REVIEW article
Front. Pharmacol.
Sec. Inflammation Pharmacology
The Role of Immune Regulation in Peripheral Nerve Regeneration: Functions of Inflammatory Cells and Cytokines
Provisionally accepted- Affiliated Zhongshan Hospital of Dalian University, Dalian, China
Select one of your emails
You have multiple emails registered with Frontiers:
Notify me on publication
Please enter your email address:
If you already have an account, please login
You don't have a Frontiers account ? You can register here
Background: The regenerative repair following peripheral nerve injury is a complex pathophysiological process in which the immune regulatory network plays a crucial role. Conventional understanding posits that inflammatory responses impede nerve regeneration; however, recent studies reveal that immune reactions constitute a "double-edged sword": a well-timed and moderate inflammatory response is essential for initiating regeneration, whereas excessive or persistent inflammation deteriorates the regenerative microenvironment and hampers repair. This review systematically elaborates the dynamic responses of the innate and adaptive immune systems after peripheral nerve injury. We focus particularly on the phenotypic switch of macrophages from the pro-inflammatory M1 to the anti-inflammatory/reparative M2 type, the early debris-clearing function of neutrophils, the interactions between T lymphocytes and Schwann cells, as well as the intricate signaling networks formed by cytokines and chemokines. The article delves into how these immune cells and factors precisely regulate key processes in Schwann cells—such as dedifferentiation, proliferation, migration, and myelination-thereby influencing axonal regeneration and functional recovery. Finally, this review prospects the translational potential of optimizing the immune microenvironment by targeting specific immune cells or signaling pathways for treating peripheral nerve injuries. Deciphering these delicate immune regulatory mechanisms will provide a critical theoretical foundation for developing novel immunomodulatory strategies to enhance nerve regeneration. Summary: In this review, we outline current understanding of the immune mechanisms underlying peripheral nerve regeneration, spanning from established paradigms to emerging therapeutic approaches, such as targeted immunomodulation, biomaterial-assisted microenvironment reshaping, and adoptive immune cell therapy, all of which represent promising avenues for improving functional recovery after nerve injury. Key Messages: The integration of immunology and nerve regeneration research is opening new frontiers for treatment. Harnessing the regenerative potential of the immune system while restraining its detrimental effects—through approaches such as precision modulation of macrophage polarization, neutrophil extracellular trap (NET) regulation, and T cell-Schwann cell crosstalk targeting—offers encouraging prospects for overcoming the current challenges in peripheral nerve repair.
Keywords: Cytokines, Immune Regulation, Inflammation, Macrophage polarization, Peripheral nerve regeneration, Schwann Cells, Signaling Pathways
Received: 30 Oct 2025; Accepted: 11 Feb 2026.
Copyright: © 2026 Zhang, Zhang, Su, Nuo, Wu, Jiang and Meng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Yun Su
Xiangjun Meng
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
