Evidence map›Paper›PMID 12368336›Full record

ArticleJournal of virology2002

Inhibition of HLA-DR assembly, transport, and loading by human cytomegalovirus glycoprotein US3: a novel mechanism for evading major histocompatibility complex class II antigen presentation.

Nagendra R Hegde, Roman A Tomazin, Todd W Wisner, Claire Dunn, Jessica M Boname, David M Lewinsohn, David C Johnson

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

58 citing papers in PubMed, 121 citations in OpenAlex.

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  3. The immune response to human cytomegalovirus: impact of age, co-morbidities and the significance of anti-viral activity assessment.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
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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.

Nagendra R HegdeDepartment of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, Oregon 97239, USA.
Roman A Tomazin
Todd W Wisner
Claire Dunn
Jessica M Boname
David M Lewinsohn
David C Johnson
Oregon Health & Science University · USPortland VA Medical Center · USUniversity of Cambridge · GB

Funding

INHIBITION OF CLASS I ANTIGEN PRESENTATION BY HSV ICP47R01EY011245 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOHNSON, DAVID C. · 1996 to 2008
$3.6M
NEI NIH HHS EY11245NEI NIH HHS R01 EY011245
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) establishes persistent lifelong infections and replicates slowly. To withstand robust immunity, HCMV utilizes numerous immune evasion strategies. The HCMV gene cassette encoding US2 to US11 encodes four homologous glycoproteins, US2, US3, US6, and US11, that inhibit the major histocompatibility complex class I (MHC-I) antigen presentation pathway, probably inhibiting recognition by CD8(+) T lymphocytes. US2 also inhibits the MHC-II antigen presentation pathway, causing degradation of human leukocyte antigen (HLA)-DR-alpha and -DM-alpha and preventing recognition by CD4(+) T cells. We investigated the effects of seven of the US2 to US11 glycoproteins on the MHC-II pathway. Each of the glycoproteins was expressed by using replication-defective adenovirus vectors. In addition to US2, US3 inhibited recognition of antigen by CD4(+) T cells by a novel mechanism. US3 bound to class II alpha/beta complexes in the endoplasmic reticulum (ER), reducing their association with Ii. Class II molecules moved normally from the ER to the Golgi apparatus in US3-expressing cells but were not sorted efficiently to the class II loading compartment. As a consequence, formation of peptide-loaded class II complexes was reduced. We concluded that US3 and US2 can collaborate to inhibit class II-mediated presentation of endogenous HCMV antigens to CD4(+) T cells, allowing virus-infected cells to resist recognition by CD4(+) T cells.

Indexed as

Antigen PresentationBiological TransportCD4-Positive T-LymphocytesCytomegalovirusDimerizationEndoplasmic ReticulumGlycoproteinsGolgi ApparatusHistocompatibility Antigens Class IIHLA-DR AntigensHumansImmediate-Early ProteinsLysosomesMembrane GlycoproteinsMembrane ProteinsPeptidesGlycoproteinsHistocompatibility Antigens Class IIHLA-DR AntigensImmediate-Early ProteinsMembrane GlycoproteinsMembrane ProteinsPeptidesRNA-Binding ProteinsUS10 glycoprotein, Human herpesvirus 5US11 protein, herpesvirusUS3 protein, cytomegalovirusUS7 glycoprotein, Human herpesvirus 5US8 protein, Human herpesvirus 5US9 protein, Human herpesvirus 5Viral Proteins

Identifiers

PMID12368336
PMCPMC136637
OpenAlexW1988607262

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.