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Record W2911503195 · doi:10.1016/j.bbmt.2018.12.464

A New Specific Promoter Allow Hematopoietic Stem Cell Immunotherapy Approach Against Acute Lymphoblastic Leukemia Using Chimeric Antigen Receptor

2019· article· en· W2911503195 on OpenAlexaff
A. Colamartino, Panojot Bifsha, Chloé Colas, Camille Tremblay‐Laganière, Simon Nicoletti, Mélanie Guiot, Andrei Boldici, Yuanyi Li, Élie Haddad

Bibliographic record

VenueBiology of Blood and Marrow Transplantation · 2019
Typearticle
Languageen
FieldMedicine
TopicCAR-T cell therapy research
Canadian institutionsCentre Hospitalier Universitaire Sainte-JustineUniversité de Montréal
Fundersnot available
KeywordsChimeric antigen receptorJurkat cellsBiologyCytotoxic T cellHaematopoiesisInterleukin 21Molecular biologyStem cellTransfectionT cellNucleofectionCancer researchCell biologyCell cultureImmunologyIn vitroImmune system

Abstract

fetched live from OpenAlex

Although efficient, Chimeric Antigen Receptor (CAR)-T cells therapy still presents several drawbacks including exhaustion and loss of engineered cells, and the cytokine release syndrome. To circumvent these issues, we envisioned to engineer hematopoietic stem cells (HSCs) to provide a continuous replenishment of CAR-T and CAR-NK cells. However, this would result in a potentially dangerous pan-hematopoietic expression of the CAR transgene. To avoid this, we designed a T-cell specific and a NK-cell specific synthetic promoter in order to restrict the CAR expression only to the cytotoxic cells progeny issued from CAR-modified HSCs. We assessed the efficacy of our promoters in vitro and in vivo in humanized mice. Methods Potential sequences for T-cell or NK-cell specific expression were designed in silico and then cloned in a GFP-reporter vector to test their specificity. We assessed in vitro the expression of the reporter gene using cell lines from various lineages and primary cells isolated from peripheral blood. We then transduced CD34 + cell and humanized NSG mice engrafted with a human thymus. Results Upon transfection with GFP under the control of our synthetic promoter, only Jurkat (T cells) for our T-specific promoter and NK-92 (NK cells) for the NK-specific promoter, expressed GFP. Consistently, nucleofection of PBMC with the T-cell specific promoter resulted in a GFP expression in T cells but not in B cells or monocytes. The promoter specificity was validated in vivo as progeny from engineered human HSCs injected in NSG showed the same T-cell specific expression pattern (Fig. 1). Using an in vitro artificial organoid thymic differentiation system, we observed that our synthetic promoter was active as early as CD7 + C + D1 progenitor cells. We also showed that T cells transduced with our specific promoter retained CAR T-cell toxicity when facing their targets, despite a lower CAR expression than with classic strong promoter. Conclusion Our results show that we were able to generate new synthetic promoters with a lineage specificity. We are currently testing our strategy in vivo against human B-ALL cells lines and primary patients' blasts. We are also validating our new NK-specific promoter in vivo . This new strategy could help overcome side effects while improving CAR-T cells persistence, and could be used for both hematological malignancies and solid tumors after autologous transplantation.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.003

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.016
GPT teacher head0.248
Teacher spread0.233 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations3
Published2019
Admission routes1
Has abstractyes

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