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Cell‐mediated cell lysis <i>in vitro</i>: genetic control of killer cell production and target specificities in the mouse
236
Citations
25
References
1974
Year
Lymphocyte DevelopmentApoptosisImmunologyCell DeathImmunodominanceLytic ActivityImmunologic MechanismImmune SystemKiller Cell PopulationNatural Killer CellsCellular PhysiologyKiller Cell ProductionHematologyCell SignalingImmune SurveillanceImmune FunctionCell BiologyGenetic ControlImmune Cell DevelopmentCell ControlCellular Immune ResponseMedicineCell DevelopmentTarget Specificities
Abstract The requirements for killer cell production in the course of a mixed leukocyte reaction and the specificity of target cell (PHA‐blasts) lysis in the mouse were investigated using inbred strains carrying intra‐ H ‐ 2 recombinant chromosomes. Strong lytic activity was generated in all, and only those, responder‐stimulator combinations which differed at either the H ‐ 2D or the H ‐ 2K , or both regions, even if the MLR incompatibility between responder and stimulator was very weak. Killing activity was specific and directed against determinants controlled by genes in the H ‐ 2K and H ‐ 2D regions. The slope of the killer dose‐response curves is the same for either type of specificity. Quantitative comparison of the lytic activity of a given killer cell population on different targets demonstrated a dose effect of the number of specificities recognized. No significant killing against the Ir or the Ss ‐ Slp regions of the H ‐ 2 complex could be detected. AntiH2 sera, if directed against the killer cells, do not inhibit their activity, while they can block killing, if directed against the target. This inhibition is specific in that a serum that blocks killing against the H ‐ 2K specificity of a given target does not inhibit the lytic activity directed against the H ‐ 2D determinants on the same target.
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