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  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
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We are analyzing https://link.springer.com/article/10.1007/s11926-012-0254-6.

Title:
Biologic Differences Between Various Inhibitors of the BLyS/BAFF Pathway: Should We Expect Differences Between Belimumab and Other Inhibitors in Development? | Current Rheumatology Reports
Description:
For the first time in more than 50 years, the US Food and Drug Administration has approved a drug specifically for the treatment of systemic lupus erythematosus (SLE). This drug, belimumab, is a monoclonal antibody that neutralizes the B-cell survival factor, B-lymphocyte stimulator (BLyS). Although belimumab has demonstrated a very favorable safety profile, many SLE patients have failed to clinically improve from belimumab therapy. Three additional BLyS antagonists (atacicept, blisibimod, tabalumab) are currently undergoing clinical testing. These antagonists subtly differ from belimumab in their biologic targets, and each is administered through a route (subcutaneous) that differs from the route through which belimumab is currently delivered (intravenous). Whether these differences will have meaningful consequences for efficacy and safety remains to be determined.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Education
  • Science
  • Health & Fitness

Content Management System {๐Ÿ“}

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 {๐Ÿ“ˆ}

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

๐ŸŒ  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? {๐Ÿ’ธ}

We don't see any clear sign of profit-making.

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 might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {๐Ÿ”}

article, google, scholar, pubmed, cas, systemic, lupus, belimumab, erythematosus, cells, sle, baff, cell, immunol, stimulator, arthritis, stohl, blys, patients, lymphocyte, april, rheum, factor, phase, tumor, mice, development, exp, med, disease, study, differences, necrosis, receptor, bliss, privacy, cookies, content, antibody, safety, bcma, jacob, human, murine, regulatory, furie, publish, research, search, biologic,

Topics {โœ’๏ธ}

neutralizing anti-b-lymphocyte stimulator month download article/chapter b-cell survival factor ifn-ฮฑ-exaggerated disease b-cell autoimmune disease systemic lupus erythematosus systemic lupus erythematosus full article pdf sle responder index privacy choices/manage cookies b-lymphocyte stimulator cellular competition independent april-deficient mice humoral immune response caml-interacting member cell receptor repertoire european economic area jt merrill undergoing clinical testing antagonists subtly differ related subjects nucleic acids res baker kp enter forbidden follicular marginal zone niches progressive multifocal leukoencephalopathy 1500 patient-year experience lupus-prone sustained disease improvement cell maturation antigen receptor homologues bcma conditions privacy policy tnf homologue implicated concurrent neutralization/elimination mol cell biol article stohl april neutralization/elimination nonselective baff blockade excess baff rescues post-hoc analysis quinn iii wj dose-escalating trial proinflammatory th17 cells pathogenic th17 cells lymphocyte stimulator enhancement multicenter phase ib article log human genome sciences baff mediates survival dose-ranging study

Questions {โ“}

  • Biologic Differences Between Various Inhibitors of the BLyS/BAFF Pathway: Should We Expect Differences Between Belimumab and Other Inhibitors in Development?
  • Biologic Differences Between Various Inhibitors of the BLyS/BAFF Pathway: Should We Expect Differences Between Belimumab and Other Inhibitors in Development?

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:Biologic Differences Between Various Inhibitors of the BLyS/BAFF Pathway: Should We Expect Differences Between Belimumab and Other Inhibitors in Development?
         description:For the first time in more than 50ย years, the US Food and Drug Administration has approved a drug specifically for the treatment of systemic lupus erythematosus (SLE). This drug, belimumab, is a monoclonal antibody that neutralizes the B-cell survival factor, B-lymphocyte stimulator (BLyS). Although belimumab has demonstrated a very favorable safety profile, many SLE patients have failed to clinically improve from belimumab therapy. Three additional BLyS antagonists (atacicept, blisibimod, tabalumab) are currently undergoing clinical testing. These antagonists subtly differ from belimumab in their biologic targets, and each is administered through a route (subcutaneous) that differs from the route through which belimumab is currently delivered (intravenous). Whether these differences will have meaningful consequences for efficacy and safety remains to be determined.
         datePublished:2012-05-01T00:00:00Z
         dateModified:2012-05-01T00:00:00Z
         pageStart:303
         pageEnd:309
         sameAs:https://doi.org/10.1007/s11926-012-0254-6
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            Atacicept
            BCMA
            Belimumab
            Blisbimod (A-623)
            BLyS/BAFF
            BR3
            Systemic lupus erythematosus
            Tabalumab (LY2127399)
            TACI
            SLE
            Rheumatology
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         isPartOf:
            name:Current Rheumatology Reports
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            volumeNumber:14
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            name:Current Science Inc.
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               name:William Stohl
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                     name:University of Southern California Keck School of Medicine
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      headline:Biologic Differences Between Various Inhibitors of the BLyS/BAFF Pathway: Should We Expect Differences Between Belimumab and Other Inhibitors in Development?
      description:For the first time in more than 50ย years, the US Food and Drug Administration has approved a drug specifically for the treatment of systemic lupus erythematosus (SLE). This drug, belimumab, is a monoclonal antibody that neutralizes the B-cell survival factor, B-lymphocyte stimulator (BLyS). Although belimumab has demonstrated a very favorable safety profile, many SLE patients have failed to clinically improve from belimumab therapy. Three additional BLyS antagonists (atacicept, blisibimod, tabalumab) are currently undergoing clinical testing. These antagonists subtly differ from belimumab in their biologic targets, and each is administered through a route (subcutaneous) that differs from the route through which belimumab is currently delivered (intravenous). Whether these differences will have meaningful consequences for efficacy and safety remains to be determined.
      datePublished:2012-05-01T00:00:00Z
      dateModified:2012-05-01T00:00:00Z
      pageStart:303
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      sameAs:https://doi.org/10.1007/s11926-012-0254-6
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         Systemic lupus erythematosus
         Tabalumab (LY2127399)
         TACI
         SLE
         Rheumatology
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            name:William Stohl
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                  name:University of Southern California Keck School of Medicine
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                     name:Division of Rheumatology, University of Southern California Keck School of Medicine, Los Angeles, USA
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      name:Current Science Inc.
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            name:University of Southern California Keck School of Medicine
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External Links {๐Ÿ”—}(164)

Analytics and Tracking {๐Ÿ“Š}

  • Google Tag Manager

Libraries {๐Ÿ“š}

  • Bliss.js
  • Clipboard.js
  • Prism.js

CDN Services {๐Ÿ“ฆ}

  • Crossref

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