Evidence map›Paper›PMID 39263923›Full record

Trial reportHuman vaccines & immunotherapeutics2024

Single and two-dose typhoid conjugate vaccine safety and immunogenicity in HIV-exposed uninfected and HIV-unexposed uninfected Malawian children.

Nginache Nampota-Nkomba, Osward M Nyirenda, Victoria Mapemba, Rhoda Masonga, Priyanka D Patel, Theresa Misiri, Felistas Mwakiseghile, Richard Wachepa, John M Ndaferankhande, Bright Lipenga and 11 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Human vaccines & immunotherapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

21 authors.

Nginache Nampota-NkombaBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.
Osward M NyirendaBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.
Victoria MapembaBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.
Rhoda MasongaBlantyre Malaria Project, Kamuzu University of Health Sciences, Blantyre, Malawi.
Priyanka D PatelMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Theresa MisiriMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Felistas MwakiseghileMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Richard WachepaMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
John M NdaferankhandeMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Bright LipengaMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Pratiksha PatelMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Happy BandaMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Jennifer OshinskyCenter 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.
Robert S HeydermanMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Leslie P JamkaCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Divya HosangadiGraduate Program in Life Sciences, University of Maryland School of Medicine, Baltimore, MD, USA.
Shrimati DattaCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Melita A GordonMalawi-Liverpool-Wellcome Program, Kamuzu University of Health Sciences, Blantyre, Malawi.
Kathleen M NeuzilCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Matthew B LaurensCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID 0000-0003-3874-581X

Funding

Wellcome Trust
6 · The paper itself

Abstract

Vaccine safety and immunogenicity data in human immunodeficiency virus (HIV)-exposed uninfected (HEU) children are important for decision-making in HIV and typhoid co-endemic countries. In an open-label study, we recruited Malawian HEU and HIV unexposed uninfected (HUU) infants aged 9 - 11 months. HEU participants were randomized to receive Vi-tetanus toxoid conjugate vaccine (Vi-TT) at 9 months, Vi-TT at 15 months, or Vi-TT at 9 and 15 months. HUU participants received Vi-TT at 9 and 15 months. Safety outcomes included solicited and unsolicited adverse events (AE) and serious AEs (SAEs) within 7 days, 28 days, and 6 months of vaccination, respectively. Serum was collected before and at day 28 after each vaccination to measure anti-Vi IgG antibodies by enzyme-linked immunosorbent assay (ELISA). Cohort 1 (66 participants) enrollment began 02 December 2019, and follow-up was terminated before completion due to the COVID-19 pandemic. Cohort 2 (100 participants) enrollment began 25 March 2020. Solicited AEs were mostly mild, with no significant differences between HEU and HUU participants or one- and two-dose groups. All six SAEs were unrelated to vaccination. Anti-Vi geometric mean titers (GMT) increased significantly from 4.1 to 4.6 ELISA units (EU)/mL at baseline to 2572.0 - 4117.6 EU/mL on day 28 post-vaccination, and similarly between HEU and HUU participants for both one- and two-dose schedules. All participants seroconverted (>4-fold increase in GMT) by the final study visit. Our findings of comparable safety and immunogenicity of Vi-TT in HUU and HEU children support country introductions with single-dose Vi-TT in HIV-endemic countries.

Indexed as

Antibodies, BacterialHIV InfectionsImmunogenicity, VaccineTyphoid FeverTyphoid-Paratyphoid VaccinesVaccines, ConjugateFemaleHumansImmunization ScheduleImmunoglobulin GInfantMalawiMaleTetanus ToxoidVaccinationAntibodies, BacterialImmunoglobulin GTetanus ToxoidTyphoid-Paratyphoid VaccinesVaccines, ConjugateHIV-exposed uninfected childrenimmunogenicitysafetysub-Saharan Africatyphoid conjugate vaccineTyphoid fevertyphoid vaccine

Identifiers

PMID39263923
PMCPMC11404620

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.