Evidence map›Paper›PMID 36779802›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

Persons with HIV Develop Spike-Specific Lymph Node Germinal Center Responses following SARS-CoV-2 Vaccination.

Michael Quinn, Luis Parra-Rodriguez, Wafaa B Alsoussi, Chapelle Ayres, Michael K Klebert, Chang Liu, Teresa Suessen, Suzanne M Scheaffer, William D Middleton, Sharlene A Teefey and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

17 authors at 2 institutions in 1 country.

Michael QuinnDivision of Infectious Diseases, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO.
Luis Parra-RodriguezDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0003-1746-0743
Wafaa B AlsoussiDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO.
Chapelle AyresClinical Trials Unit, Washington University School of Medicine, St. Louis, MO.
Michael K KlebertClinical Trials Unit, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0003-3329-3674
Chang LiuDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-6624-1454
Teresa SuessenMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Suzanne M ScheafferDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
William D MiddletonMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Sharlene A TeefeyMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
William G PowderlyDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-7808-3086
Michael S DiamondDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-8791-3165
Rachel M PrestiDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.
Ali H EllebedyDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO.
Jackson S TurnerDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO.
Jane A O'HalloranDivision of Infectious Diseases, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-8265-9471
Philip A MuddCenter for Vaccines and Immunity to Microbial Pathogens, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-3860-5473
Washington University in St. Louis · USMallinckrodt (United States) · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Household Respiratory Virus SARS-CoV-2 Transmission and Immunity Sub-Study (HRTS)U01AI144616 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GORDON, AUBREE L, THOMAS, PAUL G. · 2019 to 2025
$43.7M
Human antibody-based countermeasures against the Wuhan Coronavirus SARS-CoV-2R01AI157155 · NIAID · WASHINGTON UNIVERSITY · PI BARIC, RALPH S, CROWE, JAMES E · 2020 to 2024
$6.0M
DYNAMICS AND EVOLUTION OF IMMUNE RESPONSES TO INFLUENZA VIRUSESU01AI150747 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI, ANTIA, RUSTOM NOSHIR · 2020 to 2024
$5.9M
Programming Durable Immune Responses To VaccinationU01AI141990 · NIAID · WASHINGTON UNIVERSITY · PI Ali Hassan Ellebedy · 2019 to 2026
$5.3M
Structural interrogation of vaccine- and infection-induced B cell responsesR01AI168178 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Goran Bajic · 2022 to 2026
$3.9M
Pediatric Infectious Diseases and Immunity Training ProgramT32AI106688 · NIAID · WASHINGTON UNIVERSITY · PI Megan Anne Cooper, DAVID HUNSTAD · 2014 to 2026
$1.9M
NCATS NIH HHS UL1 TR002345NIAID NIH HHS R01 AI157155NIAID NIH HHS R01 AI168178NIAID NIH HHS T32 AI106688NIAID NIH HHS U01 AI141990NIAID NIH HHS U01 AI144616NIAID NIH HHS U01 AI150747
6 · The paper itself

Abstract

COVID-19 disproportionately affects persons with HIV (PWH) in worldwide locations with limited access to SARS-CoV-2 vaccines. PWH exhibit impaired immune responses to some, but not all, vaccines. Lymph node (LN) biopsies from PWH demonstrate abnormal LN structure, including dysregulated germinal center (GC) architecture. It is not clear whether LN dysregulation prevents PWH from mounting Ag-specific GC responses in the draining LN following vaccination. To address this issue, we longitudinally collected blood and draining LN fine needle aspiration samples before and after SARS-CoV-2 vaccination from a prospective, observational cohort of 11 PWH on antiretroviral therapy: 2 who received a two-dose mRNA vaccine series and 9 who received a single dose of the Ad26.COV2.S vaccine. Following vaccination, we observed spike-specific Abs, spike-specific B and T cells in the blood, and spike-specific GC B cell and T follicular helper cell responses in the LN of both mRNA vaccine recipients. We detected spike-specific Abs in the blood of all Ad26.COV2.S recipients, and one of six sampled Ad26.COV2.S recipients developed a detectable spike-specific GC B and T follicular helper cell response in the draining LN. Our data show that PWH can mount Ag-specific GC immune responses in the draining LN following SARS-CoV-2 vaccination. Due to the small and diverse nature of this cohort and the limited number of available controls, we are unable to elucidate all potential factors contributing to the infrequent vaccine-induced GC response observed in the Ad26.COV2.S recipients. Our preliminary findings suggest this is a necessary area of future research.

Indexed as

COVID-19COVID-19 VaccinesAd26COVS1Antibodies, ViralGerminal CenterHumansLymph NodesProspective StudiesSARS-CoV-2VaccinationAd26COVS1Antibodies, ViralCOVID-19 Vaccines

Identifiers

PMID36779802
PMCPMC10038880
OpenAlexW4320485764

What OpenQuestion holds

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LicenceTDM
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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.