Immune niches in brain metastases contain TCF1+ stem-like T cells, are associated with disease control and are modulated by preoperative SRS.
Zachary BuchwaldCaroline S JansenRoshan PrabhuMeghana PagadalaPrasanthi ChappaSubir GoyalChengjing ZhouStewart NeillNataliya ProkhnevskaMaria CardenasKimberley HoangJim ZhongSuzanna LoganJeffrey OlsonEdjah NduomLuke Del BalzoKirtesh PatelStuart BurriAnthony AsherScott WilkinsonRoss LakeKristin HigginsPretesh PatelVishal DhereAdam G SowalskyMohammad KhanHaydn T KissickPublished in: Research square (2023)
The CD8 + T-cell response is prognostic for survival outcomes in several tumor types. However, whether this extends to tumors in the brain, an organ with barriers to T cell entry, remains unclear. Here, we analyzed immune infiltration in 67 brain metastasis (BrM) and found high frequencies of PD1 + TCF1 + stem-like CD8 + T-cells and TCF1- effector-like cells. Importantly, the stem-like cells aggregate with antigen presenting cells in immune niches, and niches were prognostic for local disease control. Standard of care for BrM is resection followed by stereotactic radiosurgery (SRS), so to determine SRS’s impact on the BrM immune response, we examined 76 BrM treated with pre-operative SRS (pSRS). pSRS acutely reduced CD8 + T cells at 3 days. However, CD8 + T cells rebounded by day 6, driven by increased frequency of effector-like cells. This suggests that the immune response in BrM can be regenerated rapidly, likely by the local TCF1 + stem-like population.
Keyphrases
- immune response
- brain metastases
- dendritic cells
- small cell lung cancer
- white matter
- healthcare
- induced apoptosis
- regulatory t cells
- resting state
- multiple sclerosis
- cerebral ischemia
- type iii
- cell death
- endoplasmic reticulum stress
- palliative care
- case report
- cell cycle arrest
- signaling pathway
- blood brain barrier
- affordable care act
- subarachnoid hemorrhage