Target intelligence / Profile preview

Heat shock protein receptor (dendritic cell)

Molecular classification
Receptor, Scavenger receptor, Endocytic receptor
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Overview

Heat shock proteins (HSPs) are molecular chaperones that, when released from stressed or dying cells, form complexes with antigenic peptides. These complexes are recognized and internalized by dendritic cells primarily via surface receptors such as CD91 and SREC-I. The process is known as heat shock protein receptor-mediated uptake and is pivotal for the activation and maturation of dendritic cells, polarizing immune responses towards Th1 phenotypes, stimulating cytokine secretion, and initiating adaptive immunity. This mechanism is being explored in vaccine development and cancer immunotherapy, due to its ability to efficiently present antigens and elicit robust cellular immune responses.

Other names
HSP receptorSREC-I (scavenger receptor expressed by endothelial cell I)CD91 (also called LDL receptor-related protein 1, LRP1)various scavenger receptors
02

Mechanism of action

Facilitation of antigen uptake and cross-presentation, resulting in T cell activation Promotion of dendritic cell maturation and cytokine/chemokine production

03

Biological functions

Immune responseAntigen presentationDendritic cell maturationSignal transduction
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Disease associations

CancerInfectionInflammation
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Safety considerations

Overstimulation may lead to excessive inflammation or autoimmunitypotential for off-target activation of other immune responses
06

Interacting drugs

There are currently no approved drugs that specifically target the generic "heat shock protein receptor" pathway, but experimental vaccine adjuvants and recombinant HSP-antigen complexes interact with this system.
07

Biomarkers

Elevated expression of dendritic cell activation markers (such as CCR7, CXCR4, IL-12p70)upregulation of MHCsecretion of proinflammatory cytokines (e.g., IL-1β, TNF-α, IP-10)

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