Evidence map›Paper›PMID 35310500›Full record

ArticleChemical science2022

Retaining the structural integrity of disulfide bonds in diphtheria toxoid carrier protein is crucial for the effectiveness of glycoconjugate vaccine candidates.

Filippo Carboni, Annabel Kitowski, Charlotte Sorieul, Daniele Veggi, Marta C Marques, Davide Oldrini, Evita Balducci, Barbara Brogioni, Linda Del Bino, Alessio Corrado and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Monomeric crystal structure of the vaccine carrier protein CRMActa crystallographica. Section F, Structural biology communications · 2023
    Article
  3. Site-Specific Multi-Functionalization of the Carrier Protein CRMChembiochem : a European journal of chemical biology · 2022
    Article
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

16 authors at 2 institutions in 3 countries.

Filippo CarboniGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Annabel KitowskiInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa Lisboa Portugal gbernardes@medicina.ulisboa.pt.ORCID https://orcid.org/0000-0002-8001-5928
Charlotte SorieulGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.ORCID https://orcid.org/0000-0003-1999-6007
Daniele VeggiGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Marta C MarquesInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa Lisboa Portugal gbernardes@medicina.ulisboa.pt.
Davide OldriniGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Evita BalducciGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Barbara BrogioniGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Linda Del BinoGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Alessio CorradoGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Francesca AngioliniGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Lucia Dello IaconoGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Immaculada MargaritGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Maria Rosaria RomanoGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.
Gonçalo J L BernardesInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa Lisboa Portugal gbernardes@medicina.ulisboa.pt.ORCID https://orcid.org/0000-0001-6594-8917
Roberto AdamoGSK Via Fiorentina 10 53100 Siena Italy roberto.x.adamo@gsk.com.ORCID https://orcid.org/0000-0001-5228-6088
Toscana Life Sciences · ITUniversity of Lisbon · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The introduction of glycoconjugate vaccines marks an important point in the fight against various infectious diseases. The covalent conjugation of relevant polysaccharide antigens to immunogenic carrier proteins enables the induction of a long-lasting and robust IgG antibody response, which is not observed for pure polysaccharide vaccines. Although there has been remarkable progress in the development of glycoconjugate vaccines, many crucial parameters remain poorly understood. In particular, the influence of the conjugation site and strategy on the immunogenic properties of the final glycoconjugate vaccine is the focus of intense research. Here, we present a comparison of two cysteine selective conjugation strategies, elucidating the impact of both modifications on the structural integrity of the carrier protein, as well as on the immunogenic properties of the resulting glycoconjugate vaccine candidates. Our work suggests that conjugation chemistries impairing structurally relevant elements of the protein carrier, such as disulfide bonds, can have a dramatic effect on protein immunogenicity.

Identifiers

PMID35310500
PMCPMC8864718
OpenAlexW4211024409

What OpenQuestion holds

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LicenceCC BY-NC
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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.