<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">LAG3 Protein (CD223)</th>
</tr>
<tr>
<td class="label">Approach</td>
<td>Mechanism</td>
</tr>
<tr>
<td class="label">Blocking antibodies</td>
<td>Prevent fibril binding/uptake</td>
</tr>
<tr>
<td class="label">Soluble LAG3</td>
<td>Decoy receptor for fibrils</td>
</tr>
<tr>
<td class="label">Small molecule inhibitors</td>
<td>Block LAG3-fibril interaction</td>
</tr>
<tr>
<td class="label">Interacting Partner</td>
<td>Type</td>
</tr>
<tr>
<td class="label">MHC Class II</td>
<td>Physiological</td>
</tr>
<tr>
<td class="label">Alpha-synuclein fibrils</td>
<td>Pathological</td>
</tr>
<tr>
<td class="label">Tau fibrils</td>
<td>Pathological</td>
</tr>
<tr>
<td class="label">Fibrinogen-like protein 1</td>
<td>Physiological</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">6 edges</a></td>
</tr>
</table>
<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">LAG3 Protein (CD223)</th>
</tr>
<tr>
<td class="label">Approach</td>
<td>Mechanism</td>
</tr>
<tr>
<td class="label">Blocking antibodies</td>
<td>Prevent fibril binding/uptake</td>
</tr>
<tr>
<td class="label">Soluble LAG3</td>
<td>Decoy receptor for fibrils</td>
</tr>
<tr>
<td class="label">Small molecule inhibitors</td>
<td>Block LAG3-fibril interaction</td>
</tr>
<tr>
<td class="label">Interacting Partner</td>
<td>Type</td>
</tr>
<tr>
<td class="label">MHC Class II</td>
<td>Physiological</td>
</tr>
<tr>
<td class="label">Alpha-synuclein fibrils</td>
<td>Pathological</td>
</tr>
<tr>
<td class="label">Tau fibrils</td>
<td>Pathological</td>
</tr>
<tr>
<td class="label">Fibrinogen-like protein 1</td>
<td>Physiological</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">6 edges</a></td>
</tr>
</table>
<div style="float: right; width: 280px; background: #f8f9fa; border: 1px solid #ddd; padding: 12px; margin: 0 0 1em 1em; font-size: 0.9em;">
<h4 style="margin-top: 0; color: #3366cc;">LAG3 (CD223)</h4>
<table style="width: 100%; border-collapse: collapse;">
<tr><td style="padding: 4px; border-bottom: 1px solid #eee;"><strong>UniProt ID</strong></td><td style="padding: 4px; border-bottom: 1px solid #eee;">[P18627](https://www.uniprot.org/uniprotkb/P18627)</td></tr>
<tr><td style="padding: 4px; border-bottom: 1px solid #eee;"><strong>Gene</strong></td><td style="padding: 4px; border-bottom: 1px solid #eee;">[LAG3](/genes/lag3)</td></tr>
<tr><td style="padding: 4px; border-bottom: 1px solid #eee;"><strong>MW</strong></td><td style="padding: 4px; border-bottom: 1px solid #eee;">~57 kDa</td></tr>
<tr><td style="padding: 4px; border-bottom: 1px solid #eee;"><strong>Location</strong></td><td style="padding: 4px; border-bottom: 1px solid #eee;">Cell membrane, immune cells</td></tr>
<tr><td style="padding: 4px; border-bottom: 1px solid #eee;"><strong>PDB</strong></td><td style="padding: 4px; border-bottom: 1px solid #eee;">[1Z2M](https://www.rcsb.org/structure/1Z2M)</td></tr>
</table>
</div>
LAG3 Protein is a protein that lag3 is primarily expressed on activated t cells, regulatory t cells (tregs), natural killer cells, and to a lesser extent on b cells and dendritic cells. its canonical functions include:[@woo2012]. This page describes its structure, normal nervous system function, role in neurodegenerative disease, and potential as a therapeutic target.
LAG3 (Lymphocyte Activation Gene 3, also known as CD223) is a cell surface receptor protein belonging to the immunoglobulin superfamily that has emerged as a critical mediator of pathological protein spreading in neurodegenerative diseases, particularly [Parkinson's disease](/diseases/parkinsons-disease).[@mao2016]
LAG3 is a type I transmembrane glycoprotein composed of:
LAG3 is primarily expressed on activated T cells, regulatory T cells (Tregs), natural killer cells, and to a lesser extent on B cells and dendritic cells. Its canonical functions include:[@woo2012]
The discovery that LAG3 serves as a receptor for pathological [alpha-synuclein](/proteins/alpha-synuclein) fibrils represents a major breakthrough in understanding disease propagation in [Parkinson's disease](/diseases/parkinsons-disease):[@mao2016]
The interaction occurs primarily through the D1 domain of LAG3. Antibodies blocking this interaction prevent fibril uptake and seeding in experimental models.
LAG3 has also been implicated in [tau](/proteins/tau) spreading:[@holmes2013]
Beyond protein spreading, LAG3 contributes to neurodegeneration through immune modulation:[@mckinney2021]
LAG3 represents a promising therapeutic target for neurodegenerative diseases:
LAG3-targeting antibodies (relatlimab) are FDA-approved for cancer immunotherapy, providing clinical validation of the target. However, these agents are designed to activate LAG3's immune checkpoint function, whereas neurodegeneration therapy would require blocking the receptor's binding to pathological proteins.[@tawbi2022]
The following diagram shows the key molecular relationships involving LAG3 Protein (CD223) discovered through SciDEX knowledge graph analysis: