Abstract
Graft-versus-host disease (GVHD) was induced in (CBA X C57BL/6) F1 mice by i.v. injection of 50 X 10(6) parental spleen cells. The GVHD induced an enhanced NK (anti-YAC-1) cytotoxicity during the first 2 weeks after the spleen cell transfusion. This cytotoxic activity was shown to be mediated by asialo GM1-positive, partially Thy-1-positive and nylon-wool (NW) non-adherent cells, thus being classical NK cells. Depletion of NK-cell activity from donor and/or recipient mice with anti-asialo GM1 antibody prior to the spleen cell transfer did not prevent the GVHD as judged by the splenomegaly assay. Also, when NK activity was potentiated with polyinosinic-polycytidylic acid (pIC), no effect on the GVHD was seen. These data suggest that NK cells are not crucial for the development of GVHD in this model.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bainbridge D. R. Elimination of allogeneic lymphocytes by mice. Immunol Rev. 1983;73:5–34. doi: 10.1111/j.1600-065x.1983.tb01076.x. [DOI] [PubMed] [Google Scholar]
- Beck B. N., Gillis S., Henney C. S. Display of the neutral glycolipid ganglio-n-tetraosylceramide (asialo GM1) on cells of the natural killer and T lineages. Transplantation. 1982 Feb;33(2):118–122. doi: 10.1097/00007890-198202000-00003. [DOI] [PubMed] [Google Scholar]
- 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]
- Filipovich A. H., McGlave P. B., Ramsay N. K., Goldstein G., Warkentin P. I., Kesey J. H. Pretreatment of donor bone marrow with monoclonal antibody OKT3 for prevention of acute graft-versus-host disease in allogeneic histocompatible bone-marrow transplantation. Lancet. 1982 Jun 5;1(8284):1266–1269. doi: 10.1016/s0140-6736(82)92840-9. [DOI] [PubMed] [Google Scholar]
- 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]
- Herberman R. B., Nunn M. E., Holden H. T. Low density of Thy 1 antigen on mouse effector cells mediating natural cytotoxicity against tumor cells. J Immunol. 1978 Jul;121(1):304–309. [PubMed] [Google Scholar]
- 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]
- Kiessling R., Klein E., Wigzell H. "Natural" killer cells in the mouse. I. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Specificity and distribution according to genotype. Eur J Immunol. 1975 Feb;5(2):112–117. doi: 10.1002/eji.1830050208. [DOI] [PubMed] [Google Scholar]
- Korngold R., Sprent J. Lethal graft-versus-host disease after bone marrow transplantation across minor histocompatibility barriers in mice. Prevention by removing mature T cells from marrow. J Exp Med. 1978 Dec 1;148(6):1687–1698. doi: 10.1084/jem.148.6.1687. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lopez C., Kirkpatrick D., Livnat S., Storb R. Natural killer cells in bone marrow transplantation. Lancet. 1980 Nov 8;2(8202):1025–1025. doi: 10.1016/s0140-6736(80)92177-7. [DOI] [PubMed] [Google Scholar]
- Meredith R. F., Okunewick J. P. Possibility of graft-vs-leukemia determinants independent of the major histocompatibility complex in allogeneic marrow transplantation. Transplantation. 1983 Apr;35(4):378–385. doi: 10.1097/00007890-198304000-00023. [DOI] [PubMed] [Google Scholar]
- Pattengale P. K., Ramstedt U., Gidlund M., Orn A., Axberg I., Wigzell H. Natural killer activity in (C57BL/6 X DBA/2)F1 hybrids undergoing acute and chronic graft-vs.-host reaction. Eur J Immunol. 1983 Nov;13(11):912–919. doi: 10.1002/eji.1830131110. [DOI] [PubMed] [Google Scholar]
- Prentice H. G., Blacklock H. A., Janossy G., Bradstock K. F., Skeggs D., Goldstein G., Hoffbrand A. V. Use of anti-T-cell monoclonal antibody OKT3 to prevent acute graft-versus-host disease in allogeneic bone-marrow transplantation for acute leukaemia. Lancet. 1982 Mar 27;1(8274):700–703. doi: 10.1016/s0140-6736(82)92619-8. [DOI] [PubMed] [Google Scholar]
- Ptak W., Hanczakowska M., Skowron-Cendrzak A. Cytotoxic macrophage in graft-versus-host reaction. Transplantation. 1975 Jan;19(1):12–19. doi: 10.1097/00007890-197501000-00003. [DOI] [PubMed] [Google Scholar]
- 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]
- SIMONSEN M. Graft versus host reactions. Their natural history, and applicability as tools of research. Prog Allergy. 1962;6:349–467. [PubMed] [Google Scholar]
- Storb R., Thomas E. D. Allogeneic bone-marrow transplantation. Immunol Rev. 1983;71:77–102. doi: 10.1111/j.1600-065x.1983.tb01069.x. [DOI] [PubMed] [Google Scholar]