Evidence map›Paper›PMID 35667914›Full record

ArticleVaccine2022

Durable antibody responses elicited by 1 dose of Ad26.COV2.S and substantial increase after boosting: 2 randomized clinical trials.

Jerald Sadoff, Mathieu Le Gars, Boerries Brandenburg, Vicky Cárdenas, Georgi Shukarev, Nathalie Vaissiere, Dirk Heerwegh, Carla Truyers, Anne Marit de Groot, Mandy Jongeneelen and 9 more

2 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Vaccine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 7% 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.

NCT04436276 phase1 / phase2completednot on this map

A Randomized, Double-blind, Placebo-controlled Phase 1/2a Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Ad26COVS1 in Adults Aged 18 to 55 Years Inclusive and Adults Aged 65 Years and Older

TypeinterventionalSponsorJanssen Vaccines & Prevention B.V.Ran2020 to 2023Enrolled1,085ConditionsCovid-19 PreventionArmsAd26.COV2.S, Placebo
NCT04535453 phase2completednot on this map

A Randomized, Double-blind, Placebo-controlled Phase 2a Study to Evaluate a Range of Dose Levels and Vaccination Intervals of Ad26.COV2.S in Healthy Adults Aged 18 to 55 Years Inclusive and Adults Aged 65 Years and Older and to Evaluate 2 Dose Levels of Ad26.COV2.S in Healthy Adolescents Aged 12 to 17 Years Inclusive

TypeinterventionalSponsorJanssen Vaccines & Prevention B.V.Ran2020 to 2022Enrolled635ConditionsHealthyArmsAd26.COV2.S, Placebo
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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  20. Booster or additional vaccination doses in patients vaccinated against COVID-19.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2022
    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

19 authors at 3 institutions in 3 countries.

Jerald SadoffJanssen Vaccines and Prevention, Leiden, The Netherlands. Electronic address: jsadoff@its.jnj.com.
Mathieu Le GarsJanssen Vaccines and Prevention, Leiden, The Netherlands.
Boerries BrandenburgJanssen Vaccines and Prevention, Leiden, The Netherlands.
Vicky CárdenasJanssen Research and Development, Spring House, PA, USA.
Georgi ShukarevJanssen Vaccines and Prevention, Leiden, The Netherlands.
Nathalie VaissiereJanssen Research and Development, Beerse, Belgium.
Dirk HeerweghJanssen Research and Development, Beerse, Belgium.
Carla TruyersJanssen Research and Development, Beerse, Belgium.
Anne Marit de GrootJanssen Vaccines and Prevention, Leiden, The Netherlands.
Mandy JongeneelenJanssen Vaccines and Prevention, Leiden, The Netherlands.
Krisztian KaszasJanssen Vaccines and Prevention, Leiden, The Netherlands.
Jeroen TolboomJanssen Vaccines and Prevention, Leiden, The Netherlands.
Gert ScheperJanssen Vaccines and Prevention, Leiden, The Netherlands.
Jenny HendriksJanssen Vaccines and Prevention, Leiden, The Netherlands.
Javier Ruiz-GuiñazúJanssen Research and Development, Beerse, Belgium.
Frank StruyfJanssen Research and Development, Beerse, Belgium.
Johan Van HoofJanssen Vaccines and Prevention, Leiden, The Netherlands.
Macaya DouoguihJanssen Vaccines and Prevention, Leiden, The Netherlands.
Hanneke SchuitemakerJanssen Vaccines and Prevention, Leiden, The Netherlands.
Janssen (Netherlands) · NLJanssen (Belgium) · BEJanssen (United States) · US

Funding

ASPR HHS HHSO100201700018C
6 · The paper itself

Abstract

backgroundAd26.COV2.S is a well-tolerated and effective vaccine against COVID-19. We evaluated durability of anti-SARS-CoV-2 antibodies elicited by single-dose Ad26.COV2.S and the impact of boosting.

methodsIn randomized, double-blind, placebo-controlled, phase 1/2a and phase 2 trials, participants received single-dose Ad26.COV2.S (5 × 10

resultsData were analyzed from phase 1/2a participants enrolled from 22 July-18 December 2020 (Cohort 1a, 18-55 years [y], N = 25; Cohort 2a, 18-55y, N = 17; Cohort 3, ≥65y, N = 22), and phase 2 participants from 14 to 22 September 2020 (18-55y and ≥ 65y, N = 73). Single-dose Ad26.COV2.S elicited stable neutralizing antibodies for at least 8-9 months and stable binding antibodies for at least 6 months, irrespective of age. A 5 × 10

conclusionsSingle-dose Ad26.COV2.S elicited durable antibody responses for at least 8 months and elicited immune memory. Booster-elicited binding and neutralizing antibody responses were rapid and robust, even with a quarter vaccine dose, and stronger with a longer interval since primary vaccination.

trial registrationClinicalTrials.gov Identifier: NCT04436276, NCT04535453.

Indexed as

Ad26COVS1COVID-19Antibodies, NeutralizingAntibodies, ViralAntibody FormationCOVID-19 VaccinesHumansRandomized Controlled Trials as TopicSARS-CoV-2Ad26COVS1Antibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesAd26.COV2.SAntibodyCOVID-19Enzyme-linked immunosorbent assayVaccineVirus neutralization assay

Identifiers

PMID35667914
PMCPMC9165876
OpenAlexW4281621690

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.