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. Author manuscript; available in PMC: 2024 Nov 15.
Published in final edited form as: J Immunol. 2023 Nov 15;211(10):1526–1539. doi: 10.4049/jimmunol.2300294

Figure 4. ThCTL cell expansion develops over the course of infection in B6 mice but remains muted across time in PWD mice.

Figure 4.

B6 and PWD mice were i.p. infected MHV-68 as described in Figure 1. At 5 (D5) (4F + 4M B6 and 4F + 3M PWD), 9 (D9) (3F + 2M B6 and 3F + 2M PWD), 16 (D16) (2F + 2M B6 and 4F + 2M PWD), or 35 (D35) (4F + 4M B6 and 4F + 4M PWD) days post infection splenic leukocytes were isolated and flow cytometry was preformed to determine ThCTL kinetics during MHV-68 Infection (see Materials and Methods). Male and female data were pooled by genotype. (A) Kinetics of the CX3CR1+KLRG1+ cell subset frequency in CD4 T cells (TCRβ+CD4+CD11bCD19) during MHV-68 infection in B6 mice. Comparison of (B) Cx3CR1+KLRG1+, (C) CX3CR1+, (D) KLRG1+, (E) IFNγ+, and (F) GZMB+ cell populations as frequency of total CD4 T cells (TCRβ+CD4+CD11bCD19) in B6 and PWD mice over the course of MHV-68 infection. Significance of differences between B6 and PWD mice at each time point was determined via multiple unpaired T-tests and are indicated by the brackets where significant (p<0.05).