Abstract
Four different combinations of F1 hybrid mice [(C57BL/10 X B10.A)F1, (C57BL/10 X B10.BR)F1, B6D2F1, and AKD2F1] were injected intravenously with spleen cells from parental strains. The T-cell-mediated cytotoxic potential of spleen cells from the injected F1 mice was assessed from 4 to 21 d later by in vitro sensitization with trinitrophenyl-modified parental or syngeneic F1 spleen cells (TNP-self) or with allogeneic spleen cells. The cytotoxic potential of the F1 mice to TNP-self as well as to alloantigens was abolished or severely depressed throughout this period when the respective H-2k,a,d parental spleen cells were injected. In contrast, the cytotoxic potential was unaffected or only marginally reduced when H-2b parental cells were injected. The induction of depressed cytotoxic activity was shown to be a result of a population of parental radiosensitive T lymphocytes. The results should be discussed with respect to (a) the genetic and mechanistic parameters associated with the differential depressive effects of parental cells expressing H-2b vs. H-2k,a,d antigens, and (b) the use of this system for investigating allogeneic receptors on T-lymphocyte populations.
MeSH Terms
Animals
Brain
Cytotoxicity, Immunologic
Epitopes
Histocompatibility Antigens
Hybridization, Genetic
Immune Sera
Immunosuppression Therapy
Lymphocyte Culture Test, Mixed
Lymphocytes/immunology
Male
Mice
Rabbits/immunology
Spleen/cytology
Chemicals
Epitopes
Histocompatibility Antigens
Immune Sera
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Shearer G M
Polisson R P
References (13)
13 references, click to expand
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