Evidence map›Paper›PMID 14657218›Full record

ArticleThe Journal of experimental medicine2003

Dendritic cells initiate immune control of epstein-barr virus transformation of B lymphocytes in vitro.

Kara Bickham, Kiera Goodman, Casper Paludan, Sarah Nikiforow, Ming Li Tsang, Ralph M Steinman, Christian Münz

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. LANA-specific CD4Nature communications · 2025
    Article
  3. Transdermal delivery for gene therapy.Drug delivery and translational research · 2022
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Immune control of oncogenic γ-herpesviruses.Current opinion in virology · 2015
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

7 authors at 2 institutions in 1 country.

Kara BickhamLaboratory of Cellular Physiology and Immunology, The Rockefeller University, New York, NY 10021, USA.
Kiera Goodman
Casper Paludan
Sarah Nikiforow
Ming Li Tsang
Ralph M Steinman
Christian Münz
Rockefeller University · USYale University · US

Funding

Dendritic Cells and the Pathogenesis of HIV-1 InfectionR37AI040045 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH MARVIN · 2001 to 2010
$6.1M
Identification and vaccine adjuvant responses of dendritic cells in humansR56AI040045 · NIAID · ROCKEFELLER UNIVERSITY · PI SCHLESINGER, SARAH JANE · 2011 to 2011
$520k
DENDRITIC CELLS AND THE PATHOGENESIS OF HIV-1 INFECTIONR01AI040045 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1996 to 2000
$457k
EBNA1-specific CD4+T helper 1 CellsK08AI049958 · NIAID · ROCKEFELLER UNIVERSITY · PI BICKHAM, KARA · 2001 to 2002
$194k
NIAID NIH HHS AI40045NIAID NIH HHS AI49958NIAID NIH HHS N01 AI040045
6 · The paper itself

Abstract

The initiation of cell-mediated immunity to Epstein-Barr virus (EBV) has been analyzed with cells from EBV-seronegative blood donors in culture. The addition of dendritic cells (DCs) is essential to prime naive T cells that recognize EBV-latent antigens in enzyme-linked immunospot assays for interferon gamma secretion and eradicate transformed B cells in regression assays. In contrast, DCs are not required to control the outgrowth of EBV-transformed B lymphocytes from seropositive donors. Enriched CD4+ and CD8+ T cells mediate regression of EBV-transformed cells in seronegative and seropositive donors, but the kinetics of T-dependent regression occurs with much greater speed with seropositives. EBV infection of DCs cannot be detected by reverse transcription-polymerase chain reaction with primers specific for mRNA for the EBNA1 U and K exons. Instead, DCs capture B cell debris and generate T cells specific for EBV latency antigens. We suggest that the cross-presentation of EBV-latent antigens from infected B cells by DCs is required for the initiation of EBV-specific immune control in vivo and that future EBV vaccine strategies should target viral antigens to DCs.

Indexed as

Base SequenceB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Transformation, ViralCoculture TechniquesDendritic CellsDNA PrimersHerpesvirus 4, HumanHumansPhagocytosisDNA Primers

Identifiers

PMID14657218
PMCPMC2194129
OpenAlexW2144562339

What OpenQuestion holds

Textmetadata
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.