Evidence map›Paper›PMID 29276518›Full record

ReviewFrontiers in immunology2017

How B-Cell Receptor Repertoire Sequencing Can Be Enriched with Structural Antibody Data.

Aleksandr Kovaltsuk, Konrad Krawczyk, Jacob D Galson, Dominic F Kelly, Charlotte M Deane, Johannes Trück

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Article
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  4. Computational detection of antigen-specific B cell receptors following immunization.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  5. Article
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  7. Review
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  12. Review
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  15. How repertoire data are changing antibody science.The Journal of biological chemistry · 2020
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors.

Aleksandr KovaltsukDepartment of Statistics, University of Oxford, Oxford, United Kingdom.
Konrad KrawczykDepartment of Statistics, University of Oxford, Oxford, United Kingdom.
Jacob D GalsonDivision of Immunology and the Children's Research Center, University Children's Hospital, University of Zürich, Zürich, Switzerland.
Dominic F KellyOxford Vaccine Group, Department of Paediatrics, University of Oxford and the NIHR Oxford Biomedical Research Center, Oxford, United Kingdom.
Charlotte M DeaneDepartment of Statistics, University of Oxford, Oxford, United Kingdom.
Johannes TrückDivision of Immunology and the Children's Research Center, University Children's Hospital, University of Zürich, Zürich, Switzerland.

Funding

Biotechnology and Biological Sciences Research Council BB/M011224/1
6 · The paper itself

Abstract

Next-generation sequencing of immunoglobulin gene repertoires (Ig-seq) allows the investigation of large-scale antibody dynamics at a sequence level. However, structural information, a crucial descriptor of antibody binding capability, is not collected in Ig-seq protocols. Developing systematic relationships between the antibody sequence information gathered from Ig-seq and low-throughput techniques such as X-ray crystallography could radically improve our understanding of antibodies. The mapping of Ig-seq datasets to known antibody structures can indicate structurally, and perhaps functionally, uncharted areas. Furthermore, contrasting naïve and antigenically challenged datasets using structural antibody descriptors should provide insights into antibody maturation. As the number of antibody structures steadily increases and more and more Ig-seq datasets become available, the opportunities that arise from combining the two types of information increase as well. Here, we review how these data types enrich one another and show potential for advancing our knowledge of the immune system and improving antibody engineering.

Indexed as

Antibodiesantibody modelingB cellcomputational modelingDevelopabilityIg-seqNext-generation sequencing

Identifiers

PMID29276518
PMCPMC5727015

What OpenQuestion holds

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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.