Table 1. Characterization of the chimeric immune system.
Blood | Bone marrow | Spleen | |
% hCD45/total CD45 | 22.6±2.1 | 29.6±3.2 | 12.8±0.9 |
Monocytes | |||
% total hMono/hCD45 | 15.1±2.2 | 7.4±0.7 | |
% CD14high hMono/hCD45 | 8.7±1.7 | ||
% CD14low hMono/hCD45 | 6.3±2.7 | ||
% CD11b+CD14−/hCD45 | 12.0±1.6 | ||
% CD11b+CD14+/hCD45 | 20.8±2.6 | ||
Granulocytes | |||
% total hGranulo/hCD45 | 15.4±2.1 | ||
% hCD66b+neutrophil/hCD45 | 8.75±1.95 | ||
% CD16+ neutrophil/hCD45 | 11.4±1.9 | ||
% hCD15+ neutrophil/hCD45 | 10.8±2.1 | 3.8±0.4 | |
% hGranulo/total Granulo | 33.0±3.9 | ||
Myeloid cells | |||
% CD11b+/hCD45 | 47.1±5.2 | ||
% CD11b−/hCD45 | 52.9±5.2 | ||
NK cells | |||
% hNK cells/hCD45 | 2.2±0.4 | ||
%hCD56+ hNK cells/hCD45 | 3.3±0.7 | ||
T lymphocytes | |||
% hCD3/hCD45 | 0.34±0.10 | 1.9±0.3 | |
B lymphocytes | |||
% hCD19+/hCD45 | 57.1±3.9 | 65.4±2.5 |
Blood, bone marrow and splenic digests were analysed by flow cytometry to define the leukocyte populations (n = 26 mice). Treatment groups were matched by degree of peripheral blood chimerism prior to IgG injection. hMono = human monocytes. There was no significant difference in degree of chimerism or human granulocyte reconstitution between the experimental groups.