Evidence map›Paper›PMID 21458073›Full record

ArticleMolecular immunology2011

Human cytomegalovirus decreases constitutive transcription of MHC class II genes in mature Langerhans cells by reducing CIITA transcript levels.

Andrew W Lee, Nan Wang, Tara M C Hornell, James J Harding, Chetan Deshpande, Laura Hertel, Vashti Lacaille, Achal Pashine, Claudia Macaubas, Edward S Mocarski and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular immunology, 2011. 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
1.5field-weighted citation impact, top 19% 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, 31 citations in OpenAlex.

  1. 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

11 authors at 1 institution in 1 country.

Andrew W LeeDepartment of Pediatrics, Program in Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Nan Wang
Tara M C Hornell
James J Harding
Chetan Deshpande
Laura Hertel
Vashti Lacaille
Achal Pashine
Claudia Macaubas
Edward S Mocarski
Elizabeth D Mellins
Stanford University · US

Funding

Postnatal ontogeny of HCMV-specific CD4 T cell immunityP01AI048212 · NIAID · STANFORD UNIVERSITY · PI ARVIN, ANN M · 2000 to 2003
$3.6M
CYTOMEGALOVIRUS PATHOGENESIS IN IMMUNODEFICIENCYR01AI030363 · NIAID · STANFORD UNIVERSITY · PI EDWARD S MOCARSKI, EDWARD S. · 1991 to 2011
$2.7M
PROCESSING OF ANTIGENS FOR HLA RESTRICTED PRESENTATIONR01AI028809 · NIAID · STANFORD UNIVERSITY · PI MELLINS, ELIZABETH D · 1995 to 1999
–
NIAID NIH HHS P01 AI048212NIAID NIH HHS R01 AI028809NIAID NIH HHS R01 AI030363
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) productively infects CD34(+) progenitor-derived, mature Langerhans-type dendritic cells (matLC) and reduces surface expression of MHC class II complexes (MHC II) by increasing intracellular retention of these molecules. To determine whether HCMV also inhibits MHC II expression by other mechanisms, we assessed mRNA levels of the class II transcriptional regulator, CIITA, and several of its target genes in infected matLC. Levels of CIITA, HLA-DRA (DRA) and DRB transcripts, and new DR protein synthesis were compared in mock-infected and HCMV-infected cells by quantitative PCR and pulse-chase immunoprecipitation analyses, respectively. CIITA mRNA levels were significantly lower in HCMV-infected matLC as compared to mock-infected cells. When assessed in the presence of Actinomycin D, the stability of CIITA transcripts was not diminished by HCMV. Analysis of promoter-specific CIITA isoforms revealed that types I, III and IV all were decreased by HCMV, a result that differs from changes after incubation of these cells with lipopolysaccharide (LPS). Exposure to UV-inactivated virus failed to reduce CIITA mRNA levels, implicating de novo viral gene expression in this effect. HCMV-infected matLC also expressed lower levels of DR transcripts and reduced DR protein synthesis rates compared to mock-infected matLC. In summary, we demonstrate that HCMV infection of a human dendritic cell subset inhibits constitutive CIITA expression, most likely at the transcriptional level, resulting in reduced MHC II biosynthesis. We suggest this represents a new mechanism of modulation of mature LC by HCMV.

Indexed as

Transcription, GeneticCell DifferentiationCytomegalovirusCytomegalovirus InfectionsHistocompatibility Antigens Class IIHLA-DR alpha-ChainsHLA-DR AntigensHumansLangerhans CellsNuclear ProteinsProtein BiosynthesisProtein IsoformsRNA, MessengerRNA StabilityTrans-ActivatorsHistocompatibility Antigens Class IIHLA-DR alpha-ChainsHLA-DR AntigensMHC class II transactivator proteinNuclear ProteinsProtein IsoformsRNA, MessengerTrans-Activators

Identifiers

PMID21458073
PMCPMC3086682
OpenAlexW2028711697

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.