A. Bertotto et al., LYMPHOCYTES BEARING THE GAMMA-DELTA T-CELL RECEPTOR IN ACUTE BRUCELLA-MELITENSIS INFECTION, European Journal of Immunology, 23(5), 1993, pp. 1177-1180
A phenotypical analysis carried out by indirect immunofluorescence and
two-color cytofluorometry showed that the number of lymphocytes beari
ng the gammadelta T cell receptor (TcR) heterodimer was dramatically i
ncreased in the blood of six children with Brucella melitensis infecti
on. Most in vivo expanded gammadelta T cells reacted with a monoclonal
antibody which identifies Vdelta2 gene products and a significant pro
portion expressed CD25 and HLA-DR activation antigens. In addition, wh
ereas only a few gammadelta T lymphocytes were CD8+, nearly all were C
D4-. Highly enriched populations of both alphabeta and gammadelta T ce
lls were obtained by negative immunoselection from three subjects with
brucellosis sampled during convalescence. Despite the different form
of their TcR, the proliferation of these two major T cell subsets in r
esponse to a mitogenic anti-CD3 monoclonal reagent (OKT3) was optimal.
In contrast, alphabeta, but not gammadelta, T lymphocytes proliferate
d vigorously in response to the antigenic stimulus elicited by heat-ki
lled Brucella. Further studies are, therefore, needed to determine whe
ther the selective expansion of the gammadelta T cell subpopulation ob
served during the clinical course of the infection is driven by antige
nic determinant(s) borne by the pathogen in vivo or is due to host-der
ived stimuli, such as autologous heat-shock proteins expressed on the
surface of the infected cells.