Many clues point to a role for T lymphocytes in the pathogenesis of rh
eumatoid arthritis (RA), although the importance of these cells and th
eir position within the rheumatoid pathogenic scheme remain unknown. E
ncouraged by data from animal models of T-lymphocyte-mediated autoimmu
nity, a major focus of research into the role of T lymphocytes in RA h
as been the usage of T cell receptor V genes in rheumatoid synovitis.
Despite many methodologic problems, involving choice of patients and c
ontrols, choice of specimens, and technical factors, several conclusio
ns can be drawn from the published research. In particular, synovial T
lymphocyte populations, as a whole, frequently show biased V gene usa
ge and restricted clonality within those T lymphocyte subsets that uti
lize overrepresented V gene families. Continued research into these sy
novial T lymphocyte subsets should provide important insights into the
pathogenesis of RA, particularly if solutions to the identified metho
dologic problems are implemented.