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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s12016-025-09039-0.

Title:
Immune Memory: A New Frontier in Treating Recurrent Inflammatory Skin Diseases | Clinical Reviews in Allergy & Immunology
Description:
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.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Technology & Computing

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

We find it hard to spot revenue streams.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

pubmed, article, google, scholar, cas, memory, central, cells, immunol, cell, skin, wang, httpsdoiorgs, zhang, inflammatory, immune, diseases, nat, rev, chen, immunity, liu, epigenetic, stem, kim, front, med, tissueresident, clin, resident, cancer, psoriasis, dermatol, huang, trained, van, allergy, drug, treatment, vitiligo, nature, innate, arthritis, yang, atopic, httpsdoiorgfimmu, res, human, park, sci,

Topics {✒️}

tumor-microenvironment-responsive bispecific nanobody-protacs ifn-gamma-producing effector cd8+ cd8+cd103+ tissue-resident memory hif-1α–mediated aerobic glycolysis month download article/chapter psoriasis-specific il-17-producing αβ open-label pilot study glucocorticoid-dependent polymyalgia rheumatica lymphopenia-induced memory cd8 aim2-driven inflammasome activation il-10-producing regulatory cd4+ skin-resident memory cd8+ antigen-specific immune memory promise-ebf study group interleukin 17a-producing potential long-lived immunological memory human tissue-resident memory tissue-resident memory cd8 rapid allergen-induced interleukin-17 skin-mediated drug delivery cutaneous lupus erythematosus cells produces antigen-inexperienced autoimmune-related skin diseases graft-versus-host disease article clinical reviews jak/stat signaling controls single-cell multi-omics tumor-resident cd8+ arts rjw bcg-induced trained immunity inflammatory skin disorders long-term adverse effects long-lasting stem cell full article pdf il-23/il-17 signaling pathway carbone fr disease-naïve nonlesional sites induced aerobic glycolysis human memory cd8+ elevated ifn-γ interferon-γ secretion resident cutaneous memory inflammatory skin diseases mulder wjm acute myeloid leukemia cd8 resident memory adaptive immune memory chronic inflammatory diseases dna methylation landscape cd8+ effector memory

Questions {❓}

  • Ong PY (2022) Atopic dermatitis: Is innate or adaptive immunity in control?

Schema {🗺️}

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         headline:Immune Memory: A New Frontier in Treating Recurrent Inflammatory Skin Diseases
         description: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.
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      description: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.
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External Links {🔗}(804)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
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CDN Services {📦}

  • Crossref

5.13s.