H. Yang et Rme. Parkhouse, DIFFERENTIAL EXPRESSION OF CD8 EPITOPES AMONGST PORCINE CD8-POSITIVE FUNCTIONAL LYMPHOCYTE SUBSETS, Immunology, 92(1), 1997, pp. 45-52
The swine is a useful model for immunobiological studies as it has a h
ighly heterogeneous lymphocyte pool, containing several subsets not ea
sily accessible in humans and rodents. In particular, the CD8-positive
(CD8(+)) cells contain a variety of lymphocyte subsets, such as alpha
beta-T cells, gamma delta-T cells, CD4 CD8 double-positive (DP) cells
and natural killer (NK) cells. In order to define these subsets furth
er, we have selected four monoclonal antibodies (mAb) with differentia
l reactivity on CD8(+) cells. Thus, mAb CD8.1 (PPT20) bound to CD8(hi)
and CD8(lo) subpopulations in a similar way to the conventional anti-
CD8. The mAb CD8.2 (PPT21), though binding to all of the CD8(+) cells,
reacted preferably with CD8(hi). Two other mAb, CD8.3 (PPT22) and CD8
.4 (PPT23), were specific for CD8(hi) alpha beta-T-cell subpopulation.
These results, complemented by immunoprecipitation, co-modulation and
enzyme-linked immunosorbent assay experiments, suggest that CD8.1 and
CD8.2 react putatively with the CD8 alpha-chain and CD8.3 and CD8.4 w
ith the CD8 beta-chain. Tissue distribution studies revealed that CD8(
+) thymocytes and peripheral CD8(hi) alpha beta-T cells expressed both
putative CD8 alpha- and beta-chains while peripheral CD4(+)CD8(+) alp
ha beta-T cells, CD8(lo) gamma delta-T cells and NK cells expressed on
ly putative CD8 alpha-chain. Functional studies indicated that the CD8
(hi) alpha beta-T and CD8(lo) gamma delta-T cells were effector cells
in the CD3-redirected cytotoxicity.