Evidence map›Paper›PMID 22588271›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2012

PD-1/PD-L1 blockade can enhance HIV-1 Gag-specific T cell immunity elicited by dendritic cell-directed lentiviral vaccines.

Bingbing Dai, Liang Xiao, Paul D Bryson, Jinxu Fang, Pin Wang

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. T-cell therapies for HIV.Immunotherapy · 2013
    Review
  18. Prospects for treatment of latent HIV.Clinical pharmacology and therapeutics · 2013
    Review
  19. Review
  20. 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

5 authors at 1 institution in 1 country.

Bingbing DaiMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California, USA.
Liang XiaoMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California, USA.
Paul D BrysonMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California, USA.
Jinxu FangMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California, USA.
Pin WangMork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California, USA; Department of Biomedical Engineering, University of Southern California, Los Angeles, California, USA; Department of Pharmacology and Pharmaceutical Sciences, University of Southern California, Los Angeles, California, USA. Electronic address: pinwang@usc.edu.
University of Southern California · US

Funding

Transduction of Hematopoietic Stem Cells for Enhanced Immunotherapy of MelanomaP01CA132681 · NCI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BALTIMORE, DAVID · 2010 to 2014
$14.4M
Targeting lentiviruses to infect chosen cellsR01AI068978 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI WANG, PIN · 2006 to 2010
$2.9M
NCI NIH HHS P01 CA132681NIAID NIH HHS R01 AI068978
6 · The paper itself

Abstract

Exhaustion of CD8(+) T cells and upregulation of programmed death 1 (PD-1), a negative regulator of T cell activation, are characteristic features of individuals chronically infected with human immunodeficiency virus type 1. In a previous study, we showed in mice that a dendritic cell-directed lentiviral vector (DCLV) system encoding the human immunodeficiency virus (HIV)-1 Gag protein was an efficient vaccine modality to induce a durable Gag-specific T cell immune response. In this study, we demonstrate that blocking of the PD-1/PD-1 ligand (PD-L) inhibitory signal via an anti-PD-L1 antibody generated an enhanced HIV-1 Gag-specific CD8(+) immune response following both a single round of DCLV immunization and a homologous prime/boost regimen. The prime/boost regimen combined with PD-L1 blockade generated very high levels of Gag-specific CD8(+) T cells comprising several valuable features: improved ability to produce multiple cytokines, responding to a broader range of Gag-derived epitopes, and long-lasting memory. This enhanced cellular immune response generated by DCLV immunization combined with anti-PD-L1 blockade correlated with improved viral control following challenge with Gag-expressing vaccinia virus. Taken together, our studies offer evidence to support the use of PD-1/PD-L1 blockade as an adjuvant modality to enhance antigen-specific immune responses elicited by T cell-based immunizations such as DCLV.

Indexed as

AIDS VaccinesAnimalsAntigens, DifferentiationB7-H1 AntigenCD8-Positive T-LymphocytesDendritic CellsEpitopes, T-LymphocyteFemalegag Gene Products, Human Immunodeficiency VirusGenetic VectorsHIV-1HIV InfectionsHumansImmunity, CellularImmunization, SecondaryLentivirusAIDS VaccinesAntigens, DifferentiationB7-H1 AntigenCd274 protein, mouseEpitopes, T-Lymphocytegag Gene Products, Human Immunodeficiency VirusPdcd1 protein, mouseProgrammed Cell Death 1 Receptor

Identifiers

PMID22588271
PMCPMC3437589
OpenAlexW2006365597

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.