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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. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s00210-025-04315-4.

Title:
Beyond the tumor: the gut microbiome as a key player in immunotherapy efficacy and resistance | Naunyn-Schmiedeberg's Archives of Pharmacology
Description:
Cancer immunotherapy aims to use the immune system of the body for improved therapeutic effects on tumors. Currently, one of the more encouraging interventions under evaluation involves the use of immune checkpoint blockade, which offers longer benefit periods and greater patient tolerance than previous interventions for solid malignancies. Nevertheless, a majority of patients never respond or gradually acquire resistance; hence, a suboptimal effect of the therapy ensues. Resistance to such treatments may arise from tumor-specific factors, host factors, and environmental influences. There is growing evidence that the gut microbiome is an important modulator not only of the efficacy of these treatments but also of toxicities. Current studies are focused on the identification of key microbial profiles from both preclinical and clinical samples associated with immunotherapeutic response and antitumor activities. Elucidation of this complex interaction may provide ways to modulate gut microbial communities to improve patient outcomes. The current review addresses the components responsible for resistance against immune checkpoint inhibitors and highlights the crucial linkage between gut microbiome-immune interactions. We further summarize some recent clinical findings and explore prospective avenues for research in this evolving area of cancer treatment.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

  • Health & Fitness
  • Education
  • Science

Content Management System {šŸ“}

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 {šŸ“ˆ}

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.
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How Does Link.springer.com Make Money? {šŸ’ø}

We can't figure out the monetization strategy.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com could have a money-making trick up its sleeve, but it's undetectable for now.

Keywords {šŸ”}

pubmed, article, google, scholar, cas, cancer, central, gut, immune, immunotherapy, microbiota, microbiome, patients, checkpoint, cell, response, oncol, nat, inhibitors, med, immunol, resistance, therapy, res, wang, efficacy, clinical, fecal, york, antipd, bacteria, liu, blockade, rev, melanoma, lung, advanced, yang, front, carcinoma, science, lactobacillus, metastatic, study, human, nivolumab, tumor, effects, effect, clin,

Topics {āœ’ļø}

immunoadjuvant-functionalized metal-organic frameworks 2-amino-1-methyl-6-phenyl-1h-imidazo[4 modulating ido1/kyn/ahr axis facilitates anti–pd-l1 efficacy il-17-producing t-helper cells anti-pd-1/pd-l1 immunotherapy month download article/chapter 2-amino-3-methyl-3h-imidazo[4 tumor microenvironment–responsive nanoplatforms low-birth-weight piglets pseudo germ-free rats immune-related adverse events pd-1/pd-l1 pathway small-cell lung cancer phase ii trial anti-pd-1 based immunotherapy bile acid-microbiota crosstalk food mutagen trp-p-2 bifidobacterium strain-specific enhances reduce tumour burden anti-pd-1 refractory patients short-chain fatty acids gut microbiome-immune interactions article naunyn-schmiedeberg' full article pdf antibiotic-disrupted gut microbiome immunotherapy-refractory melanoma patients lactic acid bacteria increasing intestinal development anti-pd-1 inhibitor immune checkpoint inhibitors checkpoint inhibitor immunotherapy butyrate-producing bacterium anti-pd-1 immunotherapy privacy choices/manage cookies randomized clinical trial prevent helicobacter pylori tumor-bearing mice article zhao immune checkpoint blockade fecal microbiota transplant explore prospective avenues pd-1-based immunotherapy gradually acquire resistance cancer prev official immune checkpoints inhibitors advanced renal cell lung cancer treatment anti-pd-1 therapy fecal microbiota transplantation

Schema {šŸ—ŗļø}

WebPage:
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         headline:Beyond the tumor: the gut microbiome as a key player in immunotherapy efficacy and resistance
         description:Cancer immunotherapy aims to use the immune system of the body for improved therapeutic effects on tumors. Currently, one of the more encouraging interventions under evaluation involves the use of immune checkpoint blockade, which offers longer benefit periods and greater patient tolerance than previous interventions for solid malignancies. Nevertheless, a majority of patients never respond or gradually acquire resistance; hence, a suboptimal effect of the therapy ensues. Resistance to such treatments may arise from tumor-specific factors, host factors, and environmental influences. There is growing evidence that the gut microbiome is an important modulator not only of the efficacy of these treatments but also of toxicities. Current studies are focused on the identification of key microbial profiles from both preclinical and clinical samples associated with immunotherapeutic response and antitumor activities. Elucidation of this complex interaction may provide ways to modulate gut microbial communities to improve patient outcomes. The current review addresses the components responsible for resistance against immune checkpoint inhibitors and highlights the crucial linkage between gut microbiome-immune interactions. We further summarize some recent clinical findings and explore prospective avenues for research in this evolving area of cancer treatment.
         datePublished:2025-06-03T00:00:00Z
         dateModified:2025-06-03T00:00:00Z
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         sameAs:https://doi.org/10.1007/s00210-025-04315-4
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            Gut microbiome
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            Neurosciences
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      headline:Beyond the tumor: the gut microbiome as a key player in immunotherapy efficacy and resistance
      description:Cancer immunotherapy aims to use the immune system of the body for improved therapeutic effects on tumors. Currently, one of the more encouraging interventions under evaluation involves the use of immune checkpoint blockade, which offers longer benefit periods and greater patient tolerance than previous interventions for solid malignancies. Nevertheless, a majority of patients never respond or gradually acquire resistance; hence, a suboptimal effect of the therapy ensues. Resistance to such treatments may arise from tumor-specific factors, host factors, and environmental influences. There is growing evidence that the gut microbiome is an important modulator not only of the efficacy of these treatments but also of toxicities. Current studies are focused on the identification of key microbial profiles from both preclinical and clinical samples associated with immunotherapeutic response and antitumor activities. Elucidation of this complex interaction may provide ways to modulate gut microbial communities to improve patient outcomes. The current review addresses the components responsible for resistance against immune checkpoint inhibitors and highlights the crucial linkage between gut microbiome-immune interactions. We further summarize some recent clinical findings and explore prospective avenues for research in this evolving area of cancer treatment.
      datePublished:2025-06-03T00:00:00Z
      dateModified:2025-06-03T00:00:00Z
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         Immunotherapy
         Immune checkpoint inhibitors
         Gut microbiome
         Therapeutic resistance
         Pharmacology/Toxicology
         Neurosciences
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            name:Yuemei Zhao
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            name:Weidong Liu
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                     name:Department of Surgery and Critical Care Medicine, Shaoxing People’s Hospital, ShaoxingShaoxing City, China
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               name:Department of Surgery and Critical Care Medicine, Shaoxing People’s Hospital, ShaoxingShaoxing City, China
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      name:Weidong Liu
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            name:Shaoxing People’s Hospital
            address:
               name:Department of Surgery and Critical Care Medicine, Shaoxing People’s Hospital, ShaoxingShaoxing City, China
               type:PostalAddress
            type:Organization
      name:Yuehong Hu
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            name:Shaoxing People’s Hospital
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               name:Department of Surgery and Critical Care Medicine, Shaoxing People’s Hospital, ShaoxingShaoxing City, China
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      name:Department of Surgery and Critical Care Medicine, Shaoxing People’s Hospital, ShaoxingShaoxing City, China
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External Links {šŸ”—}(434)

Analytics and Tracking {šŸ“Š}

  • Google Tag Manager

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