Evidence map›Paper›PMID 41739814›Full record

Trial reportThe Journal of infectious diseases2026

Immunogenicity of Two Versus Three Doses of Hepatitis B Vaccine When Administered to Children Aged 2-18 Months: A Randomized Clinical Trial.

Koffi Barnabé Kegbevi, Yossi Febriani, Chantal Sauvageau, Marie-Michelle Ursu, Caroline Quach, Michaël Desjardins, Julie Bestman-Smith, Vladimir Gilca, Nicholas Brousseau

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Koffi Barnabé KegbeviDépartement de médecine sociale et préventive, Faculté de médecine, Université Laval, Québec, Québec, Canada.ORCID 0009-0005-2086-0408
Yossi FebrianiAxe maladies infectieuses et immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Québec, Québec, Canada.
Chantal SauvageauDépartement de médecine sociale et préventive, Faculté de médecine, Université Laval, Québec, Québec, Canada.ORCID 0000-0002-4300-1658
Marie-Michelle UrsuDépartement de microbiologie, infectiologie et immunologie, Faculté de médecine, Université de Montréal, Montréal, Québec, Canada.ORCID 0009-0004-4541-2567
Caroline QuachDépartement de microbiologie, infectiologie et immunologie, Faculté de médecine, Université de Montréal, Montréal, Québec, Canada.ORCID 0000-0002-1170-9475
Michaël DesjardinsDépartement de microbiologie, infectiologie et immunologie, Faculté de médecine, Université de Montréal, Montréal, Québec, Canada.ORCID 0000-0003-4028-8507
Julie Bestman-SmithAxe maladies infectieuses et immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Québec, Québec, Canada.
Vladimir GilcaDirection des risques biologiques, Institut national de santé publique du Québec, Québec, Québec, Canada.
Nicholas BrousseauDépartement de médecine sociale et préventive, Faculté de médecine, Université Laval, Québec, Québec, Canada.ORCID 0000-0001-6042-3177

Funding

CHU de Québec-Université Laval Research Center CRC-2019-00055Fonds de recherche du Québec (FRQ)Quebec Ministry of Health and Social Services
6 · The paper itself

Abstract

backgroundA 2-dose hepatitis B vaccination schedule is highly immunogenic in children aged ≥1 year, but data for infants are scarce. Our goal was to compare the immunogenicity of 2- and 3-dose hepatitis B vaccination schedules in this population.

methodsChildren in the experimental group were recruited at 2 months of age and randomized to receive a homologous (Infanrix-hexa/Infanrix-hexa) or heterologous (Infanrix-hexa/Twinrix) 2-dose schedule at 2 and 12 months. Children in the control group were recruited at 18 months and had received a homologous 3-dose schedule (Infanrix-hexa/Infanrix-hexa/Infanrix-hexa) at 2, 4, and 18 months. All groups received a challenge dose (Twinrix) 3 years later.

resultsOne month after the primary series, seroprotection rates (anti-HBs ≥10 mIU/mL) were high and similar among the 3 groups (heterologous 2-dose, 91.7%; homologous 2-dose, 90.9%; 3-dose, 94.2%). Geometric mean titers (GMTs) were lower in the 2-dose groups than in the 3-dose group. Post-challenge dose, the majority exhibited an anamnestic response, similar across all 3 groups (heterologous 2-dose, 97.2%; homologous 2-dose, 95.5%; 3-dose, 92.7%). GMTs were numerically higher in the heterologous 2-dose group (9380.5 mIU/mL) than in the 3-dose group (6900.6 mIU/mL) (P = .4). The proportion exhibiting local reactions was significantly lower after the heterologous 2-dose schedule than after the homologous 2-dose schedule.

conclusionsThe anamnestic response 3 years after 2-dose (2 and 12 months) and 3-dose (2, 4, and 18 months) hepatitis B vaccination schedules was similar. The heterologous 2-dose schedule was more immunogenic and less reactogenic than the homologous 2-dose schedule.

Indexed as

Diphtheria-Tetanus-Pertussis VaccineHaemophilus VaccinesHepatitis BHepatitis B AntibodiesHepatitis B VaccinesImmunization ScheduleImmunogenicity, VaccineFemaleHumansInfantMaleVaccinationVaccines, Combineddiphtheria-tetanus-acellular pertussis-Hib-hepatitis B vaccineDiphtheria-Tetanus-Pertussis VaccineHaemophilus VaccinesHepatitis B AntibodiesHepatitis B VaccinesVaccines, Combinedclinical trialhepatitis B vaccinesimmunizationinfantsreduced-dose schedule

Identifiers

PMID41739814
PMCPMC13537124

What OpenQuestion holds

Textmetadata
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.