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• W2036606193 abstract "Human cytomegalovirus (HCMV) infection, including primary infection resulting from transmission from a seropositive donor to a seronegative recipient (D+/R−), remains a significant problem in the setting of peripheral blood stem cell transplantation (PBSCT). The lack of a suitable animal model for studying HCMV transmission after PBSCT is a major barrier to understanding this process and, consequently, developing novel interventions to prevent HCMV infection. Our previous work demonstrated that human CD34+ progenitor cell–engrafted NOD-scid IL2Rγcnull (NSG) mice support latent HCMV infection after direct inoculation and reactivation after treatment with granulocyte colony-stimulating factor. To more accurately recapitulate HCMV infection in the D+/R− PBSCT setting, granulocyte colony-stimulating factor–mobilized peripheral blood stem cells from seropositive donors were used to engraft NSG mice. All recipient mice demonstrated evidence of HCMV infection in liver, spleen, and bone marrow. These findings validate the NSG mouse model for studying HCMV transmission during PBSCT." @default.
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• W2036606193 date "2014-01-01" @default.
• W2036606193 modified "2023-09-27" @default.
• W2036606193 title "HCMV Infection of Humanized Mice after Transplantation of G-CSF–Mobilized Peripheral Blood Stem Cells from HCMV-Seropositive Donors" @default.
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• W2036606193 doi "https://doi.org/10.1016/j.bbmt.2013.10.019" @default.
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