The development of respiratory inflammation in children

Paediatric Respiratory Reviews

Volumn 7, Issue 2, 2006, Pages 89-96

  Prescott, Susan L ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

Airway inflammation; Airway remodelling; Allergy; Asthma; Childhood; Mucosal immune system; Type 2 T helper cell cytokines

Indexed keywords

CD14 ANTIGEN; ENDOTHELIN 1; FIBROBLAST GROWTH FACTOR; FISH OIL; GAMMA INTERFERON; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; HOUSE DUST ALLERGEN; INTERLEUKIN 12; INTERLEUKIN 13; INTERLEUKIN 1BETA; INTERLEUKIN 4; INTERLEUKIN 5; INTERLEUKIN 9; PLACEBO; PLATELET DERIVED GROWTH FACTOR; TOLL LIKE RECEPTOR; TOLL LIKE RECEPTOR 2; TOLL LIKE RECEPTOR 4; TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA2;

ALLERGIC ASTHMA; ALLERGIC RHINITIS; ASTHMA; CELL HYPERPLASIA; CELLULAR IMMUNITY; CLINICAL FEATURE; CLINICAL TRIAL; CYTOKINE PRODUCTION; DIET SUPPLEMENTATION; DISEASE COURSE; DISEASE PREDISPOSITION; FOOD ALLERGY; HIGH RISK POPULATION; HUMAN; IMMUNOLOGICAL TOLERANCE; IMMUNOREGULATION; IMMUNOTHERAPY; INFLAMMATORY INFILTRATE; INNATE IMMUNITY; LUNG FIBROSIS; NONHUMAN; PASSIVE SMOKING; PATHOPHYSIOLOGY; PERINATAL PERIOD; PRENATAL PERIOD; PRIMARY PREVENTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; RESPIRATORY TRACT INFECTION; RESPIRATORY TRACT INFLAMMATION; REVIEW; RISK FACTOR; RISK REDUCTION; SENSITIZATION; SIGNAL TRANSDUCTION; TH2 CELL; VIRUS INFECTION; WHEEZING;

ANIMALS; ASTHMA; CHILD; CHILD, PRESCHOOL; CYTOKINES; HUMANS; HYPERSENSITIVITY; IMMUNITY, MUCOSAL; INFANT; INFLAMMATION; RESPIRATORY TRACT DISEASES; TH2 CELLS;

EID: 33744524818     PISSN: 15260542     EISSN: 15260550     Source Type: Journal    
DOI: 10.1016/j.prrv.2006.03.001     Document Type: Review

References (63)

1. Lau S., Illi S., Sommerfeld C., Niggemann B., et al. Early exposure to house-dust mite and cat allergens and development of childhood asthma: a cohort study. Multicentre Allergy Study Group. Lancet 356 (2000) 1392-1397
2. Pohunek P., Warner J.O., Turzikova J., Kudrmann J., and Roche W.R. Markers of eosinophilic inflammation and tissue re-modelling in children before clinically diagnosed bronchial asthma. Pediatr Allergy Immunol 16 (2005) 43-51
3. Eichenfield L.F., Hanifin J.M., Beck L.A., et al. Atopic dermatitis and asthma: parallels in the evolution of treatment. Pediatrics 111 (2003) 608-616
4. Guilbert T.W., Morgan W.J., Zeiger R.S., et al. Atopic characteristics of children with recurrent wheezing at high risk for the development of childhood asthma. J Allergy Clin Immunol 114 (2004) 1282-1287
5. Cutz E., Levison H., and Cooper D.M. Ultrastructure of airways in children with asthma. Histopathology 2 (1978) 407-421
6. van den Toorn L.M., Overbeek S.E., de Jongste J.C., Leman K., Hoogsteden H.C., and Prins J.B. Airway inflammation is present during clinical remission of atopic asthma. Am J Respir Crit Care Med 164 (2001) 2107-2113
7. Morgan W.J., Stern D.A., Sherrill D.L., et al. Outcome of asthma and wheezing in the first 6 years of life: follow-up through adolescence. Am J Respir Crit Care Med 172 (2005) 1253-1258
8. Rasmussen F., Taylor D.R., Flannery E.M., et al. Risk factors for airway remodeling in asthma manifested by a low postbronchodilator FEV1/vital capacity ratio: a longitudinal population study from childhood to adulthood. Am J Respir Crit Care Med 165 (2002) 1480-1488
9. Bibi H.S., Feigenbaum D., Hessen M., and Shoseyov D. Do current treatment protocols adequately prevent airway remodeling in children with mild intermittent asthma?. Respir Med 100 (2006) 458-462
10. Merkus P.J., van Pelt W., van Houwelingen J.C., et al. Inhaled corticosteroids and growth of airway function in asthmatic children. Eur Respir J 23 (2004) 861-868
11. Holgate S.T. Epithelial damage and response. Clin Exp Allergy 30 suppl 1 (2000) 37-41
12. Martinez F.D., and Helms P.J. Types of asthma and wheezing. Eur Respir J Suppl 27 (1998) 3s-8s
13. Tschernig T., Debertin A.S., Paulsen F., Kleemann W.J., and Pabst R. Dendritic cells in the mucosa of the human trachea are not regularly found in the first year of life. Thorax 56 (2001) 427-431
14. Nelson D., McMenamin C., McWilliam A., Brenan M., and Holt P. Development of the airway intraepithelial dendritic cell network in the rat from class II MHC (Ia) negative precursors: differential regulation of Ia expression at different levels of the respiratory tract. J Exp Med 179 (1994) 203-212
15. Nelson D., and Holt P. Defective regional immunity in the respiratory tract of neonates is attributable to hyporesponsiveness of local dendritic cells to activation signals. J Immunol 155 (1995) 3517-3524
16. Huh J.C., Strickland D.H., Jahnsen F.L., et al. Bidirectional interactions between antigen-bearing respiratory tract dendritic cells (DCs) and T cells precede the late phase reaction in experimental asthma: DC activation occurs in the airway mucosa but not in the lung parenchyma. J Exp Med 198 (2003) 19-30
17. Jahnsen F.L., Moloney E.D., Hogan T., Upham J.W., Burke C.M., and Holt P.G. Rapid dendritic cell recruitment to the bronchial mucosa of patients with atopic asthma in response to local allergen challenge. Thorax 56 (2001) 823-826
18. Stampfli M.R., Wiley R.E., Neigh G.S., et al. GM-CSF transgene expression in the airway allows aerosolized ovalbumin to induce allergic sensitization in mice. J Clin Invest 102 (1998) 1704-1714
19. Yamamoto N., Suzuki S., Shirai A., et al. Dendritic cells are associated with augmentation of antigen sensitization by influenza A virus infection in mice. Eur J Immunol 30 (2000) 316-326
20. Stumbles P.A., Thomas J.A., Pimm C.L., et al. Resting respiratory tract dendritic cells preferentially stimulate T helper cell type 2 (Th2) responses and require obligatory cytokine signals for induction of Th1 immunity. J Exp Med 188 (1998) 2019-2031
21. Upham J.W., Lee P.T., Holt B.J., et al. Development of interleukin-12-producing capacity throughout childhood. Infect Immun 70 (2002) 6583-6588
22. Bienenstock J., and Befus D. Gut- and bronchus-associated lymphoid tissue. Am J Anat 170 (1984) 437-445
23. Vancikova Z., Lodinova-Zadnikova R., Radl J., and Tlaskalova-Hogenova H. The early postnatal development of salivary antibody and immunoglobulin response in children orally colonized with a nonpathogenic, probiotic strain of E. coli. Folia Microbiol (Praha) 48 (2003) 281-287
24. Sopo S.M., Macchiaiolo M., Zorzi G., and Tripodi S. Sublingual immunotherapy in asthma and rhinoconjunctivitis; systematic review of paediatric literature. Arch Dis Child 89 (2004) 620-624
25. Novembre E., Galli E., Landi F., et al. Coseasonal sublingual immunotherapy reduces the development of asthma in children with allergic rhinoconjunctivitis. J Allergy Clin Immunol 114 (2004) 851-857
26. Bachert C., and van Cauwenberge P. The WHO ARIA (allergic rhinitis and its impact on asthma) initiative. Chem Immunol Allergy 82 (2003) 119-126
27. Ciprandi G., Cirillo I., Tosca M.A., and Vizzaccaro A. Bronchial hyperreactivity and spirometric impairment in patients with perennial allergic rhinitis. Int Arch Allergy Immunol 133 (2004) 14-18
28. Nayak A.S. The asthma and allergic rhinitis link. Allergy Asthma Proc 24 (2003) 395-402
29. Crystal-Peters J., Neslusan C., Crown W.H., and Torres A. Treating allergic rhinitis in patients with comorbid asthma: the risk of asthma-related hospitalizations and emergency department visits. J Allergy Clin Immunol 109 (2002) 57-62
30. Wills-Karp M., Luyimbazi J., Xu X., et al. Interleukin-13: central mediator of allergic asthma. Science 282 (1998) 2258-2261
31. Richter A., Puddicombe S.M., Lordan J.L., et al. The contribution of interleukin (IL)-4 and IL-13 to the epithelial-mesenchymal trophic unit in asthma. Am J Respir Cell Mol Biol 25 (2001) 385-391
32. Hansen G., Berry G., DeKruyff R.H., and Umetsu D.T. Allergen-specific Th1 cells fail to counterbalance Th2 cell-induced airway hyperreactivity but cause severe airway inflammation. J Clin Invest 103 (1999) 175-183
33. Corrigan C.J., and Kay A.B. CD4 T-lymphocyte activation in acute severe asthma. Relationship to disease severity and atopic status. Am Rev Respir Dis 141 (1990) 970-977
34. Calhoun W.J., Bates M.E., Schrader L., Sedgwick J.B., and Busse W.W. Characteristics of peripheral blood eosinophils in patients with nocturnal asthma. Am Rev Respir Dis 145 (1992) 577-581
35. Martinez F., Wright A., Taussig L., et al. Asthma and wheezing in the first six years of life. N Eng J Med 332 (1995) 133-138
36. Stick S.M., Burton P.R., Gurrin L., Sly P.D., and LeSouef P.N. Effects of maternal smoking during pregnancy and a family history of asthma on respiratory function in newborn infants. Lancet 348 (1996) 1060-1064
37. Gilliland F.D., Berhane K., Li Y.F., Rappaport E.B., and Peters J.M. Effects of early onset asthma and in utero exposure to maternal smoking on childhood lung function. Am J Respir Crit Care Med 167 (2003) 917-924
38. Prescott S., Macaubas C., Holt B., et al. Transplacental priming of the human immune system to environmental allergens: universal skewing of initial T-cell responses towards Th-2 cytokine profile. J Immunol 160 (1998) 4730-4737
39. Prescott S.L. Early origins of allergic disease: a review of processes and influences during early immune development. Curr Opin Allergy Clin Immunol 3 (2003) 125-132
40. Devereux G., Barker R.N., and Seaton A. Antenatal determinants of neonatal immune responses to allergens. Clin Exp Allergy 32 (2002) 43-50
41. Dunstan J., Mori T.A., Barden A., et al. Fish oil supplementation in pregnancy modifies neonatal allergen-specific immune responses and clinical outcomes in infants at high risk of atopy: a randomised controlled trial. J Allergy Clin Immunol 112 (2003) 1178-1184
42. Noakes P.S., Holt P.G., and Prescott S.L. Maternal smoking in pregnancy alters neonatal cytokine responses. Allergy 58 (2003) 1053-1058
43. Matsuoka T., Matsubara T., Katayama K., Takeda K., Koga M., and Furukawa S. Increase of cord blood cytokine-producing T cells in intrauterine infection. Pediatr Int 43 (2001) 453-457
44. Prescott S., Jenmalm M., Bjorksten B., and Holt P. Effects of maternal allergen-specific IgG in cord blood on early postnatal development of allergen-specific T-cell immunity. Allergy 55 (2000) 470-475
45. Edelbauer M., Loibichler C., Nentwich I., Gerstmayr M., Urbanek R., and Szepfalusi Z. Maternally delivered nutritive allergens in cord blood and in placental tissue of term and preterm neonates. Clin Exp Allergy 34 (2004) 189-193
46. Woodcock A., Lowe L.A., Murray C.S., et al. Early life environmental control: effect on symptoms, sensitization, and lung function at age 3 years. Am J Respir Crit Care Med 170 (2004) 433-439
47. Lau S., Nickel R., Niggemann B., et al. The development of childhood asthma: lessons from the German Multicentre Allergy Study (MAS). Paediatr Respir Rev 3 (2002) 265-272
48. Stein R.T., Sherrill D., Morgan W.J., et al. Respiratory syncytial virus in early life and risk of wheeze and allergy by age 13 years. Lancet 354 (1999) 541-545
49. Oddy W.H., de Klerk N.H., Sly P.D., and Holt P.G. The effects of respiratory infections, atopy, and breastfeeding on childhood asthma. Eur Respir J 19 (2002) 899-905
50. Strachan D.P. Family size, infection and atopy: the first decade of the "hygiene hypothesis". Thorax 55 suppl 1 (2000) S2-S10
51. Blumer N., Herz U., Wegmann M., and Renz H. Prenatal lipopolysaccharide-exposure prevents allergic sensitisation and airway inflammation, but not airway responsiveness in a murine model of experimental asthma. Clin Exp Allergy 35 (2005) 397-402
52. Tulic M.K., Wale J.L., Holt P.G., and Sly P.D. Modification of the inflammatory response to allergen challenge after exposure to bacterial lipopolysaccharide. Am J Respir Cell Mol Biol 22 (2000) 604-612
53. Arkwright P.D., and David T.J. Intradermal administration of a killed Mycobacterium vaccae suspension (SRL 172) is associated with improvement in atopic dermatitis in children with moderate-to-severe disease. J Allergy Clin Immunol 107 (2001) 531-534
54. Weston S., Halbert A., Richmond P., and Prescott S.L. Effects of probiotics on atopic dermatitis: a randomised controlled trial. Arch Dis Child 90 (2005) 892-897
55. Prescott S.L., Dunstan J., Hale J., et al. Clinical effects of probiotics are associated with increased interferon-gamma responses in very young children with atopic dermatitis. Clin Exp Allergy 35 (2005) 1557-1564
56. Baldini M., Lohman I.C., Halonen M., Erickson R.P., Holt P.G., and Martinez F.D. A Polymorphism in the 5{radical dot} flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E. Am J Respir Cell Mol Biol 20 (1999) 976-983
57. Eder W., Klimecki W., Yu L., et al. Toll-like receptor 2 as a major gene for asthma in children of European farmers. J Allergy Clin Immunol 113 (2004) 482-488
58. Weiss S.T., Tager I.B., Munoz A., and Speizer F.E. The relationship of respiratory infections in early childhood to the occurrence of increased levels of bronchial responsiveness and atopy. Am Rev Respir Dis 131 (1985) 573-578
59. Martinez F.D., Antognoni G., Macri F., et al. Parental smoking enhances bronchial responsiveness in nine-year-old children. Am Rev Respir Dis 138 (1988) 518-523
60. Ronchetti R., Macri F., Ciofetta G., et al. Increased serum IgE and increased prevalence of eosinophilia in 9-year-old children of smoking parents. J Allergy Clin Immunol 86 (1990) 400-407
61. Cook D.G., Carey I.M., Whincup P.H., et al. Effect of fresh fruit consumption on lung function and wheeze in children. Thorax 52 (1997) 628-633
62. Peat J., van-den-Berg R., Green W., Mellis C., Leeder S., and Woolcock A. Changing prevalence of asthma in Australian school children. Br Med J 308 (1994) 1591-1596
63. Peat J.K., Mihrshahi S., Kemp A.S., et al. Three-year outcomes of dietary fatty acid modification and house dust mite reduction in the Childhood Asthma Prevention Study. J Allergy Clin Immunol 114 (2004) 807-813