본문 바로가기
KERD
논문KCI 등재

Innate immune recognition of respiratory syncytial virus infection

2

조회

0

다운로드

4

인용

0

참고문헌

키워드

주제분류화학

초록

Respiratory syncytial virus (RSV) is the leading cause ofrespiratory infection in infants and young children. Severeclinical manifestation of RSV infection is a bronchiolitis, whichis common in infants under six months of age. Recently, RSVhas been recognized as an important cause of respiratoryinfection in older populations with cardiovascular morbidity orimmunocompromised patients. However, neither a vaccinenor an effective antiviral therapy is currently available. Moreover, the interaction between the host immune systemand the RSV pathogen during an infection is not wellunderstood. The innate immune system recognizes RSVthrough multiple mechanisms. The first innate immune RSVdetectors are the pattern recognition receptors (PRRs),including toll-like receptors (TLRs), retinoic acid-induciblegene-I (RIG-I)-like receptors (RLRs), and nucleotide-bidingoligomerization domain (NOD)-like receptors (NLRs). Thefollowing is a review of studies associated with various PRRsthat are responsible for RSV virion recognition and subsequentinduction of the antiviral immune response during RSV infection.

Abstract

Respiratory syncytial virus (RSV) is the leading cause ofrespiratory infection in infants and young children. Severeclinical manifestation of RSV infection is a bronchiolitis, whichis common in infants under six months of age. Recently, RSVhas been recognized as an important cause of respiratoryinfection in older populations with cardiovascular morbidity orimmunocompromised patients. However, neither a vaccinenor an effective antiviral therapy is currently available. Moreover, the interaction between the host immune systemand the RSV pathogen during an infection is not wellunderstood. The innate immune system recognizes RSVthrough multiple mechanisms. The first innate immune RSVdetectors are the pattern recognition receptors (PRRs),including toll-like receptors (TLRs), retinoic acid-induciblegene-I (RIG-I)-like receptors (RLRs), and nucleotide-bidingoligomerization domain (NOD)-like receptors (NLRs). Thefollowing is a review of studies associated with various PRRsthat are responsible for RSV virion recognition and subsequentinduction of the antiviral immune response during RSV infection.

참고문헌 (67)

  1. Blount, R. E., Jr, "Recovery of cytopathogenic agent from chimpanzees with coryza", Proc. Soc. Exp. Biol. Med, 92, pp.544~549 (1956)
  2. Chanock, R., "Recovery from infants with respiratory illness of a virus related to chimpanzee coryza agent (CCA). I. Isolation, properties and characterization", Am. J. Hyg, 66, pp.281~290 (1957)
  3. Chanock, R., "Recovery from infants with respiratory illness of a virus related to chimpanzee coryza agent (CCA). II. Epidemiologic aspects of infection in infants and young children", Am. J. Hyg, 66, pp.291~300 (1957)
  4. Collins, P. L., "Viral and host factors in human respiratory syncytial virus pathogenesis", J. Virol, 82, pp.2040~2055 (2008)
  5. Walsh, E. E., "Immunization with glycoprotein subunits of respiratory syncytial virus to protect cotton rats against viral infection", J. Infect. Dis, 155, pp.1198~1204 (1987)
  6. Connors, M., "Respiratory syncytial virus (RSV) F, G, M2 (22K), and N proteins each induce resistance to RSV challenge, but resistance induced by M2 and N proteins is relatively short-lived", J. Virol, 65, pp.1634~1637 (1991)
  7. Lo, M. S., "Respiratory syncytial virus nonstructural proteins NS1 and NS2 mediate inhibition of Stat2 expression and alpha", beta interferon responsiveness, 2005, pp.79, 9315~9319
  8. Conzelmann, K. K., "Transcriptional activation of alpha", beta interferon genes: interference by nonsegmented negative-strand RNA viruses, 2005, pp.79, 5241~5248
  9. Ramaswamy, M., "Specific inhibition of type I interferon signal transduction by respiratory syncytial virus", Am. J. Respir. Cell. Mol. Biol, 30, pp.893~900 (2004)
  10. Fulginiti, V. A., "Respiratory virus immunization. I. A field trial of two inactivated respiratory virus vaccines; an aqueous trivalent parainfluenza virus vaccine and an alum-precipitated respiratory syncytial virus vaccine", Am. J. Epidemiol, 89, pp.435~448 (1969)
  11. Crowe, J. E., Jr., "Respiratory syncytial virus vaccine development", Vaccine, 20(Suppl 1), pp.S32~S37 (2001)
  12. 장준, "Current progress on development of respiratory syncytial virus vaccine", BMB Reports, 44(4), pp.232~237 (2011), 생화학분자생물학회
  13. Haynes, L. M., "Progress and challenges in RSV prophylaxis and vaccine development", J. Infect. Dis, 208(Suppl 3), pp.S177~S183 (2013)
  14. Ventre, K, "Ribavirin for respiratory syncytial virus infection of the lower respiratory tract in infants and young children", Cochrane Database Syst. Rev, pp.Cd000181~ (2007)
  15. Kumar, H., "Pathogen recognition by the innate immune system", Int. Rev. Immunol, 30, pp.16~34 (2011)
  16. Arnold, R., "Peroxisome proliferator- activated receptor-gamma agonists inhibit the replication of respiratory syncytial virus (RSV) in human lung epithelial cells", Virology, 350, pp.335~346 (2006)
  17. Liu, P., "Retinoic Acid-Inducible Gene I Mediates Early Antiviral Response and Toll-Like Receptor 3 Expression in Respiratory Syncytial Virus-Infected Airway Epithelial Cells", J. Virol, 81, pp.1401~1411 (2007)
  18. Inoue, Y., "Toll-Like Receptor 2 as a Functional Receptor to Respiratory Syncytial Virus", J. Allergy Clin. Immunol, 117, pp.S210~ (2006)
  19. Murawski, M. R., "Respiratory syncytial virus activates innate immunity through Toll-like receptor 2", J. Virol, 83, pp.1492~1500 (2009)
  20. Kurt-Jones, E. A., "Pattern recognition receptors TLR4 and CD14 mediate response to respiratory syncytial virus", Nat. Immunol, 1, pp.398~401 (2000)
  21. Haynes, L. M., "Involvement of toll-like receptor 4 in innate immunity to respiratory syncytial virus", J. Virol, 75, pp.10730~10737 (2001)
  22. Haeberle, H. A., "Respiratory Syncytial Virus-Induced Activation of Nuclear Factor-κB in the Lung Involves Alveolar Macrophages and Toll-Like Receptor 4-Dependent Pathways", J. Infect. Dis, 186, pp.1199~1206 (2002)
  23. Ehl, S., "The role of Toll-like receptor 4 versus interleukin-12 in immunity to respiratory syncytial virus", Eur. J. Immunol, 34, pp.1146~1153 (2004)
  24. Monick, M. M., "Respiratory Syncytial Virus Up-regulates TLR4 and Sensitizes Airway Epithelial Cells to Endotoxin", J. Biol. Chem, 278, pp.53035~53044 (2003)
  25. Gagro, A., "Increased Toll-like receptor 4 expression in infants with respiratory syncytial virus bronchiolitis", Clin. Exp. Immunol, 135, pp.267~272 (2004)
  26. Marr, N., "Role of human TLR4 in respiratory syncytial virus-induced NF-κB activation, viral entry and replication", Innate. Immun, 18, pp.856~865 (2012)
  27. Tal, G., "Association between common Toll-like receptor 4 mutations and severe respiratory syncytial virus disease", J. Infect. Dis, 189, pp.2057~2063 (2004)
  28. Awomoyi, A. A., "Association of TLR4 polymorphisms with symptomatic respiratory syncytial virus infection in high-risk infants and young children", J. Immunol, 179, pp.3171~3177 (2007)
  29. Puthothu, B., "TLR-4 and CD14 polymorphisms in respiratory syncytial virus associated disease", Dis. Markers, 22, pp.303~308 (2006)
  30. Paulus, S. C., "Common human Toll-like receptor 4 polymorphisms-Role in susceptibility to respiratory syncytial virus infection and functional immunological relevance", Clin. Immunol, 123, pp.252~257 (2007)
  31. Dou, Y., "Respiratory syncytial virus infection induces higher Toll-like receptor-3 expression and TNF-alpha production than human metapneumovirus infection", PLoS One, 8, pp.e73488~ (2013)
  32. Rudd, B. D., "Differential Role for TLR3 in Respiratory Syncytial Virus-Induced Chemokine Expression", J. Virol, 79, pp.3350~3357 (2005)
  33. Groskreutz, D. J., "Respiratory Syncytial Virus Induces TLR3 Protein and Protein Kinase R, Leading to Increased Double- Stranded RNA Responsiveness in Airway Epithelial Cells", J. Immunol, 176, pp.1733~1740 (2006)
  34. Huang, S., "Upregulation of TLR7 and TLR3 gene expression in the lung of respiratory syncytial virus infected mice", Wei Sheng Wu Xue Bao, 49, pp.239~245 (2009)
  35. Chen, L. F., "F-kappaB RelA phosphorylation regulates RelA acetylation", Mol. Cell. Biol, 25, pp.7966~7975 (2005)
  36. Sasaki, C. Y., "Phosphorylation of RelA", p65 on serine 536 defines an I{kappa}B{alpha}-independent NF-{kappa}B pathway, 2005, pp.280, 34538~34547
  37. Vermeulen, L., "Transcriptional activation of the NF-kappaB p65 subunit by mitogen- and stress-activated protein kinase-1 (MSK1)", EMBO J, 22, pp.1313~1324 (2003)
  38. Zhong, H., "Phosphorylation of NF-kappa B p65 by PKA stimulates transcriptional activity by promoting a novel bivalent interaction with the coactivator CBP", p300, 1998, pp.1, 661~671
  39. Shingai, M., "Soluble G protein of respiratory syncytial virus inhibits Toll-like receptor 3", 4-mediated IFN-beta induction, 2008, pp.20, 1169~1180
  40. Rudd, B. D., "Deletion of TLR3 Alters the Pulmonary Immune Environment and Mucus Production during Respiratory Syncytial Virus Infection", J. Immunol, 176, pp.1937~1942 (2006)
  41. Schlender, J., "Inhibition of Toll-Like Receptor 7- and 9-Mediated Alpha", Beta Interferon Production in Human Plasmacytoid Dendritic Cells by Respiratory Syncytial Virus and Measles Virus, 2005, pp.79, 5507~5515
  42. Davidson, S., "Plasmacytoid dendritic cells promote host defense against acute pneumovirus infection via the TLR7-MyD88-dependent signaling pathway", J. Immunol, 186, pp.5938~5948 (2011)
  43. Phipps, S., "Eosinophils contribute to innate antiviral immunity and promote clearance of respiratory syncytial virus", Blood, 110, pp.1578~1586 (2007)
  44. Lukacs, N. W., "Respiratory Virus-Induced TLR7 Activation Controls IL-17-Associated Increased Mucus via IL-23 Regulation", J. Immunol, 185, pp.2231~2239 (2010)
  45. Hornung, V., "5'-Triphosphate RNA is the ligand for RIG-I", Science, 314, pp.994~997 (2006)
  46. Pichlmair, A., "RIG-I-mediated antiviral responses to single-stranded RNA bearing 5'-phosphates", Science, 314, pp.997~1001 (2006)
  47. Wu, B., "Structural basis for dsRNA recognition, filament formation, and antiviral signal activation by MDA5", Cell, 152, pp.276~289 (2013)
  48. Rehwinkel, J., "RIG-I detects viral genomic RNA during negative-strand RNA virus infection", Cell, 140, pp.397~408 (2010)
  49. Loo, Y. M., "Distinct RIG-I and MDA5 signaling by RNA viruses in innate immunity", J. Virol, 82, pp.335~345 (2008)
  50. Scagnolari, C., "Gene expression of nucleic acid-sensing pattern recognition receptors in children hospitalized for respiratory syncytial virus- associated acute bronchiolitis", Clin. Vaccine Immunol, 16, pp.816~823 (2009)
  51. Marr, N., "Attenuation of Respiratory Syncytial Virus-Induced and RIG-I-Dependent Type I IFN Responses in Human Neonates and Very Young Children", J. Immunol, 192, pp.948~957 (2014)
  52. Bhoj, V. G., "MAVS and MyD88 are essential for innate immunity but not cytotoxic T lymphocyte response against respiratory syncytial virus", Proc. Natl. Acad. Sci. U. S. A, 105, pp.14046~14051 (2008)
  53. Demoor, T., "IPS-1 signaling has a nonredundant role in mediating antiviral responses and the clearance of respiratory syncytial virus", J. Immunol, 189, pp.5942~5953 (2012)
  54. Zandi, E., "Bridging the gap: composition, regulation, and physiological function of the IkappaB kinase complex", Mol. Cell Biol, 19, pp.4547~4551 (1999)
  55. Dejardin, E., "The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways", Immunity, 17, pp.525~535 (2002)
  56. Xiao, G., "Induction of p100 processing by NF-kappaB-inducing kinase involves docking IkappaB kinase alpha (IKKalpha) to p100 and IKKalpha-mediated phosphorylation", J. Biol. Chem, 279, pp.30099~30105 (2004)
  57. Xiao, G., "NF-kappaB-inducing kinase regulates the processing of NF-kappaB2 p100", Mol. Cell, 7, pp.401~409 (2001)
  58. Liu, P., "Respiratory syncytial virus induces RelA release from cytoplasmic 100-kDa NF-kappa B2 complexes via a novel retinoic acid-inducible gene-I{middle dot}NF- kappa B-inducing kinase signaling pathway", J. Biol. Chem, 283, pp.23169~23178 (2008)
  59. Jamaluddin, M., "Respiratory syncytial virus infection induces a reactive oxygen species-MSK1-phospho-Ser-276 RelA pathway required for cytokine expression", J. Virol, 83, pp.10605~10615 (2009)
  60. Yoboua, F., "Respiratory syncytial virus-mediated NF-kappa B p65 phosphorylation at serine 536 is dependent on RIG-I, TRAF6, and IKK beta", J. Virol, 84, pp.7267~7277 (2010)
  61. Sabbah, A., "Activation of innate immune antiviral responses by Nod2", Nat. Immunol, 10, pp.1073~1080 (2009)
  62. Inohara, N., "Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease", J. Biol. Chem, 278, pp.5509~5512 (2003)
  63. Vissers, M., "Respiratory syncytial virus infection augments NOD2 signaling in an IFN-beta-dependent manner in human primary cells", Eur. J. Immunol, 42, pp.2727~2735 (2012)
  64. Pang, I. K., "Inflammasomes as mediators of immunity against influenza virus", Trends Immunol, 32, pp.34~41 (2011)
  65. Takeuchi, R, "Respiratory syncytial virus infection of human alveolar epithelial cells enhances interferon regulatory factor 1 and interleukin-1beta-convertInnate immune recognition of respiratory syncytial virus infection Tae Hoon Kim and Heung Kyu Lee http:", J. Virol, pp.1998, 72[DOI]
  66. Triantafilou, K., "Human respiratory syncytial virus viroporin SH: a viral recognition pathway used by the host to signal inflammasome activation", Thorax, 68, pp.66~75 (2013)
  67. Segovia, J., "TLR2", MyD88, ASC inflammasome during respiratory syncytial virus infection, pp.PLoS One, 2012[DOI]

관련 논문AI추천

이 간행물의 다른 논문 (9건)