Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1990 Sep;65(9):946–952. doi: 10.1136/adc.65.9.946

Latent sensitisation to respiratory syncytial virus during acute bronchiolitis and lung function after recovery.

S J Caswell 1, A H Thomson 1, S P Ashmore 1, C S Beardsmore 1, H Simpson 1
PMCID: PMC1792096  PMID: 2221967

Abstract

To determine whether latent sensitivity to respiratory syncytial virus antigen(s) occurs after infection, 27 infants with acute bronchiolitis were studied and compared with 15 hospital controls. Blood was collected for whole blood challenge, and histamine release was measured by a high performance liquid chromatography technique with fluorometric detection. There was a significantly greater histamine release to respiratory syncytial virus antigen(s) in those with bronchiolitis than in controls, expressed either in amount (median 154 nmol/l compared with 104 nmol/l) or percentage release (median 20% compared with 3%). There was a significant difference between index and control groups in terms of individual histamine responses. These findings strongly suggest that infants develop latent sensitivity to respiratory syncytial virus antigen(s) during the course of acute bronchiolitis. Serial lung function tests were performed in 15 infants. All infants had abnormalities of lung function at some stage, but the small numbers of subjects precluded comparison between 'sensitised' and 'non-sensitised' infants. Further study is indicated to define the relation of latent sensitisation and subsequent bronchial hyper-responsiveness after respiratory syncytial virus infection in infants.

Full text

PDF
946

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ashmore S. P., Thomson A. H., Simpson H. High-performance liquid chromatographic technique for the rapid determination of histamine in both the plasma and cellular components of blood. J Chromatogr. 1989 Nov 24;496(2):435–440. doi: 10.1016/s0378-4347(00)82592-x. [DOI] [PubMed] [Google Scholar]
  2. Hall C. B., Douglas R. G., Jr, Geiman J. M. Respiratory syncytial virus infections in infants: quantitation and duration of shedding. J Pediatr. 1976 Jul;89(1):11–15. doi: 10.1016/s0022-3476(76)80918-3. [DOI] [PubMed] [Google Scholar]
  3. Haydik I. B., Ma W. S. Basophil histamine release. Assays and interpretation. Clin Rev Allergy. 1988 Summer;6(2):141–162. [PubMed] [Google Scholar]
  4. Henry R. L., Milner A. D., Stokes G. M., Hodges I. G., Groggins R. C. Lung function after acute bronchiolitis. Arch Dis Child. 1983 Jan;58(1):60–63. doi: 10.1136/adc.58.1.60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Isaacs D., Bangham C. R., McMichael A. J. Cell-mediated cytotoxic response to respiratory syncytial virus in infants with bronchiolitis. Lancet. 1987 Oct 3;2(8562):769–771. doi: 10.1016/s0140-6736(87)92502-5. [DOI] [PubMed] [Google Scholar]
  6. Kocka F. E., Chittom A. L., Sanders L., Hernandez L., Soriano E., Jacobs N., Carey R. B. Nutritionally variant Streptococcus pyogenes from a periorbital abscess. J Clin Microbiol. 1987 Apr;25(4):736–737. doi: 10.1128/jcm.25.4.736-737.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lesouëf P. N., Geelhoed G. C., Turner D. J., Morgan S. E., Landau L. I. Response of normal infants to inhaled histamine. Am Rev Respir Dis. 1989 Jan;139(1):62–66. doi: 10.1164/ajrccm/139.1.62. [DOI] [PubMed] [Google Scholar]
  8. McLaughlan P., Coombs R. R. Latent anaphylactic sensitivity of infants to cow's milk proteins. Histamine release from blood basophils. Clin Allergy. 1983 Jan;13(1):1–9. doi: 10.1111/j.1365-2222.1983.tb02560.x. [DOI] [PubMed] [Google Scholar]
  9. Mok J. Y., Simpson H. Outcome of acute lower respiratory tract infection in infants: preliminary report of seven-year follow-up study. Br Med J (Clin Res Ed) 1982 Jul 31;285(6338):333–337. doi: 10.1136/bmj.285.6338.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Norrby E., Mufson M. A., Sheshberadaran H. Structural differences between subtype A and B strains of respiratory syncytial virus. J Gen Virol. 1986 Dec;67(Pt 12):2721–2729. doi: 10.1099/0022-1317-67-12-2721. [DOI] [PubMed] [Google Scholar]
  11. PARISH W. E., BARRETT A. M., COOMBS R. R., GUNTHER M., CAMPS F. E. Hypersensitivity to milk and sudden death in infancy. Lancet. 1960 Nov 19;2(7160):1106–1110. doi: 10.1016/s0140-6736(60)92187-5. [DOI] [PubMed] [Google Scholar]
  12. Prendiville A., Green S., Silverman M. Bronchial responsiveness to histamine in wheezy infants. Thorax. 1987 Feb;42(2):92–99. doi: 10.1136/thx.42.2.92. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pruzansky J. J., Patterson R. Histamine release from leukocytes of hypersensitive individuals. II. Reduced sensitivity of leukocytes after injection therapy. J Allergy. 1967 Jan;39(1):44–50. doi: 10.1016/0021-8707(67)90126-8. [DOI] [PubMed] [Google Scholar]
  14. Pullan C. R., Hey E. N. Wheezing, asthma, and pulmonary dysfunction 10 years after infection with respiratory syncytial virus in infancy. Br Med J (Clin Res Ed) 1982 Jun 5;284(6330):1665–1669. doi: 10.1136/bmj.284.6330.1665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Respiratory syncytial virus infection: admissions to hospital in industrial, urban, and rural areas. Report to the Medical Research Council Subcommittee on Respiratory Syncytial Virus Vaccines. Br Med J. 1978 Sep 16;2(6140):796–798. doi: 10.1136/bmj.2.6140.796. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Schulman E. S., MacGlashan D. W., Jr, Schleimer R. P., Peters S. P., Kagey-Sobotka A., Newball H. H., Lichtenstein L. M. Purified human basophils and mast cells: current concepts of mediator release. Eur J Respir Dis Suppl. 1983;128(Pt 1):53–61. [PubMed] [Google Scholar]
  17. Scott D. J., Gardner P. S., McQuillin J., Stanton A. N., Downham M. A. Respiratory viruses and cot death. Br Med J. 1978 Jul 1;2(6129):12–13. doi: 10.1136/bmj.2.6129.12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Scott R., Pullan C. R., Scott M., McQuillin J. Cell-mediated immunity in respiratory syncytial virus disease. J Med Virol. 1984;13(1):105–114. doi: 10.1002/jmv.1890130112. [DOI] [PubMed] [Google Scholar]
  19. Seidenberg J., Masters I. B., Hudson I., Olinsky A., Phelan P. D. Disturbance in respiratory mechanics in infants with bronchiolitis. Thorax. 1989 Aug;44(8):660–667. doi: 10.1136/thx.44.8.660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Silverman M., Prendiville A., Green S. Partial expiratory flow-volume curves in infancy: technical aspects. Bull Eur Physiopathol Respir. 1986 May-Jun;22(3):257–262. [PubMed] [Google Scholar]
  21. Taylor G., Stott E. J., Bew M., Fernie B. F., Cote P. J., Collins A. P., Hughes M., Jebbett J. Monoclonal antibodies protect against respiratory syncytial virus infection in mice. Immunology. 1984 May;52(1):137–142. [PMC free article] [PubMed] [Google Scholar]
  22. Toms G. L., Scott R. Respiratory syncytial virus and the infant immune response. Arch Dis Child. 1987 Jun;62(6):544–546. doi: 10.1136/adc.62.6.544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Welliver R. C., Kaul T. N., Ogra P. L. The appearance of cell-bound IgE in respiratory-tract epithelium after respiratory-syncytial-virus infection. N Engl J Med. 1980 Nov 20;303(21):1198–1202. doi: 10.1056/NEJM198011203032103. [DOI] [PubMed] [Google Scholar]
  24. Welliver R. C., Kaul T. N., Sun M., Ogra P. L. Defective regulation of immune responses in respiratory syncytial virus infection. J Immunol. 1984 Oct;133(4):1925–1930. [PubMed] [Google Scholar]
  25. Welliver R. C., Wong D. T., Sun M., Middleton E., Jr, Vaughan R. S., Ogra P. L. The development of respiratory syncytial virus-specific IgE and the release of histamine in nasopharyngeal secretions after infection. N Engl J Med. 1981 Oct 8;305(15):841–846. doi: 10.1056/NEJM198110083051501. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES