Evidence map›Paper›PMID 10393955›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Dichotomy between naïve and memory CD4(+) T cell responses to Fas engagement.

J Desbarats, T Wade, W F Wade, M K Newell

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 84 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Life in the Fas lane: differential outcomes of Fas signaling.Cellular and molecular life sciences : CMLS · 2013
    Review
  6. Death receptor-ligand systems in cancer, cell death, and inflammation.Cold Spring Harbor perspectives in biology · 2013
    Review
  7. The role of apoptosis-induced proliferation for regeneration and cancer.Cold Spring Harbor perspectives in biology · 2012
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Mutation in the Fas pathway impairs CD8+ T cell memory.Journal of immunology (Baltimore, Md. : 1950) · 2008
    Article
  14. Cellular metabolism as a basis for immune privilege.Journal of immune based therapies and vaccines · 2006
    Article
  15. Article
  16. Article
  17. FADD adaptor in cancer.Medical immunology (London, England) · 2005
    Article
  18. Article
  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

4 authors at 1 institution in 1 country.

J DesbaratsUniversity of Vermont College of Medicine, Burlington, VT 05405, USA.
T Wade
W F Wade
M K Newell
University of Vermont · US

Funding

FUNCTION OF MHC CLASS II ON AGED MICER03AG014782 · NIA · DARTMOUTH COLLEGE · PI WADE, WILLIAM FRANKLIN · 1997 to 1997
–
NIA NIH HHS AG-14782PHS HHS A1-33470
6 · The paper itself

Abstract

Engagement of Fas (APO-1, CD95), a member of the tumor necrosis factor receptor superfamily, can induce apoptotic cell death. However, Fas engagement also can costimulate lymphocyte proliferation. The physiologic regulation of these two outcomes is poorly understood. Here, we have used two systems, the first in vitro and the second in vivo, to demonstrate that naïve and memory CD4(+) T cells display dichotomous responses to Fas ligation. Naïve CD4(+) T cells (CD44(lo), CD45RB+, CD62L+) die as a consequence of Fas ligation in the presence of anti-CD3 antibody, whereas memory T cells (CD44(hi), CD45RB-, CD62L-), freshly isolated from the same starting population and subjected to the same stimulation conditions, are costimulated to proliferate by Fas ligation. In vitro, we demonstrate that CD28-mediated signals or T helper 1 and T helper 2 differentiation cytokines alter the response of naïve T cells, but not of memory T cells, to Fas ligation. In vivo experiments in hen egg lysozyme (HEL) T cell receptor transgenic mice show that CD4(+) T cells from HEL-naïve mice are killed by Fas ligation, but CD4(+) T cells from long-term HEL-exposed mice are costimulated by Fas ligation. Thus, the physiological outcome of Fas ligation in CD4(+) T cells is determined primarily by the antigenic history of the T cell.

Indexed as

Immunologic MemoryAnimalsAntigens, Differentiation, T-LymphocyteApoptosisCD28 AntigensCD4-Positive T-LymphocytesCell CycleCells, CulturedFas Ligand Proteinfas ReceptorImmunophenotypingLymphocyte ActivationMembrane GlycoproteinsMiceMice, Inbred C57BLMice, Inbred MRL lprAntigens, Differentiation, T-LymphocyteCD28 AntigensFas Ligand ProteinFasl protein, mousefas ReceptorMembrane GlycoproteinsReceptors, Antigen, T-Cell

Identifiers

PMID10393955
PMCPMC22195
OpenAlexW2038915318

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.