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Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1993 Jan;91(1):54–57. doi: 10.1111/j.1365-2249.1993.tb03353.x

Relationship of in vitro phagocytosis of serotype 14 Streptococcus pneumoniae to specific class and IgG subclass antibody levels in healthy adults.

J E Lortan 1, A S Kaniuk 1, M A Monteil 1
PMCID: PMC1554633  PMID: 8419085

Abstract

The role of specific IgG2 antibody in the protection against serious infection with Streptococcus pneumoniae is unclear. We therefore decided to investigate the relationship between serum antibody levels and opsonization and phagocytosis of this microorganism. We have measured serum IgM, IgA and IgG subclass antibody specific for pneumococcal capsular polysaccharide and in vitro phagocytosis of serotype 14 pneumococcus by polymorphs, in healthy adults before and after immunization with Pneumovax II. IgM and IgG2 were the predominant anti-pneumococcal antibodies seen, IgA and IgG1 being present at low titre. No significant relationship of phagocytosis with specific IgM and IgA antibodies was found. However, both specific IgG1 and IgG2 antibodies in post-immunization sera correlated significantly with phagocytosis of the pneumococcus in the presence of complement (r = 0.57, P = 0.029 and r = 0.59, P = 0.022 respectively). After heat-inactivation, the remaining opsonic activity of sera correlated only with levels of specific IgG2 antibody (r = 0.61, P = 0.0006). Whereas phagocytosis supported by specific IgG1 and IgG2 antibody to serotype 14 pneumococcus after immunization is mediated by complement activation, IgG2-specific antibody in high titre may also be able to function by complement-independent interaction with Fc gamma receptors on polymorphs.

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Selected References

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  1. Albrechtsen M., Yeaman G. R., Kerr M. A. Characterization of the IgA receptor from human polymorphonuclear leucocytes. Immunology. 1988 Jun;64(2):201–205. [PMC free article] [PubMed] [Google Scholar]
  2. Bardardottir E., Jonsson S., Jonsdottir I., Sigfusson A., Valdimarsson H. IgG subclass response and opsonization of Streptococcus pneumoniae after vaccination of healthy adults. J Infect Dis. 1990 Aug;162(2):482–488. doi: 10.1093/infdis/162.2.482. [DOI] [PubMed] [Google Scholar]
  3. Barrett D. J., Ayoub E. M. IgG2 subclass restriction of antibody to pneumococcal polysaccharides. Clin Exp Immunol. 1986 Jan;63(1):127–134. [PMC free article] [PubMed] [Google Scholar]
  4. Bjornson A. B., Lobel J. S. Direct evidence that decreased serum opsonization of Streptococcus pneumoniae via the alternative complement pathway in sickle cell disease is related to antibody deficiency. J Clin Invest. 1987 Feb;79(2):388–398. doi: 10.1172/JCI112824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bruyn G. A., Zegers B. J., van Furth R. Mechanisms of host defense against infection with Streptococcus pneumoniae. Clin Infect Dis. 1992 Jan;14(1):251–262. doi: 10.1093/clinids/14.1.251. [DOI] [PubMed] [Google Scholar]
  6. Chudwin D. S., Artrip S. G., Korenblit A., Schiffman G., Rao S. Correlation of serum opsonins with in vitro phagocytosis of Streptococcus pneumoniae. Infect Immun. 1985 Oct;50(1):213–217. doi: 10.1128/iai.50.1.213-217.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chudwin D. S., Artrip S. G., Schiffman G. Immunoglobulin G class and subclass antibodies to pneumococcal capsular polysaccharides. Clin Immunol Immunopathol. 1987 Jul;44(1):114–121. doi: 10.1016/0090-1229(87)90057-2. [DOI] [PubMed] [Google Scholar]
  8. Giebink G. S., Verhoef J., Peterson P. K., Quie P. G. Opsonic requirements for phagocytosis of Streptococcus pneumoniae types VI, XVIII, XXIII, and XXV. Infect Immun. 1977 Nov;18(2):291–297. doi: 10.1128/iai.18.2.291-297.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jefferis R., Kumararatne D. S. Selective IgG subclass deficiency: quantification and clinical relevance. Clin Exp Immunol. 1990 Sep;81(3):357–367. doi: 10.1111/j.1365-2249.1990.tb05339.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lawrence E. M., Edwards K. M., Schiffman G., Thompson J. M., Vaughn W. K., Wright P. F. Pneumococcal vaccine in normal children. Primary and secondary vaccination. Am J Dis Child. 1983 Sep;137(9):846–850. doi: 10.1001/archpedi.1983.02140350024007. [DOI] [PubMed] [Google Scholar]
  11. Lortan J. E., Vellodi A., Jurges E. S., Hugh-Jones K. Class- and subclass-specific pneumococcal antibody levels and response to immunization after bone marrow transplantation. Clin Exp Immunol. 1992 Jun;88(3):512–519. doi: 10.1111/j.1365-2249.1992.tb06480.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Lucisano Valim Y. M., Lachmann P. J. The effect of antibody isotype and antigenic epitope density on the complement-fixing activity of immune complexes: a systematic study using chimaeric anti-NIP antibodies with human Fc regions. Clin Exp Immunol. 1991 Apr;84(1):1–8. doi: 10.1111/j.1365-2249.1991.tb08115.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Musher D. M., Luchi M. J., Watson D. A., Hamilton R., Baughn R. E. Pneumococcal polysaccharide vaccine in young adults and older bronchitics: determination of IgG responses by ELISA and the effect of adsorption of serum with non-type-specific cell wall polysaccharide. J Infect Dis. 1990 Apr;161(4):728–735. doi: 10.1093/infdis/161.4.728. [DOI] [PubMed] [Google Scholar]
  14. Russell M. W., Lue C., van den Wall Bake A. W., Moldoveanu Z., Mestecky J. Molecular heterogeneity of human IgA antibodies during an immune response. Clin Exp Immunol. 1992 Jan;87(1):1–6. doi: 10.1111/j.1365-2249.1992.tb06404.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Winkelstein J. A., Shin H. S., Wood W. B., Jr Heat labile opsonins to Pneumococcus. 3. The participation of immunoglobulin and of the alternate pathway of C3 activation. J Immunol. 1972 Jun;108(6):1681–1689. [PubMed] [Google Scholar]

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