B-chronic lymphocytic leukaemia (B-CLL) is characterised by the progressive
accumulation of monoclonal B cells, which may be the result of several fac
tors leading to extended B-CLL cell lifespan, increased proliferative capac
ity and diminished cell death. Here we review the implications of several s
ignals mediated by receptors, such as surface IgM, CD6 and CD40, for the B-
CLL cell survival, together with data on gene modulation in relation to the
apoptosis process in B-CLL cells. We also describe some features of the Fa
s/FasL system in B-CLL that hypothetically might contribute to the accumula
tion of leukaemic cells and the progression of the disease, by downregulati
ng the apoptotic response or avoiding the autologous immune response.