K. Robbins et al., IMMUNOLOGICAL EFFECTS OF INSULIN-LIKE GROWTH FACTOR-I - ENHANCEMENT OF IMMUNOGLOBULIN-SYNTHESIS, Clinical and experimental immunology, 95(2), 1994, pp. 337-342
In addition to its activity as a metabolic hormone and a regulator of
somatic growth, insulin-like growth factor-I (IGF-I) has cytokine-like
activities on lymphoid cells. A 14-day infusion of recombinant human
(rh)IGF-I increased lymphocyte numbers in all the peripheral lymphoid
organs examined. This increase was apparent for up to 3 weeks followin
g cessation of hormone treatment. A second administration of rhIGF-I,
given when the lymphocyte numbers in the rhIGF-I-treated mice had retu
rned to control values, resulted in similar increases in the periphera
l T and B cell populations. This increase in lymphocyte numbers had fu
nctional significance, since rhIGF-I-treated mice produced elevated an
tibody titres following primary or secondary antigen challenge compare
d with controls. In addition, when rhIGF-I-treated mice were immunized
with a suboptimal dose of antigen they produced antibody titres which
were equivalent to those generated by immunization with optimal doses
of antigen. When examined in vitro, addition of rhIGF-I alone to cult
ures of splenocytes from antigen-primed mice stimulated immunoglobulin
synthesis. These studies suggest that IGF-I produced locally by thymi
c and bone marrow stromal cells may be a natural component of B and T
cell lymphopoiesis.