Ra. Collins et al., BOVINE GAMMA DELTA TCR(+) T-LYMPHOCYTES ARE STIMULATED TO PROLIFERATEBY AUTOLOGOUS THEILERIA ANNULUTA-INFECTED CELLS IN THE PRESENCE OF INTERLEUKIN-2/, Scandinavian journal of immunology, 44(5), 1996, pp. 444-452
An in vitro model system has been developed in which freshly isolated
resting WCl+ gamma/delta TcR(+) T cells proliferate in response to cel
ls transformed by the protozoan parasite Theileria annulata, providing
a strategy in which the basis of activation of naive gamma/delta T ce
lls can be investigated. Irradiated parasite-transformed cells stimula
te the proliferation, but not cytolytic activity, of autologous periph
eral blood mononuclear cells (PBMC) from non-immune animals. The proli
ferating cells are mainly WCl+- gamma/delta T cells. The majority of W
Cl+ gamma/gamma T cells in freshly isolated PBMC express CD25 at a low
level that increases when stimulated with T. annulata-infected cells.
Purified WCl+ gamma/delta T cells fail to proliferate when cultured w
ith irradiated T. annulata-infected cells and produce a small prolifer
ative response to IL-2, but proliferate strongly to irradiated or ligh
tly fixed Theileria-infected cells in combination with IL-2. The Theil
eria-infected cells express cytokine transcripts encoding IL-1 alpha,
IL-1 beta, IL-6 and IL-10, but not IFN gamma, IL-2, IL-4 and IL-7. Pur
ified WCl+ gamma/delta T cells stimulated with T. annulata-infected ce
lls with or without IL-2 fail to produce IL-2 transcripts, but do prod
uce those for TNF alpha. These experiments show that WCl+ gamma/delta
T cells recognize a surface determinant on T. annulata-infected cells,
that together with a second signal, which can be provided by exogenou
s IL-2, stimulates their proliferation.