Evidence map›Paper›PMID 36656773›Full record

ArticlemedRxiv : the preprint server for health sciences2023

The time between vaccination and infection impacts immunity against SARS-CoV-2 variants.

Timothy A Bates, Hans C Leier, Savannah K McBride, Devin Schoen, Zoe L Lyski, David X Lee, William B Messer, Marcel E Curlin, Fikadu G Tafesse

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Timothy A BatesDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.
Hans C LeierDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.
Savannah K McBrideDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.
Devin SchoenDivision of Infectious Diseases, Oregon Health & Science University; Portland, OR 97239, United States.
Zoe L LyskiDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.
David X LeeDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.
William B MesserDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.
Marcel E CurlinDivision of Infectious Diseases, Oregon Health & Science University; Portland, OR 97239, United States.
Fikadu G TafesseDepartment of Molecular Microbiology & Immunology, Oregon Health & Science University; Portland, OR 97239, United States.

Funding

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
NHLBI NIH HHS T32 HL083808NIAID NIH HHS R01 AI141549NIAID NIH HHS R01 AI145835
6 · The paper itself

Abstract

As the COVID-19 pandemic continues, long-term immunity against SARS-CoV-2 will be globally important. Official weekly cases have not dropped below 2 million since September of 2020, and continued emergence of novel variants have created a moving target for our immune systems and public health alike. The temporal aspects of COVID-19 immunity, particularly from repeated vaccination and infection, are less well understood than short-term vaccine efficacy. In this study, we explore the impact of combined vaccination and infection, also known as hybrid immunity, and the timing thereof on the quality and quantity of antibodies produced by a cohort of 96 health care workers. We find robust neutralizing antibody responses among those with hybrid immunity against all variants, including Omicron BA.2, and we further found significantly improved neutralizing titers with longer vaccine-infection intervals up to 400 days. These results indicate that anti-SARS-CoV-2 antibody responses undergo continual maturation following primary exposure by either vaccination or infection for at least 400 days after last antigen exposure. We show that neutralizing antibody responses improved upon secondary boosting with greater impact seen after extended intervals. Our findings may also extend to booster vaccine doses, a critical consideration in future vaccine campaign strategies.

Identifiers

PMID36656773
PMCPMC9844016

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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.