Tcr Gene Transduction

TCR gene transduction is a genetic engineering technique that gives T lymphocytes a new, antigen-specific T-cell receptor (TCR), enabling targeted immune recognition. Typically, a viral vector delivers genes encoding the TCR alpha and beta chains into isolated T cells, which are then expanded and tested for receptor expression, antigen binding, and functional activation. In immunology and infection research, this approach helps investigate how T cells recognize pathogen-derived peptides presented by major histocompatibility complex molecules. It also supports the development of adoptive cell therapies and provides a way to study T-cell specificity, signaling, and immune responses.

Tcr Gene Transduction - Related Videos

Research

JoVE EoE - Leukemia

Retroviral-Mediated Transduction: A Method to Introduce Target Gene into Cancer Cells

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2023

This video describes the protocol for genetic validation by transferring target genes using retroviruses in chronic myeloid leukemia cell lines. The retroviruses act as a mediator to transfer genetic material into the leukemia cell through the process called transduction, which enables long term expression of target gene.This method can be applied to any target cells for genetic validation and therapeutic development.

Research

JoVE Journal - Immunology and Infection
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Retroviral Transduction of T-cell Receptors in Mouse T-cells

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Cited by 21 •

2010

We present a protocol to produce antigen-specific mouse T-cells using retroviral...

Measuring TCR-pMHC Binding In Situ using a FRET-based Microscopy Assay

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Cited by 9 •

2015

This manuscript describes how to conduct (single molecule) Förster Resonance Energy Transfer (FRET)- based assays to measure the binding dynamics between T-cell antigen receptor (TCR) and antigenic peptide-loaded MHC molecules as they occur within the immunological synapse of a T-cell in contact with a functionalized planar supported lipid bilayer.

Generating De Novo Antigen-specific Human T Cell Receptors by Retroviral Transduction of Centric Hemichain

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Cited by 3 •

2016

Herein we describe a novel method to generate antigen-specific T cell receptors (TCRs) by pairing the TCRα or TCRβ of an existing TCR, possessing the antigen-specificity of interest, with complementary hemichain of the peripheral T cell receptor repertoire. The de novo generated TCRs retain antigen-specificity with varying affinity.

Retroviral Mediated Gene Transduction: A Gene Transfer Technique to Deliver a Transgene in Cultured Cells Using Engineered Retroviral Vectors

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2025

In this video, we demonstrate magnetically-guided transfection of plasmid DNA in primary neuronal cell culture. Magnetofection uses an external magnetic field to guide the delivery of plasmids bound to magnetic nanoparticles into cell cytoplasm.

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