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Therapeutic vaccine candidates using viral vectors encoding LMP2 have properly induced virus-particular CD8⁺ T cell responses in early-period scientific trials. On top of that, adoptive T mobile therapies like posoleucel also focus on LMP2 together with other latency proteins such as EBNA1, reinforcing its importance as a conserved and immunodominant antigen.
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EBNA-3a appears to manage a subset of cell genes, lots of which overlap with Gentlemen and ladies managed by EBNA2. The two proteins can act antagonistically or cooperatively to regulate gene expression.
Between these latency proteins, EBNA-3a performs a supportive but non-important position in B mobile transformation: EBV mutants missing EBNA-3a can even now renovate B cells, but with noticeably lessened performance.
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