Evidence map›Paper›PMID 24927530›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

An evolving autoimmune microenvironment regulates the quality of effector T cell restimulation and function.

Rachel S Friedman, Robin S Lindsay, Jason K Lilly, Vinh Nguyen, Caitlin M Sorensen, Jordan Jacobelli, Matthew F Krummel

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Immune cell trafficking to the islets during type 1 diabetes.Clinical and experimental immunology · 2019
    Review
  10. β-Cell Maturation and Identity in Health and Disease.International journal of molecular sciences · 2019
    Review
  11. Article
  12. CD11cFrontiers in immunology · 2019
    Article
  13. Article
  14. Establishment of human pluripotent stem cell-derived pancreatic β-like cells in the mouse pancreas.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Imaging the emergence and natural progression of spontaneous autoimmune diabetes.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  20. CD4Frontiers in immunology · 2017
    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 3 institutions in 1 country.

Rachel S FriedmanDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;Department of Immunology, University of Colorado Denver, Aurora, CO 80045; and friedmanr@njhealth.org.
Robin S LindsayDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;Department of Immunology, University of Colorado Denver, Aurora, CO 80045; and.
Jason K LillyDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;Department of Immunology, University of Colorado Denver, Aurora, CO 80045; and.
Vinh NguyenDepartments of Surgery and.
Caitlin M SorensenPathology, University of California, San Francisco, CA 94143.
Jordan JacobelliDepartment of Biomedical Research, National Jewish Health, Denver, CO 80206;Department of Immunology, University of Colorado Denver, Aurora, CO 80045; and.
Matthew F KrummelPathology, University of California, San Francisco, CA 94143.
National Jewish Health · USUniversity of California, San Francisco · USUniversity of Colorado Denver · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defining the processes of autoimmune attack of tissues is important for inhibiting continued tissue destruction. In type 1 diabetes, it is not known how cytotoxic effector T cell responses evolve over time in the pancreatic islets targeted for destruction. We used two-photon microscopy of live, intact, individual islets to investigate how progression of islet infiltration altered the behavior of infiltrating islet-specific CD8(+) T cells. During early-islet infiltration, T-cell interactions with CD11c(+) antigen-presenting cells (APCs) were stable and real-time imaging of T cell receptor (TCR) clustering provided evidence of TCR recognition in these stable contacts. Early T cell-APC encounters supported production of IFN-γ by T effectors, and T cells at this stage also killed islet APCs. At later stages of infiltration, T-cell motility accelerated, and cytokine production was lost despite the presence of higher numbers of infiltrating APCs that were able to trigger T-cell signaling in vitro. Using timed introduction of effector T cells, we demonstrate that elements of the autoimmune-tissue microenvironment control the dynamics of autoantigen recognition by T cells and their resulting pathogenic effector functions.

Indexed as

AnimalsAntigen-Presenting CellsCD8-Positive T-LymphocytesCell CommunicationCells, CulturedCellular MicroenvironmentDiabetes Mellitus, Type 1Interferon-gammaMiceReceptors, Antigen, T-CellSignal TransductionInterferon-gammaReceptors, Antigen, T-Cell2-photon microscopyautoimmunityT-lymphocyte reactivation

Identifiers

PMID24927530
PMCPMC4078867
OpenAlexW2017327665

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.