The purpose of this work was twofold: 1) to learn whether rats transge
nic for HLA-B27 and the human beta2-microglobulin gene HB2M can mount
B27-restricted cytolytic T lymphocyte (CTL) responses to the male H-Y
antigen, and 2) to learn whether such CTLs would recognize both rat an
d mouse H-Y in the context of HLA-B27. Female rats of the B27/HB2M tra
nsgenic line 21-4L were primed in vivo with cells from males of the sa
me line. CTL effectors were generated from lymph node cells of these f
emales following culture with irradiated antigen-presenting cells from
either male 21-4L rats or male mice of the B27/HB2M transgenic 56-3 l
ine. The CTLs showed male-specific, B27-specific lysis of both rat and
mouse targets. Lysis of B27 targets was inhibitable by monoclonal ant
ibodies specific for B27 or rat CD8. Specific lysis of male B27 rat an
d mouse targets was inhibitable equally by either rat or mouse male B2
7 cold targets, but not significantly by female or nontransgenic cold
targets. The B27-restficted CTLs neither recognized nor were inhibited
by B27+ or B27 male or female human targets. These results demonstrat
e that CD8+, B27-restricted, anti-H-Y CTLs recognize an evolutionarily
conserved H-Y peptide antigen in both rats and mice. In addition, the
y establish the transgenic rat as a model system for examining the T-c
ell response to antigen presented by class I HLA molecules.