Skip to main content
Immunology logoLink to Immunology
. 1985 Aug;55(4):621–628.

In vivo polyclonal stimulation of antibody secretion by two types of bacteria.

D Levitt, M A Bach
PMCID: PMC1453786  PMID: 3894223

Abstract

We previously proposed that one benefit of early polyclonal antibody secretion after bacterial infection might be the formation of antibodies protective against infection by a second pathogen. In order to analyse this possibility, the polyclonal and anti-phosphorylcholine (PC) plaque-forming cell (PFC) response induced by Staphylococcus aureus Cowan I (SA) was compared with the same responses stimulated by unencapsulated Streptococcus pneumonia strain R36a. S. aureus stimulated significant anti-PC PFCs, despite an inability to detect immunoassay-reactive PC on the surface of SA (present on R36a). The induction of these antibodies appeared very similar to the mechanism for producing polyclonal responses. R36a also stimulated both anti-PC and polyclonal PFCs, but by different means. In summary, our data suggest that each type of bacteria induces polyclonal and anti-PC responses through different mechanisms, and that the polyclonal antibody response stimulated by one group of bacteria can contain antibodies directed towards a second and different genus of bacteria.

Full text

PDF
621

Selected References

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

  1. Andersson J., Sjöberg O., Möller G. Induction of immunoglobulin and antibody synthesis in vitro by lipopolysaccharides. Eur J Immunol. 1972 Aug;2(4):349–353. doi: 10.1002/eji.1830020410. [DOI] [PubMed] [Google Scholar]
  2. Bach M. A., Beckmann E., Levitt D. Pneumococcal cell wall phosphorylcholine elicits polyclonal antibody secretion in mice. Eur J Immunol. 1984 Jul;14(7):589–594. doi: 10.1002/eji.1830140702. [DOI] [PubMed] [Google Scholar]
  3. Bach M. A., Kohler H., Levitt D. Binding of phosphorylcholine by non-immunoglobulin molecules on mouse B cells. J Immunol. 1983 Jul;131(1):365–369. [PubMed] [Google Scholar]
  4. Beckmann E., Bach M. A., Levitt D. Phosphorylcholine on isologous red blood cells induces polyclonal but not anti-phosphorylcholine plaque-forming cells in mice. Eur J Immunol. 1984 Jul;14(7):595–598. doi: 10.1002/eji.1830140703. [DOI] [PubMed] [Google Scholar]
  5. Beckmann E., Levitt D. In vitro plaque-forming cell responses induced by Streptococcus pneumoniae in humans. Scand J Immunol. 1984 Jan;19(1):1–10. doi: 10.1111/j.1365-3083.1984.tb00894.x. [DOI] [PubMed] [Google Scholar]
  6. Beckmann E., Levitt D. Phosphorylcholine on Streptococcus pneumoniae R36a is responsible for in vitro polyclonal antibody secretion by human peripheral blood lymphocytes. J Immunol. 1984 May;132(5):2174–2176. [PubMed] [Google Scholar]
  7. Briles D. E., Nahm M., Schroer K., Davie J., Baker P., Kearney J., Barletta R. Antiphosphocholine antibodies found in normal mouse serum are protective against intravenous infection with type 3 streptococcus pneumoniae. J Exp Med. 1981 Mar 1;153(3):694–705. doi: 10.1084/jem.153.3.694. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cosenza H., Köhler H. Specific inhibition of plaque formation to phosphorylcholine by antibody against antibody. Science. 1972 Jun 2;176(4038):1027–1029. doi: 10.1126/science.176.4038.1027. [DOI] [PubMed] [Google Scholar]
  9. Cosenza H., Quintáns J., Lefkovits I. Antibody response to phosphorylcholine in vitro. I. Studies on the frequency of precursor cells, average clone size and cellular cooperation. Eur J Immunol. 1975 May;5(5):343–349. doi: 10.1002/eji.1830050510. [DOI] [PubMed] [Google Scholar]
  10. Falkoff R. J., Zhu L. P., Fauci A. S. Separate signals for human B cell proliferation and differentiation in response to Staphylococcus aureus: evidence for a two-signal model of B cell activation. J Immunol. 1982 Jul;129(1):97–102. [PubMed] [Google Scholar]
  11. Gearhart P. J., Sigal N. H., Klinman N. R. Heterogeneity of the BALB/c antiphosphorylcholine antibody response at the precursor cell level. J Exp Med. 1975 Jan 1;141(1):56–71. doi: 10.1084/jem.141.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Ho P. L., Levitt D. A rapid method for quantitation of cell surface IgM by an enzyme-linked immunosorbent assay. J Immunol Methods. 1982;51(3):331–340. doi: 10.1016/0022-1759(82)90400-8. [DOI] [PubMed] [Google Scholar]
  13. Köhler H. The response to phosphorylcholine: dissecting an immune response. Transplant Rev. 1975;27:24–56. [PubMed] [Google Scholar]
  14. Mold C., Rodgers C. P., Kaplan R. L., Gewurz H. Binding of human C-reactive protein to bacteria. Infect Immun. 1982 Oct;38(1):392–395. doi: 10.1128/iai.38.1.392-395.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Poxton I. R., Tarelli E., Baddiley J. The structure of C-polysaccharide from the walls of Streptococcus pneumoniae. Biochem J. 1978 Dec 1;175(3):1033–1042. doi: 10.1042/bj1751033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Quintáns J., Kaplan R. B. Failure of CBA/N mice to respond to thymus-dependent and thymus-independent phosphorylcholine antigens. Cell Immunol. 1978 Jul;38(2):294–301. doi: 10.1016/0008-8749(78)90060-6. [DOI] [PubMed] [Google Scholar]
  17. Rittenberg M. B., Pratt K. L. Antitrinitrophenyl (TNP) plaque assay. Primary response of Balb/c mice to soluble and particulate immunogen. Proc Soc Exp Biol Med. 1969 Nov;132(2):575–581. doi: 10.3181/00379727-132-34264. [DOI] [PubMed] [Google Scholar]
  18. Romagnani S., Giudizi M. G., del Prete G., Maggi E., Biagiotti R., Almerigogna F., Ricci M. Demonstration on protein A of two distinct immunoglobulin-binding sites and their role in the mitogenic activity of Staphylococcus aureus Cowan I on human B cells. J Immunol. 1982 Aug;129(2):596–602. [PubMed] [Google Scholar]
  19. Tipple M. A., Beem M. O., Saxon E. M. Clinical characteristics of the afebrile pneumonia associated with Chlamydia trachomatis infection in infants less than 6 months of age. Pediatrics. 1979 Feb;63(2):192–197. [PubMed] [Google Scholar]
  20. Waldmann T. A., Broder S. Polyclonal B-cell activators in the study of the regulation of immunoglobulin synthesis in the human system. Adv Immunol. 1982;32:1–63. doi: 10.1016/s0065-2776(08)60720-8. [DOI] [PubMed] [Google Scholar]
  21. Yother J., Forman C., Gray B. M., Briles D. E. Protection of mice from infection with Streptococcus pneumoniae by anti-phosphocholine antibody. Infect Immun. 1982 Apr;36(1):184–188. doi: 10.1128/iai.36.1.184-188.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Immunology are provided here courtesy of British Society for Immunology

RESOURCES