Evidence map›Paper›PMID 35368573›Full record

ArticleKidney3602022

SARS-CoV-2 Neutralizing Monoclonal Antibodies for the Treatment of COVID-19 in Kidney Transplant Recipients.

Aileen X Wang, Stephan Busque, Jamie Kuo, Upinder Singh, Katharina Röeltgen, Benjamin A Pinsky, Glenn M Chertow, John D Scandling, Colin R Lenihan

Open access · diamondAbstract read
In one paragraph

Article in Kidney360, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 57% 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

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

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Aileen X WangDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-1097-9270
Stephan BusqueDivision of Abdominal Transplantation, Department of Surgery, Stanford University School of Medicine, Stanford, California.ORCID 0000-0003-1048-1621
Jamie KuoPharmacy Manager of Clinical Effectiveness, Department of Pharmacy, Stanford Health Care, Stanford, California.
Upinder SinghDivision of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.ORCID 0000-0003-0630-0306
Katharina RöeltgenDepartment of Pathology, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-1582-1720
Benjamin A PinskyDivision of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California.ORCID 0000-0001-8751-4810
Glenn M ChertowDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-7599-0534
John D ScandlingDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Colin R LenihanDivision of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Stanford University · USStanford Health Care · US

Funding

Stanford TRANSFORM I2T ProgramR25AI147369 · NIAID · STANFORD UNIVERSITY · PI CHERTOW, GLENN MATTHEW, SINGH, UPINDER · 2019 to 2023
$1.8M
NIAID NIH HHS R25 AI147369
6 · The paper itself

Abstract

Background: Morbidity and mortality associated with coronavirus disease 2019 (COVID-19) infection in kidney transplant recipients are high and early outpatient interventions to prevent progression to severe disease are needed. SARS-CoV-2 neutralizing mAbs, including bamlanivimab and casirivimab-imdevimab, received emergency use authorization in the United States in November 2020 for treatment of mild to moderate COVID-19 disease. Methods: We performed a retrospective analysis of 27 kidney transplant recipients diagnosed with COVID-19 between July 2020 and February 2021 who were treated with bamlanivimab or casirivimab-imdevimab and immunosuppression reduction. We additionally identified 13 kidney transplant recipients with COVID-19 who had mild to moderate disease at presentation, who did not receive mAbs, and had SARS-CoV-2 serology testing available. Results: There were no deaths or graft failures in either group. Both infusions were well tolerated. Four of the 27 patients treated with mAbs required hospitalization due to COVID-19. Four of 13 patients who did not receive mAbs required hospitalization due to COVID-19. Patients who received mAbs demonstrated measurable anti-SARS-CoV-2 IgG with angiotensin-converting enzyme 2 (ACE2) receptor blocking activity at the highest level detectable at 90 days postinfusion, whereas ACE2 blocking activity acquired from natural immunity in the mAb-untreated group was weak. Conclusions: Bamlanivimab and casirivimab-imdevimab combined with immunosuppression reduction were well tolerated and associated with favorable clinical outcomes in kidney transplant recipients diagnosed with mild to moderate COVID-19.

Indexed as

COVID-19Kidney TransplantationAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingHumansRetrospective StudiesSARS-CoV-2Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingbamlanivimabcasirivimabimdevimabCOVID-19immunosuppressionkidney transplantmonoclonal antibodiesSARS-CoV-2transplantation

Identifiers

PMID35368573
PMCPMC8967616
OpenAlexW3205426853

What OpenQuestion holds

Textmetadata
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.