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

We are analyzing https://link.springer.com/article/10.1007/s00262-003-0409-4.

Title:
Naturally occurring B-cell responses to breast cancer | Cancer Immunology, Immunotherapy
Description:
As demonstrated by the effectiveness of trastuzumab, antibodies against breast cancer antigens are a potentially potent mechanism of tumor control. While trastuzumab is administered exogenously, its efficacy suggests that induction of very high titer antibody responses in vivo might also be therapeutic. Both naturally occurring and vaccine-induced antibody responses to some breast cancer antigens are associated with improved survival in some cases. However, the improvement in survival associated with antibody responses to breast cancer is modest, and tumor regression is not known to be associated with the natural antitumor antibody response, indicating a need for improved understanding of the natural antitumor antibody response. Naturally occurring B-cell responses in the form of serum antibody, tumor reactive lymph node B cells, and tumor-infiltrating B cells have been described, and a variety of breast tumor–associated antigens have been identified based on reactivity of patient antibodies. This review discusses current knowledge of humoral immunity to breast cancer with regard to specific antigens and the basis for their immunogenicity, and the contexts (tumor, lymph node, serum) in which responses are observed. With few exceptions, "tumor-associated antigens" identified with naturally occurring antibodies may be overexpressed on tumor but are in fact nonspecific autoantigens. This suggests that while overexpression or aberrant processing can increase immunogenicity in some cases, the immunogenicity of many or even most tumor-associated antigens is a function of expression in tumor or the result of ancillary tumor factors.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Health & Fitness
  • Education
  • 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 can't figure out the monetization strategy.

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. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

google, scholar, pubmed, cas, cancer, breast, article, human, res, patients, cells, antibodies, tumor, carcinoma, antibody, immunol, immune, clin, monoclonal, cell, mammary, protein, antigens, response, med, lymph, responses, humoral, natl, expression, oncol, antigen, muc, sci, int, proc, acad, mucin, lymphocytes, biol, survival, reactive, treat, medullary, herneu, exp, immunother, node, tumorassociated, eur,

Topics {✒️}

granulocyte/monocyte-colony stimulating factor month download article/chapter e75-specific tumor-lytic ctls tnf-alpha-induced tu-11 gene antigen-induced b-cell death orbital tissue-infiltrating b-cells ferritin h-chain mrna mouse mammary tumor-virus von mensdorff-pouilly enzyme-linked immunosorbent assay v-fos transformation effector high density o-glycosylation vaccine-induced antibody responses low-dose intravenous cyclophosphamide anti-her2 monoclonal antibodies direct intra-tumor injection igg-recognizing shed tumor phage-displayed cdna libraries monoclonal antibody-defined phenotypes anti-erbb-2 monoclonal antibodies anti-tumor antibody produced tumour-draining lymph nodes c-myc oncogene product anti-sialyl-tn antibodies human b-cell line vivo anti-tumour effects fas-induced apoptosis analyzed cd40 ligand-positive cd8+ 2/neu protein-specific antibody critical review--part ii sialyl-tn epitopes correlate phage-displayed cdna library germinal-centre immune responses 2/neu-targeted immune responses tamoxifen-resistant tumorigenic growth nucleic-acid-binding protein early-stage breast cancer her2/neu extracellular domain antigen-driven clonal proliferation anti-malignin antibody test c-terminal region infiltrating dendritic/langerhans cells antigen-driven oligoclonal expansion article coronella-wood chemokine response profiles early-onset breast carcinomas antigen-specific immunotherapy full article pdf humanized monoclonal antibody c-erbb-2 product

Questions {❓}

  • Dion AS, Girardi AJ, Williams CC, Pomenti AA, Redfield ES (1987) Responses of serum from breast cancer patients to murine mammary tumor virus: fact or artifact?
  • Selenko N, Majdic O, Jager U, Sillaber C, Stockl J, Knapp W (2002) Cross-priming of cytotoxic T cells promoted by apoptosis-inducing tumor cell reactive antibodies?

Schema {🗺️}

WebPage:
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         headline:Naturally occurring B-cell responses to breast cancer
         description:As demonstrated by the effectiveness of trastuzumab, antibodies against breast cancer antigens are a potentially potent mechanism of tumor control. While trastuzumab is administered exogenously, its efficacy suggests that induction of very high titer antibody responses in vivo might also be therapeutic. Both naturally occurring and vaccine-induced antibody responses to some breast cancer antigens are associated with improved survival in some cases. However, the improvement in survival associated with antibody responses to breast cancer is modest, and tumor regression is not known to be associated with the natural antitumor antibody response, indicating a need for improved understanding of the natural antitumor antibody response. Naturally occurring B-cell responses in the form of serum antibody, tumor reactive lymph node B cells, and tumor-infiltrating B cells have been described, and a variety of breast tumor–associated antigens have been identified based on reactivity of patient antibodies. This review discusses current knowledge of humoral immunity to breast cancer with regard to specific antigens and the basis for their immunogenicity, and the contexts (tumor, lymph node, serum) in which responses are observed. With few exceptions, "tumor-associated antigens" identified with naturally occurring antibodies may be overexpressed on tumor but are in fact nonspecific autoantigens. This suggests that while overexpression or aberrant processing can increase immunogenicity in some cases, the immunogenicity of many or even most tumor-associated antigens is a function of expression in tumor or the result of ancillary tumor factors.
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      headline:Naturally occurring B-cell responses to breast cancer
      description:As demonstrated by the effectiveness of trastuzumab, antibodies against breast cancer antigens are a potentially potent mechanism of tumor control. While trastuzumab is administered exogenously, its efficacy suggests that induction of very high titer antibody responses in vivo might also be therapeutic. Both naturally occurring and vaccine-induced antibody responses to some breast cancer antigens are associated with improved survival in some cases. However, the improvement in survival associated with antibody responses to breast cancer is modest, and tumor regression is not known to be associated with the natural antitumor antibody response, indicating a need for improved understanding of the natural antitumor antibody response. Naturally occurring B-cell responses in the form of serum antibody, tumor reactive lymph node B cells, and tumor-infiltrating B cells have been described, and a variety of breast tumor–associated antigens have been identified based on reactivity of patient antibodies. This review discusses current knowledge of humoral immunity to breast cancer with regard to specific antigens and the basis for their immunogenicity, and the contexts (tumor, lymph node, serum) in which responses are observed. With few exceptions, "tumor-associated antigens" identified with naturally occurring antibodies may be overexpressed on tumor but are in fact nonspecific autoantigens. This suggests that while overexpression or aberrant processing can increase immunogenicity in some cases, the immunogenicity of many or even most tumor-associated antigens is a function of expression in tumor or the result of ancillary tumor factors.
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External Links {🔗}(565)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

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