Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Mar 18;68(1):31.
doi: 10.1007/s12016-025-09039-0.

Immune Memory: A New Frontier in Treating Recurrent Inflammatory Skin Diseases

Affiliations
Review

Immune Memory: A New Frontier in Treating Recurrent Inflammatory Skin Diseases

Hang Yin et al. Clin Rev Allergy Immunol. .

Abstract

The recurrence of inflammatory skin diseases represents a significant challenge in clinical practice, primarily mediated by immune memory. In inflammatory skin diseases, immune memory encompasses adaptive immune memory, trained immunity, and inflammatory memory, which are conducted by adaptive immune cells, innate immune cells, and structural cells, respectively. Adaptive immune memory is established through gene rearrangement, leading to antigen-specific immune memory. In contrast, trained immunity and inflammatory memory are formed through epigenetic and metabolic reprogramming, resulting in non-specific immune memory. Different types of immune memory work synergistically to aggravate localized inflammation in recurrent inflammatory skin diseases. However, immune memory in specific cells, such as macrophages, may also play an immunoregulatory role under certain conditions. We reviewed the immune memory mechanisms in different inflammatory skin diseases and discussed future strategies for targeted regulation of the molecular mechanisms underlying immune memory, such as targeted biological agents and epigenetic modifications. Additionally, we explored the potential for precise regulation of immune memory and its application in personalized treatment for recurrent inflammatory skin diseases.

Keywords: Immune memory; Inflammatory memory; Inflammatory skin diseases; Trained immunity.

PubMed Disclaimer

Conflict of interest statement

Declarations. Competing Interests: The authors declare no competing interests.

Similar articles

Cited by

References

    1. Picardo M, Dell’Anna ML, Ezzedine K, Hamzavi I, Harris JE, Parsad D, Taieb A (2015) Vitiligo. Nat Rev Dis Primer 1:15011. https://doi.org/10.1038/nrdp.2015.11 - DOI
    1. Griffiths CEM, Armstrong AW, Gudjonsson JE, Barker JNWN (2021) Psoriasis. The Lancet 397:1301–1315. https://doi.org/10.1016/S0140-6736(20)32549-6 - DOI
    1. Chovatiya R, Paller AS (2021) JAK inhibitors in the treatment of atopic dermatitis. J Allergy Clin Immunol 148:927–940. https://doi.org/10.1016/j.jaci.2021.08.009 - DOI - PubMed - PMC
    1. Azzolino V, Zapata L, Garg M, Gjoni M, Riding RL, Strassner JP, Richmond JM, Harris JE (2021) Jak inhibitors reverse vitiligo in mice but do not deplete skin resident memory T cells. J Invest Dermatol 141:182-184.e1. https://doi.org/10.1016/j.jid.2020.04.027 - DOI - PubMed
    1. Lin CM, Cooles FA, Isaacs JD (2020) Basic mechanisms of JAK inhibition. Mediterr J Rheumatol 31:100–104. https://doi.org/10.31138/mjr.31.1.100 - DOI - PubMed - PMC

LinkOut - more resources