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T helper 2 cell; T helper 17 cell (Th2 cell; Th17 cell)

Target
Th2 cell; Th17 cell
Molecular classification
Other (Immune cell subtypes; specifically, CD4+ T cell subsets)
01

Overview

T helper 2 cell (Th2) and T helper 17 cell (Th17) are differentiated subtypes of CD4+ T lymphocytes within the adaptive immune system. Th2 cells drive humoral immunity, antibody production, and allergic responses via secretion of IL-4, IL-5, and IL-13, principally targeting extracellular parasites and playing a key role in allergy and asthma. Th17 cells are defined by secretion of IL-17A, IL-17F, and IL-22, orchestrate neutrophil recruitment, and defend against extracellular bacteria and fungi, while aberrations in their activation underlie many autoimmune and chronic inflammatory diseases. Although they are central to immunopharmacology and are modulated by many drugs, neither Th2 nor Th17 cells are a canonical molecular drug target; instead, they represent immune populations influenced by small molecule or antibody therapies through upstream or downstream signaling proteins, cytokine receptors, or transcription factors[3][6][2][1][7].

Other names
Th2 cell (for T helper 2 cell)Th17 cell (for T helper 17 cell)
02

Mechanism of action

Inhibition of Th2 cytokines (e.g., IL-4, IL-5, IL-13) reduces allergic inflammation or asthma symptoms - Inhibition of Th17 effector cytokines (IL-17A, IL-17F) reduces autoimmunity and chronic inflammation - Inhibition of cytokines necessary for differentiation (IL-23 inhibition impacts Th17 cell survival/proliferation)

03

Biological functions

Regulation of antibody-mediated (humoral) immunityResponse to extracellular parasites and allergensPromotion of IgE class switchingModulation of eosinophil, basophil, and mast cell activationMediation of allergies and asthmaRegulation of mucosal immunity and barrier protection[6][1][2]Response to extracellular bacteria and fungiMediation of neutrophil recruitment[7]Pathogenesis of autoimmunity and chronic inflammation
04

Disease associations

Allergy (Th2 cell)[3]Asthma (Th2 cell)[3]Autoimmune diseases (Th17 cell): multiple sclerosis, rheumatoid arthritis, Crohn’s disease, psoriasis[6][7][1][2]Chronic inflammatory diseases (Th17 cell)Infection: Parasitic (Th2 cell); bacterial and fungal (Th17 cell)[1][3][6][7]
05

Safety considerations

Suppressing these pathways can increase infection risk (especially fungal and respiratory for Th17-targeted therapy)[6][7]Suppression of Th2 activity can reduce defense against parasites[3]Risk of immune imbalance, hypersensitivity, or secondary autoimmunity[6][7]
06

Interacting drugs

Monoclonal antibodies against IL-4, IL-5, IL-13 (Th2-associated cytokines; e.g., dupilumab, mepolizumab)[3]

2 more in the full profile.

07

Biomarkers

Th2 cytokines or IgE (as markers of Th2 activity)[3]Th17 cytokines (IL-17A, IL-17F, IL-22) as markers of Th17 cell activity or autoimmune disorders[6][7]Cell surface markers (CCR6, CD161, RORγt for Th17 in research/clinical context)[6][1]

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