Harnessing CD8+CD28- Regulatory T Cells as a Tool to Treat Autoimmune Disease

被引:10
|
作者
Ceeraz, Sabrina [1 ]
Thompson, Charlotte R. [2 ]
Beatson, Richard [3 ]
Choy, Ernest H. [4 ]
机构
[1] Carisma Therapeut, Philadelphia, PA 19104 USA
[2] Univ Sussex, Brighton & Sussex Med Sch, Brighton BN1 9RH, E Sussex, England
[3] Kings Coll London, Fac Life Sci & Med, Sch Canc & Pharmaceut Sci, London SE1 9RT, England
[4] Cardiff Univ, Sch Med, Div Infect & Immun, CREATE Ctr, Cardiff CF14 4XN, Wales
基金
英国医学研究理事会;
关键词
CD8; Treg; autoimmunity; immunoregulation; DIFFERENT LY COMPONENTS; X-LINKED SYNDROME; IMMUNE-RESPONSES; RHEUMATOID-ARTHRITIS; HELPER ACTIVITIES; SUPPRESSOR-CELLS; CD8+CD28-T CELLS; EPITHELIAL-CELLS; MURINE LUPUS; LYMPHOCYTES;
D O I
10.3390/cells10112973
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
T regulatory cell therapy presents a novel therapeutic strategy for patients with autoimmune diseases or who are undergoing transplantation. At present, the CD4(+) Treg population has been extensively characterized, as a result of defined phenotypic and functional readouts. In this review article, we discuss the development and biology of CD8(+) Tregs and their role in murine and human disease indications. A subset of CD8(+) Tregs that lack the surface expression of CD28 (CD8(+)CD28(-) Treg) has proved efficacious in preclinical models. CD8(+)CD28(-) Tregs are present in healthy individuals, but their impaired functionality in disease renders them less effective in mediating immunosuppression. We primarily focus on harnessing CD8(+) Treg cell therapy in the clinic to support current treatment for patients with autoimmune or inflammatory conditions.
引用
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页数:11
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