Evidence map›Paper›PMID 36252569›Full record

ArticleCell reports2022

BNT162b2-induced neutralizing and non-neutralizing antibody functions against SARS-CoV-2 diminish with age.

Timothy A Bates, Pei Lu, Ye Jin Kang, Devin Schoen, Micah Thornton, Savannah K McBride, Chanhee Park, Daehwan Kim, William B Messer, Marcel E Curlin and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

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  12. Antigen specificity shapes antibody functions in tuberculosis.bioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Timothy A BatesDepartment of Molecular Microbiology and Immunology, Oregon Health and Sciences University, Portland, OR 97239, USA.
Pei LuDivision of Infectious Diseases and Geographic Medicine, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Ye Jin KangDivision of Infectious Diseases and Geographic Medicine, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Devin SchoenDepartment of Occupational Health, Oregon Health and Sciences University, Portland, OR 97239, USA.
Micah ThorntonLyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Savannah K McBrideDepartment of Molecular Microbiology and Immunology, Oregon Health and Sciences University, Portland, OR 97239, USA.
Chanhee ParkLyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Daehwan KimLyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX 75390, USA.
William B MesserDepartment of Molecular Microbiology and Immunology, Oregon Health and Sciences University, Portland, OR 97239, USA.
Marcel E CurlinDepartment of Occupational Health, Oregon Health and Sciences University, Portland, OR 97239, USA. Electronic address: curlin@ohsu.edu.
Fikadu G TafesseDepartment of Molecular Microbiology and Immunology, Oregon Health and Sciences University, Portland, OR 97239, USA. Electronic address: tafesse@ohsu.edu.
Lenette L LuDivision of Infectious Diseases and Geographic Medicine, Department of Internal Medicine, UT Southwestern Medical Center, Dallas, TX 75390, USA; Department of Immunology, UT Southwestern Medical Center, Dallas, TX 75390, USA; Parkland Health & Hospital System, Dallas, TX 75235, USA. Electronic address: lenette.lu@utsouthwestern.edu.
Oregon Health & Science University · USSouthwestern Medical Center · USParkland Health & Hospital System · US

Funding

Oregon Clinical and Translational Research Institute - The National COVID Cohort Collaborative (N3C)UL1TR002369 · NCATS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Cynthia D Morris, Christopher G. Slatore · 2017 to 2026
$78.4M
Multidisciplinary Research Training in Pulmonary MedicineT32HL083808 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DAVID M., SLATORE, CHRISTOPHER G. · 2008 to 2025
$5.3M
Long Term Immunity Following Yellow Fever VaccinationR01AI145835 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI MESSER, WILLIAM · 2020 to 2024
$3.2M
Determining the role of sphingolipids in Mycobacterium tuberculosis infectionR01AI141549 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI TAFESSE, FIKADU G. · 2020 to 2025
$2.4M
NCATS NIH HHS UL1 TR002369NHLBI NIH HHS T32 HL083808NIAID NIH HHS R01 AI141549NIAID NIH HHS R01 AI145835
6 · The paper itself

Abstract

Each severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variant renews concerns about decreased vaccine neutralization weakening efficacy. However, while prevention of infection varies, protection from disease remains and implicates immunity beyond neutralization in vaccine efficacy. Polyclonal antibodies function through Fab domains that neutralize virus and Fc domains that induce non-neutralizing responses via engagement of Fc receptors on immune cells. To understand how vaccines promote protection, we leverage sera from 51 SARS-CoV-2 uninfected individuals after two doses of the BNT162b2 mRNA vaccine. We show that neutralizing activities against clinical isolates of wild-type and five SARS-CoV-2 variants, including Omicron BA.2, link to FcγRIIIa/CD16 non-neutralizing effector functions. This is associated with post-translational afucosylation and sialylation of vaccine-specific antibodies. Further, polyfunctional neutralizing and non-neutralizing breadth, magnitude, and coordination diminish with age. Thus, studying Fc functions in addition to Fab-mediated neutralization provides greater insight into vaccine efficacy for vulnerable populations, such as the elderly, against SARS-CoV-2 and novel variants.

Indexed as

COVID-19Viral VaccinesAgedAntibodies, NeutralizingAntibodies, ViralBNT162 VaccineHumansmRNA VaccinesReceptors, FcSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralBNT162 VaccinemRNA VaccinesReceptors, FcViral Vaccinesantibody glycosylationCOVID-19CP: ImmunologyFc effector functionsFc receptorneutralizationOmicronSARS-CoV-2vaccine

Identifiers

PMID36252569
PMCPMC9533669
OpenAlexW4302009647

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.