Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1969 Jan 31;129(2):371–391. doi: 10.1084/jem.129.2.371

A NEW METHOD FOR THE ENUMERATION OF ANTIGEN-REACTIVE CELLS RESPONSIVE TO A PURIFIED PROTEIN ANTIGEN

W D Armstrong 1, E Diener 1
PMCID: PMC2138602  PMID: 5762049

Abstract

A new technique for the enumeration of antigen-reactive cells (ARC) responsive to the polymer antigen of S. adelaide flagellin (POL) is described for two strains of mice. Foci have been shown to be antibody dependent, may be mimicked by IgM as well as IgG antibodies, and contain specific antibody-forming cells (AFC). The use of POL offers a system unencumbered by relatively high numbers of background foci which, when present, appear to be basically different from those found using the SRBC antigen. The response of 1 antigen-reactive cell (ARC) focus/1 x 106 CBAT6T6 mouse spleen cells is linearly related to the injected number between 1 x 106–3 x 106 donor spleen cells and since 5% of injected cells remain in the spleen, there are an estimated 2400 ARC/spleen. The number of ARC foci does not increase significantly after the 5th postantigen day, and by the 8th day the AFC progeny of ARC have reached the maximum mean of 280 AFC/ARC focus. In response to increasing antigen concentrations, an initial rise in the number of AFC as well as ARC is observed, resulting in a relatively constant AFC/ARC ratio. This suggests that the number of ARC stimulated determines the total number of AFC produced under these conditions rather than a variable mitotic rate of the ARC offspring. The main significance of this technique is that it will allow a study of the kinetics of the ARC in the primary and secondary immune response as well as in immunological tolerance.

Full Text

The Full Text of this article is available as a PDF (1.1 MB).

Selected References

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

  1. ADA G. L., NOSSAL G. J., PYE J., ABBOT A. ANTIGENS IN IMMUNITY. I. PREPARATION AND PROPERTIES OF FLAGELLAR ANTIGENS FROM SALMONELLA ADELAIDE. Aust J Exp Biol Med Sci. 1964 Jun;42:267–282. [PubMed] [Google Scholar]
  2. Cheng V., Trentin J. J. Enteric bacteria as a possible cause of hemolytic antibody-forming cells in normal mouse spleens. Proc Soc Exp Biol Med. 1967 Nov;126(2):467–470. doi: 10.3181/00379727-126-32479. [DOI] [PubMed] [Google Scholar]
  3. Claman H. N., Chaperon E. A., Triplett R. F. Thymus-marrow cell combinations. Synergism in antibody production. Proc Soc Exp Biol Med. 1966 Aug-Sep;122(4):1167–1171. doi: 10.3181/00379727-122-31353. [DOI] [PubMed] [Google Scholar]
  4. Diener E. A new method for the enumeration of single antibody-producing cells. J Immunol. 1968 May;100(5):1062–1070. [PubMed] [Google Scholar]
  5. HELMREICH E., KERN M., EISEN H. N. The secretion of antibody by isolated lymph node cells. J Biol Chem. 1961 Feb;236:464–473. [PubMed] [Google Scholar]
  6. Kennedy J. C., Siminovitch L., Till J. E., McCulloch E. A. A transplantation assay for mouse cells responsive to antigenic stimulation by sheep erythrocytes. Proc Soc Exp Biol Med. 1965 Dec;120(3):868–873. doi: 10.3181/00379727-120-30678. [DOI] [PubMed] [Google Scholar]
  7. Kennedy J. C., Till J. E., Siminovitch L., McCulloch E. A. The proliferative capacity of antigen-sensitive precursors of hemolytic plaque-forming cells. J Immunol. 1966 Jun;96(6):973–980. [PubMed] [Google Scholar]
  8. Kind P., Campbell P. A. Differentiation of antibody-forming cells. I. Ratio of precursor cells to antibody-forming cells in the mouse spleen. J Immunol. 1968 Jan;100(1):55–60. [PubMed] [Google Scholar]
  9. Lang P. G., Ada G. L. Antigen in tissues. IV. The effect of antibody on the retention and localization of antigen in rat lymph nodes. Immunology. 1967 Nov;13(5):523–534. [PMC free article] [PubMed] [Google Scholar]
  10. MCILWAIN H., BUDDLE H. L. Techniques in tissue metabolism. I. A mechanical chopper. Biochem J. 1953 Feb;53(3):412–420. doi: 10.1042/bj0530412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. NOSSAL G. J. Antibody production by single cells. Br J Exp Pathol. 1958 Oct;39(5):544–551. [PMC free article] [PubMed] [Google Scholar]
  12. NOSSAL G. J. Studies on the transfer of antibody-producing capacity. I. The transfer of antibody-producing cells to young animals. Immunology. 1959 Apr;2(2):137–147. [PMC free article] [PubMed] [Google Scholar]
  13. Playfair J. H., Papermaster B. W., Cole L. J. Focal antibody production by transferred spleen cells in irradiated mice. Science. 1965 Aug 27;149(3687):998–1000. doi: 10.1126/science.149.3687.998. [DOI] [PubMed] [Google Scholar]
  14. Sercarz E. E., Byers V. S. The X-Y-Z scheme of immunocyte maturation. 3. Early IgM memory and the nature of the memory cell. J Immunol. 1967 Apr;98(4):836–843. [PubMed] [Google Scholar]
  15. Wortis H. H., Taylor R. B., Dresser D. W. Antibody production studied by means of the LHG assay. I. The splenic response of CBA mice to sheep erythrocytes. Immunology. 1966 Dec;11(6):603–616. [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES