Figure 2
Figure 2. Expansion of licensed but not unlicensed Ly49H+ NK cells with increased IFNγ production post-HSCT in MHC-disparate recipients following MCMV infection. (A) Example flow plots of CD3-NK1.1+ NK cells gated on H-2d vs H-2b MHC-I haplotypes from splenocytes of B10.D2 (H-2d), B10 (H-2b), and C57BL/6 (H-2b) host mice 7 days post-MCMV infection and that underwent allo-HSCT 10 or 17 days prior to MCMV infection. (B-D) Splenocytes were stained for CD3, NK1.1, Ly49H, Ly49C/I, and Ly49G2 7 days after infection post-HSCT and compared with noninfected mice. Percentage of CD3− NK1.1+ Ly49C/I+/H+ and Ly49G2+/H+ cells in (B) B10, (C) B10.D2, (D) C57BL/6 infected and noninfected host mice are illustrated. (E-G) The percentage of CD3− NK1.1+ Ly49H+ IFNγ+ Ly49G2+ or Ly49C/I+ NK cells was determined from infected and noninfected mice after allo-HSCT in (E) B10, (F) B10.D2, and (G) C57BL/6 mice. Data are representative of 2 to 3 experiments with 4 mice per group. The error bars represent the standard error of the mean. Statistical analysis was performed using 1-way ANOVA and Tukey posttest.*P < .05; **P < .01.

Expansion of licensed but not unlicensed Ly49H+ NK cells with increased IFNγ production post-HSCT in MHC-disparate recipients following MCMV infection. (A) Example flow plots of CD3-NK1.1+ NK cells gated on H-2d vs H-2b MHC-I haplotypes from splenocytes of B10.D2 (H-2d), B10 (H-2b), and C57BL/6 (H-2b) host mice 7 days post-MCMV infection and that underwent allo-HSCT 10 or 17 days prior to MCMV infection. (B-D) Splenocytes were stained for CD3, NK1.1, Ly49H, Ly49C/I, and Ly49G2 7 days after infection post-HSCT and compared with noninfected mice. Percentage of CD3 NK1.1+ Ly49C/I+/H+ and Ly49G2+/H+ cells in (B) B10, (C) B10.D2, (D) C57BL/6 infected and noninfected host mice are illustrated. (E-G) The percentage of CD3 NK1.1+ Ly49H+ IFNγ+ Ly49G2+ or Ly49C/I+ NK cells was determined from infected and noninfected mice after allo-HSCT in (E) B10, (F) B10.D2, and (G) C57BL/6 mice. Data are representative of 2 to 3 experiments with 4 mice per group. The error bars represent the standard error of the mean. Statistical analysis was performed using 1-way ANOVA and Tukey posttest.*P < .05; **P < .01.

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