Evidence map›Paper›PMID 25080481›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2014

Nanoparticle-mediated combinatorial targeting of multiple human dendritic cell (DC) subsets leads to enhanced T cell activation via IL-15-dependent DC crosstalk.

Kartik Sehgal, Ragy Ragheb, Tarek M Fahmy, Madhav V Dhodapkar, Kavita M Dhodapkar

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Combined strategies for tumor immunotherapy with nanoparticles.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2019
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Nanomedicine approaches to improve cancer immunotherapy.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  14. Liposomal adjuvant development for leishmaniasis vaccines.Therapeutic advances in vaccines · 2017
    Review
  15. Article
  16. Review
  17. Article
  18. Article
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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 2 institutions in 1 country.

Kartik SehgalDepartment of Pediatrics, Yale School of Medicine, Yale University, New Haven, CT 06510; Department of Medicine, Yale School of Medicine, Yale University, New Haven, CT 06510;
Ragy RaghebDepartment of Biomedical Engineering, Yale School of Engineering, Yale University, New Haven, CT 06510;
Tarek M FahmyDepartment of Biomedical Engineering, Yale School of Engineering, Yale University, New Haven, CT 06510; Department of Immunobiology, Yale School of Medicine, Yale University, New Haven, CT 06510; and.
Madhav V DhodapkarDepartment of Medicine, Yale School of Medicine, Yale University, New Haven, CT 06510; Department of Immunobiology, Yale School of Medicine, Yale University, New Haven, CT 06510; and Yale Cancer Center, Yale School of Medicine, Yale University, New Haven, CT 06510.
Kavita M DhodapkarDepartment of Pediatrics, Yale School of Medicine, Yale University, New Haven, CT 06510; Yale Cancer Center, Yale School of Medicine, Yale University, New Haven, CT 06510 kavita.dhodapkar@yale.edu.
Yale University · USYale Cancer Center · US

Funding

HARNESSING HOST RESPONSE TO PREVENT MYELOMAR35CA197603 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2016 to 2022
$5.8M
Understanding Hemotopoietic Neoplasias using Humanized MiceR01CA156689 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V, FLAVELL, RICHARD A · 2010 to 2014
$5.0M
RED BLOOD CELL DISEASES, HEMOSTASIS, AND BLOOD BANKINGT32HL007262 · NHLBI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 1985 to 2011
$4.0M
Yale Autoimmunity Center of ExcellenceU19AI082713 · NIAID · YALE UNIVERSITY · PI CHO, JUDY H. · 2009 to 2013
$3.6M
Anti-Tumor immunity in myelomaR01CA106802 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2004 to 2016
$3.3M
Targeting the vascularity for delivery of inhibitors of metastasis in ovarian cancer.R01CA199004 · NCI · YALE UNIVERSITY · PI LIU, HAIPENG, MOR, GIL G · 2015 to 2019
$2.5M
Targeting Thrombospondin 1 in Bone ResorptionR01AR060322 · NIAMS · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V, INSOGNA, KARL LEONARD · 2011 to 2015
$1.8M
Targeting CaMK4 in SLER01AR064350 · NIAMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TSOKOS, GEORGE C · 2013 to 2017
$1.8M
Fcgamma mediated regulation of dendritic cell functionR01AI079222 · NIAID · YALE UNIVERSITY · PI DHODAPKAR, KAVITA MADHAV · 2009 to 2012
$1.6M
Targeting myeloma via dendritic cellsR01CA109465 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2005 to 2009
$1.6M
Immunity to stem cell antigens in preneoplastic gammopathyR01CA135110 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2008 to 2013
$1.6M
Immune resistance to glioma via dendritic cellsK08AI054375 · NIAID · YALE UNIVERSITY · PI DHODAPKAR, KAVITA MADHAV · 2004 to 2008
$631k
NCI NIH HHS CA106802NCI NIH HHS CA135110NCI NIH HHS R01 CA106802NCI NIH HHS R01 CA109465NCI NIH HHS R01 CA135110NCI NIH HHS R01 CA156689NCI NIH HHS R01 CA199004NCI NIH HHS R35 CA197603NHLBI NIH HHS T32 HL007262NIAID NIH HHS K08 AI054375NIAID NIH HHS R01 AI079222NIAID NIH HHS R01AI079222NIAID NIH HHS R21 AI101918NIAID NIH HHS U19AI082713NIAMS NIH HHS R01 AR060322NIAMS NIH HHS R01 AR064350NIAMS NIH HHS R01AR064350
6 · The paper itself

Abstract

Most vaccines depend on coadministration of Ags and adjuvants that activate APCs. Nanoparticles (NPs) have emerged as an attractive vehicle for synchronized delivery of Ags and adjuvants to APCs and can be targeted to specific cell types, such as dendritic cells (DCs), which are potent APCs. Which subset of human DCs should be targeted for optimal activation of T cell immunity, however, remains unknown. In this article, we describe a poly-lactic-coglycolic acid-based NP platform, wherein avidin-decorated NPs can be targeted to multiple human DC subsets via biotinylated Abs. Both BDCA3(+) and monocyte-derived DC-SIGN(+) NP-loaded DCs were equally effective at generating Ag-specific human T cells in culture, including against complex peptide mixtures from viral and tumor Ags across multiple MHC molecules. Ab-mediated targeting of NPs to distinct DC subsets led to enhanced T cell immunity. However, combination targeting to both DC-SIGN and BDCA3(+) DCs led to significantly greater activation of T cells compared with targeting either DC subset alone. Enhanced T cell activation following combination targeting depended on DC-mediated cytokine release and was IL-15 dependent. These data demonstrate that simultaneous targeting of multiple DC subsets may improve NP vaccines by engaging DC crosstalk and provides a novel approach to improving vaccines against pathogens and tumors.

Indexed as

NanoparticlesAntigens, SurfaceCell Adhesion MoleculesCell CommunicationCells, CulturedDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsFemaleHumansInterleukin-15Lectins, C-TypeLymphocyte ActivationMaleReceptors, Cell SurfaceThrombomodulinT-LymphocytesAntigens, SurfaceCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinIL15 protein, humanInterleukin-15Lectins, C-TypeReceptors, Cell SurfaceTHBD protein, humanThrombomodulin

Identifiers

PMID25080481
PMCPMC6195217
OpenAlexW1939617698

What OpenQuestion holds

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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.