H-2-associated specificity of virus-immune cytotoxic T cells from H-2 mutant and wild-type mice: M523 (H-2Kka) and M505(H-2Kbd) do, M504 (H-2Dda) and M506(H-2Kfa) do not crossreact with wild-type H-2K or H-2D

Rolf M. Zinkernagel, Jan Klein

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Abstract

B10.A(3R) (H-2Kb) mice infected with lymphocytic choriomeningitis virus (LCMV) or vaccinia virus generate cytotoxic T cells capable of specifically lysing virus-infected macrophage target cells from H-2Kb mutant mice M505 (H-2Kbd), and vice versa. Similarly, virus-immune B10.A(4R) (H-2Kk) T cells specifically lyse infected targets from M523 (H-2Kka), and vice versa. In contrast, virus-specific cytotoxic T cells from neither M504 (H-2Dda) and B10.A(5R) (H-2Dd) nor M506 (H-2Kfa) and B10.M(11R) (H-2Kf) mutually crossreact at the cytotoxic effector-cell level. As far as tested, the crossreactivity patterns between wild-type and mutant K or D specificities are identical for LCMV- and vaccinia virus-immune spleen cells. Although this finding is no proof for either the altered self nor the dual recognition concept of T-cell recognition, it may be compatible with the latter model.

Original languageEnglish (US)
Pages (from-to)581-590
Number of pages10
JournalImmunogenetics
Volume4
Issue number1
DOIs
StatePublished - Dec 1 1977

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Satellite Viruses
Lymphocytic choriomeningitis virus
T-Lymphocytes
Vaccinia virus
Viruses
Spleen
Macrophages

All Science Journal Classification (ASJC) codes

  • Immunology
  • Genetics

Cite this

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title = "H-2-associated specificity of virus-immune cytotoxic T cells from H-2 mutant and wild-type mice: M523 (H-2Kka) and M505(H-2Kbd) do, M504 (H-2Dda) and M506(H-2Kfa) do not crossreact with wild-type H-2K or H-2D",
abstract = "B10.A(3R) (H-2Kb) mice infected with lymphocytic choriomeningitis virus (LCMV) or vaccinia virus generate cytotoxic T cells capable of specifically lysing virus-infected macrophage target cells from H-2Kb mutant mice M505 (H-2Kbd), and vice versa. Similarly, virus-immune B10.A(4R) (H-2Kk) T cells specifically lyse infected targets from M523 (H-2Kka), and vice versa. In contrast, virus-specific cytotoxic T cells from neither M504 (H-2Dda) and B10.A(5R) (H-2Dd) nor M506 (H-2Kfa) and B10.M(11R) (H-2Kf) mutually crossreact at the cytotoxic effector-cell level. As far as tested, the crossreactivity patterns between wild-type and mutant K or D specificities are identical for LCMV- and vaccinia virus-immune spleen cells. Although this finding is no proof for either the altered self nor the dual recognition concept of T-cell recognition, it may be compatible with the latter model.",
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AU - Zinkernagel, Rolf M.

AU - Klein, Jan

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N2 - B10.A(3R) (H-2Kb) mice infected with lymphocytic choriomeningitis virus (LCMV) or vaccinia virus generate cytotoxic T cells capable of specifically lysing virus-infected macrophage target cells from H-2Kb mutant mice M505 (H-2Kbd), and vice versa. Similarly, virus-immune B10.A(4R) (H-2Kk) T cells specifically lyse infected targets from M523 (H-2Kka), and vice versa. In contrast, virus-specific cytotoxic T cells from neither M504 (H-2Dda) and B10.A(5R) (H-2Dd) nor M506 (H-2Kfa) and B10.M(11R) (H-2Kf) mutually crossreact at the cytotoxic effector-cell level. As far as tested, the crossreactivity patterns between wild-type and mutant K or D specificities are identical for LCMV- and vaccinia virus-immune spleen cells. Although this finding is no proof for either the altered self nor the dual recognition concept of T-cell recognition, it may be compatible with the latter model.

AB - B10.A(3R) (H-2Kb) mice infected with lymphocytic choriomeningitis virus (LCMV) or vaccinia virus generate cytotoxic T cells capable of specifically lysing virus-infected macrophage target cells from H-2Kb mutant mice M505 (H-2Kbd), and vice versa. Similarly, virus-immune B10.A(4R) (H-2Kk) T cells specifically lyse infected targets from M523 (H-2Kka), and vice versa. In contrast, virus-specific cytotoxic T cells from neither M504 (H-2Dda) and B10.A(5R) (H-2Dd) nor M506 (H-2Kfa) and B10.M(11R) (H-2Kf) mutually crossreact at the cytotoxic effector-cell level. As far as tested, the crossreactivity patterns between wild-type and mutant K or D specificities are identical for LCMV- and vaccinia virus-immune spleen cells. Although this finding is no proof for either the altered self nor the dual recognition concept of T-cell recognition, it may be compatible with the latter model.

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