Evidence map›Paper›PMID 39192583›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

Blunting specific T-dependent antibody responses with engineered "decoy" B cells.

Ragan A Pitner, Jaime L Chao, Noelle P Dahl, Meng-Ni Fan, Xiaohe Cai, Nathan G Avery, Kelsey Roe, P Clint Spiegel, Carol H Miao, Michael Y Gerner and 2 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Inhibiting the inhibitors at the cellular level.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    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

12 authors.

Ragan A PitnerDepartment of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA; Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Jaime L ChaoDepartment of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
Noelle P DahlCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Meng-Ni FanCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Xiaohe CaiCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Nathan G AveryDepartment of Chemistry, Western Washington University, Bellingham, WA 98225, USA.
Kelsey RoeCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA.
P Clint SpiegelDepartment of Chemistry, Western Washington University, Bellingham, WA 98225, USA.
Carol H MiaoCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA 98195, USA.
Michael Y GernerDepartment of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA.
Richard G JamesCenter for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA 98195, USA.
David J RawlingsDepartment of Immunology, University of Washington School of Medicine, Seattle, WA 98109, USA; Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA 98101, USA; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address: drawling@uw.edu.

Funding

NRSA Training CoreTL1TR002318 · NCATS · UNIVERSITY OF WASHINGTON · PI Megan Moore · 2017 to 2026
$8.4M
RESEARCH TRAINING IN RHEUMATOLOGYT32AR007108 · NIAMS · UNIVERSITY OF WASHINGTON · PI Shaun Jackson, Tomas M Mustelin · 1986 to 2026
$6.6M
Ultrasound-mediated gene delivery to achieve therapeutic correction of hemophilia AR01HL151077 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI MIAO, CAROL H · 2020 to 2023
$3.2M
Gene Editing for Hemophilia A Treatment Using Lipid NanoparticlesR01HL169793 · NHLBI · SEATTLE CHILDREN'S HOSPITAL · PI Carol H Miao · 2024 to 2026
$2.2M
NCATS NIH HHS TL1 TR002318NHLBI NIH HHS R01 HL151077NHLBI NIH HHS R01 HL169793NIAMS NIH HHS T32 AR007108
6 · The paper itself

Abstract

Antibody inhibitors pose an ongoing challenge to the treatment of subjects with inherited protein deficiency disorders, limiting the efficacy of both protein replacement therapy and corrective gene therapy. Beyond their central role as producers of serum antibody, B cells also exhibit many unique properties that could be exploited in cell therapy applications, notably including antigen-specific recognition and the linked capacity for antigen presentation. Here we employed CRISPR-Cas9 to demonstrate that ex vivo antigen-primed Blimp1-knockout "decoy" B cells, incapable of differentiation into plasma cells, participated in and downregulated host antigen-specific humoral responses after adoptive transfer. Following ex vivo antigen pulse, adoptively transferred high-affinity antigen-specific decoy B cells were diverted into germinal centers en masse, thereby reducing participation by endogenous antigen-specific B cells in T-dependent humoral responses and suppressing both cognate and linked antigen-specific immunoglobulin (Ig)G following immunization with conjugated antigen. This effect was dose-dependent and, importantly, did not impact concurrent unrelated antibody responses. We demonstrated the therapeutic potential of this approach by treating factor VIII (FVIII)-knockout mice with antigen-pulsed decoy B cells prior to immunization with an FVIII conjugate protein, thereby blunting the production of serum FVIII-specific IgG by an order of magnitude as well as reducing the proportion of animals exhibiting functional FVIII inhibition by 6-fold.

Indexed as

Antibody FormationB-LymphocytesMice, KnockoutPositive Regulatory Domain I-Binding Factor 1Adoptive TransferAnimalsCRISPR-Cas SystemsFactor VIIIGerminal CenterHumansImmunoglobulin GMiceT-LymphocytesFactor VIIIImmunoglobulin GPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseantibodyantibody inhibitorsB cell engineeringBlimp1cell therapyCRISPRgene therapygerminal centershemophiliaimmune tolerance

Identifiers

PMID39192583
PMCPMC11489556

What OpenQuestion holds

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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.