Evidence map›Paper›PMID 37553068›Full record

ArticleACS synthetic biology2023

A Cell-Free Protein Synthesis Platform to Produce a Clinically Relevant Allergen Panel.

Ariel Helms Thames, Clayton H Rische, Yun Cao, Rebecca A Krier-Burris, Fei Li Kuang, Robert G Hamilton, Charles Bronzert, Bruce S Bochner, Michael C Jewett

Abstract readLetter
In one paragraph

Article in ACS synthetic biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Ariel Helms ThamesMedical Scientist Training Program, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.ORCID 0000-0001-5418-6048
Clayton H RischeCenter for Synthetic Biology, Northwestern University, 2145 Sheridan Road, Tech B486, Evanston, Illinois 60208, United States.ORCID 0000-0003-3610-2116
Yun CaoDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.
Rebecca A Krier-BurrisDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.
Fei Li KuangDivision of Allergy and Immunology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.
Robert G HamiltonDivision of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224, United States.
Charles BronzertDivision of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224, United States.
Bruce S BochnerMedical Scientist Training Program, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.ORCID 0000-0002-9411-6009
Michael C JewettMedical Scientist Training Program, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, United States.ORCID 0000-0003-2948-6211

Funding

Deciphering the roles of eosinophils and T lymphocytes in EGIDK23AI171085 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Fei Li Kuang · 2023 to 2026
$764k
Combining Bacterial Glycosylation Tools and Nanotechnology to Optimize Siglec Ligands for the Treatment of Allergy and AnaphylaxisF31AI165279 · NIAID · NORTHWESTERN UNIVERSITY · PI THAMES, ARIEL · 2021 to 2023
$70k
NIAID NIH HHS F31 AI165279NIAID NIH HHS K23 AI171085
6 · The paper itself

Abstract

Allergens are used in the clinical diagnosis (e.g., skin tests) and treatment (e.g., immunotherapy) of allergic diseases. With growing interest in molecular allergy diagnostics and precision therapies, new tools are needed for producing allergen-based reagents. As a step to address this need, we demonstrate a cell-free protein synthesis approach for allergen production of a clinically relevant allergen panel composed of common allergens spanning a wide range of phylogenetic kingdoms. We show that allergens produced with this approach can be recognized by allergen-specific immunoglobulin E (IgE), either monoclonals or in patient sera. We also show that a cell-free expressed allergen can activate human cells such as peripheral blood basophils and CD34+ progenitor-derived mast cells in an IgE-dependent manner. We anticipate that this cell-free platform for allergen production will enable diagnostic and therapeutic technologies, providing useful tools and treatments for both the allergist and allergic patient.

Indexed as

AllergensImmunoglobulin EHumansPhylogenyAllergensImmunoglobulin Eallergenbasophilscell-free protein synthesisIgE recognitionmast cells

Identifiers

PMID37553068
PMCPMC10768853

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Registered trials

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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.