Experimental models demonstrate leukemia cell migration in the central nervous system, highlighting lymphatic interactions.
Central nervous system (CNS) involvement frequently occurs in acute lymphoblastic leukemia (ALL), but many questions remain about how leukemia cells access, persist in, and exploit the CNS. The CNS is protected by the meninges, which are fluid filled membranes that surround the brain. Within the meninges, meningeal lymphatic vessels drain cerebrospinal fluid to cervical lymph nodes for immunosurveillance, a potential pathway for leukemia cell migration into or egress from the CNS. Here, we utilize tissue engineered models of the meningeal lymphatics and lymph node stroma to probe how leukemia cells interact with these key tissues. We first demonstrate that standard-of-care chemotherapeutics can damage meningeal lymphatic barriers. Next, we showed that soluble factors from the meningeal lymphatics can support leukemia cell growth while soluble factors from the lymph node model under flow can promote leukemia cell migration. Finally, we show that leukemia cells migrate through the lymph node model under both static and flow conditions. Overall, we have demonstrated the feasibility of using engineered lymphatic models to study leukemia cell behavior in the CNS with the goal of expanding the available experimental platforms for understanding CNS metastasis and relapse.
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Hammel et al. (2025) studied this question.
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