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We are analyzing https://link.springer.com/article/10.1186/s12943-019-1055-6.

Title:
Neoantigen vaccine: an emerging tumor immunotherapy | Molecular Cancer
Description:
Genetic instability of tumor cells often leads to the occurrence of a large number of mutations, and expression of non-synonymous mutations can produce tumor-specific antigens called neoantigens. Neoantigens are highly immunogenic as they are not expressed in normal tissues. They can activate CD4+ and CD8+ T cells to generate immune response and have the potential to become new targets of tumor immunotherapy. The development of bioinformatics technology has accelerated the identification of neoantigens. The combination of different algorithms to identify and predict the affinity of neoantigens to major histocompatibility complexes (MHCs) or the immunogenicity of neoantigens is mainly based on the whole-exome sequencing technology. Tumor vaccines targeting neoantigens mainly include nucleic acid, dendritic cell (DC)-based, tumor cell, and synthetic long peptide (SLP) vaccines. The combination with immune checkpoint inhibition therapy or radiotherapy and chemotherapy might achieve better therapeutic effects. Currently, several clinical trials have demonstrated the safety and efficacy of these vaccines. Further development of sequencing technologies and bioinformatics algorithms, as well as an improvement in our understanding of the mechanisms underlying tumor development, will expand the application of neoantigen vaccines in the future.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
  • Education
  • Health & Fitness

Content Management System {πŸ“}

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 {πŸ“ˆ}

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 7,642,828 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

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

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 revenue plan, but it's either invisible or we haven't found it.

Keywords {πŸ”}

pubmed, tumor, google, scholar, article, cells, cas, cancer, central, neoantigens, vaccines, immune, cell, vaccine, neoantigen, patients, tumors, response, mutations, sequencing, immunotherapy, therapy, med, antigen, antitumor, res, clinical, effect, development, melanoma, identification, xiong, wang, antigens, targeting, sci, immunol, zhang, combination, therapeutic, human, specific, clin, bioinformatics, rna, carcinoma, peptide, types, showed, genome,

Topics {βœ’οΈ}

granulocyte/macrophage-colony stimulating factor-secreting neoantigen-specific t-cell responses cancer-specific t-cell receptors anti-pd-1/pd-l1 therapy article download pdf anti-pd-l1 antibodies [116] t-cell receptor targeting post-operative wound healing itim motif-carrying immunoreceptor donor t-cell repertoires related rho/rock signaling de bruin ec adoptive kras g12d-specific computer-simulated epitope prediction emerging anti-tumor immunotherapy anti-pd-l1 antibody pd-l1/b7h-1 inhibits pd-1/pd-l1 blockade mutant peptide-mhc complex targetable tumor-specific antigens foxp3/aml1 interaction inhibits high-throughput sequencing techniques adoptively transferred tumor-reactive cancer-immune set point high-throughput neoantigen prediction adoptive t-cell therapy central south university anti-tumor immune response myeloid-derived suppressor cells mutated tumor-related antigen generate anti-tumor response long-term therapeutic effects express p1a-specific receptor distant immune-controlled tumors tumor cell-mediated inhibition achieve anti-tumor response central immunological tolerance high-throughput sequencing technology inoculated amph-pepviii vaccine p1a-expressing tumor cells mhc-neoantigen-peptide complexes frame-shift mutations account effectively induce tumor-specific disease-free survival period van buuren mm tumour-specific cytotoxic single-molecule targeted therapy potassium-induced immune suppression made considerable progress mutated hla-ii antigen

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Neoantigen vaccine: an emerging tumor immunotherapy
         description:Genetic instability of tumor cells often leads to the occurrence of a large number of mutations, and expression of non-synonymous mutations can produce tumor-specific antigens called neoantigens. Neoantigens are highly immunogenic as they are not expressed in normal tissues. They can activate CD4+ and CD8+ T cells to generate immune response and have the potential to become new targets of tumor immunotherapy. The development of bioinformatics technology has accelerated the identification of neoantigens. The combination of different algorithms to identify and predict the affinity of neoantigens to major histocompatibility complexes (MHCs) or the immunogenicity of neoantigens is mainly based on the whole-exome sequencing technology. Tumor vaccines targeting neoantigens mainly include nucleic acid, dendritic cell (DC)-based, tumor cell, and synthetic long peptide (SLP) vaccines. The combination with immune checkpoint inhibition therapy or radiotherapy and chemotherapy might achieve better therapeutic effects. Currently, several clinical trials have demonstrated the safety and efficacy of these vaccines. Further development of sequencing technologies and bioinformatics algorithms, as well as an improvement in our understanding of the mechanisms underlying tumor development, will expand the application of neoantigen vaccines in the future.
         datePublished:2019-08-23T00:00:00Z
         dateModified:2019-08-23T00:00:00Z
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            Tumor
            Vaccine
            Malignancy
            Immunotherapy
            Cancer Research
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ScholarlyArticle:
      headline:Neoantigen vaccine: an emerging tumor immunotherapy
      description:Genetic instability of tumor cells often leads to the occurrence of a large number of mutations, and expression of non-synonymous mutations can produce tumor-specific antigens called neoantigens. Neoantigens are highly immunogenic as they are not expressed in normal tissues. They can activate CD4+ and CD8+ T cells to generate immune response and have the potential to become new targets of tumor immunotherapy. The development of bioinformatics technology has accelerated the identification of neoantigens. The combination of different algorithms to identify and predict the affinity of neoantigens to major histocompatibility complexes (MHCs) or the immunogenicity of neoantigens is mainly based on the whole-exome sequencing technology. Tumor vaccines targeting neoantigens mainly include nucleic acid, dendritic cell (DC)-based, tumor cell, and synthetic long peptide (SLP) vaccines. The combination with immune checkpoint inhibition therapy or radiotherapy and chemotherapy might achieve better therapeutic effects. Currently, several clinical trials have demonstrated the safety and efficacy of these vaccines. Further development of sequencing technologies and bioinformatics algorithms, as well as an improvement in our understanding of the mechanisms underlying tumor development, will expand the application of neoantigen vaccines in the future.
      datePublished:2019-08-23T00:00:00Z
      dateModified:2019-08-23T00:00:00Z
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         Neoantigen
         Tumor
         Vaccine
         Malignancy
         Immunotherapy
         Cancer Research
         Oncology
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