Evidence map›Paper›PMID 35261995›Full record

ArticleMed (New York, N.Y.)2022

Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants.

Sho Miyamoto, Takeshi Arashiro, Yu Adachi, Saya Moriyama, Hitomi Kinoshita, Takayuki Kanno, Shinji Saito, Harutaka Katano, Shun Iida, Akira Ainai and 26 more

Open access · bronzeAbstract read
In one paragraph

Article in Med (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 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

36 authors at 1 institution in 1 country.

Sho MiyamotoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Takeshi ArashiroDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Yu AdachiResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Saya MoriyamaResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Hitomi KinoshitaDepartment of Virology I, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Takayuki KannoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Shinji SaitoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Harutaka KatanoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Shun IidaDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Akira AinaiDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Ryutaro KotakiResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Souichi YamadaDepartment of Virology I, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Yudai KurodaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Tsukasa YamamotoDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Keita IshijimaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Eun-Sil ParkDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Yusuke InoueDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Yoshihiro KakuDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Minoru TobiumeDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Naoko Iwata-YoshikawaDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Nozomi Shiwa-SudoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Kenzo TokunagaDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Seiya OzonoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Takuya HemmiDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Akira UenoDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Noriko KishidaCenter for Influenza and Respiratory Virus Research, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Shinji WatanabeCenter for Influenza and Respiratory Virus Research, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Kiyoko NojimaDepartment of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, 208-0011, Japan.
Yohei SekiDepartment of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, 208-0011, Japan.
Takuo MizukamiDepartment of Safety Research on Blood and Biological Products, National Institute of Infectious Diseases, 208-0011, Japan.
Hideki HasegawaCenter for Influenza and Respiratory Virus Research, National Institute of Infectious Diseases, Tokyo 208-0011, Japan.
Hideki EbiharaDepartment of Virology I, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Ken MaedaDepartment of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Shuetsu FukushiDepartment of Virology I, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Yoshimasa TakahashiResearch Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
Tadaki SuzukiDepartment of Pathology, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.
National Institute of Infectious Diseases · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The immune profile against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has dramatically diversified due to a complex combination of exposure to vaccines and infection by various lineages/variants, likely generating a heterogeneity in protective immunity in a given population. To further complicate this, the Omicron variant, with numerous spike mutations, has emerged. These circumstances have created the need to assess the potential of immune evasion by Omicron in individuals with various immune histories. Methods: The neutralization susceptibility of the variants, including Omicron and their ancestors, was comparably assessed using a panel of plasma/serum derived from individuals with divergent immune histories. Blood samples were collected from either mRNA vaccinees or from those who suffered from breakthrough infections of Alpha/Delta with multiple time intervals following vaccination. Findings: Omicron was highly resistant to neutralization in fully vaccinated individuals without a history of breakthrough infections. In contrast, robust cross-neutralization against Omicron was induced in vaccinees that experienced breakthrough infections. The time interval between vaccination and infection, rather than the variant types of infection, was significantly correlated with the magnitude and potency of Omicron-neutralizing antibodies. Conclusions: Immune histories with breakthrough infections can overcome the resistance to infection by Omicron, with the vaccination-infection interval being the key determinant of the magnitude and breadth of neutralization. The diverse exposure history in each individual warrants a tailored and cautious approach to understanding population immunity against Omicron and future variants. Funding: This study was supported by grants from the Japan Agency for Medical Research and Development (AMED).

Indexed as

COVID-19SARS-CoV-2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesHumansPostoperative ComplicationsVaccinationAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesBNT162b2 mRNA vaccinebreakthrough infectionCOVID-19 vaccineneutralizing antibodyOmicron variantSARS-CoV-2

Identifiers

PMID35261995
PMCPMC8894731
OpenAlexW4220709043

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.