Evidence map›Paper›PMID 36182684›Full record

ArticleCell reports. Medicine2022

Enhanced antibody responses in fully vaccinated individuals against pan-SARS-CoV-2 variants following Omicron breakthrough infection.

Hye Won Jeong, Se-Mi Kim, Min Kyung Jung, Ji Yun Noh, Ji-Seung Yoo, Eun-Ha Kim, Young-Il Kim, Kwangmin Yu, Seung-Gyu Jang, Juryeon Gil and 17 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.1field-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.

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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. High-resolution map of the Fc functions mediated by COVID-19-neutralizing antibodies.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. 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

27 authors at 7 institutions in 2 countries.

Hye Won JeongCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju 28644, Republic of Korea.
Se-Mi KimCenter for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Min Kyung JungThe Center for Viral Immunology, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Ji Yun NohDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Seoul 08308, Republic of Korea.
Ji-Seung YooCenter for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Eun-Ha KimCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea.
Young-Il KimCenter for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Kwangmin YuCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea.
Seung-Gyu JangCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Center for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Juryeon GilCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea.
Mark Anthony CaselCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Center for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Rollon RareCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Center for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Jeong Ho ChoiCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea.
Hee-Sung KimCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Department of Internal Medicine, Chungbuk National University Hospital, Cheongju 28644, Republic of Korea.
Jun Hyoung KimDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju 28644, Republic of Korea.
Jihye UmPublic Health Research Institute, National Medical Center, Seoul 04564, Republic of Korea.
Chaeyoon KimThe Center for Viral Immunology, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea.
Yeonjae KimDivision of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul 04564, Republic of Korea.
Bum Sik ChinDivision of Infectious Diseases, Department of Internal Medicine, National Medical Center, Seoul 04564, Republic of Korea.
Sungmin JungGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.
Jun Yong ChoiDepartment of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Kyoung-Ho SongDivision of Infectious Diseases, Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Republic of Korea.
Yong-Dae KimCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Chungbuk Regional Cancer Center, Chungbuk National University Hospital, Cheongju 28644, Republic of Korea.
Jun-Sun ParkPublic Health Research Institute, National Medical Center, Seoul 04564, Republic of Korea.
Joon Young SongDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Seoul 08308, Republic of Korea. Electronic address: infection@korea.ac.kr.
Eui-Cheol ShinThe Center for Viral Immunology, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea. Electronic address: ecshin@kaist.ac.kr.
Young Ki ChoiCollege of Medicine and Medical Research Institute, Chungbuk National University, Cheongju 28644, Republic of Korea; Center for Study of Emerging and Re-emerging Viruses, Korea Virus Research Institute, Institute for Basic Science (IBS), Daejeon 34126, Republic of Korea. Electronic address: choiki55@ibs.re.kr.
Chungbuk National University · KRInstitute for Basic Science · KRNational Medical Center · KRKorea Advanced Institute of Science and Technology · KRKorea University · KRChungbuk National University Hospital · KRSeoul National University Bundang Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Omicron has become the globally dominant severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant, creating additional challenges due to its ability to evade neutralization. Here, we report that neutralizing antibodies against Omicron variants are undetected following COVID-19 infection with ancestral or past SARS-CoV-2 variant viruses or after two-dose mRNA vaccination. Compared with two-dose vaccination, a three-dose vaccination course induces broad neutralizing antibody responses with improved durability against different SARS-CoV-2 variants, although neutralizing antibody titers against Omicron remain low. Intriguingly, among individuals with three-dose vaccination, Omicron breakthrough infection substantially augments serum neutralizing activity against a broad spectrum of SARS-CoV-2 variants, including Omicron variants BA.1, BA.2, and BA.5. Additionally, after Omicron breakthrough infection, memory T cells respond to the spike proteins of both ancestral and Omicron SARS-CoV-2 by producing cytokines with polyfunctionality. These results suggest that Omicron breakthrough infection following three-dose mRNA vaccination induces pan-SARS-CoV-2 immunity that may protect against emerging SARS-CoV-2 variants of concern.

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralAntibody FormationBroadly Neutralizing AntibodiesCytokinesHumansRNA, MessengerSpike Glycoprotein, CoronavirusViral Envelope ProteinsAntibodies, ViralBroadly Neutralizing AntibodiesCytokinesRNA, MessengerSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Envelope Proteinsancestralbreakthrough infectioncross-neutralizationD614GmRNA vaccineOmicron BA.1Omicron BA.2recovered patientSARS-CoV-2T cell immune responsevariants of concern

Identifiers

PMID36182684
PMCPMC9482837
OpenAlexW4296260830

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.