Abstract
F1 hybrid mice are capable of rejecting inbred parental strain bone marrow grafts after a single lethal exposure to X-rays. The incompatibility is genetically controlled by the Hybrid-histocompatibility-1 (Hh-1) locus in or near the D end of the Histocompatibility-2 (H-2) region. The onset of parental graft rejection begins 9–12 hr after transplantation and is completed by 24 hr. Maturation of hybrid resistance does not occur until the 22nd day of life. In adults, the resistance to parental marrow grafts can be temporarily abrogated or weakened by administration of cyclophosphamide or dead cultures of Corynebacterium parvum, acute supralethal exposures to radiation, or by split-dose irradiation with 6–37-day intervals. Parental marrow grafts elicit a transplantation reaction in irradiated F1 mice which is indistinguishable from that elicited in irradiated allogeneic (H-2-incompatible) hosts. Because of this immunogenetic similarity, the following question is raised: are the same or different alloantigens responsible for rejection of parental and allogeneic marrow grafts? In the first case, Hh-1 alleles would be recessive determinants of tissue-specific transplantation antigens, whereas in the second case they would be the determinants of parental- and tissue-specific antigens subject to genetic suppression in Hh-1 heterozygotes. Although the available evidence is not conclusive in excluding one of the two possibilities, it favors the concept that allograft reactivity to hemopoietic cells is elicited by recessive tissue-specific antigens.
Full Text
The Full Text of this article is available as a PDF (872.3 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bennett M., Cudkowicz G., Foster R. S., Jr, Metcalf D. Hemopoietic progenitor cells of W anemic mice studies in vivo and in vitro. J Cell Physiol. 1968 Jun;71(3):211–226. doi: 10.1002/jcp.1040710304. [DOI] [PubMed] [Google Scholar]
- Bennett M. Graft-versus-host reactions in mice. I. Kinetic and immunogenetic studies of alloantigen-sensitive units of lymphoid tissue. Transplantation. 1971 Feb;11(2):158–169. [PubMed] [Google Scholar]
- CELADA F., WELSHONS W. J. Demonstration of F1 hybrid anti-parent immunological reaction. Proc Natl Acad Sci U S A. 1962 Mar 15;48:326–331. doi: 10.1073/pnas.48.3.326. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CUDKOWICZ G. Evidence for immunization of F-1 hybrid mice against parental transplantation antigens. Proc Soc Exp Biol Med. 1961 Aug-Sep;107:968–972. doi: 10.3181/00379727-107-26812. [DOI] [PubMed] [Google Scholar]
- CUDKOWICZ G., STIMPFLING J. H. DEFICIENT GROWTH OF C57BL MARROW CELLS TRANSPLANTED IN F1 HYBRID MICE. ASSOCIATION WITH THE HISTOCOMPATIBILITY-2 LOCUS. Immunology. 1964 May;7:291–306. [PMC free article] [PubMed] [Google Scholar]
- CUDKOWICZ G., STIMPFLING J. H. INDUCTION OF IMMUNITY AND OF UNRESPONSIVENESS TO PARENTAL MARROW GRAFTS IN ADULT F-1 HYBRID MICE. Nature. 1964 Oct 31;204:450–453. doi: 10.1038/204450a0. [DOI] [PubMed] [Google Scholar]
- Chiller J. M., Habicht G. S., Weigle W. O. Kinetic differences in unresponsiveness of thymus and bone marrow cells. Science. 1971 Feb 26;171(3973):813–815. doi: 10.1126/science.171.3973.813. [DOI] [PubMed] [Google Scholar]
- Claman H. N., Chaperon E. A., Hayes L. L. Thymus-marrow immunocompetence. IV. The growth and immunocompetence of transferred marrow, thymus, and spleen cells in parent and F1 hybrid mice. Transplantation. 1969 Feb;7(2):87–98. [PubMed] [Google Scholar]
- Cudkowicz G., Bennett M. Peculiar immunobiology of bone marrow allografts. I. Graft rejection by irradiated responder mice. J Exp Med. 1971 Jul 1;134(1):83–102. doi: 10.1084/jem.134.1.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cudkowicz G. Genetic control of bone marrow graft rejection. I. Determinant-specific difference of reactivity in two pairs of inbred mouse strains. J Exp Med. 1971 Jul 1;134(1):281–293. doi: 10.1084/jem.134.1.281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gregory S. A., Fried W., Knospe W. H., Trobaugh F. E., Jr Accelerated regeneration of transplanted hematopoietic stem cells in irradiated mice pretreated with cyclophosphamide. Blood. 1971 Feb;37(2):196–203. [PubMed] [Google Scholar]
- Lotzová E., Cudkowicz G. Hybrid resistance to parental NZW bone marrow grafts: association with the D end of H-2. Transplantation. 1971 Aug;12(2):130–138. doi: 10.1097/00007890-197108000-00005. [DOI] [PubMed] [Google Scholar]
- NEVEU T., BRANELLEC A., BIOZZI G. PROPRI'ET'ES ADJUVANTES DE CORYNEBACTERIUM PARVUM SUR LA PRODUCTION D'ANTICORPS ET SUR L'INDUCTION DE L'HYPERSENSIBILIT'E RETARD'EE ENVERS LES PROT'EINES CONJUGU'EES. Ann Inst Pasteur (Paris) 1964 May;106:771–777. [PubMed] [Google Scholar]
- SNELL G. D., JACKSON R. B. Histocompatibility genes of the mouse. II. Production and analysis of isogenic resistant lines. J Natl Cancer Inst. 1958 Nov;21(5):843–877. [PubMed] [Google Scholar]
- SNELL G. D., STEVENS L. C. Histocompatibility genes of mice. III. H-1 and H-4, two histocompatibility loci in the first linkage group. Immunology. 1961 Oct;4:366–379. [PMC free article] [PubMed] [Google Scholar]
- Shadduck R. K., Rickard K. A., Howard D. E., Stohlman F., Jr The effect of preirradiation of recipient mice on the proliferation of transplanted hemopoietic stem cells. Blood. 1971 Mar;37(3):330–339. [PubMed] [Google Scholar]
- Wolf N. S., Trentin J. J. Hemopoietic colony studies. V. Effect of hemopoietic organ stroma on differentiation of pluripotent stem cells. J Exp Med. 1968 Jan 1;127(1):205–214. doi: 10.1084/jem.127.1.205. [DOI] [PMC free article] [PubMed] [Google Scholar]