Evidence map›Paper›PMID 38260484›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Impact of COVID-19 vaccination on symptoms and immune phenotypes in vaccine-naïve individuals with Long COVID.

Connor B Grady, Bornali Bhattacharjee, Julio Silva, Jillian Jaycox, Lik Wee Lee, Valter Silva Monteiro, Mitsuaki Sawano, Daisy Massey, César Caraballo, Jeff R Gehlhausen and 22 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. 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, 7 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

32 authors at 8 institutions in 2 countries.

Connor B GradyDepartment of Biostatistics, Epidemiology, and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0001-8407-846X
Bornali BhattacharjeeDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Julio SilvaDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Jillian JaycoxDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Lik Wee LeeAdaptive Biotechnologies, Seattle, WA, USA.
Valter Silva MonteiroDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Mitsuaki SawanoCenter for Outcomes Research and Evaluation, Yale New Haven Hospital, New Haven, Connecticut.
Daisy MasseyCenter for Outcomes Research and Evaluation, Yale New Haven Hospital, New Haven, Connecticut.
César CaraballoCenter for Outcomes Research and Evaluation, Yale New Haven Hospital, New Haven, Connecticut.
Jeff R GehlhausenDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Alexandra TabachnikovaDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Tianyang MaoDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Carolina LucasDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Mario A Peña-HernandezDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Lan XuDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Tiffany J TzengDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Takehiro TakahashiDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Jeph HerrinDepartment of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Diana Berrent GütheSurvivor Corps.
Athena AkramiSainsbury Wellcome Centre, University College London, London, UK.
Gina AssafPatient-Led Research Collaborative.
Hannah DavisPatient-Led Research Collaborative.
Karen HarrisSurvivor Corps.
Lisa McCorkellPatient-Led Research Collaborative.
Wade L SchulzCenter for Infection and Immunity, Yale School of Medicine, New Haven, Connecticut.
Daniel GrffinDepartment of Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York City, New York.
Hannah WeiPatient-Led Research Collaborative.
Aaron M RingDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Leying GuanCenter for Infection and Immunity, Yale School of Medicine, New Haven, Connecticut.
Charles Dela CruzDepartment of Microbial Pathogenesis, Yale University School of Medicine, New Haven, Connecticut, USA.
Akiko IwasakiDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.
Harlan M KrumholzCenter for Infection and Immunity, Yale School of Medicine, New Haven, Connecticut.ORCID 0000-0003-2046-127X
Yale University · USYale New Haven Hospital · USPatient-Led Research CollaborativeAdaptive Biotechnologies (United States) · USColumbia University · USHarvard University · USHoward Hughes Medical Institute · USSainsbury Laboratory · GB

Funding

Yale-Mayo FDA Center for Excellence in Regulatory Science and InnovationU01FD005938 · FDA · YALE UNIVERSITY · PI Joseph Solomon Ross · 2016 to 2026
$25.4M
Viral and immune-mediated CNS pathology during SARS-CoV-2 infectionR01AI157488 · NIAID · YALE UNIVERSITY · PI FARHADIAN, SHELLI, IWASAKI, AKIKO · 2020 to 2024
$4.7M
FDA HHS U01 FD005938NIAID NIH HHS R01 AI157488
6 · The paper itself

Abstract

Background: Long COVID contributes to the global burden of disease. Proposed root cause hypotheses include the persistence of SARS-CoV-2 viral reservoir, autoimmunity, and reactivation of latent herpesviruses. Patients have reported various changes in Long COVID symptoms after COVID-19 vaccinations, leaving uncertainty about whether vaccine-induced immune responses may alleviate or worsen disease pathology. Methods: In this prospective study, we evaluated changes in symptoms and immune responses after COVID-19 vaccination in 16 vaccine-naïve individuals with Long COVID. Surveys were administered before vaccination and then at 2, 6, and 12 weeks after receiving the first vaccine dose of the primary series. Simultaneously, SARS-CoV-2-reactive TCR enrichment, SARS-CoV-2-specific antibody responses, antibody responses to other viral and self-antigens, and circulating cytokines were quantified before vaccination and at 6 and 12 weeks after vaccination. Results: Self-report at 12 weeks post-vaccination indicated 10 out of 16 participants had improved health, 3 had no change, 1 had worse health, and 2 reported marginal changes. Significant elevation in SARS-CoV-2-specific TCRs and Spike protein-specific IgG were observed 6 and 12 weeks after vaccination. No changes in reactivities were observed against herpes viruses and self-antigens. Within this dataset, higher baseline sIL-6R was associated with symptom improvement, and the two top features associated with non-improvement were high IFN-β and CNTF, among soluble analytes. Conclusions: Our study showed that in this small sample, vaccination improved the health or resulted in no change to the health of most participants, though few experienced worsening. Vaccination was associated with increased SARS-CoV-2 Spike protein-specific IgG and T cell expansion in most individuals with Long COVID. Symptom improvement was observed in those with baseline elevated sIL-6R, while elevated interferon and neuropeptide levels were associated with a lack of improvement.

Identifiers

PMID38260484
PMCPMC10802754
OpenAlexW4390822170

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.