Cargando…
In situ conversion of defective Treg into SuperTreg cells to treat advanced IPEX-like disorders in mice
Mutations disrupting regulatory T (Treg) cell function can cause IPEX and IPEX-related disorders, but whether established disease can be reversed by correcting these mutations is unclear. Treg-specific deletion of the chromatin remodeling factor Brg1 impairs Treg cell activation and causes fatal aut...
Autores principales: | Li, Yongqin, Chen, Yuxin, Mao, Shaoshuai, Kaundal, Ravinder, Jing, Zhengyu, Chen, Qin, Wang, Xinxin, Xia, Jing, Liu, Dahai, Sun, Jianlong, Wang, Haopeng, Chi, Tian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271236/ https://www.ncbi.nlm.nih.gov/pubmed/32493900 http://dx.doi.org/10.1038/s41467-020-15836-2 |
Ejemplares similares
-
Author Correction: In situ conversion of defective Treg into SuperTreg cells to treat advanced IPEX-like disorders in mice
por: Li, Yongqin, et al.
Publicado: (2021) -
Mutations from patients with IPEX ported to mice reveal different patterns of FoxP3 and Treg dysfunction
por: Leon, Juliette, et al.
Publicado: (2023) -
Super-Treg: Toward a New Era of Adoptive Treg Therapy Enabled by Genetic Modifications
por: Amini, Leila, et al.
Publicado: (2021) -
IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom
por: Al Maawali, Ali, et al.
Publicado: (2020) -
GATA3, HDAC6, and BCL6 Regulate FOXP3+ Treg Plasticity and Determine Treg Conversion into Either Novel Antigen-Presenting Cell-Like Treg or Th1-Treg
por: Xu, Keman, et al.
Publicado: (2018)