LAUSR

Humanized mouse models have been developed to study cell-mediated immune responses to human pathogens in vivo. How immunocompetent human T cells are selected in a murine thymus in such humanized mice remains poorly explored. To gain insights into this mechanism, we investigated the differentiation of human immune compartments in mouse MHC class II deficient immune compromised mice (humanized Ab0 mice). We observed a strong reduction in human CD4+ T cell development but despite this reduction Ab0 mice had no disadvantage during Epstein Barr virus (EBV) infection. Viral loads were equally well controlled in humanized Ab0 mice compare to humanized NSG mice, and improved T cell recognition of autologous EBV-transformed B cells (LCLs) was observed, especially with respect to cytotoxicity. MHC class II blocking experiments with CD4+ T cells from humanized Ab0 mice demonstrated MHC class II restriction of LCL recognition. These findings suggest that a small number of CD4+ T cells in humanized mice can be solely selected on human MHC class II molecules, presumably expressed by reconstituted human immune cells, leading to improved effector functions. This article is protected by copyright. All rights reserved.