Humanized mice mount specific adaptive and innate immune responses to EBV and TSST-1 - PubMed (original) (raw)
. 2006 Nov;12(11):1316-22.
doi: 10.1038/nm1431. Epub 2006 Oct 22.
Affiliations
- PMID: 17057712
- DOI: 10.1038/nm1431
Humanized mice mount specific adaptive and innate immune responses to EBV and TSST-1
Michael W Melkus et al. Nat Med. 2006 Nov.
Abstract
Here we show that transplantation of autologous human hematopoietic fetal liver CD34+ cells into NOD/SCID mice previously implanted with human fetal thymic and liver tissues results in long-term, systemic human T-cell homeostasis. In addition, these mice show systemic repopulation with human B cells, monocytes and macrophages, and dendritic cells (DCs). T cells in these mice generate human major histocompatibility complex class I- and class II-restricted adaptive immune responses to Epstein-Barr virus (EBV) infection and are activated by human DCs to mount a potent T-cell immune response to superantigens. Administration of the superantigen toxic shock syndrome toxin 1 (TSST-1) results in the specific systemic expansion of human Vbeta2+ T cells, release of human proinflammatory cytokines and localized, specific activation and maturation of human CD11c+ dendritic cells. This represents the first demonstration of long-term systemic human T-cell reconstitution in vivo allowing for the manifestation of the differential response by human DCs to TSST-1.
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