# Integrin alpha L: structure, cellular functions, and emerging role in human diseases

**Authors:** Xianglin Wang, Guoya Yang, Yanpei Chen, Fang Zhu, Fuming Lian, Wenzhi Shen, Dehong Luo

PMC · DOI: 10.3389/fimmu.2025.1707291 · Frontiers in Immunology · 2026-01-12

## TL;DR

This review explores the role of Integrin α L in immune processes, disease mechanisms, and potential as a biomarker for various conditions including cancer.

## Contribution

The paper provides a comprehensive review of Integrin α L's structure, functions, and emerging roles in both tumor and non-tumor-related diseases.

## Key findings

- Integrin α L is essential for leukocyte adhesion and migration through interactions with ICAMs.
- Its expression patterns correlate with tumor cell invasion, metastasis, and immune evasion.
- Integrin α L is implicated in non-cancerous diseases like atherosclerosis and rheumatoid arthritis.

## Abstract

As an integral component of Lymphocyte Function-associated Antigen 1 (LFA-1), Integrin α L is crucial for the processes of leukocyte adhesion and migration. It engages in specific interactions with Inter-Cellular Adhesion Molecules (ICAMs), thereby playing a significant role in intercellular adhesion, signal transduction, immune response regulation, inflammatory pathways, and the intricate formation of the tumor microenvironment. While preliminary studies have begun to elucidate the phenotypic diversity and bioinformatic characteristics of Integrin α L across various diseases, there remains a paucity of comprehensive reviews addressing the functional roles and underlying mechanisms of Integrin α L in different pathological contexts. This review aims to delineate the fundamental structure and function of Integrin α L, while also summarizing the relationship between its expression patterns and functional attributes with respect to the invasive potential, metastatic capabilities, immune evasion strategies, and clinical outcomes of tumor cells and patients across a spectrum of tumor types. Furthermore, we highlight the significant involvement of Integrin α L in non-tumor-related diseases, including atherosclerosis, systemic sclerosis, depression, and rheumatoid arthritis. Additionally, we assess the potential of Integrin α L as a molecular biomarker for the diagnosis of specific diseases and tumors, which may pave the way for novel therapeutic targets in the treatment of associated conditions and malignancies.

## Linked entities

- **Proteins:** ITGAL (integrin subunit alpha L)
- **Diseases:** atherosclerosis (MONDO:0005311), systemic sclerosis (MONDO:0005100), depression (MONDO:0002050), rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** ITGAL (integrin subunit alpha L) [NCBI Gene 3683] {aka CD11A, EV6, HNA-5, LFA-1, LFA1A}
- **Diseases:** malignancies (MESH:D009369), rheumatoid arthritis (MESH:D001172), systemic sclerosis (MESH:D012595), atherosclerosis (MESH:D050197), depression (MESH:D003866), inflammatory (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12832350/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12832350/full.md

## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832350/full.md

---
Source: https://tomesphere.com/paper/PMC12832350