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Infection and Immunity, May 1999, p. 2241-2249, Vol. 67, No. 5
International Livestock Research Institute
(ILRI), Nairobi, Kenya,1 and Department
of Veterinary Microbiology and Pathology, Washington State University,
Pullman, Washington2
Received 26 June 1998/Returned for modification 13 August
1998/Accepted 26 February 1999
T cells bearing the
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Bovine

T-Cell Responses to the Intracellular
Protozoan Parasite Theileria parva


antigen receptor (
T cells) can
constitute up to 50% of T cells in the peripheral blood and lymphoid organs of young cattle. We present data showing that 
T cells are
involved in immune responses against Theileria parva.

T cells isolated from peripheral blood mononuclear cells (PBMC) of T. parva-naive and -immune cattle proliferated in the
presence of fixed or unfixed autologous T. parva-infected
lymphoblasts (TpL) and heat-stressed concanavalin A (ConA)-induced
blasts (ConA blasts) but not untreated ConA blasts. The specificity of
response was further evaluated with a panel of 
T-cell lines and
clones. T-cell reactivity was blocked by GB21A, a monoclonal antibody (MAb) specific for the 
T-cell receptor, but not by MAbs specific for class I and class II major histocompatibility complex (MHC) molecules. In addition, TpL but not ConA blasts from a variety of
MHC-mismatched animals induced proliferation of the 
T-cell lines
and clones. These 
T cells were found to respond to TpL infected
with several different parasite stocks and failed to recognize TpL
after elimination of the parasite by the theilericidal drug BW 720C.
Assays for cytotoxic activity of 
T cells sorted from bulk
cultures of immune PBMC restimulated several times with autologous TpL
demonstrated that effector cells whose specificity is similar to that
of proliferating cells are generated. These results suggest that bovine

T cells are activated by and lyse T. parva-infected
cells by recognizing conserved parasite-induced or parasite-derived
antigens in an MHC-unrestricted fashion.
*
Corresponding author. Present address: Swiss Tropical
Institute, Postfach, CH 4002 Basel, Switzerland. Phone: 41 61 284 8236. Fax: 41 61 271 8654. E-mail:
Daubenberger{at}ubaclu.unibas.ch.
This is ILRI publication no. 98026.
Present address: City of Hope National Medical Center, Duarte, CA 91010.
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