Skip to main content
Immunology logoLink to Immunology
. 1987 Jun;61(2):179–183.

Experimental studies of immunologically mediated enteropathy. II. Role of natural killer cells in the intestinal phase of murine graft-versus-host reaction.

A M Mowat, M V Felstein
PMCID: PMC1453377  PMID: 3596637

Abstract

This study has investigated whether natural killer (NK) cells play a protective or an effector role in unirradiated mice with graft-versus-host reaction (GvHR). Treatment of (CBA X BALB/c)F1 mice with anti-asialo GM1 (ASGM1) antibody produced a profound depletion of resting NK-cell activity and also inhibited the normal enhancement of NK activity found after induction of a GvHR with CBA spleen cells. Compared with normal hosts, mice treated with anti-AsGM1 developed less splenomegaly in GvHR and did not show the crypt hyperplasia normally found in this model of GvHR. Anti-AsGM1 also produced a small but significant reduction of intraepithelial lymphocyte (IEL) numbers in the jejunum of control mice. We conclude that intestinal NK cells are an essential component of the local delayed-type hypersensitivity (DTH) reaction which is responsible for the intestinal phase of GvHR in unirradiated mice.

Full text

PDF
179

Selected References

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

  1. Benner R., Wolters E. A., Bril H., Molendijk A., van Oudenaren A. Regulation of delayed type hypersensitivity to host histocompatibility antigens during graft-versus-host reactions. Immunol Rev. 1985 Dec;88:25–57. doi: 10.1111/j.1600-065x.1985.tb01152.x. [DOI] [PubMed] [Google Scholar]
  2. Borland A., Mowat A. M., Parrott D. M. Augmentation of intestinal and peripheral natural killer cell activity during the graft-versus-host reaction in mice. Transplantation. 1983 Nov;36(5):513–519. doi: 10.1097/00007890-198311000-00009. [DOI] [PubMed] [Google Scholar]
  3. Carman P. S., Ernst P. B., Rosenthal K. L., Clark D. A., Befus A. D., Bienenstock J. Intraepithelial leukocytes contain a unique subpopulation of NK-like cytotoxic cells active in the defense of gut epithelium to enteric murine coronavirus. J Immunol. 1986 Mar 1;136(5):1548–1553. [PubMed] [Google Scholar]
  4. Charley M. R., Mikhael A., Bennett M., Gilliam J. N., Sontheimer R. D. Prevention of lethal, minor-determinate graft-host disease in mice by the in vivo administration of anti-asialo GM1. J Immunol. 1983 Nov;131(5):2101–2103. [PubMed] [Google Scholar]
  5. Dennert G., Anderson C. G., Warner J. T killer cells play a role in allogeneic bone marrow graft rejection but not in hybrid resistance. J Immunol. 1985 Dec;135(6):3729–3734. [PubMed] [Google Scholar]
  6. Dillon S. B., MacDonald T. T. Functional characterization of Con A-responsive Lyt2-positive mouse small intestinal intraepithelial lymphocytes. Immunology. 1986 Nov;59(3):389–396. [PMC free article] [PubMed] [Google Scholar]
  7. Elson C. O., Reilly R. W., Rosenberg I. H. Small intestinal injury in the graft versus host reaction: an innocent bystander phenomenon. Gastroenterology. 1977 May;72(5 Pt 1):886–889. [PubMed] [Google Scholar]
  8. Habu S., Fukui H., Shimamura K., Kasai M., Nagai Y., Okumura K., Tamaoki N. In vivo effects of anti-asialo GM1. I. Reduction of NK activity and enhancement of transplanted tumor growth in nude mice. J Immunol. 1981 Jul;127(1):34–38. [PubMed] [Google Scholar]
  9. Hackett J., Jr, Tutt M., Lipscomb M., Bennett M., Koo G., Kumar V. Origin and differentiation of natural killer cells. II. Functional and morphologic studies of purified NK-1.1+ cells. J Immunol. 1986 Apr 15;136(8):3124–3131. [PubMed] [Google Scholar]
  10. Handa K., Suzuki R., Matsui H., Shimizu Y., Kumagai K. Natural killer (NK) cells as a responder to interleukin 2 (IL 2). II. IL 2-induced interferon gamma production. J Immunol. 1983 Feb;130(2):988–992. [PubMed] [Google Scholar]
  11. Kasahara T., Djeu J. Y., Dougherty S. F., Oppenheim J. J. Capacity of human large granular lymphocytes (LGL) to produce multiple lymphokines: interleukin 2, interferon, and colony stimulating factor. J Immunol. 1983 Nov;131(5):2379–2385. [PubMed] [Google Scholar]
  12. Kasai M., Iwamori M., Nagai Y., Okumura K., Tada T. A glycolipid on the surface of mouse natural killer cells. Eur J Immunol. 1980 Mar;10(3):175–180. doi: 10.1002/eji.1830100304. [DOI] [PubMed] [Google Scholar]
  13. Kiessling R., Hochman P. S., Haller O., Shearer G. M., Wigzell H., Cudkowicz G. Evidence for a similar or common mechanism for natural killer cell activity and resistance to hemopoietic grafts. Eur J Immunol. 1977 Sep;7(9):655–663. doi: 10.1002/eji.1830070915. [DOI] [PubMed] [Google Scholar]
  14. Korngold R., Sprent J. Surface markers of T cells causing lethal graft-vs-host disease to class I vs class II H-2 differences. J Immunol. 1985 Nov;135(5):3004–3010. [PubMed] [Google Scholar]
  15. Kubota E., Ishikawa H., Saito K. Modulation of F1 cytotoxic potentials by GvHR. Host- and donor-derived cytotoxic lymphocytes arise in the unirradiated F1 host spleens under the condition of GvHR-associated immunosuppression. J Immunol. 1983 Sep;131(3):1142–1148. [PubMed] [Google Scholar]
  16. Like A. A., Biron C. A., Weringer E. J., Byman K., Sroczynski E., Guberski D. L. Prevention of diabetes in BioBreeding/Worcester rats with monoclonal antibodies that recognize T lymphocytes or natural killer cells. J Exp Med. 1986 Oct 1;164(4):1145–1159. doi: 10.1084/jem.164.4.1145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mowat A. M., Borland A., Parrott D. M. Augmentation of natural killer cell activity by anti-host delayed-type hypersensitivity during the graft-versus-host reaction in mice. Scand J Immunol. 1985 Oct;22(4):389–399. doi: 10.1111/j.1365-3083.1985.tb01897.x. [DOI] [PubMed] [Google Scholar]
  18. Mowat A. M., Borland A., Parrott D. M. Hypersensitivity reactions in the small intestine. VII. Induction of the intestinal phase of murine graft-versus-host-reaction by Lyt 2- T cells activated by I-A alloantigens. Transplantation. 1986 Feb;41(2):192–198. [PubMed] [Google Scholar]
  19. Mowat A. M., Ferguson A. Hypersensitivity reactions in the small intestine. 6. Pathogenesis of the graft-versus-host reaction in the small intestinal mucosa of the mouse. Transplantation. 1981 Sep;32(3):238–243. doi: 10.1097/00007890-198109000-00011. [DOI] [PubMed] [Google Scholar]
  20. Mowat A. M., Ferguson A. Intraepithelial lymphocyte count and crypt hyperplasia measure the mucosal component of the graft-versus-host reaction in mouse small intestine. Gastroenterology. 1982 Aug;83(2):417–423. [PubMed] [Google Scholar]
  21. Nakano T., Imai Y., Naiki M., Osawa T. Characterization of mouse helper and suppressor T cell subsets separated by lectins. J Immunol. 1980 Nov;125(5):1928–1932. [PubMed] [Google Scholar]
  22. Nemlander A., Saksela E., Häyry P. Are "natural killer" cells involved in allograft rejection? Eur J Immunol. 1983 Apr;13(4):348–350. doi: 10.1002/eji.1830130415. [DOI] [PubMed] [Google Scholar]
  23. Roy C., Ghayur T., Kongshavn P. A., Lapp W. S. Natural killer activity by spleen, lymph node, and thymus cells during the graft-versus-host reaction. Transplantation. 1982 Sep;34(3):144–146. doi: 10.1097/00007890-198209000-00006. [DOI] [PubMed] [Google Scholar]
  24. Shields J. G., Parrott D. M. Appearance of delayed-type hypersensitivity effector cells in murine gut mucosa. Immunology. 1985 Apr;54(4):771–776. [PMC free article] [PubMed] [Google Scholar]
  25. Stein K. E., Schwarting G. A., Marcus D. M. Glycolipid markers of murine lymphocyte subpopulations. J Immunol. 1978 Feb;120(2):676–679. [PubMed] [Google Scholar]
  26. Stitz L., Baenziger J., Pircher H., Hengartner H., Zinkernagel R. M. Effect of rabbit anti-asialo GM1 treatment in vivo or with anti-asialo GM1 plus complement in vitro on cytotoxic T cell activities. J Immunol. 1986 Jun 15;136(12):4674–4680. [PubMed] [Google Scholar]
  27. Suttles J., Schwarting G. A., Stout R. D. Flow cytometric analysis reveals the presence of asialo GM1 on the surface membrane of alloimmune cytotoxic T lymphocytes. J Immunol. 1986 Mar 1;136(5):1586–1591. [PubMed] [Google Scholar]
  28. Wilson A. D., Stokes C. R., Bourne F. J. Morphology and functional characteristics of isolated porcine intraepithelial lymphocytes. Immunology. 1986 Sep;59(1):109–113. [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES