Evidence map›Paper›PMID 34127854›Full record

ArticleNature medicine2021

Evidence for increased breakthrough rates of SARS-CoV-2 variants of concern in BNT162b2-mRNA-vaccinated individuals.

Talia Kustin, Noam Harel, Uriah Finkel, Shay Perchik, Sheri Harari, Maayan Tahor, Itamar Caspi, Rachel Levy, Michael Leshchinsky, Shifra Ken Dror and 19 more

Abstract read
In one paragraph

Article in Nature medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 233 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
233citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

233 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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173 more citing papers are in PubMed but not listed here.

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

29 authors.

Talia Kustin *The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.ORCID http://orcid.org/0000-0001-5677-4150
Noam Harel *The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Uriah FinkelClalit Research Institute, Innovation Division, Clalit Health Services, Ramat Gan, Israel.
Shay PerchikClalit Research Institute, Innovation Division, Clalit Health Services, Ramat Gan, Israel.
Sheri HarariThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Maayan TahorThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Itamar CaspiThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Rachel LevyThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Michael LeshchinskyClalit Research Institute, Innovation Division, Clalit Health Services, Ramat Gan, Israel.
Shifra Ken DrorClalit Health Services, Central Laboratories, Haifa and Western Galilee, Nesher, Israel.
Galit BergerzonClalit Health Services, Central Laboratories, Haifa and Western Galilee, Nesher, Israel.
Hala GadbanClalit Health Services, Central Laboratories, Haifa and Western Galilee, Nesher, Israel.
Faten GadbanClalit Health Services, Central Laboratories, Haifa and Western Galilee, Nesher, Israel.
Eti EliassianProgenin Laboratories, Jerusalem District, Clalit Health Services, Tel Aviv, Israel.
Orit ShimronProgenin Laboratories, Jerusalem District, Clalit Health Services, Tel Aviv, Israel.
Loulou SalehMicrobiology lab, Rabin Medical Center, Beilinson Hospital, Petah Tiqva, Israel.
Haim Ben-ZviMicrobiology lab, Rabin Medical Center, Beilinson Hospital, Petah Tiqva, Israel.
Elena Keren TaradayCentral Laboratory, Clalit Health Services, Tel Aviv, Israel.
Doron AmichayCentral Laboratory, Clalit Health Services, Tel Aviv, Israel.
Anat Ben-DorCentral Laboratory, Clalit Health Services, Tel Aviv, Israel.
Dana SagasMicrobiology Laboratory, Emek Medical Center, Afula, Israel.
Merav StraussMicrobiology Laboratory, Emek Medical Center, Afula, Israel.
Yonat Shemer AvniLaboratory of Clinical Virology, Soroka University Medical Center, Beersheba, Israel.
Amit HuppertThe Bio-statistical and Bio-mathematical Unit, The Gertner Institute for Epidemiology and Health Policy Research, Chaim Sheba Medical Center, Tel HaShomer, Ramat Gan, Israel.
Eldad KeptenClalit Research Institute, Innovation Division, Clalit Health Services, Ramat Gan, Israel.
Ran D BalicerClalit Research Institute, Innovation Division, Clalit Health Services, Ramat Gan, Israel.
Doron Netzer *Clalit Health Services, Tel Aviv, Israel.
Shay Ben-Shachar *Clalit Research Institute, Innovation Division, Clalit Health Services, Ramat Gan, Israel. shayb@clalit.org.il.ORCID http://orcid.org/0000-0001-7994-5805
Adi SternThe Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel. sternadi@tauex.tau.ac.il.ORCID http://orcid.org/0000-0002-2919-3542

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 852223
6 · The paper itself

Abstract

The BNT162b2 mRNA vaccine is highly effective against SARS-CoV-2. However, apprehension exists that variants of concern (VOCs) may evade vaccine protection, due to evidence of reduced neutralization of the VOCs B.1.1.7 and B.1.351 by vaccine sera in laboratory assays. We performed a matched cohort study to examine the distribution of VOCs in infections of BNT162b2 mRNA vaccinees from Clalit Health Services (Israel) using viral genomic sequencing, and hypothesized that if vaccine effectiveness against a VOC is reduced, its proportion among breakthrough cases would be higher than in unvaccinated controls. Analyzing 813 viral genome sequences from nasopharyngeal swabs, we showed that vaccinees who tested positive at least 7 days after the second dose were disproportionally infected with B.1.351, compared with controls. Those who tested positive between 2 weeks after the first dose and 6 days after the second dose were disproportionally infected by B.1.1.7. These findings suggest reduced vaccine effectiveness against both VOCs within particular time windows. Our results emphasize the importance of rigorously tracking viral variants, and of increasing vaccination to prevent the spread of VOCs.

Indexed as

AdolescentAdultAgedAged, 80 and overBNT162 VaccineChildChild, PreschoolCOVID-19COVID-19 VaccinesFemaleHumansInfantInfant, NewbornMaleMiddle AgedRNA, MessengerBNT162 VaccineCOVID-19 VaccinesRNA, Messenger

Identifiers

PMID34127854
PMCPMC8363499

What OpenQuestion holds

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LicenceCC BY
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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.