Evidence map›Paper›PMID 10775582›Full record

ArticleJournal of virology2000

Expression of herpes simplex virus ICP47 and human cytomegalovirus US11 prevents recognition of transgene products by CD8(+) cytotoxic T lymphocytes.

C Berger, S Xuereb, D C Johnson, K S Watanabe, H P Kiem, P D Greenberg, S R Riddell

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Oncolytic Virotherapy in Solid Tumors: A Current Review.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Oncolytic Viral Therapy for Mesothelioma.Frontiers in oncology · 2017
    Review
  8. Review
  9. Oncolytic viruses: a new class of immunotherapy drugs.Nature reviews. Drug discovery · 2015
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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

7 authors at 3 institutions in 2 countries.

C BergerFred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
S Xuereb
D C Johnson
K S Watanabe
H P Kiem
P D Greenberg
S R Riddell
Fred Hutch Cancer Center · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAOregon Health & Science University · US

Funding

VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Geoffrey Roger HILL · 1985 to 2026
$128.4M
INHIBITION OF CLASS I ANTIGEN PRESENTATION BY HSV ICP47R01EY011245 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOHNSON, DAVID C. · 1996 to 2008
$3.6M
TREATMENT OF HIV WITH GENE MODIFIED CD8+ T CELL CLONESP01AI043650 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GREENBERG, PHILIP D · 1998 to 2001
$2.9M
RECONSTITUTION OF CMV IMMUNITY IN HIV-INFECTED HOSTSR01AI041754 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RIDDELL, STANLEY R · 1997 to 2001
$1.8M
NCI NIH HHS CA18029NCI NIH HHS P01 CA018029NEI NIH HHS R01 EY011245NIAID NIH HHS AI41754NIAID NIH HHS AI43650
6 · The paper itself

Abstract

The in vivo persistence of gene-modified cells may be limited by the development of a host immune response to vector-encoded proteins. Herpesviruses evade cytotoxic T-lymphocyte (CTL) recognition by expressing genes which interfere selectively with presentation of viral antigens by class I major histocompatibility complex (MHC) molecules. Here, we studied the use of retroviral vectors encoding herpes simplex virus ICP47, human cytomegalovirus (HCMV) US3, or HCMV US11 to decrease presentation of viral proteins and transgene products to CD8(+) CTL. Human fibroblasts and T cells transduced to express the ICP47, US3, or US11 genes alone exhibited a decrease in cell surface class I MHC expression. The combination of ICP47 and US11 rendered fibroblasts negative for surface class I MHC and allowed a class I MHC-low population of T cells to be sorted by flow cytometry. Fibroblasts and T cells expressing both ICP47 and US11 were protected from CTL-mediated lysis and failed to stimulate specific memory T-cell responses to transgene products in vitro. Our findings suggest that expression of immunoregulatory viral gene products could be a potential strategy to prolong transgene expression in vivo.

Indexed as

TransgenesAnimalsAntigen PresentationCells, CulturedCytomegalovirusCytotoxicity, ImmunologicFibroblastsGene ExpressionGenetic VectorsGlycoproteinsHerpesviridaeHumansImmediate-Early ProteinsKiller Cells, NaturalLymphocyte ActivationMembrane ProteinsGlycoproteinshygromycin-B kinaseICP47 protein, Herpes simplex virusImmediate-Early ProteinsMembrane ProteinsPhosphotransferases (Alcohol Group Acceptor)Recombinant ProteinsRNA-Binding ProteinsUS11 protein, herpesvirusUS3 protein, cytomegalovirusViral Proteins

Identifiers

PMID10775582
PMCPMC111967
OpenAlexW2131720677

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.