Evidence map›Paper›PMID 16051832›Full record

ArticleJournal of virology2005

Vaccinia virus tropism for primary hematolymphoid cells is determined by restricted expression of a unique virus receptor.

Ann Chahroudi, Rahul Chavan, Natalia Kozyr, Natalia Koyzr, Edmund K Waller, Guido Silvestri, Mark B Feinberg

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of virology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.4field-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

48 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Mpox (formerly monkeypox): pathogenesis, prevention, and treatment.Signal transduction and targeted therapy · 2023
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Targeting Head and Neck Cancer by Vaccination.Frontiers in immunology · 2018
    Review
  15. Article
  16. Generalized Vaccinia After Smallpox Vaccination With Concomitant Primary Epstein Barr Virus Infection.Federal practitioner : for the health care professionals of the VA, DoD, and PHS · 2017
    Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
    Koyzr, Natalia [corrected to Kozyr, Natalia]
5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Ann ChahroudiEmory Vaccine Center, Emory University School of Medicine, Atlanta, Georgia 30329, USA.
Rahul Chavan
Natalia Kozyr
Natalia Koyzr
Edmund K Waller
Guido Silvestri
Mark B Feinberg
Piedmont Cancer Institute · USWinship Cancer InstituteEmory and Henry College · USEmory University · US

Funding

Project Coordination and Product DevelopmentU19AI061728 · NIAID · EMORY UNIVERSITY · PI PRIDDY, FRANCES H · 2004 to 2008
$14.3M
RECOMBINANT YELLOW FEVER VIRUS AS A CANDIDATE AIDS VACCINEP01AI046007 · NIAID · UNIVERSITY OF ZURICH · PI FEINBERG, MARK B. · 1999 to 2003
$6.7M
NIAID NIH HHS P01 AI046007NIAID NIH HHS P01-AI46007NIAID NIH HHS U19 AI061728NIAID NIH HHS U19-AI061728
6 · The paper itself

Abstract

The presumed broad tropism of poxviruses has stymied attempts to identify both the cellular receptor(s) and the viral determinant(s) for binding. Detailed studies of poxvirus binding to and infection of primary human cells have not been conducted. In particular, the determinants of target cell infection and the consequences of infection for cells involved in the generation of antiviral immune responses are incompletely understood. In this report, we show that vaccinia virus (VV) exhibits a more restricted tropism for primary hematolymphoid human cells than has been previously recognized. We demonstrate that vaccinia virus preferentially infects antigen-presenting cells (dendritic cells, monocytes/macrophages, and B cells) and activated T cells, but not resting T cells. The infection of activated T cells is permissive, with active viral replication and production of infectious progeny. Susceptibility to infection is determined by restricted expression of a cellular receptor that is induced de novo upon T-cell activation and can be removed from the cell surface by either trypsin or pronase treatment. The VV receptor expressed on activated T cells displays unique characteristics that distinguish it from the receptor used to infect cell lines in culture. The observed restricted tropism of VV may have significant consequences for the understanding of natural poxvirus infection and immunity and for poxvirus-based vaccine development.

Indexed as

AnimalsFemaleGene ExpressionLymphocyte ActivationMiceMice, Inbred BALB CPronaseReceptors, VirusT-LymphocytesTropismTrypsinVaccinia virusPronaseReceptors, VirusTrypsin

Identifiers

PMID16051832
PMCPMC1182677
OpenAlexW2156065256

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.