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. Author manuscript; available in PMC: 2019 Apr 18.
Published in final edited form as: Cell Rep. 2019 Apr 9;27(2):537–548.e5. doi: 10.1016/j.celrep.2019.03.059

Figure 7. Loss of Qa-1 Negatively Impacts the Non-classical CD8+ T Cell Response and Their Protective Capabilities.

Figure 7.

(A and B) Frequency (A) and absolute number (B) of non-classical CD8+ T cells in the spleen, liver, and blood of KbDb−/−Qa-1+/+, KbDb−/−Qa-1+/−, and KbDb−/−Qa-1−/− mice on day 7 post-MCMV infection (n = 9–11).

(C–G) KLRG1+CD127 (C), KLRG1+CX3CR1+ (D), and NKG2A/C/E+ (E) non-classical CD8+ T cells and KLRG1+ (F) and NKG2A/C/E+ NK (G) cells on day 7 post-MCMV infection from indicated organs of KbDb−/−Qa1+/+, KbDb−/−Qa1+/−, and KbDb−/−Qa1−/− mice (n = 9–11).

(H and I) Frequency (H) and absolute number (I) of CD8+ T cells from the spleen and liver of long-term infected KbDb−/−Qa1+/+ (DKO) and KbDb−/−Qa1−/− (TKO) mice (n = 5–7).

(J) Survival of RAG1−/−KbDb−/− mice with (—, n = 5) or without (- -, n = 6) adoptive transfer of 5 × 104 sorted CD8+ TM cells (KLRG1CD27+) from long-term infected KbDb−/−Qa-1−/− mice. Statistical analysis determined by Mantel-Cox test.

Data are pooled from two (H and I) or three independent experiments (A–G) or representative of three independent experiments (J). Data represent mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001, and ****p < 0.0001.

See also Figure S4.