Evidence map›Paper›PMID 15085201›Full record

ArticleThe Journal of clinical investigation2004

Suppression of autoimmune disease after vaccination with autoreactive T cells that express Qa-1 peptide complexes.

Vily Panoutsakopoulou, Katharina M Huster, Nami McCarty, Evan Feinberg, Rijian Wang, Kai W Wucherpfennig, Harvey Cantor

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.4field-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

30 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Towards Clinical Translation of CD8International journal of molecular sciences · 2019
    Review
  5. Article
  6. Alloactivation of Naïve CD4Frontiers in immunology · 2019
    Article
  7. Overlapping Peptide Library to Map Qa-1 Epitopes in a Protein.Journal of visualized experiments : JoVE · 2017
    Article
  8. Molecular mechanisms underlying Th1-like Treg generation and function.Cellular and molecular life sciences : CMLS · 2017
    Review
  9. Memory CD4American journal of translational research · 2017
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. CD8(+) Tregs in autoimmunity: learning "self"-control from experience.Cellular and molecular life sciences : CMLS · 2011
    Review
  18. Review
  19. Article
  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

7 authors at 2 institutions in 1 country.

Vily PanoutsakopoulouDepartment of Cancer Immunology & AIDS, Dana-Farber Cancer Institute, and Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Katharina M Huster
Nami McCarty
Evan Feinberg
Rijian Wang
Kai W Wucherpfennig
Harvey Cantor
Dana-Farber Cancer Institute · USHarvard University Press · US

Funding

IMMUNOLOGIC MECHANISMS THAT PREVENT AUTOIMMUNITYR01AI037562 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 1996 to 2021
$9.4M
THE T-CELL RESPONSE TO ANTIGENR01AI048125 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 2000 to 2021
$5.1M
IMMUNOBIOLOGY OF LY+ T-CELL SUBCLASSESR01AI013600 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 1985 to 2003
$1.5M
NIAID NIH HHS AI13600NIAID NIH HHS AI37562NIAID NIH HHS AI48125NIAID NIH HHS R01 AI013600NIAID NIH HHS R01 AI037562NIAID NIH HHS R01 AI048125
6 · The paper itself

Abstract

The ability of autoreactive T cells to provoke autoimmune disease is well documented. The finding that immunization with attenuated autoreactive T cells (T cell vaccination, or TCV) can induce T cell-dependent inhibition of autoimmune responses has opened the possibility that regulatory T cells may be harnessed to inhibit autoimmune disease. Progress in the clinical application of TCV, however, has been slow, in part because the underlying mechanism has remained clouded in uncertainty. We have investigated the molecular basis of TCV-induced disease resistance in two murine models of autoimmunity: herpes simplex virus-1 (KOS strain)-induced herpes stromal keratitis and murine autoimmune diabetes in non-obese diabetic (NOD) mice. We find that the therapeutic effects of TCV depend on activation of suppressive CD8 cells that specifically recognize Qa-1-bound peptides expressed by autoreactive CD4 cells. We clarify the molecular interaction between Qa-1 and self peptides that generates biologically active ligands capable of both inducing suppressive CD8 cells and targeting them to autoreactive CD4 cells. These studies suggest that vaccination with peptide-pulsed cells bearing the human equivalent of murine Qa-1 (HLA-E) may represent a convenient and effective clinical approach to cellular therapy of autoimmune disease.

Indexed as

Immunotherapy, AdoptiveAnimalsAutoimmune DiseasesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell CommunicationCell LineageDNA-Binding ProteinsFemaleHistocompatibility Antigens Class IMiceMice, Inbred BALB CMice, Inbred NODReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesVaccinationDNA-Binding ProteinsHistocompatibility Antigens Class IQ surface antigensRag2 protein, mouseReceptors, Antigen, T-Cell, alpha-betaV(D)J recombination activating protein 2

Identifiers

PMID15085201
PMCPMC385407
OpenAlexW1986553367

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.