Cytolytic T cells activated by H-2-controlled E molecules cross-react with A molecules |
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Authors: | Ivica Vu?ak Antonio Jureti? Zoltan A Nagy Jan Klein |
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Institution: | (1) Abteilung Immungenetik, Max-Planck-Institut für Biologie, Corrensstrasse 42, D-7400 Tübingen, Germany;(2) Present address: Department of Physiology, Faculty of Medicine, University of Zagreb, alata 3, Zagreb, Yugoslavia |
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Abstract: | Cell-mediated lymphocytotoxicity was generated in four strain combinations differing only by the cell-surface expression of the class II E molecule controlled by the H-2 complex. The four combinations were: B10.D2(R107) anti-B10.A(3R), B10.A(4R) anti-B10.A(2R), B10.GD anti-B10.D2(R101), and B10.S(7R) anti-B10.S(9R). In all four of these combinations, the stimulator expresses E molecules on the cell surface, while the responder does not. The cytolytic T lymphocytes generated in the B10.D2(R107) anti-B10.A(3R) and B10.A(4R) anti-B10.A(2R) combinations reacted not only with the stimulator but also with strains that do not express cell-surface E molecules, in particular, strains carrying the H-2
f
and H-2
q
haplotypes. The cross-reactivity with E-negative strains could be blocked by monoclonal antibodies specific for the Af or Aq molecules but not by antibodies recognizing determinants on E or class I (K) molecules. The anti-H-2f cross-reactivity could be inhibited by H-2
q
cold targets and, reciprocally, the anti-H-2q reactivity could be blocked by H-2
f
cold targets. These findings are interpreted as indicating that the cytolytic T lymphocytes stimulated by E molecules can recognize and lyse cells lacking E molecules but expressing A molecules. The observed E-A cross-reactivity supports the notion of structural and functional relatedness between the A and E molecules and suggests a common evolutionary origin of the A- and E-encoding loci. |
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