Target intelligence / Profile preview

Apolipoprotein B-100 peptide P210–MHC complex (P210–MHC complex)

Target
P210–MHC complex
Molecular classification
Peptide-MHC complex, Antigen, Self-antigen
01

Overview

The P210–MHC complex is a molecular assembly consisting of a specific 20-amino acid peptide (P210, derived from residues 3136–3155 of Apolipoprotein B-100) bound to a Major Histocompatibility Complex (MHC) molecule, typically HLA-A*02:01. This complex is presented on the surface of antigen-presenting cells (APCs), such as dendritic cells, where it serves as a critical recognition element for the adaptive immune system. In the context of atherosclerosis, the P210 peptide acts as a self-antigen that can trigger both pro-inflammatory and regulatory immune responses. Therapeutic strategies targeting this complex aim to modulate the immune system's reaction to low-density lipoprotein (LDL) components. Experimental vaccines, such as P210-loaded peptide amphiphile micelles (P210-PAM), are designed to promote the expansion of P210-specific regulatory T cells (Tregs) and dampen the activity of pro-inflammatory CD8+ and CD4+ T cells. By inducing immune tolerance or protective immunity against this specific epitope, these therapies seek to reduce arterial inflammation and stabilize or shrink atherosclerotic plaques. This approach represents a novel immunotherapeutic paradigm for treating cardiovascular diseases beyond traditional lipid-lowering statin therapies.

Other names
ApoB-100 P210–MHC complexPeptide 210–HLA complexApolipoprotein B-100 (3136–3155) peptide–MHC complexP210–HLA-A*02:01 complex
02

Mechanism of action

Induction of antigen-specific regulatory T cells (Tregs) and modulation of pro-inflammatory T-cell responses to reduce vascular inflammation and atherosclerotic plaque formation.

03

Biological functions

Antigen presentationImmune responseT-cell activationImmune tolerance inductionRegulatory T-cell modulation
04

Disease associations

AtherosclerosisCardiovascular diseaseHypercholesterolemia
05

Safety considerations

Potential for inducing autoimmune responsesMHC restriction (efficacy limited to specific HLA types)Immune evasion through MHC downregulationVariability in individual immune repertoires
06

Interacting drugs

P210-PAM (Peptide Amphiphile Micelles)

2 more in the full profile.

07

Biomarkers

P210-specific CD8+ T-cell frequencyHLA-A*02:01 genotypeApoB-100 autoantibody levelsC-reactive protein (CRP)

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