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. 1979 Feb;23(2):276–281. doi: 10.1128/iai.23.2.276-281.1979

Cell-free and cell-bound antibody in nasal secretions from infants with respiratory syncytial virus infection.

K McIntosh, J McQuillin, P S Gardner
PMCID: PMC414160  PMID: 422241

Abstract

Twenty-two infants under 9 months of age hospitalized with bronchiolitis or pneumonia due to respiratory syncytial virus (RSV) were serially sampled to determine the pattern of secretory antibody response. Using double labeling techniques, we found several types of immunoglobulin in secretions: cell-free antibody to RSV of the immunoglobulin A (IgA), immunoglobulin G (IgG), and immunoglobulin M (IgM) classes; and immunoglobulins of all three classes bound to RSV-infected cells shed from the nasal epithelium (presumably cell-bound antibody to RSV). IgA attached to RSV-infected epithelial cells was almost always detected in the first available nasal sample (day 1 or 2 of hospitalization). In contrast, cell-free anti-RSV IgA first appeared an average of 3.5 days later at a time when virus antigen was disappearing from the secretion. IgG and IgM attached to RSV-infected cells appeared more irregularly. The titer of cell-free anti-RSV IgM was often higher than that of IgA early in the illness and declined as the infection resolved. Cell-free anti-RSV IgG was usually present earlier than IgA and rose during convalescence.

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Selected References

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

  1. Dowdle W. R., Downie J. C., Laver W. G. Inhibition of virus release by antibodies to surface antigens of influenza viruses. J Virol. 1974 Feb;13(2):269–275. doi: 10.1128/jvi.13.2.269-275.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Gardner P. S., McQuillin J., Court S. D. Speculation on pathogenesis in death from respiratory syncytial virus infection. Br Med J. 1970 Feb 7;1(5692):327–330. doi: 10.1136/bmj.1.5692.327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gardner P. S., McQuillin J. The coating of respiratory syncytial (RS) virus-infected cells in the respiratory tract by immunoglobulins. J Med Virol. 1978;2(2):165–173. doi: 10.1002/jmv.1890020211. [DOI] [PubMed] [Google Scholar]
  4. Kim H. W., Bellanti J. A., Arrobio J. O., Mills J., Brandt C. D., Chanock R. M., Parrott R. H. Respiratory syncytial virus neutralizing activity in nasal secretions following natural infection. Proc Soc Exp Biol Med. 1969 Jun;131(2):658–661. doi: 10.3181/00379727-131-33946. [DOI] [PubMed] [Google Scholar]
  5. McIntosh K., Masters H. B., Orr I., Chao R. K., Barkin R. M. The immunologic response to infection with respiratory syncytial virus in infants. J Infect Dis. 1978 Jul;138(1):24–32. doi: 10.1093/infdis/138.1.24. [DOI] [PubMed] [Google Scholar]
  6. Mills J., 5th, Van Kirk J. E., Wright P. F., Chanock R. M. Experimental respiratory syncytial virus infection of adults. Possible mechanisms of resistance to infection and illness. J Immunol. 1971 Jul;107(1):123–130. [PubMed] [Google Scholar]
  7. Scott R., De Landazuri M. O., Gardner P. S., Owen J. J. Detection of antibody to respiratory syncytial virus by membrane fluorescence. Clin Exp Immunol. 1976 Oct;26(1):78–85. [PMC free article] [PubMed] [Google Scholar]
  8. Scott R., Gardner P. S. Respiratory syncytial virus neutralizing activity in nasopharyngeal secretions. J Hyg (Lond) 1970 Dec;68(4):581–588. doi: 10.1017/s0022172400042510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Scott R., Gardner P. S. The local antibody response to R.S. virus infection in the respiratory tract. J Hyg (Lond) 1974 Feb;72(1):111–120. doi: 10.1017/s0022172400023275. [DOI] [PMC free article] [PubMed] [Google Scholar]

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