Evidence map›Paper›PMID 34909634›Full record

ArticleClinical infection in practice2022

Severe breakthrough COVID-19 with a heavily mutated variant in a multiple myeloma patient 10 weeks after vaccination.

Samuel D Stampfer, Marissa-Skye Goldwater, Sean Bujarski, Bernard Regidor, Wenjuan Zhang, Aaron J Feinstein, Regina Swift, Shahrooz Eshaghian, Eric Vail, James R Berenson

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical infection in practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 5 institutions in 1 country.

Samuel D StampferDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, 954 Gatewood Rd NE, Atlanta, GA 30329, USA.
Marissa-Skye GoldwaterInstitute for Myeloma and Bone Cancer Research, 9201 Sunset Blvd #300, West Hollywood, CA 90069, USA.
Sean BujarskiInstitute for Myeloma and Bone Cancer Research, 9201 Sunset Blvd #300, West Hollywood, CA 90069, USA.
Bernard RegidorBerenson Cancer Center, 9201 Sunset Blvd #300, West Hollywood, CA 90069, USA.
Wenjuan ZhangDepartment of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, 8700 Beverly BLVD #2900A, Los Angeles, CA 90048, USA.
Aaron J FeinsteinProvidence Cedars-Sinai Tarzana Medical Center, 1831 Clark St, Tarzana, CA 91356, USA.
Regina SwiftBerenson Cancer Center, 9201 Sunset Blvd #300, West Hollywood, CA 90069, USA.
Shahrooz EshaghianDivision of Hematology and Oncology, Cedars Sinai Medical Center, 8700 Beverly BLVD #2900A, Los Angeles, CA 90048, USA.
Eric VailDepartment of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, 8700 Beverly BLVD #2900A, Los Angeles, CA 90048, USA.
James R BerensonInstitute for Myeloma and Bone Cancer Research, 9201 Sunset Blvd #300, West Hollywood, CA 90069, USA.
Cedars-Sinai Medical Center · USInstitute for Myeloma & Bone Cancer Research · USEmory University · USOncotherapeutics (United States) · USTarzana Treatment Centers · US

Funding

Training a New Generation of VaccinologistsT32AI074492 · NIAID · EMORY UNIVERSITY · PI Rama Rao Amara, Benjamin A Lopman · 2009 to 2026
$6.4M
NIAID NIH HHS T32 AI074492
6 · The paper itself

Abstract

backgroundPatients with multiple myeloma have unpredictable responses to vaccination for COVID-19. Anti-spike antibody levels can determine which patients develop antibodies at levels similar to healthy controls, and are a known correlate of protection. CASE REPORT: A multiple myeloma patient developed protective anti-spike antibodies after vaccination (608 IU/mL), but nonetheless developed severe breakthrough COVID-19 just 10 weeks following his second vaccination with mRNA-1273.

resultsSequencing of the viral isolate revealed an extensively mutated variant with 10 spike protein mutations, including E484Q and N440K. Serology testing showed a dramatic decline in anti-spike antibodies immediately prior to virus exposure.

conclusionsMultiple myeloma patients who do develop detectable antibody responses to vaccination may be at increased risk for breakthrough infections due to rapid decline in antibody levels. Viral variants with immune escape mutations such as N440K, also seen independently in the SARS-CoV-2 Omicron variant (B.1.1.529) and in viral passaging experiments, likely require a higher level of anti-spike antibodies to prevent severe COVID-19.

Indexed as

AntibodyB.1.628BreakthroughCorrelate of protectionCOVID-19E484QImmunocompromisedMultiple myelomaN440KS194LSARS-CoV-2SevereSpike

Identifiers

PMID34909634
PMCPMC8654462
OpenAlexW4200591664

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.