Target intelligence / Profile preview

Plasmodium vivax Duffy binding protein region II (PvDBP-II)

Target
PvDBP-II
Molecular classification
Adhesin (parasite ligand), Duffy-binding-like (DBL) domain protein, Member of the erythrocyte-binding-like (EBL) family
01

Overview

Plasmodium vivax Duffy binding protein region II (PvDBP-II) is a crucial surface ligand expressed by the merozoite stage of the malaria parasite P. vivax. PvDBP-II contains a Duffy-binding-like (DBL) domain that mediates the specific and necessary interaction between the parasite and the Duffy antigen receptor for chemokines (DARC) on human reticulocytes, initiating the invasion process that leads to malaria symptoms[1][2][4][5][6]. It is a primary target of naturally acquired and vaccine-induced immune responses. Antibodies that target PvDBP-II can neutralize the parasite by blocking its interaction with DARC, thereby preventing red blood cell invasion and subsequent propagation of infection. Despite its centrality to P. vivax biology, PvDBP-II is highly polymorphic, which enables the parasite to evade strain-transcending immune responses; this presents a key hurdle for global vaccine development. The region has been structurally characterized in complex with DARC and key neutralizing antibodies, guiding rational immunogen design for vaccine efforts[4][3][6]. PvDBP-II remains a leading candidate in the development of blood-stage malaria vaccines due to its indispensable role in parasite virulence[1][2][5].

Other names
Duffy Binding Protein region IIDBP-IIPvDBP region IIPlasmodium vivax Duffy binding-like domain IIPvDBPII
02

Mechanism of action

Vaccines/antibodies block PvDBP-II from binding to DARC on reticulocytes, preventing parasite invasion and halting the blood-stage infection[1][2][3][6][7]

03

Biological functions

Mediates parasite invasion of reticulocytes (immature red blood cells)Binds to human Duffy antigen receptor for chemokines (DARC)Essential for initiating merozoite entry into host red blood cellsTarget of neutralizing antibodies
04

Disease associations

Infection (malaria, specifically Plasmodium vivax malaria)Critical for parasite virulence and propagation
05

Safety considerations

High polymorphism in PvDBP-II leads to strain-specific immunity, limiting broad vaccine efficacy[2][1][5]Possibility of immune escape or reduced cross-protection against diverse P. vivax strains[2][5]
06

Interacting drugs

No approved drugs; several vaccine candidates and neutralizing monoclonal antibodies in development[6][7][3][5][1] (examples: mAbs 053054, 092096, DB1, 2D10, 2H2)
07

Biomarkers

Anti-PvDBP-II antibody titers (indicator of exposure or immune protection)[5][6]

Beyond the preview

Go deeper on Plasmodium vivax Duffy binding protein region II (PvDBP-II).

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 Plasmodium vivax Duffy binding protein region II (PvDBP-II).

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