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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
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We began analyzing https://www.nature.com/articles/nri.2016.107, but it redirected us to https://www.nature.com/articles/nri.2016.107. The analysis below is for the second page.

Title[redir]:
Immunogenic cell death in cancer and infectious disease | Nature Reviews Immunology
Description:
Initiation of an adaptive immune response depends on the detection of both antigenic epitopes and adjuvant signals. Infectious pathogens and cancer cells often avoid immune detection by limiting the release of danger signals from dying cells. When is cell death immunogenic and what are the pathophysiological implications of this process? Immunogenicity depends on two key factors: antigenicity and adjuvanticity. The presence of exogenous or mutated antigens explains why infected cells and malignant cells can initiate an adaptive immune response provided that the cells also emit adjuvant signals as a consequence of cellular stress and death. Several infectious pathogens have devised strategies to control cell death and limit the emission of danger signals from dying cells, thereby avoiding immune recognition. Similarly, cancer cells often escape immunosurveillance owing to defects in the molecular machinery that underlies the release of endogenous adjuvants. Here, we review current knowledge on the mechanisms that underlie the activation of immune responses against dying cells and their pathophysiological relevance.

Matching Content Categories {📚}

  • Science
  • Education
  • Health & Fitness

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org 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 Doi.org Make Money? {💸}

We're unsure if the website is profiting.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Doi.org might be cashing in, but we can't detect the method they're using.

Keywords {🔍}

pubmed, article, google, scholar, cas, cell, cancer, central, cells, death, immunol, nat, immunogenic, rev, immune, galluzzi, nature, kroemer, kepp, immunity, therapy, receptor, response, med, calreticulin, anticancer, autophagy, france, type, protein, dendritic, tumor, disease, guido, immunogenicity, dying, access, antitumor, exposure, radiation, paris, content, lorenzo, zitvogel, responses, signalling, buqué, danger, adaptive, molecular,

Topics {✒️}

nature portfolio permissions reprints privacy policy siric cancer research cancer research institutes author information authors advertising european research council cytosolic double-stranded dna nature 461 nature 515 nature 517 nature social media animal development interferon-dependent antitumor immunity cd4+ t-cell responses mir-133a tumor suppressor single-dose radiotherapy induces radiation fosters dose-dependent cytosolic double-stranded rna tumor-specific immune response t-cell-dependent manner ebv-induced nasopharyngeal carcinoma research cancéropôle ile-de-france rsl3-loaded nanoparticles amplify oxygen-generating nanoplatform remodels marie curie/paris vi chemotherapy-driven icd depends review current knowledge pattern-recognition receptor signalling z-vad-fmk enhanced t-cell killing immune-mediated abscopal effect cancer cell-autonomous phenotype radiation-induced immunogenic modulation antitumor immunity induced uvc-treated prostate cancer cell-extrinsic effects innate immune recognition personal data uvc light-induced apoptosis antitumor immune cells tumour immune elimination cancer cell-autonomous contribution human tumor cells data protection anti-ctla-4 treatment springerlink instant access

Questions {❓}

  • Extrinsic cell death pathway plasticity: a driver of clonal evolution in cancer?

Schema {🗺️}

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         headline:Immunogenic cell death in cancer and infectious disease
         description: Initiation of an adaptive immune response depends on the detection of both antigenic epitopes and adjuvant signals. Infectious pathogens and cancer cells often avoid immune detection by limiting the release of danger signals from dying cells. When is cell death immunogenic and what are the pathophysiological implications of this process? Immunogenicity depends on two key factors: antigenicity and adjuvanticity. The presence of exogenous or mutated antigens explains why infected cells and malignant cells can initiate an adaptive immune response provided that the cells also emit adjuvant signals as a consequence of cellular stress and death. Several infectious pathogens have devised strategies to control cell death and limit the emission of danger signals from dying cells, thereby avoiding immune recognition. Similarly, cancer cells often escape immunosurveillance owing to defects in the molecular machinery that underlies the release of endogenous adjuvants. Here, we review current knowledge on the mechanisms that underlie the activation of immune responses against dying cells and their pathophysiological relevance.
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