Evidence map›Paper›PMID 41062830›Full record

Trial reportNature medicine2025

A combination typhoid and non-typhoidal Salmonella polysaccharide conjugate vaccine in healthy adults: a randomized, placebo-controlled phase 1 trial.

Wilbur H Chen, Robin S Barnes, Michael J Sikorski, Reva Datar, Roohali Sukhavasi, Yuanyuan Liang, Rekha R Rapaka, Marcela F Pasetti, Marcelo B Sztein, Rezwanul Wahid and 13 more

Registry-linked trialAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Nature medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03981952 (Phase 1 Randomized, Placebo-Controlled, Dose-Escalation Study of the Safety, Reactogenicity, and Immunogenicity of Trivalent), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

NCT03981952 phase1completednot on this map

Phase 1 Randomized, Placebo-Controlled, Dose-Escalation Study of the Safety, Reactogenicity, and Immunogenicity of Trivalent (S. Enteritidis/S. Typhimurium/S. Typhi Vi) Conjugate Vaccine Against Invasive Salmonella Disease Administered Parenterally to Healthy U.S. Adults

TypeinterventionalSponsorUniversity of Maryland, BaltimoreRan2019 to 2021Enrolled96ConditionsRisk ReductionArmsTrivalent Invasive Salmonella Disease Vaccine (6.25 µg), Trivalent Invasive Salmonella Disease Vaccine (12 µg), Trivalent Invasive Salmonella Disease Vaccine (25 µg), Trivalent Invasive Salmonella Disease Vaccine (highest, well-tolerated dose among Cohorts A-C), Placebo
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Multivalent vaccines for invasiveInfection and immunity · 2026
    Review
  6. Development of an 8-valentFrontiers in immunology · 2026
    Article
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors.

Wilbur H ChenCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA. wilbur.chen@som.umaryland.edu.ORCID http://orcid.org/0000-0001-7741-5536
Robin S BarnesCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Michael J SikorskiCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Reva DatarCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Roohali SukhavasiCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Yuanyuan LiangDepartment of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Rekha R RapakaCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Marcela F PasettiCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Marcelo B SzteinCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Rezwanul WahidCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Sharon M TennantCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Raphael SimonCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Scott M BalibanCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
James E GalenCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Andrew LeesCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-8370-4876
Biana BernshteinRagon Institute, Harvard Medical School, Cambridge, MA, USA.
Galit AlterRagon Institute, Harvard Medical School, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-7680-9215
Raches EllaBharat Biotech International Ltd, Hyderabad, India.ORCID http://orcid.org/0000-0002-4646-4471
Krishna MohanBharat Biotech International Ltd, Hyderabad, India.
M Gangadhara NaiduBharat Biotech International Ltd, Hyderabad, India.
D Yogeswar RaoBharat Biotech International Ltd, Hyderabad, India.
Krishna M EllaBharat Biotech International Ltd, Hyderabad, India.ORCID http://orcid.org/0000-0002-0021-5082
Myron M LevineCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA. mlevine@som.umaryland.edu.ORCID http://orcid.org/0000-0002-5721-5040

Funding

UNIVERSITY OF MARYLAND GREENEBAUM CANCER CENTERSUPPORT GRANTP30CA134274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI FEYRUZ VIRGILIA RASSOOL · 2008 to 2026
$51.0M
Wild-type S. typhi Infection in Humans: Integrated Immunoprotective MechanismsU19AI082655 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI SZTEIN, MARCELO B. · 2009 to 2018
$27.8M
IMMUNE MECHANISMS OF PROTECTION IN S TYPHI VACCINESR01AI036525 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Marcelo B. Sztein · 1994 to 2026
$12.2M
Systems Biology and Biostatistics CoreU19AI181108 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Rosangela Mezghanni · 2024 to 2026
$8.0M
Johns Hopkins HIV Epidemiology and Prevention Sciences Training ProgramT32AI102623 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Shruti H Mehta · 2013 to 2026
$5.3M
Human Cellular Immune Programming Against Invasive SalmonellaK08AI143923 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI RAPAKA, REKHA R · 2019 to 2023
$798k
NCI NIH HHS P30 CA134274NIAID NIH HHS R01 AI036525NIAID NIH HHS T32 AI102623NIAID NIH HHS U19 AI082655NIAID NIH HHS U19 AI181108U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) P30CA134274U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences (NCATS) UMTR004926U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) K08AI143923U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) U19AI181108Wellcome Trust 095967Wellcome Trust (Wellcome) 095967/Z/11/Z
6 · The paper itself

Abstract

In sub-Saharan Africa, typhoidal and non-typhoidal Salmonella (NTS) are leading causes of invasive disease among young children. Trivalent Salmonella conjugate vaccine (TSCV) consists of Vi capsule polysaccharide conjugated to tetanus toxoid and core-plus-O-polysaccharides from the two most prevalent invasive NTS serovars conjugated to flagellin subunits. We conducted a first-in-human, randomized, placebo-controlled, phase 1 trial evaluating the safety and immunogenicity of TSCV. A total of 22 healthy adults aged 18-45 years were randomly allocated to 6.25-µg TSCV (n = 8), 12.5-µg TSCV (n = 10) or placebo (n = 4). The primary objective was the assessment of safety. The co-primary immunogenicity objective was the serum IgG response against the three vaccine polysaccharides and two flagellin carrier proteins. Here we show that TSCV was safe and well tolerated, meeting the prespecified safety endpoints, with the most common solicited symptom being short-lived injection site pain. For each of the three polysaccharides, immune responses, as demonstrated by ≥4-fold increases over baseline, were observed among all (100%) vaccinees, and no responses were elicited in the placebo group, meeting the prespecified immunogenicity endpoints. The two flagellin components elicited 88% (7/8) and 100% (8/8) responses among 6.25-µg and 12.5-µg TSCV recipients and no placebo recipients. These data warrant further evaluation of TSCV for protection against invasive Salmonella disease. ClinicalTrial.gov identifier: NCT03981952 .

Indexed as

Polysaccharides, BacterialSalmonella VaccinesTyphoid FeverTyphoid-Paratyphoid VaccinesAdolescentAdultAntibodies, BacterialFemaleFlagellinHealthy VolunteersHumansImmunoglobulin GMaleMiddle AgedSalmonella typhiVaccines, ConjugateAntibodies, BacterialFlagellinImmunoglobulin GPolysaccharides, BacterialSalmonella VaccinesTyphoid-Paratyphoid VaccinesVaccines, Conjugate

Identifiers

PMID41062830
PMCPMC7618460

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Registered trials

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.