# Immunomodulatory Effects of Lidocaine: Mechanisms of Actions and Therapeutic Applications

**Authors:** Jianwei Wu, Quanfu Chen, Zhiling He, Bin Yang, Zhenhua Dai, Feifei Qiu

PMC · DOI: 10.3390/ph19010134 · 2026-01-12

## TL;DR

Lidocaine, known as an anesthetic, also modulates immune responses and could be repurposed to treat immune-related diseases.

## Contribution

This paper reviews lidocaine's immunomodulatory effects on various immune cells and signaling pathways, suggesting its potential as a repurposed immunotherapy.

## Key findings

- Lidocaine modulates innate and adaptive immune cells like macrophages and T lymphocytes.
- It influences immune processes via pathways such as NF-κB and TLR4/p38 MAPK.
- Lidocaine's effects vary with concentration, duration, and microenvironment.

## Abstract

Lidocaine, an amide-type regional anesthetic, has been an important medication in the field of anesthesia since its clinical approval. Recently, lidocaine has emerged as a powerful immunomodulatory agent beyond its classical anesthetic properties. This review has summarized the recent basic and clinical studies with sufficient evidence on the multifaceted effects of lidocaine on both innate and adaptive immune cells, including macrophages, neutrophils, eosinophils, basophils, natural killer (NK) cells, mast cells, dendritic cells (DCs), monocytes, and T lymphocytes. We have also detailed how lidocaine affects critical cellular processes, such as cellular polarization, cytokine production, phagocytosis, and apoptosis, through multiple signaling pathways, including NF-κB, TLR4/p38 MAPK, voltage-sensitive sodium channels, HIF1α, TGF-β/Smad3, AMPK-SOCS3, TBK1-IRF7, and G protein-coupled receptors. These immunoregulatory effects of lidocaine are dependent on its concentration, duration of action, and the microenvironment. The immunomodulatory actions of lidocaine may contribute to its potential therapeutic value in various settings of diseases, such as cancer, sepsis, acute lung injury, asthma, organ transplantation, ischemia–reperfusion injury (IRI), and diabetes. We propose that lidocaine can be repurposed as an immunomodulator for treating immune-mediated inflammatory diseases. However, future research should define optimal dosing strategies, validate its mechanisms of action in clinical trials, and explore its novel clinical applications as a complementary immunotherapy.

## Linked entities

- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1), TLR4 (toll like receptor 4), P38mapk (p38 map kinase), HIF1A (hypoxia inducible factor 1 subunit alpha), TGFB1 (transforming growth factor beta 1), SMAD3 (SMAD family member 3), PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1), SOCS3 (suppressor of cytokine signaling 3), TBK1 (TANK binding kinase 1), IRF7 (interferon regulatory factor 7)
- **Chemicals:** Lidocaine (PubChem CID 3676)
- **Diseases:** cancer (MONDO:0004992), acute lung injury (MONDO:0006502), asthma (MONDO:0004979), ischemia–reperfusion injury (MONDO:0005203), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** TBK1 (TANK binding kinase 1) [NCBI Gene 29110] {aka AIARV, FTDALS4, IIAE8, NAK, T2K}, IRF7 (interferon regulatory factor 7) [NCBI Gene 3665] {aka IMD39, IRF-7, IRF-7H, IRF7A, IRF7B, IRF7C}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, SMAD3 (SMAD family member 3) [NCBI Gene 4088] {aka HSPC193, HsT17436, JV15-2, LDS1C, LDS3, MADH3}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562] {aka AMPK, AMPK alpha 1, AMPKa1}, SOCS3 (suppressor of cytokine signaling 3) [NCBI Gene 9021] {aka ATOD4, CIS3, Cish3, SOCS-3, SSI-3, SSI3}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}
- **Diseases:** acute lung injury (MESH:D055371), IRI (MESH:D015427), immune-mediated inflammatory diseases (MESH:C567355), diabetes (MESH:D003920), asthma (MESH:D001249), cancer (MESH:D009369), sepsis (MESH:D018805)
- **Chemicals:** amide (MESH:D000577), Lidocaine (MESH:D008012)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12845077/full.md

---
Source: https://tomesphere.com/paper/PMC12845077