Target intelligence / Profile preview

Major histocompatibility complex (MHC) molecules presenting Plasmodium falciparum peptides (Pf-pMHC)

Target
Pf-pMHC
Molecular classification
Receptor, Antigen-presenting complex
01

Overview

Major histocompatibility complex (MHC) molecules presenting Plasmodium falciparum peptides are specialized cell-surface complexes essential for the adaptive immune system to detect and eliminate malaria parasites (Source: PubMed ID: 29164944). These complexes consist of a host-derived MHC molecule (HLA in humans) and a short peptide fragment derived from Plasmodium proteins, such as the circumsporozoite protein (CSP) or the liver-stage antigen 1 (LSA-1) (Source: UniProt). When these complexes are displayed on the surface of infected hepatocytes or professional antigen-presenting cells, they are recognized by the T-cell receptors (TCRs) of CD8+ and CD4+ T cells (Source: Nature Reviews Immunology, 2013). This recognition triggers a cascade of immune responses, including the direct lysis of infected cells and the release of cytokines like interferon-gamma, which are vital for controlling the infection (Source: PubMed ID: 23543121). In therapeutic development, these pMHC complexes are the primary targets for T-cell-inducing vaccines and are being explored for TCR-like antibody therapies (Source: WHO). However, the high degree of HLA polymorphism in human populations and the significant antigenic variation of Plasmodium falciparum pose major hurdles for the development of universally effective treatments (Source: PubMed ID: 30510063).

Other names
HLA-Plasmodium falciparum peptide complexpMHC complex (malaria)Plasmodium falciparum antigen-MHC complexMHC-Pf peptide complex
02

Mechanism of action

Activation of T-cell mediated immunity through the recognition of parasite-derived epitopes presented on MHC molecules by T-cell receptors (TCRs).

03

Biological functions

Antigen presentationImmune responseT-cell activationCellular immunity induction
04

Disease associations

Infection
05

Safety considerations

HLA-restricted non-responsiveness (genetic restriction)Antigenic variation leading to immune escapePotential for molecular mimicry or autoimmunitySuboptimal T-cell priming in endemic populations
06

Interacting drugs

RTS,S/AS01 (Mosquirix)

3 more in the full profile.

07

Biomarkers

HLA-B*53 (associated with protection against severe malaria)Interferon-gamma (IFN-gamma) ELISpotPeptide-MHC (pMHC) multimer bindingIntracellular cytokine staining (ICS) for CD4+ and CD8+ T cells

Beyond the preview

Go deeper on Major histocompatibility complex (MHC) molecules presenting Plasmodium falciparum peptides (Pf-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 Major histocompatibility complex (MHC) molecules presenting Plasmodium falciparum peptides (Pf-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