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. 2012 Jan 11;7(1):e28626. doi: 10.1371/journal.pone.0028626

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.