Evidence map›Paper›PMID 31267246›Full record

ArticleGlycoconjugate journal2019

Fluorine-modified sialyl-Tn-CRM197 vaccine elicits a robust immune response.

Chengcheng Song, Xiu-Jing Zheng, Haili Guo, Yafei Cao, Fan Zhang, Qin Li, Xin-Shan Ye, Yifa Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in Glycoconjugate journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  4. Synthesis of Fluorinated Glycotope Mimetics Derived fromInternational journal of molecular sciences · 2025
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  5. Article
  6. Review
  7. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Chengcheng SongSchool of Life Sciences, Northeast Normal University, Changchun, 130024, China.
Xiu-Jing ZhengState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China.
Haili GuoSchool of Life Sciences, Northeast Normal University, Changchun, 130024, China.
Yafei CaoState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China.
Fan ZhangSchool of Life Sciences, Northeast Normal University, Changchun, 130024, China.
Qin LiState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China.
Xin-Shan YeState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China. xinshan@bjmu.edu.cn.
Yifa ZhouSchool of Life Sciences, Northeast Normal University, Changchun, 130024, China. zhouyf383@nenu.edu.cn.
Northeast Normal University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Even though a vaccine that targets tumor-associated carbohydrate antigens on epithelial carcinoma cells presents an attractive therapeutic approach, relatively poor immunogenicity limits its development. In this study, we investigated the immunological activity of a fluoro-substituted Sialyl-Tn (F-STn) analogue coupled to the non-toxic cross-reactive material of diphtheria toxin197 (CRM197). Our results indicate that F-STn-CRM197 promotes a greater immunogenicity than non-fluorinated STn-CRM197. In the presence or absence of adjuvant, F-STn-CRM197 remarkably enhances both cellular and humoral immunity against STn by increasing antigen-specific lymphocyte proliferation and inducing a mixed Th1/Th2 response leading to production of IFN-γ and IL-4 cytokines, as well as STn-specific antibodies. Furthermore, antisera produced from F-STn-CRM197 immunization significantly recognizes STn-positive tumor cells and increases cancer cell lysis induced by antibody-dependent cell-mediated cytotoxicity (ADCC) or complement-dependent cytotoxicity (CDC) pathways. Our data suggest that this F-STn vaccine may be useful for cancer immunotherapy and possibly for prophylactic prevention of cancer.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, NeoplasmAntibody-Dependent Cell CytotoxicityAntigens, Tumor-Associated, CarbohydrateBacterial ProteinsCancer VaccinesCell Line, TumorColonic NeoplasmsFemaleGene ExpressionGlycoconjugatesHalogenationHumansImmune SeraImmunity, CellularAdjuvants, ImmunologicAntibodies, NeoplasmAntigens, Tumor-Associated, CarbohydrateBacterial ProteinsCancer VaccinesCRM197 (non-toxic variant of diphtheria toxin)GlycoconjugatesIl4 protein, mouseImmune SeraInterferon-gammaInterleukin-4sialosyl-Tn antigenCancer immunotherapyGlycoconjugate vaccineSTnTACAs

Identifiers

PMID31267246
OpenAlexW2953671989

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.