Evidence map›Paper›PMID 38570727›Full record

ArticleGenes and immunity2024

Comparative single-cell transcriptomic profile of hybrid immunity induced by adenovirus vector-based COVID-19 vaccines.

Melissa García-Vega, Hui Wan, Mónica Reséndiz-Sandoval, Diana Hinojosa-Trujillo, Olivia Valenzuela, Verónica Mata-Haro, Freddy Dehesa-Canseco, Mario Solís-Hernández, Harold Marcotte, Qiang Pan-Hammarström and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

11 authors at 4 institutions in 3 countries.

Melissa García-Vega *Laboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C, Hermosillo, Sonora, 83304, Mexico.
Hui Wan *Division of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solna, SE171 65, Sweden.
Mónica Reséndiz-SandovalLaboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C, Hermosillo, Sonora, 83304, Mexico.
Diana Hinojosa-TrujilloLaboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C, Hermosillo, Sonora, 83304, Mexico.
Olivia ValenzuelaDepartamento de Ciencias Químico Biológicas, Universidad de Sonora, Hermosillo, Sonora, 83000, Mexico.
Verónica Mata-HaroLaboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C, Hermosillo, Sonora, 83304, Mexico.ORCID 0000-0002-7394-4569
Freddy Dehesa-CansecoComisión México-Estados Unidos para la Prevención de la Fiebre Aftosa y otras Enfermedades Exóticas de los Animales (CPA), SENASICA, SADER, Ciudad de México, 05010, Mexico.
Mario Solís-HernándezComisión México-Estados Unidos para la Prevención de la Fiebre Aftosa y otras Enfermedades Exóticas de los Animales (CPA), SENASICA, SADER, Ciudad de México, 05010, Mexico.
Harold MarcotteDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solna, SE171 65, Sweden.
Qiang Pan-HammarströmDivision of Immunology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solna, SE171 65, Sweden. qiang.pan-hammarstrom@ki.se.ORCID 0000-0003-1990-8804
Jesús HernándezLaboratorio de Inmunología, Centro de Investigación en Alimentación y Desarrollo, A.C, Hermosillo, Sonora, 83304, Mexico. jhdez@ciad.mx.ORCID 0000-0002-5131-3600
Centro de Investigación en Alimentación y Desarrollo · MXKarolinska Institutet · SECentro Panamericano de Fiebre Aftosa · BRUniversidad de Sonora · MX

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 101003650Vetenskapsrådet (Swedish Research Council) 2019-01302 and 2020-06116
6 · The paper itself

Abstract

In this study, antibody response and a single-cell RNA-seq analysis were conducted on peripheral blood mononuclear cells from five different groups: naïve subjects vaccinated with AZD1222 (AZ) or Ad5-nCoV (Cso), individuals previously infected and later vaccinated (hybrid) with AZD1222 (AZ-hb) or Ad5-nCoV (Cso-hb), and those who were infected and had recovered from COVID-19 (Inf). The results showed that AZ induced more robust neutralizing antibody responses than Cso. The single-cell RNA data revealed a high frequency of memory B cells in the Cso and Cso-hb. In contrast, AZ and AZ-hb groups exhibited the highest proportion of activated naïve B cells expressing CXCR4. Transcriptomic analysis of CD4

Indexed as

COVID-19COVID-19 VaccinesAdaptive ImmunityAdenoviridaeAntibodies, NeutralizingAntibodies, ViralCD8-Positive T-LymphocytesChAdOx1 nCoV-19Gene Expression ProfilingHumansLeukocytes, MononuclearAntibodies, NeutralizingAntibodies, ViralChAdOx1 nCoV-19COVID-19 Vaccines

Identifiers

PMID38570727
OpenAlexW4393869226

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.