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9V
2 T Cells in Humans and Aotus Monkeys, a Primate Infection Model for Plasmodium falciparum Malaria1 ,2




*
Department of Molecular Immunology, Swiss Tropical Institute, Basel, Switzerland;
Instituto de Inmunologia, Universidad Nacional de Colombia, Santafe de Bogota, Leticia Colombia; and
Solvias Aktiengesellschaft, Basel, Switzerland

T cells are implicated to play crucial roles during early
immune responses to pathogens. A subset of human 
T cells
carrying the V
9V
2 TCR recognize small, phosphorylated nonpeptidic
Ags. However, the precise role of these cells and the ligands
recognized in human immune responses against pathogens remains unclear
because of the lack of suitable animal models. We have analyzed the
reactivity of spleen cells of the New World monkey Aotus
nancymaae against isopentenyl pyrophosphate (IPP), a
phosphorylated microbial metabolite selectively activating V
9V
2 T
cells. Spleen cells were stimulated by IPP and the expanding cell
population expressed the V
9 TCR. TRGV-J and
TRDV-D-J rearrangements expressed by IPP-stimulated
cells of Aotus were analyzed by RT-PCR and DNA
sequencing. The TRGV-J and TRDV-D-J
rearrangements expressed by IPP-stimulated Aotus and
human 
T cells were similar with respect to 1) TCR gene segment
usage, 2) a high degree of germline sequence homology of the TCR gene
segments used, and 3) the diversity of the CDR3 regions. Phylogenetic
analysis of human, Pan troglodytes, and A.
nancymaae TRGV gene segments showed that
the interspecies differences are smaller than the intraspecies
differences with TRGV9 gene segments located on a
distinct clade of the phylogenetic tree. The structural and functional
conservation of V
9V
2 T cells in A. nancymaae and
humans implicates a functionally important and evolutionary conserved
mechanism of recognition of phosphorylated microbial
metabolites.
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