OBJECTIVE - B-cells expressing CD5 are associated with the production
of autoantibodies and are present at increased levels in several autom
immune diseases. The aim of this study was to investigate the relation
ship of these cells to the development of type I diabetes and the pres
ence of organ and non-organ-specific autoantibodies. RESEARCH DESIGN A
ND METHODS - We measured percentage levels of CD5(+) B-cells in patien
ts with recent-onset (n = 34) and long-standing (n = 21) type I diabet
es and in a cohort of 18 identical twins of patients with type I diabe
tes studied prospectively, 8 of whom became diabetic (prediabetic twin
s) during the study; the rest remained nondiabetic after at least 7 ye
ars and are now unlikely to develop the disease. Forty-seven healthy i
ndividuals were studied as control subjects. RESULTS - Percentage leve
ls of total B-cells (CD20(+)) and the proportion expressing CD5 were i
ncreased in patients with recent-onset (P < 0.001 for both) but not lo
ng-standing type I diabetes compared with control subjects. Percentage
levels of CD20(+) B-cells were increased in prediabetic twins through
out the prediabetic period (P < 0.05), and there was an increased prop
ortion of CD5-expressing B-cells that failed to reach statistical sign
ificance (P = 0.08). Percentage levels of CD20(+) B-cells and the prop
ortion expressing CD5 were normal throughout the study in twins remain
ing nondiabetic. No relationship between percentage levels of CD5+ B-c
ells and islet cell antibody, thyroid autoantibodies, or non-organ-spe
cific autoantibodies was found. CONCLUSIONS - These results show an in
crease in B-cell percentage levels at the diagnosis of type I diabetes
, which is because of an expansion of the CD5(+) subset. These changes
are also evident in twins throughout the prediabetic period, which su
ggests that they are related to the processes that lead to diabetes.