Evidence map›Paper›PMID 15270723›Full record

ArticleImmunology2004

Increased expression of the natural killer cell inhibitory receptor CD85j/ILT2 on antigen-specific effector CD8 T cells and its impact on CD8 T-cell function.

M Nedim Ince, Brooke Harnisch, Zhan Xu, Sang-Kyung Lee, Christoph Lange, Lorenzo Moretta, Michael Lederman, Judy Lieberman

Open access · greenAbstract read
In one paragraph

Article in Immunology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Review
  3. Heterogeneity of memory T cells in aging.Frontiers in immunology · 2023
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. The hallmarks of CMV-specific CD8 T-cell differentiation.Medical microbiology and immunology · 2019
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 5 institutions in 2 countries.

M Nedim InceCBR Institute for Biomedical Research and Department of Pediatrics, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
Brooke Harnisch
Zhan Xu
Sang-Kyung Lee
Christoph Lange
Lorenzo Moretta
Michael Lederman
Judy Lieberman
Harvard University · USCase Western Reserve University · USHarvard University Press · USUniversity Hospitals of Cleveland · USUniversity of Genoa · IT

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Sharon L. Hillier, JONATHAN KARN · 1994 to 2026
$50.0M
CD8 T CELL DYSFUNCTION IN HIV INFECTIONR01AI042519 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI LIEBERMAN, JUDY · 1998 to 2005
$2.2M
NIAID NIH HHS AI 36219NIAID NIH HHS AI 42519NIAID NIH HHS P30 AI036219NIAID NIH HHS R01 AI042519
6 · The paper itself

Abstract

We investigated whether inhibitory natural killer cell receptor (iNKR) expression contributes to impaired antigen-specific cytotoxicity and interferon-gamma (IFN-gamma) production by CD8 T cells during chronic infection. iNKR immunoglobulin-like transcript-2 (ILT2/CD85j) is expressed on 40-55% of cytomegalovirus (CMV)-, Epstein-Barr virus (EBV)- and human immunodeficiency virus (HIV)-specific CD8 T cells in both healthy and HIV-infected donors. Other iNKRs (CD158a, b1, e1/e2, k, CD94/NKG2A) are expressed on only a small minority of CD8 T cells and are not preferentially expressed on tetramer-staining virus-specific cells. In normal donors, ILT2 is expressed largely on perforin(+) CD27(-) effector cells. However, in HIV-infected donors, only a third of ILT2(+) cells are also perforin(+). In both normal and HIV-infected donors, ILT2(+) cells are prone to spontaneous apoptosis. Therefore, ILT2 is normally expressed during effector cytotoxic T-lymphocyte (CTL) differentiation, but can also be expressed when effector maturation is incomplete, as in HIV infection. The effect of ILT2 on CD8 cell function was assessed by preincubating effector cells with ILT2 antibody. While blocking ILT2 engagement has no appreciable effect on cytotoxicity, it increases antiviral IFN-gamma production by approximately threefold in both normal and HIV-infected donors. Thus, ILT2 expression, increased on antiviral CD8 cells in chronic infection, may interfere with protective CD8 T-cell function by suppressing IFN-gamma production.

Indexed as

Antigens, CDApoptosisCD8-Positive T-LymphocytesCell DifferentiationCytotoxicity, ImmunologicEpitopes, T-LymphocyteHIV InfectionsHumansInterferon-gammaLeukocyte Immunoglobulin-like Receptor B1Lymphocyte ActivationMembrane GlycoproteinsPerforinPore Forming Cytotoxic ProteinsReceptors, ImmunologicAntigens, CDEpitopes, T-LymphocyteInterferon-gammaLeukocyte Immunoglobulin-like Receptor B1LILRB1 protein, humanMembrane GlycoproteinsPerforinPore Forming Cytotoxic ProteinsReceptors, Immunologic

Identifiers

PMID15270723
PMCPMC1782522
OpenAlexW2122121638

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.