In schistosomiasis a systemic hyperplasia of the monomacrophagic cell
lineage is associated with its mild modifications in myelograms and he
mograms. We monitored the in vitro proliferation of myeloid precursors
obtained from bone marrow, blood, spleen, and liver. The macrophage c
olony-forming unit (M-CFU) numbers were stable in bone marrow but incr
eased progressively in spleen and in liver, reaching in each organ the
values equivalent to one femur. The bone marrow had an increased prod
uction and enhanced capacity to release M-CFU. Their quantitative incr
ease in blood and in peripheral tissues of schistosome-infected mice w
as associated with their qualitative modifications: augmented prolifer
ative capacity, enhanced adhesion, and accelerated differentiation. Th
e accelerated release of monomacrophage progenitors and their enhanced
proliferation in peripheral tissues potentially account for the relat
ively low involvement of the bone marrow and for an efficient in situ
production of phagocytes, which participate in host reactions to paras
ites.