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Targeting Hematopoietic Cells Using a Blimp-1 Promoter Helper Dependent Adenoviruses.

2004· article· en· W2588338825 on OpenAlexaff
Chang‐Xin Shi, Xiao‐Yan Wen, Dingyan Wang, Bo Gao, Gillian Sleep, Lihua Zhuang, Zhihua Li, Mary Hitt, A. Keith Stewart

Bibliographic record

VenueBlood · 2004
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicVirus-based gene therapy research
Canadian institutionsPrincess Margaret Cancer Centre
Fundersnot available
KeywordsLuciferaseGenetic enhancementMolecular biologyTransgeneBiologyViral vectorCell culturePromoterVirologyGeneGene expressionTransfectionRecombinant DNAGenetics

Abstract

fetched live from OpenAlex

Abstract B lymphocyte-induced maturation protein-1 (Blimp-1) plays a key role in the maturation of B lymphocytes into end-stage, antibody-screting plasma cells. However its promoter region has not been well characterized. As an initiative aimed at identifying plasma cell specific promoters for use in gene therapy of myeloma, we studied the function of the blimp-1 promoter in a helper-dependent adenovirus (HDAd) vector system. The advantages of employing HDAd include: 1) High capacity encompassing transgene (upto 36 kb); 2). Higher and longer transgene expression; 3). Lower cytotoxicity in vivo; 4). Improved specificity for tissue-specific promoters. Blimp-1 promoter fragments of 2.6, 4.7 and 25 kb driving the luciferase gene were cloned into HDAd precursor plasmid and then rescued into HDAd vectors. A panel of B lymphoma and myeloma cell lines were infected with these HDAd vectors and a positive control vector HDMCMV (an HDAd vector expressing luciferase under the control of MCMV promoter) at an MOI of 2,000 particles/cell. Two days after infection, very high luciferase activity was demonstrated in human myeloma cell lines (KMS11, U266, MM1, and MY5 cells), but low or no activity was seen in human B lymphoma cell lines (Namalwa and Raji). In fibroblasts, the Blimp-1 derived promoter activity appeared to be high in COS7 cells but 10 times lower in NIH3T3 cells. All three differently sized promoter fragments of Blimp-1 demonstrated similar activity. Next we further tested these three Blimp1/Luc HDAd vectors in mice using HDMCMV as a positive control. Six week old FVB mice were intravenously injected with 1X10(e11) particles per mouse. Different tissues were assayed for luciferase activity three days after injection. The control HDMCMV virus directed the highest luciferase activity in the liver because of the tropism of adenovirus. However, the Blimp-1/luciferase viruses directed highest luciferase expression in the spleen and bone marrow with lower level relative expression in the liver and trace amount or no expression in other tissues examined. After normalization, the transciptional activity of the Blimp-1 promoter is ~80 fold higher than the CMV promoter in spleen tissue. All three Blimp-1 promoters demonstrated similar activity, indicating that the 2.6 kb Blimp promoter contains the regulation element for spleen and bone marrow-specific gene expression. FACS analysis of spleen cells co-stained with luciferase antibody revealed luciferase expression in both B220+ve B and B220-ve non-B cells. Taking together, we conclude that 2.6kb blimp-1 promoter sequence is enough to direct gene expression to hematopoietic cells but is not B cell specific.

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 score0.005

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 communication0.0010.000
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 head0.020
GPT teacher head0.281
Teacher spread0.261 · 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

Citations0
Published2004
Admission routes1
Has abstractyes

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