Evidence map›Paper›PMID 20648001›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2010

Enhanced induction of HIV-specific cytotoxic T lymphocytes by dendritic cell-targeted delivery of SOCS-1 siRNA.

Sandesh Subramanya, Myriam Armant, Janelle R Salkowitz, Alice M Nyakeriga, Viraga Haridas, Maroof Hasan, Anju Bansal, Paul A Goepfert, Katherine K Wynn, Kristin Ladell and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% of its field
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Optimal delivery of RNA interference by viral vectors for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
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  16. Article
  17. Article
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  19. Article
  20. SOCS proteins in infectious diseases of mammals.Veterinary immunology and immunopathology · 2013
    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

14 authors at 5 institutions in 2 countries.

Sandesh SubramanyaImmune Disease Institute, Harvard Medical School, Boston, Massachusetts, USA.
Myriam Armant
Janelle R Salkowitz
Alice M Nyakeriga
Viraga Haridas
Maroof Hasan
Anju Bansal
Paul A Goepfert
Katherine K Wynn
Kristin Ladell
David A Price
Manjunath N
June Kan-Mitchell
Premlata Shankar
Cardiff University · GBHarvard University · USTexas Tech University · USThe University of Texas at El Paso · USUniversity of Alabama at Birmingham · US

Funding

Targeted delivery of anti HIV sRNAs/shRNAs to T cellsR01AI071882 · NIAID · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI SHANKAR, PREMLATA · 2007 to 2010
$1.5M
NIAID NIH HHS AI071882NIAID NIH HHS R01 AI071882
6 · The paper itself

Abstract

Dendritic cells (DCs) are potent antigen-presenting cells that play a critical role in the activation of T cells. RNA interference (RNAi)-mediated silencing of negative immunoregulatory molecules expressed by DCs may provide a strategy to enhance the potency of DC-based vaccines and immunotherapy. Ablation of suppressor of cytokine signaling-1 (SOCS-1) in antigen-presenting cells has been shown to enhance cellular immune response in mice. Here, we used a previously reported DC-targeting approach to deliver small interfering RNA (siRNA) against SOCS-1 to human myeloid-derived DCs (MDDCs). SOCS1-silencing in MDDCs resulted in enhanced cytokine responses to lipopolysaccharide (LPS) and a strong mixed-lymphocyte reaction. Moreover, only DCs treated with SOCS-1 siRNA, and not controls, elicited strong primary in vitro responses to well-characterized HLA-A*0201-restricted Melan-A/MART-1 and human immunodeficiency virus (HIV) Gag epitopes in naive CD8(+) T cells from healthy donors. Finally, stimulation of CD8(+) T cells from HIV-seropositive subjects with SOCS1-silenced DCs resulted in an augmented polyfunctional cytotoxic T-lymphocyte (CTL) response, suggesting that SOCS-1 silencing can restore functionally compromised T cells in HIV infection. Collectively, these results demonstrate the feasibility of DC3-9dR-mediated manipulation of DC function to enhance DC immunogenicity for potential vaccine or immunotherapeutic applications.

Indexed as

ApoptosisBlotting, WesternCell ProliferationCells, CulturedCytokinesDendritic CellsFlow CytometryHIVHIV InfectionsHLA-A2 AntigenHLA-A AntigensHumansLipopolysaccharidesMyeloid CellsPeptide FragmentsReverse Transcriptase Polymerase Chain ReactionCytokinesHLA-A*02:01 antigenHLA-A2 AntigenHLA-A AntigensLipopolysaccharidesPeptide FragmentsRNA, MessengerRNA, Small InterferingSOCS1 protein, humanSuppressor of Cytokine Signaling 1 ProteinSuppressor of Cytokine Signaling Proteins

Identifiers

PMID20648001
PMCPMC2990509
OpenAlexW2044365799

What OpenQuestion holds

Textmetadata
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.