Evidence map›Paper›PMID 25566245›Full record

ReviewFrontiers in immunology2014

Plasticity of human CD4 T cell subsets.

Jens Geginat, Moira Paroni, Stefano Maglie, Johanna Sophie Alfen, Ilko Kastirr, Paola Gruarin, Marco De Simone, Massimiliano Pagani, Sergio Abrignani

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 171 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
171citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% 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

171 citing papers in PubMed, 1 synthesis or guideline pooled it, 279 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Baseline CD4Journal of blood medicine · 2025
    Trial
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Immunomodulatory Delivery Materials for Tissue Repair.Advanced healthcare materials · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

111 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Jens GeginatFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Moira ParoniFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Stefano MaglieFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Johanna Sophie AlfenFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Ilko KastirrFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Paola GruarinFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Marco De SimoneFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Massimiliano PaganiFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Sergio AbrignaniFondazione Istituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi" INGM , Milan , Italy.
Istituto Nazionale Genetica Molecolare · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human beings are exposed to a variety of different pathogens, which induce tailored immune responses and consequently generate highly diverse populations of pathogen-specific T cells. CD4(+) T cells have a central role in adaptive immunity, since they provide essential help for both cytotoxic T cell- and antibody-mediated responses. In addition, CD4(+) regulatory T cells are required to maintain self-tolerance and to inhibit immune responses that could damage the host. Initially, two subsets of CD4(+) helper T cells were identified that secrete characteristic effector cytokines and mediate responses against different types of pathogens, i.e., IFN-γ secreting Th1 cells that fight intracellular pathogens, and IL-4 producing Th2 cells that target extracellular parasites. It is now well established that this dichotomy is insufficient to describe the complexity of CD4(+) T cell differentiation, and in particular the human CD4 compartment contains a myriad of T cell subsets with characteristic capacities to produce cytokines and to home to involved tissues. Moreover, it has become increasingly clear that these T cell subsets are not all terminally differentiated cells, but that the majority is plastic and that in particular central memory T cells can acquire different properties and functions in secondary immune responses. In addition, there is compelling evidence that helper T cells can acquire regulatory functions upon chronic stimulation in inflamed tissues. The plasticity of antigen-experienced human T cell subsets is highly relevant for translational medicine, since it opens new perspectives for immune-modulatory therapies for chronic infections, autoimmune diseases, and cancer.

Indexed as

CD4 T cellscytokinesdifferentiationplasticitytissue homing

Identifiers

PMID25566245
PMCPMC4267263
OpenAlexW1980386568

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.