Literature DB >> 28008849

[First use of CRISPR for gene therapy].

Bertrand Jordan1.   

Abstract

Two clinical trials using CRISPR technology to engineer the T cells of cancer patients by inactivating the gene for immune checkpoint molecule PD-1 are (almost) underway, one in the USA and the other in China. The less sophisticated Chinese trial seems slated to begin first, in part because of very speedy approval ; it may however trigger autoimmune reactions that could be very serious.
© 2016 médecine/sciences – Inserm.

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Year:  2016        PMID: 28008849     DOI: 10.1051/medsci/20163211024

Source DB:  PubMed          Journal:  Med Sci (Paris)        ISSN: 0767-0974            Impact factor:   0.818


  2 in total

1.  PD-1 is a haploinsufficient suppressor of T cell lymphomagenesis.

Authors:  Tim Wartewig; Zsuzsanna Kurgyis; Selina Keppler; Konstanze Pechloff; Erik Hameister; Rupert Öllinger; Roman Maresch; Thorsten Buch; Katja Steiger; Christof Winter; Roland Rad; Jürgen Ruland
Journal:  Nature       Date:  2017-11-15       Impact factor: 49.962

Review 2.  Genome-Editing Technologies: Concept, Pros, and Cons of Various Genome-Editing Techniques and Bioethical Concerns for Clinical Application.

Authors:  Sikandar Hayat Khan
Journal:  Mol Ther Nucleic Acids       Date:  2019-04-03
  2 in total

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