# Therapeutic potential of TAM receptors in autoimmune diseases: insights from original studies

**Authors:** Sheu Ibrahim Adedayo, Taiye Abdullahi Gegele, Kehinde Ahmad Adeshina, Baliqis Adejoke Olukade, Ridwanullah Abiodun Abubakar, Adullateef Abdulsalam, Toheeb Oladejo Olalekan, Mohamed Mustaf Ahmed, Kasimu Ghandi Ibrahim

PMC · DOI: 10.1093/oxfimm/iqag001 · 2026-01-22

## TL;DR

This paper explores how TAM receptors may play a role in autoimmune diseases and could be used as biomarkers or therapeutic targets.

## Contribution

The paper reviews primary studies to highlight TAM receptors as potential therapeutic targets in autoimmune diseases.

## Key findings

- TAM receptors are critical for immune homeostasis and apoptotic cell clearance.
- Dysfunction in TAM signaling contributes to autoimmune diseases like multiple sclerosis and lupus.
- TAM receptors may serve as biomarkers and therapeutic targets for autoimmune conditions.

## Abstract

TAM receptors, composed of Tyro3, Axl, and Mertk, belong to the receptor tyrosine kinase family and are activated by binding of their cognate ligands, Gas6 and Pros1. These receptor-ligand interactions mediate critical physiological processes, including the maintenance of immunological equilibrium, thrombocyte aggregation and subsequent thrombus development, apoptotic cellular debris clearance, homeostatic regulation of endothelial and vascular smooth muscle cells, and erythrocyte production. Perturbations in TAM signaling cascades have been shown to compromise the clearance of apoptotic cells, leading to persistent inflammatory responses that can contribute to the development of various autoimmune pathologies, including multiple sclerosis, rheumatoid arthritis, Sjögren’s syndrome, and systemic lupus erythematosus. We retrieved and reviewed only the primary studies addressing the roles of TAM receptors and their ligands in selected autoimmune diseases from Google Scholar, Scopus, Web of Science, and PubMed. The critical roles of TAM receptors in immune homeostasis and apoptotic cell clearance are well established. However, findings from several primary studies discussed in this review further emphasized that the loss of TAM receptor function in these processes significantly contributes to the pathogenesis and progression of autoimmune diseases. Herein, we highlight the role of TAM receptors in several autoimmune diseases, suggesting that TAM receptors are potential biomarkers for monitoring disease prognosis and therapeutic targets to improve patient outcomes.

## Linked entities

- **Genes:** TYRO3 (TYRO3 protein tyrosine kinase) [NCBI Gene 7301], AXL (AXL receptor tyrosine kinase) [NCBI Gene 558], MERTK (MER proto-oncogene, tyrosine kinase) [NCBI Gene 10461]
- **Proteins:** GAS6 (growth arrest specific 6), PROS1 (protein S)
- **Diseases:** multiple sclerosis (MONDO:0005301), rheumatoid arthritis (MONDO:0008383), systemic lupus erythematosus (MONDO:0007915)

## Full-text entities

- **Genes:** AXL (AXL receptor tyrosine kinase) [NCBI Gene 558] {aka ARK, AXL3, JTK11, Tyro7, UFO}, TYRO3 (TYRO3 protein tyrosine kinase) [NCBI Gene 7301] {aka BYK, Dtk, Etk-2, RSE, Rek, Sky}, GAS6 (growth arrest specific 6) [NCBI Gene 2621] {aka AXLLG, AXSF}, PROS1 (protein S) [NCBI Gene 5627] {aka PROS, PS21, PS22, PS23, PS24, PS25}, MERTK (MER proto-oncogene, tyrosine kinase) [NCBI Gene 10461] {aka MER, RP38, Tyro12, c-Eyk, c-mer}
- **Diseases:** inflammatory (MESH:D007249), Sjogren's syndrome (MESH:D012859), multiple sclerosis (MESH:D009103), systemic lupus erythematosus (MESH:D008180), rheumatoid arthritis (MESH:D001172), thrombus (MESH:D013927), autoimmune diseases (MESH:D001327)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12860480/full.md

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Source: https://tomesphere.com/paper/PMC12860480