M. Bijl et al., Expression of costimulatory molecules on peripheral blood lymphocytes of patients with systemic lupus erythematosus, ANN RHEUM D, 60(5), 2001, pp. 523-526
Objective-In systemic lupus erythematosus (SLE) autoantibody production is
T cell dependent. For a proper T and B cell interaction, signalling of cost
imulatory molecules on these cells is necessary. The expression of costimul
atory molecules on peripheral blood lymphocytes in patients with SLE in con
junction with disease activity was measured to evaluate whether expression
of costimulatory molecules in SLE is increased.
Methods-Thirteen patients with SLE with active disease, 10 patients with in
active disease, and 14 controls entered the study. In addition, samples fro
m 10 of the 13 patients with active disease could be studied at a moment of
inactive disease as well. Isolated peripheral blood lymphocytes were stain
ed for the lymphocyte subset markers CD4, CD8, CD19, their respective activ
ation markers CD25, HLA-DR, CD38, and the costimulatory molecules CD40L, CD
28, CD40, CD80, and CD86. Expression was measured by flow cytometry.
Results-Peripheral blood lymphocytes of patients with SLE showed signs of i
ncreased activation at the moment of active disease. Almost all CD4+ T cell
s expressed CD28, both in patients and in controls. CD80 expression on CD19
+ B cells was low in both groups and did not correlate with disease activit
y. In contrast, the percentage of CD19+ B cells expressing CD86 was increas
ed in patients with SLE even in patients with inactive disease (p=0.04) and
correlated with the SLEDAI score (p=0.0005) ana levels of anti-dsDNA (p=0.
006). No changes in CD40 or CD40L expression were found in the patients wit
h SLE.
Conclusion-In patients with SLE the expression of CD86 on CD19+ B cells is
increased and is associated with disease activity, B cell activation, and l
evels of anti-dsDNA. The increased CD86 expression will render (autoreactiv
e) B cells more susceptible for T cells. This can facilitate autoantibody p
roduction and might be a target for immunosuppressive treatments.