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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
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We are analyzing https://link.springer.com/article/10.1007/s00210-025-04131-w.

Title:
Emerging new immune checkpoint inhibitors in solid tumor immunotherapy | Naunyn-Schmiedeberg's Archives of Pharmacology
Description:
The advent of immune checkpoint inhibitors (ICIs) has revolutionised cancer therapy and has led to improved outcomes for patients with many cancers. While proven inhibitors targeting programmed cell death protein 1 (PD- 1), programmed cell death ligand 1 (PD-L1), and cytotoxic T lymphocyte-associated protein 4 (CTLA- 4) have had great success, new ICIs are on the horizon. However, data from clinical trials indicate that some patients develop resistance to ICIs targeting PD- 1/L1 and/or CTLA- 4 for multiple mechanisms. This gives rise to the idea that combining therapy by using multiple ICIs could help overcome this resistance through the inhibition of multiple pathways and immune checkpoints. Therefore, the new generation of immune checkpoint inhibitors opens up new therapeutic candidates for solid tumors. This review covers novel checkpoint agents, including T cell immunoglobulin and mucin domain 3 (TIM- 3), lymphocyte activating gene 3 (LAG- 3), and other promising pathways, including Ig V domain suppressor for T cell activation (VISTA). We review the underlying mechanisms of these targets, how they have been developed in the laboratory and clinic, and the initial efficacy and safety seen in ongoing trials. We also discuss combination strategies to further improve their therapeutic potential. By identifying challenges and opportunities with these new agents, this review explores the direction in which immunotherapy for solid tumors is headed and calls for further research in this emerging field.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

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're unsure if the website is profiting.

Not all websites are made for profit; some exist to inform or educate users. Or any other reason why people make websites. And this might be the case. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

pubmed, article, google, scholar, cas, central, cancer, cell, immune, immunol, cells, med, checkpoint, immunotherapy, tim, oncol, blockade, ctla, phase, melanoma, tumor, lag, clin, res, therapy, resistance, immunity, patients, tumors, nat, advanced, vista, combination, expression, nivolumab, antibody, antitumor, gene, sci, solid, trial, activation, human, ipilimumab, targeting, study, nature, exp, receptor, inhibitors,

Topics {✒️}

month download article/chapter galectin-9-independent ligand-binding surface tumor antigen–specific cd8+ high-risk myelodysplastic syndrome ifn-γ pathway genes acidic ph-selective ligand trans pd-l1 interaction zr-dfo-azepin-onartuzumab foxp3/nfat interaction enhances rouzbeh shams amiri intra-tumoural trbv6-6 variants constitutive clathrin-mediated endocytosis pd-1/pd-l1 blockade monotherapy single-cell rna-seq targeting stat3-vista axis peripheral t-cell tolerance human cd4 n-terminal immune-checkpoint protein vista phase ib/ii trial restore anti-tumor immunity anti-pd-1 antibody toripalimab cd80 cis-heterodimer triggers small-cell lung cancer small-cell lung cancer article naunyn-schmiedeberg' higher-risk mds treated anti-pd-l1 antibody anti-tim3 antibody promotes v-domain ig suppressor anti-lag-3 antibody lbl-007 α-pd-l1 antibody enhances t-cell function full article pdf andrews lp mhc class ii1 cancer chemo-immunotherapy resistance pembrolizumab-based combination therapy immune checkpoint modulators cd33-positive myeloid cells lymphocyte activation gene-3 lymphocyte activation gene-31 tumor-expressed ido recruits tumor-infiltrating regulatory lag-3-targeted therapy ochoa de olza accepted manuscript version cd4-related molecule suppress tumor aggression t-cell immunoglobulin open-ended story

Questions {❓}

  • Böger C et al (2017) The novel negative checkpoint regulator VISTA is expressed in gastric carcinoma and associated with PD-L1/PD-1: a future perspective for a combined gastric cancer therapy?
  • Musielak B, Kocik J, Skalniak L, Magiera-Mularz K, Sala D, Czub M, et al (2019) CA-170–a potent small-molecule PD-L1 inhibitor or not?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Emerging new immune checkpoint inhibitors in solid tumor immunotherapy
         description:The advent of immune checkpoint inhibitors (ICIs) has revolutionised cancer therapy and has led to improved outcomes for patients with many cancers. While proven inhibitors targeting programmed cell death protein 1 (PD- 1), programmed cell death ligand 1 (PD-L1), and cytotoxic T lymphocyte-associated protein 4 (CTLA- 4) have had great success, new ICIs are on the horizon. However, data from clinical trials indicate that some patients develop resistance to ICIs targeting PD- 1/L1 and/or CTLA- 4 for multiple mechanisms. This gives rise to the idea that combining therapy by using multiple ICIs could help overcome this resistance through the inhibition of multiple pathways and immune checkpoints. Therefore, the new generation of immune checkpoint inhibitors opens up new therapeutic candidates for solid tumors. This review covers novel checkpoint agents, including T cell immunoglobulin and mucin domain 3 (TIM- 3), lymphocyte activating gene 3 (LAG- 3), and other promising pathways, including Ig V domain suppressor for T cell activation (VISTA). We review the underlying mechanisms of these targets, how they have been developed in the laboratory and clinic, and the initial efficacy and safety seen in ongoing trials. We also discuss combination strategies to further improve their therapeutic potential. By identifying challenges and opportunities with these new agents, this review explores the direction in which immunotherapy for solid tumors is headed and calls for further research in this emerging field.
         datePublished:2025-04-11T00:00:00Z
         dateModified:2025-04-11T00:00:00Z
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            Pharmacology/Toxicology
            Neurosciences
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ScholarlyArticle:
      headline:Emerging new immune checkpoint inhibitors in solid tumor immunotherapy
      description:The advent of immune checkpoint inhibitors (ICIs) has revolutionised cancer therapy and has led to improved outcomes for patients with many cancers. While proven inhibitors targeting programmed cell death protein 1 (PD- 1), programmed cell death ligand 1 (PD-L1), and cytotoxic T lymphocyte-associated protein 4 (CTLA- 4) have had great success, new ICIs are on the horizon. However, data from clinical trials indicate that some patients develop resistance to ICIs targeting PD- 1/L1 and/or CTLA- 4 for multiple mechanisms. This gives rise to the idea that combining therapy by using multiple ICIs could help overcome this resistance through the inhibition of multiple pathways and immune checkpoints. Therefore, the new generation of immune checkpoint inhibitors opens up new therapeutic candidates for solid tumors. This review covers novel checkpoint agents, including T cell immunoglobulin and mucin domain 3 (TIM- 3), lymphocyte activating gene 3 (LAG- 3), and other promising pathways, including Ig V domain suppressor for T cell activation (VISTA). We review the underlying mechanisms of these targets, how they have been developed in the laboratory and clinic, and the initial efficacy and safety seen in ongoing trials. We also discuss combination strategies to further improve their therapeutic potential. By identifying challenges and opportunities with these new agents, this review explores the direction in which immunotherapy for solid tumors is headed and calls for further research in this emerging field.
      datePublished:2025-04-11T00:00:00Z
      dateModified:2025-04-11T00:00:00Z
      pageStart:1
      pageEnd:28
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         TIM- 3
         Solid tumors
         Immunotherapy
         Pharmacology/Toxicology
         Neurosciences
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         name:Naunyn-Schmiedeberg's Archives of Pharmacology
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            0028-1298
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         name:Springer Berlin Heidelberg
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                     type:PostalAddress
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                     name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
                     type:PostalAddress
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            name:Malihe Azadehrah
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                  address:
                     name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
                     type:PostalAddress
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                  name:Golestan University of Medical Sciences
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                     name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
                     type:PostalAddress
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                  name:Golestan University of Medical Sciences
                  address:
                     name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
                     type:PostalAddress
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         0028-1298
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      name:Springer Berlin Heidelberg
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      name:Golestan University of Medical Sciences
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         name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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         name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Golestan University of Medical Sciences
      address:
         name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Golestan University of Medical Sciences
      address:
         name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
         type:PostalAddress
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            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Mahboubeh Tajaldini
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            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Farahnazsadat Ahmadi
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            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Arash Tahmasebifar
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            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
               type:PostalAddress
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      name:Mahboobeh Azadehrah
      affiliation:
            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
               type:PostalAddress
            type:Organization
      name:Malihe Azadehrah
      affiliation:
            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
               type:PostalAddress
            type:Organization
      name:Amir Ghamoushiramandi
      affiliation:
            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
               type:PostalAddress
            type:Organization
      name:Rouzbeh Shams Amiri
      affiliation:
            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Vahid Khori
      affiliation:
            name:Golestan University of Medical Sciences
            address:
               name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
               type:PostalAddress
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      name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
      name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
      name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
      name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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      name:Ischemic Disorder Research Center, Golestan University of Medical Sciences, Gorgan, Iran
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External Links {🔗}(656)

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