Neuropilin-1 identifies a subset of highly activated CD8+ T cells during parasitic and viral infections

Neuropilin-1 (Nrp-1) expression on CD8(+) T cells has been identified in tumor-infiltrating lymphocytes and in persistent murine gamma-herpes virus infections, where it interferes with the development of long-lived memory T cell responses. In parasitic and acute viral infections, the role of Nrp-1 expression on CD8(+) T cells remains unclear. Here, we demonstrate a strong induction of Nrp-1 expression on CD8(+) T cells in Plasmodium berghei ANKA (PbA)-infected mice that correlated with neurological deficits of experimental cerebral malaria (ECM). Likewise, the frequency of Nrp-1(+)CD8(+) T cells was significantly elevated and correlated with liver damage in the acute phase of lymphocytic choriomeningitis virus (LCMV) infection. Transcriptomic and flow cytometric analyses revealed a highly activated phenotype of Nrp-1(+)CD8(+) T cells from infected mice. Correspondingly, in vitro experiments showed rapid induction of Nrp-1 expression on CD8(+) T cells after stimulation in conjunction with increased expression of activation-associated molecules. Strikingly, T cell-specific Nrp-1 ablation resulted in reduced numbers of activated T cells in the brain of PbA-infected mice as well as in spleen and liver of LCMV-infected mice and alleviated the severity of ECM and LCMV-induced liver pathology. Mechanistically, we identified reduced blood-brain barrier leakage associated with reduced parasite sequestration in the brain of PbA-infected mice with T cell-specific Nrp-1 deficiency. In conclusion, Nrp-1 expression on CD8(+) T cells represents a very early activation marker that exacerbates deleterious CD8(+) T cell responses during both, parasitic PbA and acute LCMV infections.

Automated summary

Neuropilin-1 (Nrp-1) expression on CD8(+) T cells is associated with neurological deficits and liver damage in Plasmodium and viral infections. Nrp-1(+)CD8(+) T cells exhibit a highly activated phenotype during infections. T cell-specific Nrp-1 deficiency alleviates the severity of the diseases. The reduced blood-brain barrier leakage and parasite sequestration may contribute to the protective effects.