Target intelligence / Profile preview

CD8+ regulatory T cell (CD8+ Treg) (CD8+ Treg)

Target
CD8+ Treg
Molecular classification
Other
01

Overview

CD8+ regulatory T cells (CD8+ Tregs) are a distinct subset of T lymphocytes responsible for maintaining immune homeostasis and preventing autoimmunity by suppressing the activity of various immune cells, including effector T cells and B cells [Mahnke et al., 2013, Immunology]. While CD4+ Tregs are more extensively characterized, CD8+ Tregs represent a potent regulatory population that utilizes mechanisms such as the secretion of inhibitory cytokines (IL-10, TGF-beta) and direct cell-to-cell contact-mediated suppression [Niederlova et al., 2021, Frontiers in Immunology]. In the context of autoimmune diseases and organ transplantation, a deficiency or dysfunction in CD8+ Tregs can lead to a loss of self-tolerance and chronic inflammation [Yu et al., 2018, Journal of Immunology Research]. Conversely, in oncology, an accumulation of CD8+ Tregs within the tumor microenvironment can hinder effective anti-tumor immune responses, making them a potential target for depletion or reprogramming [Salama et al., 2012, Journal of Clinical Oncology]. Current therapeutic approaches include the use of low-dose IL-2 or anti-CD3 antibodies to expand these cells in vivo, as well as ex vivo expansion for adoptive cell therapy [Sim et al., 2014, Journal of Autoimmunity]. Understanding the specific markers and functional plasticity of CD8+ Tregs is essential for developing targeted immunotherapies that can precisely modulate the immune system without causing broad immunosuppression.

Other names
CD8+ suppressor T cellCD8+ TregCD8+ CD25+ Foxp3+ T cellCD8+ CD28- T cellCD8+ CD122+ T cell
02

Mechanism of action

Modulation of CD8+ regulatory T cell frequency and suppressive function to restore immune tolerance or enhance anti-tumor immunity.

03

Biological functions

Immune responseImmune suppressionMaintenance of self-toleranceRegulation of inflammatory responseSuppression of effector T cell activity
04

Disease associations

CancerInflammationAutoimmune diseaseGraft-versus-host diseaseOrgan transplantation
05

Safety considerations

Systemic immunosuppressionIncreased risk of opportunistic infectionsPotential for promoting tumor growth through excessive suppression of anti-tumor immunityDifficulty in specific targeting without affecting effector CD8+ T cells
06

Interacting drugs

Teplizumab

3 more in the full profile.

07

Biomarkers

CD8Foxp3CD25CD122HeliosGITRCTLA-4

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