Evidence map›Paper›PMID 25710490›Full record

ArticleInternational immunology2015

CD1d-dependent expansion of NKT follicular helper cells in vivo and in vitro is a product of cellular proliferation and differentiation.

Pragya Rampuria, Mark L Lang

Open access · bronzeAbstract read
In one paragraph

Article in International immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Follicular Helper CD4Mediators of inflammation · 2021
    Review
  4. Use of aFrontiers in immunology · 2021
    Article
  5. Article
  6. Article
  7. Differential Control ofFrontiers in immunology · 2019
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Diacylglycerol Kinases in T Cell Tolerance and Effector Function.Frontiers in cell and developmental biology · 2016
    Review
  13. 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

2 authors at 1 institution in 1 country.

Pragya RampuriaDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Mark L LangDepartment of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA mark-lang@ouhsc.edu.
University of Oklahoma Health Sciences Center · US

Funding

Regulation of humoral immunity by NKT cellsR01AI078993 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LANG, MARK L · 2009 to 2013
$1.6M
Regulation of humoral immunity by NKT cellsR56AI078993 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI LANG, MARK L · 2014 to 2014
$404k
NIAID NIH HHS AI078993NIAID NIH HHS R56 AI078993
6 · The paper itself

Abstract

NKT follicular helper cells (NKTfh cells) are a recently discovered functional subset of CD1d-restricted NKT cells. Given the potential for NKTfh cells to promote specific antibody responses and germinal center reactions, there is much interest in determining the conditions under which NKTfh cells proliferate and/or differentiate in vivo and in vitro. We confirm that NKTfh cells expressing the canonical semi-invariant Vα14 TCR were CXCR5(+)/ICOS(+)/PD-1(+)/Bcl6(+) and increased in number following administration of the CD1d-binding glycolipid α-galactosylceramide (α-GC) to C57Bl/6 mice. We show that the α-GC-stimulated increase in NKTfh cells was CD1d-dependent since the effect was diminished by reduced CD1d expression. In vivo and in vitro treatment with α-GC, singly or in combination with IL-2, showed that NKTfh cells increased in number to a greater extent than total NKT cells, but proliferation was near-identical in both populations. Acquisition of the NKTfh phenotype from an adoptively transferred PD-1-depleted cell population was also evident, showing that peripheral NKT cells differentiated into NKTfh cells. Therefore, the α-GC-stimulated, CD1d-dependent increase in peripheral NKTfh cells is a result of cellular proliferation and differentiation. These findings advance our understanding of the immune response following immunization with CD1d-binding glycolipids.

Indexed as

Adoptive TransferAnimalsAntigens, CD1dCell DifferentiationCell ProliferationDNA-Binding ProteinsFemaleGalactosylceramidesGerminal CenterInducible T-Cell Co-Stimulator ProteinIn Vitro TechniquesMiceMice, Inbred C57BLMice, KnockoutNatural Killer T-CellsProgrammed Cell Death 1 Receptoralpha-galactosylceramideAntigens, CD1dBcl6 protein, mouseCXCR5 protein, mouseDNA-Binding ProteinsGalactosylceramidesIcos protein, mouseInducible T-Cell Co-Stimulator ProteinPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins c-bcl-6Receptors, Antigen, T-Cell, alpha-betaReceptors, CXCR5CD1dfollicular helper cellsNKT cells

Identifiers

PMID25710490
PMCPMC4406267
OpenAlexW2107453138

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.