| Popis: |
Background Why Epstein–Barr virus-related hemophagocytic lymphohistiocytosis (EBV-HLH) undergoes remission shortly after treatment and relapses rapidly and whether EBV infection in natural killer (NK)/T cells contributes to the deterioration of EBV-HLH are unknown. Methods EBV cell tropism and anti-EBV host cellular immunity were compared based on multicolor flow cytometry technique between EBV-HLH survivors and those who died to explore the key factors associated with the deterioration of HLH progression. Transcriptomics was performed to reveal the underlying mechanisms of EBV-HLH deterioration. Results In the deceased cases, EBV infection spread to NK (CD3-CD56+, 84.3%) and/or NKT (CD3 + CD56+, 67.9%) cells with a highly proliferating profile, whereas the infection was only limited to B cells in survivors. Although a similar low NK activation (Myc), proliferation (MKI67), and EBV LMP1-related carcinogenesis (TRAF2 and Jak3) genes. Conclusions Our study suggest that the oncogenicity of EBV-infected NK/NKT cells deteriorates EBV-HLH, and the spread of EBV to NK and NKT cells may indicate a prephase of NK/T lymphoma. Thus, the findings of this study may guide future therapeutic strategies for EBV-HLH. |
