Improved polymerase chain reaction (PCR)-based methods now permit a mo
re in-depth analysis of the repertoire of T cells recovered in biologi
cal samples from mice and humans. At a certain level of resolution, th
e diversity of the T-cell repertoire can be readily estimated and clon
al expansions become easily detectable. As discussed here by Christoph
e Pannetier, Jos Even and Philippe Kourilsky, these improvements allow
a better appreciation of the degree of reproducibility of immune resp
onses, both in mice and humans, and should have a significant impact o
n clinical investigations.