Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1989 Apr;57(4):1137–1141. doi: 10.1128/iai.57.4.1137-1141.1989

Adoptive transfer of gut mucosal antitoxin memory by isolated B cells 1 year after oral immunization with cholera toxin.

N Lycke 1, J Holmgren 1
PMCID: PMC313242  PMID: 2784416

Abstract

A protocol was elaborated for the adoptive transfer of lymphocytes from mice which were orally immunized with cholera toxin (CT) to enable the study of long-term gut mucosal immunological memory at the single-cell level. Mesenteric lymph node (MLN) cells were transferred 1 year after priming immunizations, and recipient animals were challenged perorally on days 1 and 2 with CT before sacrifice on day 6 to 7 following transfer of cells. Strong antitoxin ELISPOT spot-forming cell (SFC) responses were recorded in spleens, MLN, and laminae propriae (LP) of recipient mice. In contrast, no SFC were found in Peyer's patches. The magnitude of the response equaled that of the acute response seen after optimal oral CT immunization and was directly dependent on the number of transferred cells. The memory antitoxin response in MLN and LP required oral challenge with CT as opposed to the spleen SFC response, which could also be triggered by intravenous challenge with antigen. Spleen cells from mice immunized perorally with CT were as effective as MLN cells in transferring immunological memory detectable in the gut immune system. Irrespective of the tissue source of transferring immunological memory detectable in the gut immune system. Irrespective of the tissue source of the memory cells, the isotype distribution of the antitoxin SFC response in recipient mice was similar with predominantly immunoglobulin A (96%) in LP and immunoglobulin G (66%) in MLN and spleen. Transfer of antitoxic memory was completely abrogated by treatment of the cells with J11d monoclonal antibody and complement prior to their injection into recipient mice by was unaffected by treatment with anti-Thy-1.2 antibody and complement, suggesting that long-term gut mucosal memory is carried by B cells. Antitoxin B memory cells might help explain the long-term protection against recurrent disease seen in convalescents from cholera in cholera-endemic areas.

Full text

PDF
1137

Selected References

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

  1. Bienenstock J., Befus A. D. Mucosal immunology. Immunology. 1980 Oct;41(2):249–270. [PMC free article] [PubMed] [Google Scholar]
  2. Brooks K. H., Feldbush T. L. In vitro antigen-mediated clonal expansion of memory B lymphocytes. J Immunol. 1981 Sep;127(3):959–963. [PubMed] [Google Scholar]
  3. Brooks K. H., Feldbush T. L., van der Hoven A. The generation of memory B-cell subpopulations capable of proliferation and expansion of the pool: effect of time and antigen. Cell Immunol. 1980 Mar 15;50(2):392–404. doi: 10.1016/0008-8749(80)90293-2. [DOI] [PubMed] [Google Scholar]
  4. Bruce J., Symington F. W., McKearn T. J., Sprent J. A monoclonal antibody discriminating between subsets of T and B cells. J Immunol. 1981 Dec;127(6):2496–2501. [PubMed] [Google Scholar]
  5. Craig S. W., Cebra J. J. Peyer's patches: an enriched source of precursors for IgA-producing immunocytes in the rabbit. J Exp Med. 1971 Jul 1;134(1):188–200. doi: 10.1084/jem.134.1.188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Czerkinsky C. C., Nilsson L. A., Nygren H., Ouchterlony O., Tarkowski A. A solid-phase enzyme-linked immunospot (ELISPOT) assay for enumeration of specific antibody-secreting cells. J Immunol Methods. 1983 Dec 16;65(1-2):109–121. doi: 10.1016/0022-1759(83)90308-3. [DOI] [PubMed] [Google Scholar]
  7. Czinn S. J., Lamm M. E. Selective chemotaxis of subsets of B lymphocytes from gut-associated lymphoid tissue and its implications for the recruitment of mucosal plasma cells. J Immunol. 1986 May 15;136(10):3607–3611. [PubMed] [Google Scholar]
  8. Feldbrush T. L., Stewart N. Antigen modulation of the immune response. V. Generation of large memory cells in antigen draining lymph nodes. Cell Immunol. 1978 May;37(2):336–348. doi: 10.1016/0008-8749(78)90202-2. [DOI] [PubMed] [Google Scholar]
  9. Gearhart P. J., Cebra J. J. Differentiated B lymphocytes. Potential to express particular antibody variable and constant regions depends on site of lymphoid tissue and antigen load. J Exp Med. 1979 Jan 1;149(1):216–227. doi: 10.1084/jem.149.1.216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Glass R. I., Becker S., Huq M. I., Stoll B. J., Khan M. U., Merson M. H., Lee J. V., Black R. E. Endemic cholera in rural Bangladesh, 1966-1980. Am J Epidemiol. 1982 Dec;116(6):959–970. doi: 10.1093/oxfordjournals.aje.a113498. [DOI] [PubMed] [Google Scholar]
  11. Husband A. J., Gowans J. L. The origin and antigen-dependent distribution of IgA-containing cells in the intestine. J Exp Med. 1978 Nov 1;148(5):1146–1160. doi: 10.1084/jem.148.5.1146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Jalkanen S., Streeter P., Lakey E., Bargatze R., Butcher E. C. Lymphocyte and endothelial cell recognition elements that control lymphocyte traffic to mucosa-associated lymphatic tissues. Monogr Allergy. 1988;24:144–149. [PubMed] [Google Scholar]
  13. Jertborn M., Svennerholm A. M., Holmgren J. Five-year immunologic memory in Swedish volunteers after oral cholera vaccination. J Infect Dis. 1988 Feb;157(2):374–377. doi: 10.1093/infdis/157.2.374. [DOI] [PubMed] [Google Scholar]
  14. Kawanishi H., Saltzman L. E., Strober W. Mechanisms regulating IgA class-specific immunoglobulin production in murine gut-associated lymphoid tissues. I. T cells derived from Peyer's patches that switch sIgM B cells to sIgA B cells in vitro. J Exp Med. 1983 Feb 1;157(2):433–450. doi: 10.1084/jem.157.2.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kiyono H., Mosteller-Barnum L. M., Pitts A. M., Williamson S. I., Michalek S. M., McGhee J. R. Isotype-specific immunoregulation. IgA-binding factors produced by Fc alpha receptor-positive T cell hybridomas regulate IgA responses. J Exp Med. 1985 Apr 1;161(4):731–747. doi: 10.1084/jem.161.4.731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lebman D. A., Griffin P. M., Cebra J. J. Relationship between expression of IgA by Peyer's patch cells and functional IgA memory cells. J Exp Med. 1987 Nov 1;166(5):1405–1418. doi: 10.1084/jem.166.5.1405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Levine M. M., Black R. E., Clements M. L., Cisneros L., Nalin D. R., Young C. R. Duration of infection-derived immunity to cholera. J Infect Dis. 1981 Jun;143(6):818–820. doi: 10.1093/infdis/143.6.818. [DOI] [PubMed] [Google Scholar]
  18. Lycke N. A sensitive method for the detection of specific antibody production in different isotypes from single lamina propria plasma cells. Scand J Immunol. 1986 Oct;24(4):393–403. doi: 10.1111/j.1365-3083.1986.tb02127.x. [DOI] [PubMed] [Google Scholar]
  19. Lycke N., Hellström U., Holmgren J. Circulating cholera antitoxin memory cells in the blood one year after oral cholera vaccination in humans. Scand J Immunol. 1987 Aug;26(2):207–211. doi: 10.1111/j.1365-3083.1987.tb02253.x. [DOI] [PubMed] [Google Scholar]
  20. Lycke N., Holmgren J. Intestinal mucosal memory and presence of memory cells in lamina propria and Peyer's patches in mice 2 years after oral immunization with cholera toxin. Scand J Immunol. 1986 May;23(5):611–616. doi: 10.1111/j.1365-3083.1986.tb01995.x. [DOI] [PubMed] [Google Scholar]
  21. Lycke N., Holmgren J. Long-term cholera antitoxin memory in the gut can be triggered to antibody formation associated with protection within hours of an oral challenge immunization. Scand J Immunol. 1987 Apr;25(4):407–412. doi: 10.1111/j.1365-3083.1987.tb02207.x. [DOI] [PubMed] [Google Scholar]
  22. Lycke N., Holmgren J. Strong adjuvant properties of cholera toxin on gut mucosal immune responses to orally presented antigens. Immunology. 1986 Oct;59(2):301–308. [PMC free article] [PubMed] [Google Scholar]
  23. Lycke N., Lindholm L., Holmgren J. Cholera antibody production in vitro by peripheral blood lymphocytes following oral immunization of humans and mice. Clin Exp Immunol. 1985 Oct;62(1):39–47. [PMC free article] [PubMed] [Google Scholar]
  24. McDermott M. R., Horsewood P., Clark D. A., Bienenstock J. T lymphocytes in the intestinal epithelium and lamina propria of mice. Immunology. 1986 Feb;57(2):213–218. [PMC free article] [PubMed] [Google Scholar]
  25. Pierce N. F., Cray W. C., Jr Determinants of the localization, magnitude, and duration of a specific mucosal IgA plasma cell response in enterically immunized rats. J Immunol. 1982 Mar;128(3):1311–1315. [PubMed] [Google Scholar]
  26. Pierce N. F., Gowans J. L. Cellular kinetics of the intestinal immune response to cholera toxoid in rats. J Exp Med. 1975 Dec 1;142(6):1550–1563. doi: 10.1084/jem.142.6.1550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Smith M. E., Ford W. L. The recirculating lymphocyte pool of the rat: a systematic description of the migratory behaviour of recirculating lymphocytes. Immunology. 1983 May;49(1):83–94. [PMC free article] [PubMed] [Google Scholar]
  28. Svennerholm A. M., Gothefors L., Sack D. A., Bardhan P. K., Holmgren J. Local and systemic antibody responses and immunological memory in humans after immunization with cholera B subunit by different routes. Bull World Health Organ. 1984;62(6):909–918. [PMC free article] [PubMed] [Google Scholar]
  29. Svennerholm A. M., Jertborn M., Gothefors L., Karim A. M., Sack D. A., Holmgren J. Mucosal antitoxic and antibacterial immunity after cholera disease and after immunization with a combined B subunit-whole cell vaccine. J Infect Dis. 1984 Jun;149(6):884–893. doi: 10.1093/infdis/149.6.884. [DOI] [PubMed] [Google Scholar]
  30. Woodward W. E. Cholera reinfection in man. J Infect Dis. 1971 Jan;123(1):61–66. doi: 10.1093/infdis/123.1.61. [DOI] [PubMed] [Google Scholar]
  31. Yefenof E., Sanders V. M., Snow E. C., Noelle R. J., Oliver K. G., Uhr J. W., Vitetta E. S. Preparation and analysis of antigen-specific memory B cells. J Immunol. 1985 Dec;135(6):3777–3784. [PubMed] [Google Scholar]
  32. Yefenof E., Sanders V. M., Uhr J. W., Vitetta E. S. In vitro activation of murine antigen-specific memory B cells by a T-dependent antigen. J Immunol. 1986 Jul 1;137(1):85–90. [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES