Evidence map›Paper›PMID 36284110›Full record

ArticleNPJ vaccines2022

Development of antibody-dependent cellular cytotoxicity in response to recombinant and live-attenuated herpes zoster vaccines.

Seong Yeon Park, Myron J Levin, Jennifer Canniff, Michael Johnson, D Scott Schmid, Adriana Weinberg

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  12. Therapeutic vaccines for herpesviruses.The Journal of clinical investigation · 2024
    Review
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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

6 authors at 3 institutions in 2 countries.

Seong Yeon ParkDepartment of Infectious Diseases, Dongguk University Ilsan Hospital, Goyang, Republic of Korea.ORCID http://orcid.org/0000-0001-8762-7006
Myron J LevinDepartments of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Jennifer CanniffDepartments of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
Michael JohnsonDepartments of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.
D Scott SchmidCenters for Disease Control and Prevention, Division of Viral Diseases, Atlanta, GA, USA.
Adriana WeinbergDepartments of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA. adriana.weinberg@ucdenver.edu.ORCID http://orcid.org/0000-0001-6920-0623
University of Colorado Denver · USCenters for Disease Control and Prevention · USDongguk University Ilsan Hospital · KR

Funding

PERSISTENCE OF PROTECTION CONFERRED BY SHINGRIX AGAINST HERPES ZOSTER IN OLDER ADULTSU01AI141919 · NIAID · UNIVERSITY OF COLORADO DENVER · PI ADRIANA WEINBERG · 2019 to 2026
$5.8M
TBDR01AI149746 · NIAID · JACKSON LABORATORY · PI LI, SHUZHAO · 2020 to 2024
$2.6M
Division of Intramural Research, National Institute of Allergy and Infectious Diseases (Division of Intramural Research of the NIAID) 1U01AI141919-01Dongguk University (DU) Research fund of 2019GlaxoSmithKline (GlaxoSmithKline plc.) 63007497National Research Foundation of Korea (NRF) NRF-2017R1C1B2003336NIAID NIH HHS R01 AI149746NIAID NIH HHS U01 AI141919
6 · The paper itself

Abstract

Zoster vaccines generate antibody responses against varicella-zoster virus (VZV). We compared antibody-dependent cell cytotoxicity (ADCC) elicited by zoster vaccine live (ZVL) and recombinant zoster vaccine (RZV). ADCC mediated by antibodies against VZV lysate (VZV-ADCC) and recombinant glycoprotein E (gE-ADCC) was measured using plasma from 20 RZV- and 20 ZVL-recipients, including half 50-60-years-old and half ≥70-years-old. Solid phase-bound anti-VZV antibodies stimulated TNFα in NK cells as measured by flow cytometry or ELISA. VZV-ADCC pre- and post-immunization was higher in younger vaccinees. ZVL did not appreciably increase VZV-ADCC, whereas RZV increased VZV-ADCC in older vaccinees. ELISA-measured gE-ADCC was similar across groups pre-immunization; significantly increased after ZVL; and RZV and was higher in younger RZV than ZVL recipients. IgG3 antibodies increased after RZV and ZVL, with greater anti-gE than anti-VZV responses. Moreover, gE-ADCC strongly correlated with anti-gE antibody avidity, but there were no appreciable correlations between VZV-ADCC and avidity. NK cells stimulated by anti-gE antibodies showed increased IFNγ and CD107a expression, which was not observed with anti-VZV antibodies. In conclusion, anti-gE antibodies generated more robust ADCC than anti-VZV antibodies. RZV induced higher ADCC antibodies than ZVL depending on the antigen and age of vaccinees. Older adults had lower ADCC antibodies before and after vaccination than younger adults.

Identifiers

PMID36284110
PMCPMC9593992
OpenAlexW4307198162

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.