Evidence map›Paper›PMID 11781371›Full record

ArticleThe Journal of experimental medicine2002

Antitumor monoclonal antibodies enhance cross-presentation ofcCellular antigens and the generation of myeloma-specific killer T cells by dendritic cells.

Kavita M Dhodapkar, Joseph Krasovsky, Barbara Williamson, Madhav V Dhodapkar

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed, 1 pooled it
11.8field-weighted citation impact, top 1% 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

134 citing papers in PubMed, 1 synthesis or guideline pooled it, 351 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Article
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  9. Article
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  11. Article
  12. Targeting syndecan-1: new opportunities in cancer therapy.American journal of physiology. Cell physiology · 2022
    Review
  13. Review
  14. Review
  15. Review
  16. SLE-associated risk factors affect DC function.Current rheumatology reports · 2019
    Review
  17. Article
  18. Article
  19. A Restricted Role for FcγR in the Regulation of Adaptive Immunity.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  20. Review

74 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Kavita M DhodapkarLaboratory of Tumor Immunology and Immunotherapy, The Rockefeller University, New York, NY 10021, USA.
Joseph Krasovsky
Barbara Williamson
Madhav V Dhodapkar
Memorial Sloan Kettering Cancer Center · USRockefeller University · US

Funding

WOUND HEALING IN INDIVIDUALS OF DIFFERENT AGE AND GENETIC BACKGROUNDM01RR000102 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 1985 to 2006
$32.8M
EBV SPECIFIC THERAPY OF LYMPHOMA USING DENDRITIC CELLSK23CA081138 · NCI · ROCKEFELLER UNIVERSITY · PI DHODAPKAR, MADHAV V · 2000 to 2002
$447k
NCI NIH HHS CA81138NCRR NIH HHS M01 RR000102NCRR NIH HHS M0-RR00102
6 · The paper itself

Abstract

The mechanism of antitumor effect of monoclonal antibodies (mAbs) is not fully understood. Here we show that coating myeloma cells with anti-syndecan-1 antibody promotes cross-presentation of cellular antigens by dendritic cells (DCs) to autologous T cells from healthy donors. The tumor cells treated with anti-syndecan-1 or isotype-matched control antibody were fed to HLA-mismatched monocyte-derived immature DCs. Tumor cell-loaded mature DCs induced a strong CD8(+) T cell response that was specific for the cancer-testis (C-T) antigens expressed in the tumor. The CD8(+) T cells killed peptide-pulsed targets, as well as myeloma tumor cells. Importantly, mAbs-coated tumor-loaded DCs were consistently superior to DCs loaded with peptides or dying cells for eliciting tumor-specific killer T cells. This enhanced cross-presentation was not due to enhanced tumor cell uptake or to DC maturation. When mixtures of NY-Eso-1-positive and -negative myeloma cells were captured by DCs, the anti-syndecan-1 antibody had to be on the NY-Eso-1-positive cells to elicit NY-Eso-1-specific response. Cross-presentation was inhibited by pretreatment of DCs with Fc gamma receptor blocking antibodies. Targeting of mAb-coated tumors to DCs may contribute to the efficacy of tumor-reactive mAb and offers a new strategy for immunotherapy.

Indexed as

Antigen PresentationMembrane ProteinsAntibodies, MonoclonalAntibodies, NeoplasmAntigens, NeoplasmApoptosisDendritic CellsHumansImmunotherapyInterferon-gammaKiller Cells, NaturalMaleMembrane GlycoproteinsMultiple MyelomaNeoplasm ProteinsProteinsAntibodies, MonoclonalAntibodies, NeoplasmAntigens, NeoplasmCTAG1B protein, humanInterferon-gammaMAGEA3 protein, humanMembrane GlycoproteinsMembrane ProteinsNeoplasm ProteinsProteinsProteoglycansReceptors, IgGSyndecans

Identifiers

PMID11781371
PMCPMC2196013
OpenAlexW2124749346

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.