Figure 2
Figure 2. Presence of NK-cell cytotoxic activity reduces biological features of HLH-like syndrome. Rag2−/− Il2rg−/− and Rag2−/− mice were reconstituted with BM from Prf1−/− and control B6 donors. After 8 weeks, TPrf1−NKPrf1− (open bars), TPrf1−NKPrf1+ (gray bars), and TPrf1+NKPrf1+ mice (black bars) were infected with 200 PFU of LCMV-WE. (A) Spleen size expressed as percentage of body weight on day 14 postinfection. (B) Mononuclear cell (MNC) infiltration in liver on day 14 postinfection. (C) Absolute numbers of CD8+ and NK1.1+ in liver. (D) FACS analysis of MNC from liver gated on CD3− CD19− NK1.1− (left panel). Quantification of absolute numbers of CD64+ Ly6C+ in liver on day 14 postinfection. (E) Serum alanine and aspartate aminotransferase (alanine aminotransferase and aspartate aminotransferase, respectively) levels in infected mice were analyzed on day 14 postinfection. (F) Serum IFN-γ on day 8 postinfection. (G) Serum IL-6 (left panel), CCL2 (middle panel), and CCL5 levels (right panel) on day 14 postinfection. Data (mean ± SEM) are representative of 3 to 4 independent experiments with at least 3 mice in each group. Dotted lines represent minimal normal values for control mice. Statistical analysis was performed using 1-way ANOVA or Student t test. *P < .05; **P < .01.

Presence of NK-cell cytotoxic activity reduces biological features of HLH-like syndrome.Rag2/Il2rg/ and Rag2/ mice were reconstituted with BM from Prf1/ and control B6 donors. After 8 weeks, TPrf1NKPrf1 (open bars), TPrf1NKPrf1+ (gray bars), and TPrf1+NKPrf1+ mice (black bars) were infected with 200 PFU of LCMV-WE. (A) Spleen size expressed as percentage of body weight on day 14 postinfection. (B) Mononuclear cell (MNC) infiltration in liver on day 14 postinfection. (C) Absolute numbers of CD8+ and NK1.1+ in liver. (D) FACS analysis of MNC from liver gated on CD3 CD19 NK1.1 (left panel). Quantification of absolute numbers of CD64+ Ly6C+ in liver on day 14 postinfection. (E) Serum alanine and aspartate aminotransferase (alanine aminotransferase and aspartate aminotransferase, respectively) levels in infected mice were analyzed on day 14 postinfection. (F) Serum IFN-γ on day 8 postinfection. (G) Serum IL-6 (left panel), CCL2 (middle panel), and CCL5 levels (right panel) on day 14 postinfection. Data (mean ± SEM) are representative of 3 to 4 independent experiments with at least 3 mice in each group. Dotted lines represent minimal normal values for control mice. Statistical analysis was performed using 1-way ANOVA or Student t test. *P < .05; **P < .01.

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