Antigen-specific CD8 T cells in cell cycle circulate in the blood after vaccination.
Sonia SimonettiAmbra NataliniAntonella FolgoriStefania CaponeAlfredo NicosiaAngela SantoniFrancesca Di RosaPublished in: Scandinavian journal of immunology (2019)
Although clonal expansion is a hallmark of adaptive immunity, the location(s) where antigen-responding T cells enter cell cycle and complete it have been poorly explored. This lack of knowledge stems partially from the limited experimental approaches available. By using Ki67 plus DNA staining and a novel strategy for flow cytometry analysis, we distinguished antigen-specific CD8 T cells in G0 , in G1 and in S-G2 /M phases of cell cycle after intramuscular vaccination of BALB/c mice with antigen-expressing viral vectors. Antigen-specific cells in S-G2 /M were present at early times after vaccination in lymph nodes (LNs), spleen and, surprisingly, also in the blood, which is an unexpected site for cycling of normal non-leukaemic cells. Most proliferating cells had high scatter profile and were undetected by current criteria of analysis, which under-estimated up to 6 times antigen-specific cell frequency in LNs. Our discovery of cycling antigen-specific CD8 T cells in the blood opens promising translational perspectives.
Keyphrases
- cell cycle
- cell proliferation
- induced apoptosis
- flow cytometry
- cell cycle arrest
- lymph node
- healthcare
- small molecule
- type diabetes
- high intensity
- signaling pathway
- early stage
- metabolic syndrome
- sars cov
- high throughput
- oxidative stress
- stem cells
- pi k akt
- radiation therapy
- single molecule
- skeletal muscle
- neoadjuvant chemotherapy