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Male BALB/c mice were randomly divided into the conventional immunity control (NIC) team, normal resistance illness (NIA) group, resistant compromised control (CIC) group, and resistant compromised disease (CIA) group (letter = 15 for every group). Intraperitoneal injection of cyclophosphamide and intranasal instillation of A. baumannii answer were used to induce affected resistance and murine pneumonia, respectively. The mice were sacrificed at 6 and 24 h later o
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