Evidence map›Paper›PMID 39730488›Full record

ArticleScientific reports2024

SLAMF7 defines subsets of human effector CD8 T cells.

Hassen Kared, Crystal Tan, Vipin Narang, Shu Wen Tan, Chin Hui Xian, Alicia Tay Seok Wei, Josephine Lum, Ezequiel Ruiz-Mateos, Reena Rajasuriar, Adeeba Kamarulzaman and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

12 authors.

Hassen KaredSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore. kared.hassen@gmail.com.
Crystal TanSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.
Vipin NarangSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.
Shu Wen TanSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.
Chin Hui XianSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.
Alicia Tay Seok WeiSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.
Josephine LumSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.
Ezequiel Ruiz-MateosClinical Unit of Infectious Diseases, Microbiology and Preventive Medicine, Institute of Biomedicine of Seville (IBiS), Virgen del Rocío University Hospital, CSIC, University of Seville, Seville, Spain.
Reena RajasuriarCentre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia.
Adeeba KamarulzamanCentre of Excellence for Research in AIDS (CERiA), University of Malaya, Kuala Lumpur, Malaysia.
Tze Pin NgGerontology Research Programme and Department of Psychological Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Anis LarbiSingapore Immunology Network (SIgN), Agency for Science Technology and Research (A*STAR), Immunos Building, 8A Biomedical Grove, Biopolis, Republic of Singapore.

Funding

Agency for Science, Technology and Research (A*STAR) BMRC IAF 311006, BMRC transition funds#H16/99/b0/011, BMRC IAF-PP H1901a0024Agency for Science, Technology and Research (A*STAR) No. 10-036Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI16/00684Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI9/01127Ministry of Higher Education, Malaysia (MOHE) HIR/MOHE; H-20001-E000001Universiti Malaya (University of Malaya) UMRG RP029-14HTM
6 · The paper itself

Abstract

Long-term control of viral replication relies on the efficient differentiation of memory T cells into effector T cells during secondary immune responses. Recent findings have identified T cell precursors for both memory and exhausted T cells, suggesting the existence of progenitor-like effector T cells. These cells can persist without antigenic challenge but expand and acquire effector functions upon recall immune responses. In this study, we demonstrate that the combination of SLAMF7 with either CD27 or TCF-1 effectively identifies progenitor-like effector CD8 T cells, while SLAMF7 with GPR56 or TOX defines effector CD8 T cells. These markers allow for the clear segregation of these distinct cell subsets. SLAMF7

Indexed as

CD8-Positive T-LymphocytesSignaling Lymphocytic Activation Molecule FamilySTAT1 Transcription FactorAgingHepatocyte Nuclear Factor 1-alphaHumansInterleukin-15Middle AgedT-Lymphocyte SubsetsVirus DiseasesHepatocyte Nuclear Factor 1-alphaInterleukin-15Signaling Lymphocytic Activation Molecule FamilySLAMF7 protein, humanSTAT1 protein, humanSTAT1 Transcription Factor

Identifiers

PMID39730488
PMCPMC11680708

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Registered trials

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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.