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. Author manuscript; available in PMC: 2024 Dec 10.
Published in final edited form as: Cell. 2015 Apr 16;161(3):486–500. doi: 10.1016/j.cell.2015.03.005

Figure 2. Adhesion Molecules that Govern Leukocyte Trafficking in Other Organs Are Not Required for CD8 TE Accumulation in the Liver.

Figure 2.

(A) Percentage of Cor93 CD8 TE that accumulated within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) that were previously treated with anti-PSGL1, anti-CD62L or anti-CD62E Abs relative to control (control = 100%). n = 5; results are representative of two independent experiments. Similar results were obtained with Env28 CD8 TE (data not shown).

(B) Percentage of Cor93 CD8 TE that accumulated within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) that were previously treated with anti-VLA-4, anti-LFA-1 or anti-PECAM-1 Abs relative to control (control = 100%). n = 8; results are representative of two independent experiments. Similar results were obtained with Env28 CD8 TE (data not shown).(C) Percentage of Cor93 CD8 TE that accumulated WT CD44−/− within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) that were previously treated with anti-VAP-1 Abs relative to control (control = 100%). n = 5; results are representative of two independent experiments. Similar results were obtained with Env28 CD8 TE (data not shown).

(D) Percentage of CD44−/− Cor93 CD8 TE that accumulated within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) relative to WT Cor93 CD8 TE (WT = 100%). n = 10; results are representative of two independent experiments.

(E) Percentage of PTX-treated Cor93 CD8 TE that accumulated within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) relative to control Cor93 CD8 TE (control = 100%). n = 5; results are representative of two independent experiments. Similar results were obtained with Env28 CD8 TE (data not shown).

(F) Percentage of Cor93 CD8 TE that accumulated within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) that were injected 24 hr earlier with 5 × 106 Env28 CD8 TE relative to control (control = 100%). n = 5; results are representative of two independent experiments.

(G) Percentage of PTX-treated Cor93 CD8 TE (relative to untreated Cor93 CD8 TE controls) that accumulated within the liver 2 hr upon transfer into HBV replication-competent transgenic mice (H2bxd) that were treated 24 hr earlier with Env28 CD8 TE. n = 5; results are representative of two independent experiments.

Results are expressed as mean ± SEM.

See also Figure S1.