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engineered bacteriophage T7

Development stage
Unknown
Modality
Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Oncolytic Viruses → Oncolytic Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, Synthetic Biology Platforms → Engineered Microbial Therapeutics → Microbiome Therapeutics, Fresh FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Genetically Modified Bacteria → Engineered Microbial Therapeutics → Microbiome Therapeutics, Yeast Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Recombinant Proteins and Enzymes, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, Gene Therapies, Nanoparticles → Drug Delivery Systems, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics
Administration
Intravenous, Local Injection
01

Overview

Engineered bacteriophage T7 refers to bacteriophage T7 viruses that have been genetically modified for therapeutic or diagnostic purposes. Modifications include display of targeting peptides or proteins on the phage capsid, integration of genes encoding therapeutic proteins (such as granulocyte macrophage colony-stimulating factor (GM-CSF) or antimicrobial peptides like apidaecin), or enabling payload delivery (such as CRISPR–Cas systems or reporters like lacZ). These engineered T7 phages can directly lyse bacterial cells, deliver therapeutic payloads (e.g., anti-tumor peptides, cytokines), or reprogram the tumor microenvironment by recruiting immune cells. In cancer models, engineered T7 displaying tumor-homing peptides and expressing GM-CSF inhibited tumor growth and attracted anti-tumor immune cells. In infectious disease models, T7 has been engineered to express antimicrobial peptides that kill resistant bacteria, and to deliver CRISPR systems for sequence-specific bacterial killing. Key mechanisms rely on phage infection of bacteria, engineered gene expression in targeted cells, and stimulation of immune or antimicrobial responses[1][2][3][4][5][6].

Other names
engineered phage T7recombinant bacteriophage T7genetically engineered T7 phage
02

Targets

HSPA5 (Heat shock protein family A member 5)

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