Evidence map›Paper›PMID 41635086›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2026

In vivo production of an anti-HIV antibody in mice by non-viral gene knockin in primate hematopoietic stem and progenitor cells.

Jack M P Castelli, Katrina Poljakov, Youngseo Jwa, Rachel Cunningham, Molly E Cassidy, Matthew D Gray, Jocelyn N Sanchez Gaytan, Mark R Enstrom, Grady Gastelum, Zhongchen Wang and 4 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2026. 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. Article
  3. Review
4 · The record

Corrections and comments

  • Update of
    2025
5 · Who and what money

Authors and funding

14 authors.

Jack M P CastelliTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Katrina PoljakovVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Youngseo JwaTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Rachel CunninghamTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Molly E CassidyTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Matthew D GrayVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Jocelyn N Sanchez GaytanTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Mark R EnstromTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Grady GastelumTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Zhongchen WangBeirne B. Carter Center for Immunology Research, University of Virginia, Charlottesville, VA, USA; Biomedical Sciences Graduate Program, University of Virginia, Charlottesville, VA, USA.
Jonathan D LintonTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Anthony RongvauxTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Immunology, University of Washington, Seattle, WA, USA.
Justin J TaylorBeirne B. Carter Center for Immunology Research, University of Virginia, Charlottesville, VA, USA; Biomedical Sciences Graduate Program, University of Virginia, Charlottesville, VA, USA; Division of Infectious Disease and International Health, Department of Medicine, University of Virginia, Charlottesville, VA, USA.
Jennifer E AdairTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA; Department of Medical Oncology, University of Washington, Seattle, WA, USA. Electronic address: jennifer.adair@umassmed.edu.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI CONNIE L CELUM · 1988 to 2026
$104.9M
WaNPRC Macaca nemestrina SPF Breeding ColonyU42OD011123 · OD · UNIVERSITY OF WASHINGTON · PI CHARLOTTE HOTCHKISS · 2012 to 2026
$34.4M
In vivo CRISPR engineering of B cells to produce anti-HIV broadly neutralizing antibodies using novel nanoparticlesR01AI167009 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Jennifer Eileen Adair, Justin J Taylor · 2022 to 2026
$4.2M
Targeted genetic engineering of B cells to induce protective antibody responses to viral pathogensR01AI158728 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Jennifer Eileen Adair, Justin J Taylor · 2022 to 2026
$3.8M
Leveraging North-South Partnerships toAdvance Cell and Gene Therapy for HIV Research Training Capacity in Uganda (C and GT-Uganda)D43TW013052 · FIC · JOINT CLINICAL RESEARCH CENTER · PI Jennifer Eileen Adair, CISSY KITYO · 2025 to 2026
$570k
Bill & Melinda Gates Foundation INV-002613FIC NIH HHS D43 TW013052NCI NIH HHS P30 CA015704NIAID NIH HHS P30 AI027757NIAID NIH HHS R01 AI158728NIAID NIH HHS R01 AI167009NIH HHS P51 OD010425NIH HHS U42 OD011123
6 · The paper itself

Abstract

Gene editing strategies that do not rely on viral vectors are being explored for their potential to support durable biologics production. While clinical trials have shown that adeno-associated virus encoding broadly neutralizing antibodies can protect against HIV, these interventions often yield limited, short-lived responses. The development of non-viral gene editing approaches in hematopoietic stem and progenitor cells holds promise for long-term antibody production. In this study, we evaluated CRISPR-Cas9 and CRISPR-Cas12a for gene knockin at the immunoglobulin heavy chain locus in non-human primate (NHP) hematopoietic stem and progenitor cells (HSPCs). Delivering the nuclease as a protein alongside a custom DNA template, we optimized editing with Cas12a and demonstrated higher knockin efficiency and fewer non-specific edits than with Cas9. Transplantation of edited NHP HSPCs into MISTRG mice led to engraftment, B cell differentiation, and transgene expression of a reporter transgene or anti-HIV antibody after gp120 antigen immunization with detectable titers in circulation. These findings demonstrate the feasibility of using non-viral knockin in HSPCs as a potential strategy for sustained biologics production in the treatment of chronic diseases. Future work will assess the efficacy of this approach in an NHP model of HIV infection.

Indexed as

Gene Knock-In TechniquesHematopoietic Stem CellsHIV AntibodiesHIV InfectionsAnimalsAntibodies, NeutralizingB-LymphocytesCRISPR-Cas SystemsGene EditingGenetic VectorsHematopoietic Stem Cell TransplantationHumansImmunoglobulin Heavy ChainsMiceAntibodies, NeutralizingHIV AntibodiesImmunoglobulin Heavy Chainsbroadly neutralizing antibodyCRISPR-Cas12aCRISPR-Cas9gene knockingene therapyHIVHSPCMISTRG mice

Identifiers

PMID41635086
PMCPMC12947312

What OpenQuestion holds

Textmetadata
LicenceTDM
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.