Visualization of the human CD4+ T-cell response in humanized HLA-DR4-expressing NOD/Shi-scid/γcnull (NOG) mice by retrogenic expression of the human TCR gene

Abstract

The development of severe immunodeficient mouse strains containing various human genes, including cytokines or HLA, has enabled the reconstitution of functional human immune systems after transplantation of human hematopoietic stem cells (HSC). Accumulating evidence has suggested that HLA-restricted antigen-specific human T-cell responses can be generated in these humanized mice. To directly monitor immune responses of human CD4+ T cells, we introduced β-lactoglobulin (BLG)-specific T cell receptor (TCR) genes derived from CD4+ T-cell clones of cow-milk allergy patients into HSCs, and subsequently transplanted them into NOG-HLA-DR4 transgenic/I-Aβ deficient mice (NOG-DR4/I-Ao). In the thymus, thymocytes with BLG-specific TCR preferentially differentiated into CD4+CD8− single-positive cells. Adoptive transfer of mature CD4+ T cells expressing the TCR into recipient NOG-DR4/I-Ao mice demonstrated that human CD4+ T cells proliferated in response to antigenic stimulation and produced IFN-γ in vivo, suggesting that functional T-cell reactions (especially Th1-skewed responses) were induced in humanized mice.