Evidence map›Paper›PMID 35505864›Full record

ArticleClinical & translational immunology2022

Humoral immunity against SARS-CoV-2 variants including omicron in solid organ transplant recipients after three doses of a COVID-19 mRNA vaccine.

Kapil K Saharia, Jennifer S Husson, Silke V Niederhaus, Thierry Iraguha, Stephanie V Avila, Youngchae J Yoo, Nancy M Hardy, Xiaoxuan Fan, Destiny Omili, Alice Crane and 17 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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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

27 authors at 3 institutions in 1 country.

Kapil K SahariaInstitute of Human Virology University of Maryland School of Medicine Baltimore MD USA.
Jennifer S HussonInstitute of Human Virology University of Maryland School of Medicine Baltimore MD USA.
Silke V NiederhausDepartment of Surgery University of Maryland School of Medicine Baltimore MD USA.
Thierry IraguhaDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Stephanie V AvilaDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Youngchae J YooInstitute of Human Virology University of Maryland School of Medicine Baltimore MD USA.
Nancy M HardyDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Xiaoxuan FanDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Destiny OmiliDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Alice CraneDepartment of Surgery University of Maryland School of Medicine Baltimore MD USA.
Amber CarrierDepartment of Surgery University of Maryland School of Medicine Baltimore MD USA.
Wen Y XieUniversity of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Erica Vander MauseDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Kim HankeyTransplant and Cellular Therapy Program University of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Sherri BaumanTransplant and Cellular Therapy Program University of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Patricia LeshoTransplant and Cellular Therapy Program University of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Heather D MannuelUniversity of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Ashish AhujaDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Minu MathewDivison of Infectious Diseases University of Maryland School of Medicine Baltimore MD USA.
James AvruchDepartment of Surgery University of Maryland School of Medicine Baltimore MD USA.
John BaddleyInstitute of Human Virology University of Maryland School of Medicine Baltimore MD USA.
Olga GoloubevaDepartment of Epidemiology and Public Health University of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Kirti ShettyDivision of Hepatology/Liver Transplantation University of Maryland School of Medicine Baltimore MD USA.
Saurabh DahiyaDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Aaron P RapoportDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
Tim LuetkensTransplant and Cellular Therapy Program University of Maryland Greenebaum Comprehensive Cancer Center Baltimore MD USA.
Djordje AtanackovicDepartment of Medicine University of Maryland School of Medicine Baltimore MD USA.
University of Maryland, Baltimore · USU-M Rogel Cancer CenterSidney Kimmel Comprehensive Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Solid organ transplant recipients (SOTR) receiving post-transplant immunosuppression show increased COVID-19-related mortality. It is unclear whether an additional dose of COVID-19 vaccines can overcome the reduced immune responsiveness against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants. Methods: We analysed humoral immune responses against SARS-CoV-2 and its variants in 53 SOTR receiving SARS-CoV-2 vaccination. Results: Following the initial vaccination series, 60.3% of SOTR showed no measurable neutralisation and only 18.9% demonstrated neutralising activity of > 90%. More intensive immunosuppression, antimetabolites in particular, negatively impacted antiviral immunity. While absolute IgG levels were lower in SOTR than controls, antibody titres against microbial recall antigens were higher. By contrast, SOTR showed reduced vaccine-induced IgG/IgA antibody titres against SARS-CoV-2 and its delta variants and fewer linear B-cell epitopes, indicating reduced B-cell diversity. Importantly, a third vaccine dose led to an increase in anti-SARS-CoV-2 antibody titres and neutralising activity across alpha, beta and delta variants and to the induction of anti-SARS-CoV-2 CD4 Conclusion: Only a small subgroup of solid organ transplant recipients is able to generate functional antibodies after an initial vaccine series; however, an additional vaccine dose resulted in dramatically improved antibody responses against all SARS-CoV-2 variants except omicron where antibody responses and neutralising activity remained suboptimal.

Indexed as

antibody responsesCOVID‐19omicron variantSARS‐CoV‐2solid organ transplantvaccine

Identifiers

PMID35505864
PMCPMC9052011
OpenAlexW4226205218

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.