AI Article Synopsis

  • Reporter proteins are essential in biomedical research, but introducing them into mice can trigger immune rejection.
  • The study introduces a novel 'Tol' mouse model, which expresses a variety of shuffled reporter proteins from one genetic sequence, enhancing tolerance to these proteins.
  • This model reduces the immune response against specific T cells and improves the success of gene transfer experiments, making it a useful tool for future studies in cell and gene therapy.

Article Abstract

Reporter proteins have become an indispensable tool in biomedical research. However, exogenous introduction of these reporters into mice poses a risk of rejection by the immune system. Here, we describe the generation, validation and application of a multiple reporter protein tolerant 'Tol' mouse model that constitutively expresses an assembly of shuffled reporter proteins from a single open reading frame. We demonstrate that expression of the Tol transgene results in the deletion of CD8 T cells specific for a model epitope, and substantially improves engraftment of reporter-gene transduced T cells. The Tol strain provides a valuable mouse model for cell transfer and viral-mediated gene transfer studies, and serves as a methodological example for the generation of poly-tolerant mouse strains.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260180PMC
http://dx.doi.org/10.1038/s42003-020-0979-0DOI Listing

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