Selected article for: "clinical study and immune system"

Author: Endsley, Janice J.; Huante, Matthew B.; Naqvi, Kubra F.; Gelman, Benjamin B.; Endsley, Mark A.
Title: Advancing our understanding of HIV co-infections and neurological disease using the humanized mouse
  • Cord-id: 1rvkx50p
  • Document date: 2021_6_16
  • ID: 1rvkx50p
    Snippet: Humanized mice have become an important workhorse model for HIV research. Advances that enabled development of a human immune system in immune deficient mouse strains have aided new basic research in HIV pathogenesis and immune dysfunction. The small animal features facilitate development of clinical interventions that are difficult to study in clinical cohorts, and avoid the high cost and regulatory burdens of using non-human primates. The model also overcomes the host restriction of HIV for hu
    Document: Humanized mice have become an important workhorse model for HIV research. Advances that enabled development of a human immune system in immune deficient mouse strains have aided new basic research in HIV pathogenesis and immune dysfunction. The small animal features facilitate development of clinical interventions that are difficult to study in clinical cohorts, and avoid the high cost and regulatory burdens of using non-human primates. The model also overcomes the host restriction of HIV for human immune cells which limits discovery and translational research related to important co-infections of people living with HIV. In this review we emphasize recent advances in modeling bacterial and viral co-infections in the setting of HIV in humanized mice, especially neurological disease, and Mycobacterium tuberculosis and HIV co-infections. Applications of current and future co-infection models to address important clinical and research questions are further discussed. [Image: see text]

    Search related documents:
    Co phrase search for related documents
    • absence presence and active infection: 1, 2, 3
    • absence presence and active tuberculosis: 1
    • acid fast bacilli and active tuberculosis: 1, 2, 3
    • acquired aids immune deficiency syndrome and active infection: 1