Evidence map›Paper›PMID 32663199›Full record

ArticleJCI insight2020

Human C. difficile toxin-specific memory B cell repertoires encode poorly neutralizing antibodies.

Hemangi B Shah, Kenneth Smith, Edgar J Scott, Jason L Larabee, Judith A James, Jimmy D Ballard, Mark L Lang

Abstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Trial
  2. Article
  3. HumanbioRxiv : the preprint server for biology · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Gene Expression Dysregulation in Whole Blood of Patients withInternational journal of molecular sciences · 2024
    Article
  10. Article
  11. Reviewing theMicroorganisms · 2024
    Review
  12. Review
  13. Review
  14. Microbiology (Reading, England) · 2023
    Review
  15. Observational
  16. Review
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

7 authors.

Hemangi B ShahDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center (OUHSC).
Kenneth SmithArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, and.
Edgar J ScottDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center (OUHSC).
Jason L LarabeeDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center (OUHSC).
Judith A JamesArthritis and Clinical Immunology, Oklahoma Medical Research Foundation, and.
Jimmy D BallardDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center (OUHSC).
Mark L LangDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center (OUHSC).

Funding

Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TIMOTHY M VANWAGONER · 2013 to 2026
$68.2M
Tissue Pathology Shared ResourceP30CA225520 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Wade Williams · 2018 to 2026
$27.1M
Differential Effects of TcdB1 and TcdB2 in C. difficile diseaseR01AI119048 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI BALLARD, JIMMY D. · 2015 to 2024
$3.8M
NCI NIH HHS P30 CA225520NIAID NIH HHS R01 AI119048NIGMS NIH HHS U54 GM104938
6 · The paper itself

Abstract

Clostridioides difficile is a leading cause of nosocomial infection responsible for significant morbidity and mortality with limited options for therapy. Secreted C. difficile toxin B (TcdB) is a major contributor to disease pathology, and select TcdB-specific Abs may protect against disease recurrence. However, the high frequency of recurrence suggests that the memory B cell response, essential for new Ab production following C. difficile reexposure, is insufficient. We therefore isolated TcdB-specific memory B cells from individuals with a history of C. difficile infection and performed single-cell deep sequencing of their Ab genes. Herein, we report that TcdB-specific memory B cell-encoded antibodies showed somatic hypermutation but displayed limited isotype class switch. Memory B cell-encoded mAb generated from the gene sequences revealed low to moderate affinity for TcdB and a limited ability to neutralize TcdB. These findings indicate that memory B cells are an important factor in C. difficile disease recurrence.

Indexed as

AdultAgedAged, 80 and overAnimalsAntibodies, MonoclonalAntibodies, NeutralizingBacterial ProteinsBacterial ToxinsB-LymphocytesCase-Control StudiesCHO CellsClostridioides difficileClostridium InfectionsCricetulusHumansImmunoglobulin GAntibodies, MonoclonalAntibodies, NeutralizingBacterial ProteinsBacterial ToxinsImmunoglobulin GtoxB protein, Clostridium difficileBacterial infectionsB cellsImmunologyInfectious diseaseMemory

Identifiers

PMID32663199
PMCPMC7455132

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.