Figure 2
Figure 2. EμB29-Btk gene therapy restores central and peripheral B-cell development. PB, BM, spleen, and peritoneal cells from LV-treated mice and mock controls were stained for surface markers and analyzed by flow cytometry to identify B-cell subsets (supplemental Figure 2, gating strategy). (A) PB cells were first gated on live and CD11b− populations and then analyzed for B220, IgM, and IgD expression. FACS plots show representative mice from WT mock (n = 7), KO mock (n = 8), MOI 3 (n = 3), and MOI 15 to 25 (n = 12) experimental groups. (B-E) Total cell numbers in each B-cell subset were determined for BM, spleen, and peritoneal cavity. In bar graphs, KO data include both unmanipulated and mock-transplanted animals. Data represent 4 independent experiments. P values compare EμB29-Btk and KO groups: ***P < .001; **P = .001-.01; *P = .01-.05.

EμB29-Btk gene therapy restores central and peripheral B-cell development. PB, BM, spleen, and peritoneal cells from LV-treated mice and mock controls were stained for surface markers and analyzed by flow cytometry to identify B-cell subsets (supplemental Figure 2, gating strategy). (A) PB cells were first gated on live and CD11b populations and then analyzed for B220, IgM, and IgD expression. FACS plots show representative mice from WT mock (n = 7), KO mock (n = 8), MOI 3 (n = 3), and MOI 15 to 25 (n = 12) experimental groups. (B-E) Total cell numbers in each B-cell subset were determined for BM, spleen, and peritoneal cavity. In bar graphs, KO data include both unmanipulated and mock-transplanted animals. Data represent 4 independent experiments. P values compare EμB29-Btk and KO groups: ***P < .001; **P = .001-.01; *P = .01-.05.

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