Evidence map›Paper›PMID 9271582›Full record

ArticleThe Journal of experimental medicine1997

High levels of a major histocompatibility complex II-self peptide complex on dendritic cells from the T cell areas of lymph nodes.

K Inaba, M Pack, M Inaba, H Sakuta, F Isdell, R M Steinman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 286 citations in OpenAlex.

  1. Article
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  10. Article
  11. Antigen-specific immune reactions to ischemic stroke.Frontiers in cellular neuroscience · 2014
    Review
  12. Review
  13. Immunotherapy for colorectal cancer.World journal of gastroenterology · 2013
    Review
  14. Review
  15. Macrophages-Key cells in the response to wear debris from joint replacements.Journal of biomedical materials research. Part A · 2013
    Review
  16. Targeting the B7 family of co-stimulatory molecules: successes and challenges.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2013
    Review
  17. Rodent blood-stage Plasmodium survive in dendritic cells that infect naive mice.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  18. Review
  19. Article
  20. Article

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

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

6 authors at 3 institutions in 2 countries.

K InabaKyoto University, Kitashirakawa-Oiusake-cho, Kyoto 606-01, Japan.
M Pack
M Inaba
H Sakuta
F Isdell
R M Steinman
Rockefeller University · USKyoto University · JPKansai Medical University · JP

Funding

Properties of Mouse of Dendritic Cells and MacrophagesR01AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI MOJSOV, SVETLANA · 1985 to 2015
$8.9M
PROPERTIES OF MOUSE DENDRITIC CELLS AND MACROPHAGESR37AI013013 · NIAID · ROCKEFELLER UNIVERSITY · PI STEINMAN, RALPH M. · 1986 to 1995
–
NIAID NIH HHS AI-13013NIAID NIH HHS R01 AI013013NIDDK NIH HHS DK-39672
6 · The paper itself

Abstract

T lymphocytes recirculate continually through the T cell areas of peripheral lymph nodes. During each passage, the T cells survey the surface of large dendritic cells (DCs), also known as interdigitating cells. However, these DCs have been difficult to release from the lymph node. By emphasizing the use of calcium-free media, as shown by Vremec et al. (Vremec, D., M. Zorbas, R. Scollay, D.J. Saunders, C.F. Ardavin, L. Wu, and K. Shortman. 1992. J. Exp. Med. 176:47-58.), we have been able to release and enrich DCs from the T cell areas. The DCs express the CD11c leukocyte integrin, the DEC-205 multilectin receptor for antigen presentation, the intracellular granule antigens which are recognized by monoclonal antibodies M342, 2A1, and MIDC-8, very high levels of MHC I and MHC II, and abundant accessory molecules such as CD40, CD54, and CD86. When examined with the Y-Ae monoclonal which recognizes complexes formed between I-Ab and a peptide derived from I-Ealpha, the T cell area DCs expressed the highest levels. The enriched DCs also stimulated a T-T hybridoma specific for this MHC II-peptide complex, and the hybridoma underwent apoptosis. Therefore DCs within the T cell areas can be isolated. Because they present very high levels of self peptides, these DCs should be considered in the regulation of self reactivity in the periphery.

Indexed as

AnimalsAntibodies, MonoclonalAntigen PresentationAntigen-Presenting CellsAntigens, CDBone MarrowDendritic CellsEpidermisFlow CytometryHistocompatibility Antigens Class IIHybridomasImmunohistochemistryInterleukin-2Lymph NodesMiceMice, Inbred C57BLAntibodies, MonoclonalAntigens, CDHistocompatibility Antigens Class III-E-antigenInterleukin-2

Identifiers

PMID9271582
PMCPMC2199017
OpenAlexW2170293184

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.