Evidence map›Paper›PMID 36310813›Full record

ArticleAntimicrobial stewardship & healthcare epidemiology : ASHE2022

Predictors of humoral response to SARS-CoV-2 mRNA vaccine BNT162b2 in patients receiving maintenance dialysis.

Tingting Li, Sumanth Gandra, Kimberly A Reske, Margaret A Olsen, Silvana Bommarito, Candace Miller, Karl G Hock, Claire A Ballman, Christina Su, Na Le Dang and 5 more

Open access · goldAbstract read
In one paragraph

Article in Antimicrobial stewardship & healthcare epidemiology : ASHE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

15 authors at 1 institution in 1 country.

Tingting LiDivision of Nephrology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri.ORCID https://orcid.org/0000-0001-7331-9619
Sumanth GandraDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.ORCID https://orcid.org/0000-0003-1482-0854
Kimberly A ReskeDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Margaret A OlsenDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.ORCID https://orcid.org/0000-0001-7070-9320
Silvana BommaritoDivision of Nephrology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri.
Candace MillerDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Karl G HockDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri.
Claire A BallmanDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri.
Christina SuDivision of Nephrology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri.ORCID https://orcid.org/0000-0003-0968-9409
Na Le DangDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.ORCID https://orcid.org/0000-0001-7458-1264
Jennie H KwonDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
David K WarrenDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.ORCID https://orcid.org/0000-0001-8679-8241
Victoria J FraserDivision of Infectious Diseases, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.ORCID https://orcid.org/0000-0001-6251-0733
Christopher W FarnsworthDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri.
Centers for Disease Control and Prevention Epicenters Program
Washington University in St. Louis · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
NCATS NIH HHS UL1 TR002345
6 · The paper itself

Abstract

Objective: Patients on dialysis are at high risk for severe COVID-19 and associated morbidity and mortality. We examined the humoral response to SARS-CoV-2 mRNA vaccine BNT162b2 in a maintenance dialysis population. Design: Single-center cohort study. Setting and participants: Adult maintenance dialysis patients at 3 outpatient dialysis units of a large academic center. Methods: Participants were vaccinated with 2 doses of BNT162b2, 3 weeks apart. We assessed anti-SARS-CoV-2 spike antibodies (anti-S) ∼4-7 weeks after the second dose and evaluated risk factors associated with insufficient response. Definitions of antibody response are as follows: nonresponse (anti-S level, <50 AU/mL), low response (anti-S level, 50-839 AU/mL), and sufficient response (anti-S level, ≥840 AU/mL). Results: Among the 173 participants who received 2 vaccine doses, the median age was 60 years (range, 28-88), 53.2% were men, 85% were of Black race, 86% were on in-center hemodialysis and 14% were on peritoneal dialysis. Also, 7 participants (4%) had no response, 27 (15.6%) had a low response, and 139 (80.3%) had a sufficient antibody response. In multivariable analysis, factors significantly associated with insufficient antibody response included end-stage renal disease comorbidity index score ≥5 and absence of prior hepatitis B vaccination response. Conclusions: Although most of our study participants seroconverted after 2 doses of BNT162b2, 20% of our cohort did not achieve sufficient humoral response. Our findings demonstrate the urgent need for a more effective vaccine strategy in this high-risk patient population and highlight the importance of ongoing preventative measures until protective immunity is achieved.

Identifiers

PMID36310813
PMCPMC9615013
OpenAlexW4294976533

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.