Lymphocytes express antigen receptors that allow the immune system to speci
fically recognize antigens, In transplantation, T cells play a critical rol
e in the rejection process, and different protocols inhibiting T cell-media
ted alloreactivity efficiently achieve prolongation of allograft survival.
T cells can interact with alloantigens by two ways, either by the "indirect
" pathway that correspond to the physiological mechanism of T cell immune r
ecognition, or through the "direct" pathway where they recognize alloantige
ns directly on the surface of donor cells. If some T cells are specifically
activated in allorecognition, one should be able to indirectly detect this
"selection" by analyzing the T cell receptor usage that could be biased an
d reflect the preferential amplification of alloreactive lymphocyte subsets
. Nevertheless compared with disease states such as cancer or autoimmunity
the T cell receptor repertoire is still largely uncharacterized. We review
the current results available on T cell repertoire usage in transplantation
studies involving humans or various animal models. The T cell receptor rep
ertoire involved in transplantation (restricted or unrestricted) and the fe
atures potentially common to alloimmune responses will be discussed.