Interleukin-g (IL-6), although often regarded as a B-cell differentiation f
actor, was recently described as the essential survival factor for human pl
asmablasts in vivo in reactive plasmacytosis, The present study reinvestiga
ted the roles of IL-6 and IL-2 in the generation of plasma cells from human
memory B cells in vitro. The cells involved in this differentiation proces
s were identified as preplasma-blasts (CD20(+/-)CD38(+/-)CD138(-)), plasmab
lasts (CD20(-)CD38(++)CD138(-)), and early plasma cells (CD20(-)CD38(+++)CD
138(+++)). IL-2 or IL-10 induced a strong generation of plasmablasts and ea
rly plasma cells (PCs), Compared to IL-2 or IL-10, IL-6 alone was inefficie
nt at PC generation, However, when combined with IL-2 or IL-10, IL-6 enhanc
ed generation of early PCs. Moreover, anti-IL-6 monoclonal antibody markedl
y reduced IL-2-induced generation of early plasma cells, but not of plasmab
lasts. These roles of IL-2 and IL-6 were consistent with the difference in
the expression of their respective receptors (R), CD25 (IL-2R alpha) was in
creased 72 +/- 10-fold on activated B cells, but decreased and then disappe
ared on plasmablasts, Conversely, CD126 (IL-6R alpha) was barely expressed
on activated B cells, but increased 18 +/- 2-fold on preplasmablasts, Final
ly, IL-6 enhanced the proliferation (2-fold increase) of IL-2-generated pla
smablasts, In conclusion, the data indicate that IL-6 is a growth factor fo
r nonmalignant human plasmablasts, (Blood, 2001; 97:1817-1822) (C) 2001 by
The American Society of Hematology.