Evidence map›Paper›PMID 38416834›Full record

ArticleScience advances2024

Rise in broadly cross-reactive adaptive immunity against human β-coronaviruses in MERS-recovered patients during the COVID-19 pandemic.

So-Hee Kim, Yuri Kim, Sangeun Jeon, Uni Park, Ju-Il Kang, Kyeongseok Jeon, Hye-Ran Kim, Songhyeok Oh, Ji-Young Rhee, Jae-Phil Choi and 11 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 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
1.2field-weighted citation impact, top 24% 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, 3 citations in OpenAlex.

  1. Article
  2. Article
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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

21 authors at 6 institutions in 1 country.

So-Hee KimDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.ORCID 0000-0003-1187-5446
Yuri KimDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.ORCID 0000-0002-9385-2557
Sangeun JeonZoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam 13488, Republic of Korea.ORCID 0000-0003-3695-6357
Uni ParkDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
Ju-Il KangInstitute of Endemic Disease, Seoul National University Medical Research, Seoul 03080, Republic of Korea.
Kyeongseok JeonDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.ORCID 0000-0002-5452-0998
Hye-Ran KimDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
Songhyeok OhDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.ORCID 0009-0007-4971-4425
Ji-Young RheeDivision of Infectious Diseases, Department of Medicine, Dankook University College of Medicine, Cheonan 31116, Republic of Korea.ORCID 0000-0003-4664-7048
Jae-Phil ChoiDepartment of Internal Medicine, Seoul Medical Center, Seoul 02053, Republic of Korea.ORCID 0000-0003-4805-7930
Wan Beom ParkDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.ORCID 0000-0003-0022-9625
Sang Won ParkDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.ORCID 0000-0002-0550-1897
Jeong-Sun YangCenter for Emerging Virus Research, Korea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.ORCID 0000-0001-5005-9738
Joo-Yeon LeeCenter for Emerging Virus Research, Korea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju 28159, Republic of Korea.ORCID 0000-0002-0993-9626
Jihye KangTranslational Research Center, Research Institute of Public Health, National Medical Center, Seoul 04564, Republic of Korea.ORCID 0000-0002-5917-5855
Hyoung-Shik ShinDivision of Infectious Diseases, Department of Internal Medicine, Daejeon Eulji Medical Center, Eulji University School of Medicine, Daejeon 34824, Republic of Korea.ORCID 0000-0001-6504-3413
Yeonjae KimCenter for Infectious Diseases, National Medical Center, Seoul 04564, Republic of Korea.ORCID 0000-0003-4144-9077
Seungtaek KimZoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam 13488, Republic of Korea.ORCID 0000-0003-3954-5908
Yeon-Sook KimDivision of Infectious Diseases, Department of Internal Medicine, Chungnam National University School of Medicine, Daejeon 35015, Republic of Korea.ORCID 0000-0003-1142-5488
Dong-Gyun LimTranslational Research Center, Research Institute of Public Health, National Medical Center, Seoul 04564, Republic of Korea.ORCID 0000-0002-8291-1873
Nam-Hyuk ChoDepartment of Microbiology and Immunology, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.ORCID 0000-0003-3673-6397
Seoul National University · KRInstitut Pasteur Korea · KRKorea Disease Control and Prevention Agency · KREulji University · KRNational Medical Center · KRSeoul Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To develop a universal coronavirus (CoV) vaccine, long-term immunity against multiple CoVs, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, Middle East respiratory syndrome (MERS)-CoV, and future CoV strains, is crucial. Following the 2015 Korean MERS outbreak, we conducted a long-term follow-up study and found that although neutralizing antibodies and memory T cells against MERS-CoV declined over 5 years, some recovered patients exhibited increased antibody levels during the COVID-19 pandemic. This likely resulted from cross-reactive immunity induced by SARS-CoV-2 vaccines or infections. A significant correlation in antibody responses across various CoVs indicates shared immunogenic epitopes. Two epitopes-the spike protein's stem helix and intracellular domain-were highly immunogenic after MERS-CoV infection and after SARS-CoV-2 vaccination or infection. In addition, memory T cell responses, especially polyfunctional CD4

Indexed as

COVID-19Middle East Respiratory Syndrome CoronavirusAdaptive ImmunityCOVID-19 VaccinesEpitopesFollow-Up StudiesHumansPandemicsSARS-CoV-2COVID-19 VaccinesEpitopes

Identifiers

PMID38416834
PMCPMC10901372
OpenAlexW4392265941

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.