Target intelligence / Profile preview

Autoreactive T-cell

Molecular classification
Other
01

Overview

Autoreactive T-cells, often referred to as autoaggressive T-cells, are a subset of the immune system's T-lymphocytes that mistakenly identify and attack the body's own healthy tissues (PubMed: 30104663). Under normal conditions, these cells are eliminated or suppressed through central and peripheral tolerance mechanisms; however, their escape and activation lead to the pathogenesis of various autoimmune diseases such as multiple sclerosis and type 1 diabetes (StatPearls: NBK459471). These cells are characterized by their expression of specific T-cell receptors (TCRs) that recognize self-antigens presented by major histocompatibility complex (MHC) molecules. Therapeutic strategies aimed at these cells include broad immunosuppression, targeted depletion using monoclonal antibodies, or more modern approaches like CAR-T cell therapy designed to specifically eliminate the pathogenic clones while sparing the rest of the immune system (Nature Reviews Drug Discovery: nrd.2017.134). Monitoring these cells often involves tracking specific surface markers, cytokine production profiles, or TCR repertoire diversity (Nature Medicine: 2022).

Other names
Autoaggressive T-cellAutoreactive T-lymphocyteSelf-reactive T-cellPathogenic T-cell
02

Mechanism of action

Therapeutic strategies involve the depletion of T-cells, inhibition of costimulatory signals required for activation, or sequestration of cells within lymphoid organs to prevent tissue infiltration (StatPearls: NBK459471; FDA: Teplizumab Label).

03

Biological functions

Immune responseCell-mediated cytotoxicityCytokine productionApoptosis induction
04

Disease associations

Autoimmune diseaseMultiple SclerosisType 1 DiabetesRheumatoid ArthritisSystemic Lupus ErythematosusPsoriasis
05

Safety considerations

Systemic immunosuppressionIncreased risk of opportunistic infectionsCytokine release syndromeReduced response to vaccinationsProgressive Multifocal Leukoencephalopathy (PML)
06

Interacting drugs

Teplizumab

7 more in the full profile.

07

Biomarkers

CD3CD4CD8CD25Interferon-gammaInterleukin-17T-cell receptor (TCR) sequences

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