Evidence map›Paper›PMID 15194762›Full record

ArticleJournal of virology2004

Nef proteins from simian immunodeficiency virus-infected chimpanzees interact with p21-activated kinase 2 and modulate cell surface expression of various human receptors.

Frank Kirchhoff, Michael Schindler, Nicola Bailer, G Herma Renkema, Kalle Saksela, Volker Knoop, Michaela C Müller-Trutwin, Mario L Santiago, Frederic Bibollet-Ruche, Matthias T Dittmar and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

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  13. Mechanisms of HIV-1 Nef function and intracellular signaling.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2011
    Review
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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

13 authors at 7 institutions in 5 countries.

Frank KirchhoffDepartment of Virology, Universitatsklinikum, 89081 Ulm, Germany. frank.kirchhoff@medizin.uni-ulm.de
Michael Schindler
Nicola Bailer
G Herma Renkema
Kalle Saksela
Volker Knoop
Michaela C Müller-Trutwin
Mario L Santiago
Frederic Bibollet-Ruche
Matthias T Dittmar
Jonathan L Heeney
Beatrice H Hahn
Jan Münch
University of Alabama at Birmingham · USBiomedical Primate Research Centre · NLHeidelberg University · DEInstitut Pasteur · FRTampere University · FITampere University Hospital · FIUniversity of Bonn · DE

Funding

Natural SIV Reservoirs and Human Zoonotic RiskR01AI050529 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HAHN, BEATRICE H · 2001 to 2022
$6.1M
SIV-RCM AND RELATED PRIMATE LENTIVIRUSES IN WEST AFRICAR01AI044596 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI MARX, PRESTON A · 1999 to 2003
$2.4M
NIAID NIH HHS R01 AI044596NIAID NIH HHS R01 AI050529NIAID NIH HHS R01 AI 44596NIAID NIH HHS R01 AI50529
6 · The paper itself

Abstract

The accessory Nef protein allows human immunodeficiency virus type 1 (HIV-1) to persist at high levels and to cause AIDS in infected humans. The function of HIV-1 group M subtype B nef alleles has been extensively studied, and a variety of in vitro activities believed to be important for viral pathogenesis have been established. However, the function of nef alleles derived from naturally simian immunodeficiency virus (SIV)-infected chimpanzees, the original host of HIV-1, or from the HIV-1 N and O groups resulting from independent zoonotic transmissions remains to be investigated. In the present study we demonstrate that SIVcpz and HIV-1 group N or O nef alleles down-modulate CD4, CD28, and class I or II MHC molecules and up-regulate surface expression of the invariant chain (Ii) associated with immature major histocompatibility complex (MHC) class II. Furthermore, the ability of Nef to interact with the p21-activated kinase 2 was generally conserved. The functional activity of HIV-1 group N and O nef genes did not differ significantly from group M nef alleles. However, SIVcpz nef genes as a group showed a 1.8- and 2.0-fold-higher activity in modulating CD28 (P = 0.0002) and Ii (P = 0.016) surface expression, respectively, but were 1.7-fold less active in down-regulating MHC class II molecules (P = 0.006) compared to HIV-1 M nef genes. Our finding that primary SIVcpz nef alleles derived from naturally infected chimpanzees modulate the surface expression of various human cellular receptors involved in T-cell activation and antigen presentation suggests that functional nef genes helped the chimpanzee virus to persist efficiently in infected humans immediately after zoonotic transmission.

Indexed as

AdultAnimalsCD28 AntigensCD4 AntigensFemaleGene Expression RegulationGene Products, nefHistocompatibility Antigens Class IIHIV-1HIV InfectionsHumansMaleMiddle AgedMolecular Sequence Datanef Gene Products, Human Immunodeficiency Virusp21-Activated KinasesCD28 AntigensCD4 AntigensGene Products, nefHistocompatibility Antigens Class IInef Gene Products, Human Immunodeficiency Virusp21-Activated KinasesPAK2 protein, humanProtein Serine-Threonine Kinases

Identifiers

PMID15194762
PMCPMC421647
OpenAlexW2160483300

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.