Distinct Effector Programs of Brain-Homing CD8+ T Cells in Multiple Sclerosis

The effector programs of CD8(+) memory T cells are influenced by the transcription factors RUNX3, EOMES and T-bet. How these factors define brain-homing CD8(+) memory T cells in multiple sclerosis (MS) remains unknown. To address this, we analyzed blood, CSF and brain tissues from MS patients for the impact of differential RUNX3, EOMES and T-bet expression on CD8(+) T cell effector phenotypes. The frequencies of RUNX3- and EOMES-, but not T-bet-expressing CD8(+) memory T cells were reduced in the blood of treatment-naive MS patients as compared to healthy controls. Such reductions were not seen in MS patients treated with natalizumab (anti-VLA-4 Ab). We found an additional loss of T-bet in RUNX3-expressing cells, which was associated with the presence of MS risk SNP rs6672420 (RUNX3). RUNX3(+)EOMES(+)T-bet(-) CD8(+) memory T cells were enriched for the brain residency-associated markers CCR5, granzyme K, CD20 and CD69 and selectively dominated the MS CSF. In MS brain tissues, T-bet coexpression was recovered in CD20(dim) and CD69(+) CD8(+) T cells, and was accompanied by increased coproduction of granzyme K and B. These results indicate that coexpression of RUNX3 and EOMES, but not T-bet, defines CD8(+) memory T cells with a pre-existing brain residency-associated phenotype such that they are prone to enter the CNS in MS.

Automated summary

The effector programs of CD8(+) memory T cells in multiple sclerosis (MS) are influenced by transcription factors RUNX3, EOMES, and T-bet. This study found that the frequencies of RUNX3- and EOMES-expressing CD8(+) memory T cells were reduced in the blood of MS patients, but not in MS patients treated with natalizumab. CD8(+) memory T cells that co-express RUNX3 and EOMES and do not express T-bet were enriched in the MS cerebrospinal fluid and associated with brain residency-associated markers. These findings suggest that the co-expression of RUNX3 and EOMES defines CD8(+) memory T cells with a pre-existing brain residency-associated phenotype in MS.