PERITONEAL-MACROPHAGES PLAY AN IMPORTANT ROLE IN ELIMINATING HUMAN-CELLS FROM SEVERE COMBINED IMMUNODEFICIENT MICE TRANSPLANTED WITH HUMAN PERIPHERAL-BLOOD LYMPHOCYTES
S. Shibata et al., PERITONEAL-MACROPHAGES PLAY AN IMPORTANT ROLE IN ELIMINATING HUMAN-CELLS FROM SEVERE COMBINED IMMUNODEFICIENT MICE TRANSPLANTED WITH HUMAN PERIPHERAL-BLOOD LYMPHOCYTES, Immunology, 93(4), 1998, pp. 524-532
To elucidate che mechanism of human cell elimination from severe combi
ned immunodeficient (SCID) mice transplanted with human peripheral blo
od lymphocytes (hu-PBL-SCID mice), we explored the immunocytes in the
peritoneal cavity in SCID mice where human PBL were transferred. When
the phenotype of peritoneal exudate cells (PEC) was compared by flow c
ytometry among three congenic strains of SCID mice that differ in thei
r acceptability for human PBL, the PEC in NOD-scid mice, which exhibit
the highest acceptability, contained the smallest number of F4/80(lot
-)Mac-1(+)-activated macrophages. Moreover, the proportions of natural
killer cells in PEC of the three strains of SCID mice were not always
correlated with the acceptability. These findings suggest the possibi
lity that peritoneal macrophages eliminate human cells in hu-PBL-SCID
mice. To verify this hypothesis, we evaluated the engraftment of human
PBL into SCID mice that were treated with liposome-encapsulated dichl
oromethylene diphosphonate, which selectively depletes macrophages by
inducing apoptosis, or S-aminoguanidine hemisulphate salt, an inhibito
r of inducible nitric oxide synthase of macrophages. As a result, both
of these regimens improved engraftment of human PBL: indicating that
peritoneal macrophages take part in human cell elimination in the peri
toneal cavity of bu-PBL-SCID mice and that it is mediated, at least in
part, by direct macrophage cytotoxicity utilizing nitric oxide.