Evidence map›Paper›PMID 33180929›Full record

Trial reportThe Journal of experimental medicine2021

Vi-specific serological correlates of protection for typhoid fever.

Celina Jin, Jennifer Hill, Bronwyn M Gunn, Wen-Han Yu, Lindsay C Dahora, Elizabeth Jones, Mari Johnson, Malick M Gibani, Rachel L Spreng, S Munir Alam and 8 more

Open access · hybridAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Typhoid conjugate vaccines for preventing typhoid fever (enteric fever).The Cochrane database of systematic reviews · 2025
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Article
  7. Multivalent vaccines for invasiveInfection and immunity · 2026
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Longevity of immune response after a single dose of typhoid conjugate vaccine against Salmonella Typhi among children in Hyderabad, Pakistan.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2024
    Article
  15. Review
  16. Article
  17. Review
  18. Shigella-Controlled Human Infection Models: Current and Future Perspectives.Current topics in microbiology and immunology · 2024
    Review
  19. Article
  20. Typhoid fever.Nature reviews. Disease primers · 2023
    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

18 authors at 3 institutions in 2 countries.

Celina JinOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
Jennifer HillOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
Bronwyn M GunnRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, MA.
Wen-Han YuRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, MA.
Lindsay C DahoraDepartments of Immunology, Surgery, and Molecular Genetics and Microbiology, Duke Human Vaccine Institute, Duke University, Durham, NC.
Elizabeth JonesOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
Mari JohnsonOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
Malick M GibaniOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
Rachel L SprengDepartments of Immunology, Surgery, and Molecular Genetics and Microbiology, Duke Human Vaccine Institute, Duke University, Durham, NC.
S Munir AlamDepartments of Immunology, Surgery, and Molecular Genetics and Microbiology, Duke Human Vaccine Institute, Duke University, Durham, NC.
Anna NebykovaOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
Helene B JuelOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
S Moses DennisonDepartments of Immunology, Surgery, and Molecular Genetics and Microbiology, Duke Human Vaccine Institute, Duke University, Durham, NC.
Kelly E SeatonDepartments of Immunology, Surgery, and Molecular Genetics and Microbiology, Duke Human Vaccine Institute, Duke University, Durham, NC.
Jonathan K FallonRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, MA.
Georgia D TomarasDepartments of Immunology, Surgery, and Molecular Genetics and Microbiology, Duke Human Vaccine Institute, Duke University, Durham, NC.
Galit AlterRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, MA.
Andrew J PollardOxford Vaccine Group, Department of Pediatrics, University of Oxford, Oxford, UK.
National Institute for Health Research · GBDuke University · USRagon Institute of MGH, MIT and Harvard · US

Funding

Basic Immunology Training ProgramT32AI052077 · NIAID · DUKE UNIVERSITY · PI KRANGEL, MICHAEL S · 2002 to 2024
$4.2M
NIAID NIH HHS T32 AI052077Wellcome Trust
6 · The paper itself

Abstract

Typhoid Vi vaccines have been shown to be efficacious in children living in endemic regions; however, a widely accepted correlate of protection remains to be established. We applied a systems serology approach to identify Vi-specific serological correlates of protection using samples obtained from participants enrolled in an experimental controlled human infection study. Participants were vaccinated with Vi-tetanus toxoid conjugate (Vi-TT) or unconjugated Vi-polysaccharide (Vi-PS) vaccines and were subsequently challenged with Salmonella Typhi bacteria. Multivariate analyses identified distinct protective signatures for Vi-TT and Vi-PS vaccines in addition to shared features that predicted protection across both groups. Vi IgA quantity and avidity correlated with protection from S. Typhi infection, whereas higher fold increases in Vi IgG responses were associated with reduced disease severity. Targeted antibody-mediated functional responses, particularly neutrophil phagocytosis, were also identified as important components of the protective signature. These humoral markers could be used to evaluate and develop efficacious Vi-conjugate vaccines and assist with accelerating vaccine availability to typhoid-endemic regions.

Indexed as

AdultBacterial LoadHumansImmunity, HumoralImmunogenicity, VaccineImmunoglobulin GTime FactorsTyphoid FeverTyphoid-Paratyphoid VaccinesVaccines, ConjugateImmunoglobulin GTyphoid-Paratyphoid VaccinesVaccines, Conjugate

Identifiers

PMID33180929
PMCPMC7668386
OpenAlexW3101359861

What OpenQuestion 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 OpenQuestion graph.