Evidence map›Paper›PMID 22363608›Full record

ArticlePloS one2012

Preformed CD40L is stored in Th1, Th2, Th17, and T follicular helper cells as well as CD4+ 8- thymocytes and invariant NKT cells but not in Treg cells.

Yoshinobu Koguchi, Abigail C Buenafe, Timothy J Thauland, Jennifer L Gardell, Elizabeth R Bivins-Smith, David B Jacoby, Mark K Slifka, David C Parker

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Many Th Cell Subsets Have Fas Ligand-Dependent Cytotoxic Potential.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  14. Transcriptome Analysis of Mycobacteria-Specific CD4Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  15. Article
  16. CD40L Expression Allows CD8Frontiers in immunology · 2017
    Article
  17. Article
  18. Review
  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

8 authors at 1 institution in 1 country.

Yoshinobu KoguchiDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, Oregon, United States of America.
Abigail C Buenafe
Timothy J Thauland
Jennifer L Gardell
Elizabeth R Bivins-Smith
David B Jacoby
Mark K Slifka
David C Parker
Oregon Health & Science University · US

Funding

YR 50 PROJ- ROBERTS PRIMATE ISLETP51RR000163 · NCRR · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI FRUH, KLAUS J · 1985 to 2011
$140.8M
Imaging and Function of the Immunological SynapseR01AI050823 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI PARKER, DAVID C · 2002 to 2012
$2.9M
The non-canonical NF-kappaB pathway in survival and function of T lymphocytesR01AI092080 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI PARKER, DAVID C · 2011 to 2015
$1.9M
B Cell Subsets as Antigen-presenting Cells in Peripheral Self-toleranceR01AI070934 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI PARKER, DAVID C · 2007 to 2011
$1.9M
Cytokine-mediated T cell activationR01AI054458 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI SLIFKA, MARK K · 2004 to 2008
$1.6M
Mechanisms of Virus-Induced Hyperreactivity in AtopicsR01HL061013 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 1998 to 2010
$1.6M
Inflammation and T Lymphocyte ImmunoregulationT32AI078903 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI HILL, ANN B · 2009 to 2013
$1.5M
ANTIVIRAL EFFECTS OF EOSINOPHILS IN THE LUNGSR01HL071795 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2004 to 2007
$1.5M
REPRODUCTIVE STEROIDS AND EXPERIMENTAL STROKEK01RR000163 · NCRR · OREGON HEALTH AND SCIENCE UNIVERSITY · PI MURPHY, STEPHANIE J · 2000 to 2004
$479k
Airway Eosinophil Activation by Anticholinergic TherapyR21AI075064 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2008 to 2009
$424k
The Alternative NFkB Pathway in Survival and Function of Anti-Viral T CellsR21AI077032 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI PARKER, DAVID C · 2007 to 2008
$420k
NCRR NIH HHS K01 RR000163NCRR NIH HHS P51 RR000163NCRR NIH HHS RR000163NHLBI NIH HHS HL061013NHLBI NIH HHS HL071795NHLBI NIH HHS R01 HL061013NHLBI NIH HHS R01 HL071795NIAID NIH HHS AI054458NIAID NIH HHS AI075064NIAID NIH HHS R01 AI050823NIAID NIH HHS R01 AI054458NIAID NIH HHS R01 AI070934NIAID NIH HHS R01 AI092080NIAID NIH HHS R0I AI050823NIAID NIH HHS R21 AI075064NIAID NIH HHS R21 AI077032NIAID NIH HHS T32 AI078903
6 · The paper itself

Abstract

CD40L is essential for the development of adaptive immune responses. It is generally thought that CD40L expression in CD4(+) T cells is regulated transcriptionally and made from new mRNA following antigen recognition. However, imaging studies show that the majority of cognate interactions between effector CD4(+) T cells and APCs in vivo are too short to allow de novo CD40L synthesis. We previously showed that Th1 effector and memory cells store preformed CD40L (pCD40L) in lysosomal compartments and mobilize it onto the plasma membrane immediately after antigenic stimulation, suggesting that primed CD4(+) T cells may use pCD40L to activate APCs during brief encounters. Indeed, our recent study showed that pCD40L is sufficient to mediate selective activation of cognate B cells and trigger DC activation in vitro. In this study, we show that pCD40L is present in Th1 and follicular helper T cells developed during infection with lymphocytic choriomeningitis virus, Th2 cells in the airway of asthmatic mice, and Th17 cells from the CNS of animals with experimental autoimmune encephalitis (EAE). pCD40L is nearly absent in both natural and induced Treg cells, even in the presence of intense inflammation such as occurs in EAE. We also found pCD40L expression in CD4 single positive thymocytes and invariant NKT cells. Together, these results suggest that pCD40L may function in T cell development as well as an unexpectedly broad spectrum of innate and adaptive immune responses, while its expression in Treg cells is repressed to avoid compromising their suppressive activity.

Indexed as

AnimalsAntigensCD40 LigandCD8-Positive T-LymphocytesDown-RegulationInflammationInterleukin-4Intracellular SpaceLymphocyte ActivationMiceMice, Inbred C57BLNatural Killer T-CellsProtein TransportSide-Population CellsStaining and LabelingTh17 CellsAntigensCD40 LigandInterleukin-4

Identifiers

PMID22363608
PMCPMC3283616
OpenAlexW2079312631

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.