Positive selection of self- and alloreactive CD8+ T cells in Tap-1 mutant mice.
Author(s) -
Carla J. Aldrich,
HansGustaf Ljunggren,
Luc Van Kaer,
Philip G. AshtonRickardt,
Susumu Tonegawa,
James Forman
Publication year - 1994
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.91.14.6525
Subject(s) - priming (agriculture) , cd8 , cytotoxic t cell , major histocompatibility complex , in vivo , biology , microbiology and biotechnology , t cell , mutant , in vitro , immunology , antigen , immune system , gene , genetics , botany , germination
Mice with a homozygous deletion in their Tap-1 gene (-/- mice) express very low levels of cell membrane major histocompatibility complex class I molecules and have < 1% peripheral CD8+ T cells. We show that these -/- mice but not their +/- littermates display strong primary syngeneic anti-H-2Kb and -Db-specific responses mediated by CD8+ T cells. These responses are augmented by in vivo priming. Further, -/- mice primed in vivo with H-2d alloantigens generate an anti-H-2d response which appears nearly as strong as that found in +/- littermates. Both -/- anti-H-2b and anti-H-2d T cells do not recognize target cells from Tap-1 -/- animals or Tap-2-deficient RMA-S cells. Thus, some CD8+ anti-self and alloreactive T cells can be selected in the absence of Tap proteins.
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