Target intelligence / Profile preview

Idiotype-derived peptide-Major Histocompatibility Complex (Id-pMHC) (Id-pMHC)

Target
Id-pMHC
Molecular classification
Antigen-MHC complex, Major Histocompatibility Complex, Receptor-ligand complex
01

Overview

The Idiotype-derived peptide-Major Histocompatibility Complex (Id-pMHC) is a specialized antigen-presenting structure found on the surface of B-cell lineage cells, particularly in the context of B-cell malignancies like Multiple Myeloma and Follicular Lymphoma (Bogen et al., 1993). These complexes consist of peptides derived from the unique variable regions (idiotypes) of the clonal B-cell receptor (BCR) or secreted immunoglobulin, which are processed and loaded onto MHC Class I and Class II molecules (Lynch et al., 1985). Recognition of Id-pMHC by T-cell receptors (TCRs) is a cornerstone of tumor immunosurveillance, where CD4+ T cells recognize MHC II-presented idiotype peptides and CD8+ T cells recognize MHC I-presented counterparts (Corthay et al., 2005). Because the idiotype is unique to the malignant clone, these complexes serve as ideal tumor-specific antigens for precision immunotherapy. Therapeutic interventions, such as idiotype vaccines (e.g., BiovaxID) and TCR-engineered T cells, aim to stimulate or provide T cells that specifically target these complexes to eliminate cancerous cells while sparing healthy tissue (Schuster et al., 2011; Yi et al., 2000). However, challenges such as MHC downregulation by tumors and the inherent low immunogenicity of self-derived peptides remain significant hurdles in clinical application.

Other names
Idiotype-MHC complexB-cell receptor idiotype-derived peptide-MHCId-peptide-HLA complexTumor-specific idiotype antigenId-pMHC
02

Mechanism of action

Induction of idiotype-specific T-cell responses (CD4+ and CD8+) that recognize and eliminate malignant B cells presenting idiotype-derived peptides on MHC molecules.

03

Biological functions

Antigen presentationT-cell activationImmune responseAdaptive immunityImmune surveillance
04

Disease associations

B-cell lymphomaMultiple myelomaFollicular lymphomaMantle cell lymphomaB-cell malignancies
05

Safety considerations

Tumor immune escape via MHC downregulationIdiotype antigen loss or clonal evolutionLow immunogenicity of self-derived peptidesPotential for cytokine release syndrome with adoptive T-cell therapies
06

Interacting drugs

BiovaxID (Dasiprotimut-T)

3 more in the full profile.

07

Biomarkers

Clonal immunoglobulin variable region sequence (idiotype)Patient HLA genotype (e.g., HLA-DRB1, HLA-A*02:01)Idiotype-specific T-cell frequency (ELISPOT)MHC expression levels on tumor cells

Beyond the preview

Go deeper on Idiotype-derived peptide-Major Histocompatibility Complex (Id-pMHC) (Id-pMHC).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Idiotype-derived peptide-Major Histocompatibility Complex (Id-pMHC) (Id-pMHC).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call