F. Briere et al., HUMAN INTERLEUKIN-10 INDUCES NAIVE SURFACE-IMMUNOGLOBULIN D-CELLS TO SECRETE IGG1 AND IGG3( (SIGD(+)) B), The Journal of experimental medicine, 179(2), 1994, pp. 757-762
During antigen-induced immune responses, human B cells switch isotype
from immunoglobulin M (IgM)-IgD to IgG1-4, IgA1-2, or IgE. In the huma
n, no cytokines have yet been demonstrated to act as switch factors fo
r IgG1, IgG2, and IgG3. In this paper, we report that in response to i
nterleukin 10 (IL-10), anti-CD40 activated tonsillar surface IgD(+) (s
IgD(+))B cells are induced to secrete large amounts of IgM, IgG1, and
IgG3 but neither IgG2 nor IgG4. Cord blood purified B cells and lympho
cytes from Hyper-IgM patients also produced IgG1 and IgG3 after cultur
e with anti-CD40 and IL-10. In contrast, sIgD(-) isotype-committed B c
ells produce IgG1, IgG2, and IgG3 when activated through CD40 in the p
resence of IL-10. Thus, in addition to its growth-promoting and differ
entiating activities on human B cells, IL-10 may represent a switch fa
ctor for IgG1 and IgG3.