.en_US
dc.identifier.citedreferenceFallon PG, Ballantyne SJ, Mangan NE et al. Identification of an interleukin (IL)‐25‐dependent cell population that provides IL‐4, IL‐5, and IL‐13 at the onset of helminth expulsion. J Exp Med 2006; 203: 1105 – 1116.en_US
dc.identifier.citedreferenceKim EY, Battaile JT, Patel AC et al. Persistent activation of an innate immune response translates respiratory viral infection into chronic lung disease. Nat Med 2008; 14: 633 – 640.en_US
dc.identifier.citedreferenceVermaelen K, Pauwels R. Accurate and simple discrimination of mouse pulmonary dendritic cell and macrophage populations by flow cytometry: methodology and new insights. Cytometry A 2004; 61: 170 – 177.en_US
dc.identifier.citedreferenceArase H, Saito T, Phillips JH, Lanier LL. Cutting edge: the mouse NK cell‐associated antigen recognized by DX5 monoclonal antibody is CD49b (alpha 2 integrin, very late antigen‐2). J Immunol 2001; 167: 1141 – 1144.en_US
dc.identifier.citedreferenceFleming TJ, Fleming ML, Malek TR. Selective expression of Ly‐6G on myeloid lineage cells in mouse bone marrow. RB6‐8C5 mAb to granulocyte‐differentiation antigen (Gr‐1) detects members of the Ly‐6 family. J Immunol 1993; 151: 2399 – 2408.en_US
dc.identifier.citedreferenceMiller AL, Bowlin TL, Lukacs NW. Respiratory syncytial virus‐induced chemokine production: linking viral replication to chemokine production in vitro and in vivo. J Infect Dis 2004; 189: 1419 – 1430.en_US
dc.identifier.citedreferenceFoster PS, Hogan SP, Ramsay AJ, Matthaei KI, Young IG. Interleukin 5 deficiency abolishes eosinophilia, airways hyperreactivity, and lung damage in a mouse asthma model. J Exp Med 1996; 183: 195 – 201.en_US
dc.identifier.citedreferenceJohn AE, Berlin AA, Lukacs NW. Respiratory syncytial virus‐induced CCL5/RANTES contributes to exacerbation of allergic airway inflammation. Eur J Immunol 2003; 33: 1677 – 1685.en_US
dc.identifier.citedreferenceLukacs NW. Role of chemokines in the pathogenesis of asthma. Nat Rev Immunol 2001; 1: 108 – 116.en_US
dc.identifier.citedreferenceHaeberle HA, Casola A, Gatalica Z et al. IkappaB kinase is a critical regulator of chemokine expression and lung inflammation in respiratory syncytial virus infection. J Virol 2004; 78: 2232 – 2241.en_US
dc.identifier.citedreferenceJiang XB, Wang ZD, Zhu Y et al. Inhibition of CD8+ T lymphocytes attenuates respiratory syncytial virus‐enhanced allergic inflammation. Respiration 2009; 77: 76 – 84.en_US
dc.identifier.citedreferenceSmit JJ, Boon L, Lukacs NW. Respiratory virus‐induced regulation of asthma‐like responses in mice depends upon CD8 T cells and interferon‐gamma production. Am J Pathol 2007; 171: 1944 – 1951.en_US
dc.identifier.citedreferenceLloyd CM, Hawrylowicz CM. Regulatory T cells in asthma. Immunity 2009; 31: 438 – 449.en_US
dc.identifier.citedreferenceSun J, Cardani A, Sharma AK et al. Autocrine regulation of pulmonary inflammation by effector T‐cell derived IL‐10 during infection with respiratory syncytial virus. PLoS Pathog 2011; 7: e1002173.en_US
dc.identifier.citedreferenceZuany‐Amorim C, Haile S, Leduc D et al. Interleukin‐10 inhibits antigen‐induced cellular recruitment into the airways of sensitized mice. J Clin Invest 1995; 95: 2644 – 2651.en_US
dc.identifier.citedreferenceNakagome K, Dohi M, Okunishi K et al. In vivo IL‐10 gene delivery suppresses airway eosinophilia and hyperreactivity by down‐regulating APC functions and migration without impairing the antigen‐specific systemic immune response in a mouse model of allergic airway inflammation. J Immunol 2005; 174: 6955 – 6966.en_US
dc.identifier.citedreferenceRichardson JY, Ottolini MG, Pletneva L et al. Respiratory syncytial virus (RSV) infection induces cyclooxygenase 2: a potential target for RSV therapy. J Immunol 2005; 174: 4356 – 4364.en_US
dc.identifier.citedreferencePetersen BC, Budelsky AL, Baptist AP, Schaller MA, Lukacs NW. Interleukin‐25 induces type 2 cytokine production in a steroid‐resistant interleukin‐17RB+ myeloid population that exacerbates asthmatic pathology. Nat Med 2012; 18: 751 – 758.en_US
dc.identifier.citedreferenceLukacs NW, Tekkanat KK, Berlin A et al. Respiratory syncytial virus predisposes mice to augmented allergic airway responses via IL‐13‐mediated mechanisms. J Immunol 2001; 167: 1060 – 1065.en_US
dc.identifier.citedreferencePark JW, Taube C, Yang ES et al. Respiratory syncytial virus‐induced airway hyperresponsiveness is independent of IL‐13 compared with that induced by allergen. J Allergy Clin Immunol 2003; 112: 1078 – 1087.en_US
dc.identifier.citedreferenceDoucet C, Brouty‐Boye D, Pottin‐Clemenceau C, Canonica GW, Jasmin C, Azzarone B. Interleukin (IL) 4 and IL‐13 act on human lung fibroblasts. Implication in asthma. J Clin Invest 1998; 101: 2129 – 2139.en_US
dc.identifier.citedreferenceIkeda T, Sato K, Kuwada N et al. Interleukin‐10 differently regulates monocyte chemoattractant protein‐1 gene expression depending on the environment in a human monoblastic cell line, UG3. J Leukoc Biol 2002; 72: 1198 – 1205.en_US
dc.identifier.citedreferenceIp WK, Wong CK, Lam CW. Interleukin (IL)‐4 and IL‐13 up‐regulate monocyte chemoattractant protein‐1 expression in human bronchial epithelial cells: involvement of p38 mitogen‐activated protein kinase, extracellular signal‐regulated kinase 1/2 and Janus kinase‐2 but not c‐Jun NH2‐terminal kinase 1/2 signalling pathways. Clin Exp Immunol 2006; 145: 162 – 172.en_US
dc.identifier.citedreferenceCorne JM, Holgate ST. Mechanisms of virus induced exacerbations of asthma. Thorax 1997; 52: 380 – 389.en_US
dc.identifier.citedreferenceMartinez FD. Definition of pediatric asthma and associated risk factors. Pediatr Pulmonol Suppl 1997; 15: 9 – 12.en_US
dc.identifier.citedreferenceSchwarze J, Hamelmann E, Bradley KL, Takeda K, Gelfand EW. Respiratory syncytial virus infection results in airway hyperresponsiveness and enhanced airway sensitization to allergen. J Clin Invest 1997; 100: 226 – 233.en_US
dc.identifier.citedreferenceTeichtahl H, Buckmaster N, Pertnikovs E. The incidence of respiratory tract infection in adults requiring hospitalization for asthma. Chest 1997; 112: 591 – 596.en_US
dc.identifier.citedreferenceHogg JC. Childhood viral infection and the pathogenesis of asthma and chronic obstructive lung disease. Am J Respir Crit Care Med 1999; 160: S26 – 28.en_US
dc.identifier.citedreferenceHoltzman MJ, Morton JD, Shornick LP et al. Immunity, inflammation, and remodeling in the airway epithelial barrier: epithelial–viral–allergic paradigm. Physiol Rev 2002; 82: 19 – 46.en_US
dc.identifier.citedreferencePrince GA, Capiau C, Deschamps M et al. Efficacy and safety studies of a recombinant chimeric respiratory syncytial virus FG glycoprotein vaccine in cotton rats. J Virol 2000; 74: 10287 – 10292.en_US
dc.identifier.citedreferenceConnors M, Giese NA, Kulkarni AB, Firestone CY, Morse HC III, Murphy BR. Enhanced pulmonary histopathology induced by respiratory syncytial virus (RSV) challenge of formalin‐inactivated RSV‐immunized BALB/c mice is abrogated by depletion of interleukin‐4 (IL‐4) and IL‐10. J Virol 1994; 68: 5321 – 5325.en_US
dc.identifier.citedreferenceHunter CA, Ellis‐Neyes LA, Slifer T et al. IL‐10 is required to prevent immune hyperactivity during infection with Trypanosoma cruzi. J Immunol 1997; 158: 3311 – 3316.en_US
dc.identifier.citedreferenceSteidler L, Hans W, Schotte L et al. Treatment of murine colitis by Lactococcus lactis secreting interleukin‐10. Science 2000; 289: 1352 – 1355.en_US
dc.identifier.citedreferenceMurai H, Terada A, Mizuno M et al. IL‐10 and RANTES are elevated in nasopharyngeal secretions of children with respiratory syncytial virus infection. Allergol Int 2007; 56: 157 – 163.en_US
dc.identifier.citedreferenceBont L, Heijnen CJ, Kavelaars A et al. Monocyte IL‐10 production during respiratory syncytial virus bronchiolitis is associated with recurrent wheezing in a one‐year follow‐up study. Am J Respir Crit Care Med 2000; 161: 1518 – 1523.en_US
dc.identifier.citedreferenceSchuurhof A, Janssen R, de Groot H et al. Local interleukin‐10 production during respiratory syncytial virus bronchiolitis is associated with post‐bronchiolitis wheeze. Respir Res 2011; 12: 121 – 127.en_US
dc.identifier.citedreferenceChung HL, Kim WT, Kim JK et al. Relationship between atopic status and nasal interleukin 10 and 11 levels in infants with respiratory syncytial virus bronchiolitis. Ann Allergy Asthma Immunol 2005; 94: 267 – 272.en_US
dc.identifier.citedreferenceTakanashi S, Hasegawa Y, Kanehira Y et al. Interleukin‐10 level in sputum is reduced in bronchial asthma, COPD and in smokers. Eur Respir J 1999; 14: 309 – 314.en_US
dc.identifier.citedreferenceAraujo MI, Hoppe B, Medeiros M, Jr et al. Impaired T helper 2 response to aeroallergen in helminth‐infected patients with asthma. J Infect Dis 2004; 190: 1797 – 1803.en_US
dc.identifier.citedreferenceSpight D, Zhao B, Haas M, Wert S, Denenberg A, Shanley TP. Immunoregulatory effects of regulated, lung‐targeted expression of IL‐10 in vivo. Am J Physiol Lung Cell Mol Physiol 2005; 288: L251 – 265.en_US
dc.identifier.citedreferenceTekkanat KK, Maassab HF, Cho DS et al. IL‐13‐induced airway hyperreactivity during respiratory syncytial virus infection is STAT6 dependent. J Immunol 2001; 166: 3542 – 3548.en_US
dc.identifier.citedreferenceLindell DM, Lane TE, Lukacs NW. CXCL10/CXCR3‐mediated responses promote immunity to respiratory syncytial virus infection by augmenting dendritic cell and CD8(+) T cell efficacy. Eur J Immunol 2008; 38: 2168 – 2179.en_US
dc.identifier.citedreferenceSmit JJ, Lindell DM, Boon L, Kool M, Lambrecht BN, Lukacs NW. The balance between plasmacytoid DC versus conventional DC determines pulmonary immunity to virus infections. PLoS One 2008; 3: e1720.en_US
dc.identifier.citedreferenceSchaller MA, Neupane R, Rudd BD et al. Notch ligand Delta‐like 4 regulates disease pathogenesis during respiratory viral infections by modulating Th2 cytokines. J Exp Med 2007; 204: 2925 – 2934.en_US
dc.identifier.citedreferenceSteinhauser ML, Hogaboam CM, Kunkel SL, Lukacs NW, Strieter RM, Standiford TJ. IL‐10 is a major mediator of sepsis‐induced impairment in lung antibacterial host defense. J Immunol 1999; 162: 392 – 399.en_US
dc.identifier.citedreferenceMukherjee S, Lindell DM, Berlin AA et al. IL‐17‐induced pulmonary pathogenesis during respiratory viral infection and exacerbation of allergic disease. Am J Pathol 2011; 179: 248 – 258.en_US
dc.identifier.citedreferenceRudd BD, Smit JJ, Flavell RA et al. Deletion of TLR3 alters the pulmonary immune environment and mucus production during respiratory syncytial virus infection. J Immunol 2006; 176: 1937 – 1942.en_US
dc.identifier.citedreferenceTekkanat KK, Maassab H, Miller A, Berlin AA, Kunkel SL, Lukacs NW. RANTES (CCL5) production during primary respiratory syncytial virus infection exacerbates airway disease. Eur J Immunol 2002; 32: 3276 – 3284.en_US
dc.identifier.citedreferenceLukacs NW, Strieter RM, Warmington K, Lincoln P, Chensue SW, Kunkel SL. Differential recruitment of leukocyte populations and alteration of airway hyperreactivity by C‐C family chemokines in allergic airway inflammation. J Immunol 1997; 158: 4398 – 4404.en_US
dc.identifier.citedreferenceSchaller MA, Kallal LE, Lukacs NW. A key role for CC chemokine receptor 1 in T‐cell‐mediated respiratory inflammation. Am J Pathol 2008; 172: 386 – 394.en_US
dc.identifier.citedreferenceNakayama T, Yamashita M. Initiation and maintenance of Th2 cell identity. Curr Opin Immunol 2008; 20: 265 – 271.en_US
dc.identifier.citedreferenceBishop DK, Chan Wood S, Eichwald EJ, Orosz CG. Immunobiology of allograft rejection in the absence of IFN‐gamma: CD8+ effector cells develop independently of CD4+ cells and CD40–CD40 ligand interactions. J Immunol 2001; 166: 3248 – 3255.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Name:
cei12059.pdf
Size:
1.414MB
Format:
PDF
View/Open

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.