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These results indicated that a large number of effector cells accumulated in lung tissue after CD5/ LNP-FAPCAR 2.2 treatment because of T cell immune activation, which partially resulted from transient FAPCAR-T recruited in the fibrotic lung

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Thus, it is highly interesting to investigate the oligomeric state of mVP35 under the context of the MARV LVP35 complex as well as to compare the potential similarities and differences in structures and RNA synthesis mechanisms between MARV and EBOV polymerases

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