Evidence map›Paper›PMID 10727456›Full record

ArticleThe Journal of experimental medicine2000

Self-recognition of CD1 by gamma/delta T cells: implications for innate immunity.

F M Spada, E P Grant, P J Peters, M Sugita, A Melián, D S Leslie, H K Lee, E van Donselaar, D A Hanson, A M Krensky and 4 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 166 papers.

0numbers the graph read from it
0cells of the map it votes in
166citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

166 citing papers in PubMed, 370 citations in OpenAlex.

  1. Trial
  2. Article
  3. Efficient multiplex non-viral engineering and expansion of polyclonal γδ CAR-T cells for immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
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  11. Article
  12. The Evolving Portrait of γδ TCR Recognition Determinants.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Review
  13. Article
  14. Review
  15. Review
  16. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  17. Article
  18. Review
  19. The emerging roles of γδ T cells in cancer immunotherapy.Nature reviews. Clinical oncology · 2023
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 3 countries.

F M SpadaDivision of Rheumatology, Immunology, and Allergy, Department of Medicine, Brigham and Women's Hospital at Harvard Medical School, Boston, Massachusetts 02115, USA.
E P Grant
P J Peters
M Sugita
A Melián
D S Leslie
H K Lee
E van Donselaar
D A Hanson
A M Krensky
O Majdic
S A Porcelli
C T Morita
M B Brenner
Brigham and Women's Hospital · USDutch Cancer Society · NLUniversity of Iowa · USStanford University · USVirginia Mason Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The specificity of immunoglobulins and alpha/beta T cell receptors (TCRs) provides a framework for the molecular basis of antigen recognition. Yet, evolution has preserved a separate lineage of gamma/delta antigen receptors that share characteristics of both immunoglobulins and alpha/beta TCRs but whose antigens remain poorly understood. We now show that T cells of the major tissue gamma/delta T cell subset recognize nonpolymorphic CD1c molecules. These T cells proliferated in response to CD1+ presenter cells, lysed CD1c+ targets, and released T helper type 1 (Th1) cytokines. The CD1c-reactive gamma/delta T cells were cytotoxic and used both perforin- and Fas-mediated cytotoxicity. Moreover, they produced granulysin, an important antimicrobial protein. Recognition of CD1c was TCR mediated, as recognition was transferred by transfection of the gamma/delta TCR. Importantly, all CD1c-reactive gamma/delta T cells express V delta 1 TCRs, the TCR expressed by most tissue gamma/delta T cells. Recognition by this tissue pool of gamma/delta T cells provides the human immune system with the capacity to respond rapidly to nonpolymorphic molecules on professional antigen presenting cells (APCs) in the absence of foreign antigens that may activate or eliminate the APCs. The presence of bactericidal granulysin suggests these cells may directly mediate host defense even before foreign antigen-specific T cells have differentiated.

Indexed as

Amino Acid SequenceAntigen-Presenting CellsAntigens, CD1Antigens, Differentiation, T-LymphocyteAnti-Infective AgentsBase SequenceCell DifferentiationCell LineCytotoxicity, ImmunologicCytotoxicity Tests, Immunologicfas ReceptorGene Rearrangement, delta-Chain T-Cell Antigen ReceptorGene Rearrangement, gamma-Chain T-Cell Antigen ReceptorHumansImmunity, InnateLymphocyte ActivationAntigens, CD1Antigens, Differentiation, T-LymphocyteAnti-Infective Agentsfas ReceptorGNLY protein, humanMembrane GlycoproteinsPerforinPore Forming Cytotoxic ProteinsReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID10727456
PMCPMC2193122
OpenAlexW2163819348

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.