التفاصيل البيبلوغرافية
العنوان: |
Manipulating the NKG2D Receptor-Ligand Axis Using CRISPR: Novel Technologies for Improved Host Immunity |
المؤلفون: |
Eric Alves, Emily McLeish, Pilar Blancafort, Jerome D. Coudert, Silvana Gaudieri |
المصدر: |
Frontiers in Immunology, Vol 12 (2021) |
بيانات النشر: |
Frontiers Media S.A., 2021. |
سنة النشر: |
2021 |
المجموعة: |
LCC:Immunologic diseases. Allergy |
مصطلحات موضوعية: |
NKG2D, CRISPR, precision medicine, NK cells, viral infection, cancer, Immunologic diseases. Allergy, RC581-607 |
الوصف: |
The activating immune receptor natural killer group member D (NKG2D) and its cognate ligands represent a fundamental surveillance system of cellular distress, damage or transformation. Signaling through the NKG2D receptor-ligand axis is critical for early detection of viral infection or oncogenic transformation and the presence of functional NKG2D ligands (NKG2D-L) is associated with tumor rejection and viral clearance. Many viruses and tumors have developed mechanisms to evade NKG2D recognition via transcriptional, post-transcriptional or post-translational interference with NKG2D-L, supporting the concept that circumventing immune evasion of the NKG2D receptor-ligand axis may be an attractive therapeutic avenue for antiviral therapy or cancer immunotherapy. To date, the complexity of the NKG2D receptor-ligand axis and the lack of specificity of current NKG2D-targeting therapies has not allowed for the precise manipulation required to optimally harness NKG2D-mediated immunity. However, with the discovery of clustered regularly interspaced short palindromic repeats (CRISPRs) and CRISPR-associated (Cas) proteins, novel opportunities have arisen in the realm of locus-specific gene editing and regulation. Here, we give a brief overview of the NKG2D receptor-ligand axis in humans and discuss the levels at which NKG2D-L are regulated and dysregulated during viral infection and oncogenesis. Moreover, we explore the potential for CRISPR-based technologies to provide novel therapeutic avenues to improve and maximize NKG2D-mediated immunity. |
نوع الوثيقة: |
article |
وصف الملف: |
electronic resource |
اللغة: |
English |
تدمد: |
1664-3224 |
Relation: |
https://www.frontiersin.org/articles/10.3389/fimmu.2021.712722/full; https://doaj.org/toc/1664-3224 |
DOI: |
10.3389/fimmu.2021.712722 |
URL الوصول: |
https://doaj.org/article/1c461da9c4b7407a988488131fd0a08d |
رقم الانضمام: |
edsdoj.1c461da9c4b7407a988488131fd0a08d |
قاعدة البيانات: |
Directory of Open Access Journals |