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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
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We began analyzing https://www.nature.com/articles/ni.2552, but it redirected us to https://www.nature.com/articles/ni.2552. The analysis below is for the second page.

Title[redir]:
Plasticity of TH17 cells in Peyer's patches is responsible for the induction of T cell–dependent IgA responses | Nature Immunology
Description:
Nature Immunology - IgA is essential in the maintenance of mucosal host defense and intestinal homeostasis. Stockinger and colleagues show that TH17 cells acquire a follicular helper T cell...

Matching Content Categories {📚}

  • Science
  • Education
  • Telecommunications

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 how the site profits.

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. Doi.org might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

pubmed, article, cas, google, scholar, cells, nature, central, cell, immunol, helper, iga, follicular, immunology, nat, immunity, research, gut, access, content, intestinal, receptor, plasticity, lymphoid, mice, center, medical, essential, cookies, responses, differentiation, privacy, function, peyers, patches, induction, celldependent, hirota, development, germinal, production, regulatory, med, mucosal, immune, foxp, proc, natl, acad, sci,

Topics {✒️}

nature portfolio permissions reprints privacy policy biological services advertising social media dual nature merck research laboratories japan nature 481 nature 448 nature 475 nature 453 nature content high-affinity iga cell-independent iga synthesis iga-producing germinal center identifying foxp3-expressing suppressor author correspondence interferon-driven immune dysregulation lymphoid organ development medical research cell–dependent iga responses personal data springerlink instant access data protection regulatory cell-iga response permissions article hirota lymphoid development transcriptional repressor bcl6 cell–dependent iga european economic area germinal center response physiologically normal state privacy icos receptor instructs cell–dependent immunoglobulin molecular immunology cells expressing foxp3 nuclear receptor rorγ present address competing financial interests foxp3+ follicular regulatory interleukin 17-producing effector th17 cell plasticity intestinal th17 cells mucoepithelial bacterial infection follicular helper cd4 adaptive immune regulation

Schema {🗺️}

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         headline:Plasticity of TH17 cells in Peyer's patches is responsible for the induction of T cell–dependent IgA responses
         description:IgA is essential in the maintenance of mucosal host defense and intestinal homeostasis. Stockinger and colleagues show that TH17 cells acquire a follicular helper T cell phenotype in Peyer's patches and induce the development of IgA-producing B cells. Intestinal Peyer's patches are essential lymphoid organs for the generation of T cell–dependent immunoglobulin A (IgA) for gut homeostasis. Through the use of interleukin 17 (IL-17) fate-reporter mice, we found here that endogenous cells of the TH17 subset of helper T cells in lymphoid organs of naive mice 'preferentially' homed to the intestines and were maintained independently of IL-23. In Peyer's patches, such TH17 cells acquired a follicular helper T cell (TFH cell) phenotype and induced the development of IgA-producing germinal center B cells. Mice deficient in TH17 cells failed to generate antigen-specific IgA responses, which provides evidence that TH17 cells are the crucial subset required for the production of high-affinity T cell–dependent IgA.
         datePublished:2013-03-10T00:00:00Z
         dateModified:2013-03-10T00:00:00Z
         pageStart:372
         pageEnd:379
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      headline:Plasticity of TH17 cells in Peyer's patches is responsible for the induction of T cell–dependent IgA responses
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      dateModified:2013-03-10T00:00:00Z
      pageStart:372
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Social Networks {👍}(1)

External Links {🔗}(297)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Prism.js
  • Zoom.js

Emails and Hosting {✉️}

Mail Servers:

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Name Servers:

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