Evidence map›Paper›PMID 22377676›Full record

ArticlemAbs

Selective killing of Kaposi's sarcoma-associated herpesvirus lytically infected cells with a recombinant immunotoxin targeting the viral gpK8.1A envelope glycoprotein.

Deboeeta Chatterjee, Bala Chandran, Edward A Berger

Open access · goldAbstract read
In one paragraph

Article in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Targeting the Inside of Cells with Biologicals: Toxin Routes in a Therapeutic Context.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Antiviral Immunotoxin AgainstFrontiers in microbiology · 2018
    Article
  7. Article
  8. New pharmacological strategies to fight enveloped viruses.Trends in pharmacological sciences · 2014
    Review
  9. Article
  10. 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

3 authors at 3 institutions in 1 country.

Deboeeta ChatterjeeLaboratory of Viral Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, MD USA.
Bala ChandranDepartiment of Microbiology and Immunology; Rosalind Franklin University of Medicine and Science; Chicago, IL USA.
Edward A BergerLaboratory of Viral Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health; Bethesda, MD USA.
Franklin University · USGlobal Viral · USNational Institute of Allergy and Infectious Diseases · US

Funding

Interactions Of Human Immunodeficiency Virus With ReceptorsZIAAI000538 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BERGER, EDWARD · 2009 to 2019
$8.8M
Targeted Killing of Herpesvirus-Infected Cells and Ebola Virus-Infected CellsZIAAI001070 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BERGER, EDWARD · 2009 to 2017
$1.8M
Intramural NIH HHS ZIA AI001070
6 · The paper itself

Abstract

Kaposi sarcoma-associated herpesvirus (KSHV, human herpesvirus 8) is etiologically associated with three neoplastic syndromes: Kaposi sarcoma and the uncommon HIV-associated B-cell lymphoproliferative disorders primary effusion lymphoma and multicentric Castleman disease. The incidence of the latter B-cell pathology has been increasing in spite of antiretroviral therapy; its association with lytic virus replication has prompted interest in therapeutic strategies aimed at this phase of the virus life cycle. We designed and expressed a recombinant immunotoxin (2014-PE38) targeting the gpK8.1A viral glycoprotein expressed on the surface of the virion and infected cells. We show that this immunotoxin selectively kills KSHV-infected cells in dose-dependent fashion, resulting in major reductions of infectious virus release. The immunotoxin and ganciclovir, an inhibitor of viral DNA replication, showed marked reciprocal potentiation of antiviral activities. These results suggest that the immunotoxin, alone or in combination, may represent a new approach to treat diseases associated with KSHV lytic replication.

Indexed as

AnimalsAntibodies, ViralAntiviral AgentsBase SequenceChlorocebus aethiopsDNA ReplicationDNA, ViralGlycoproteinsHerpesviridae InfectionsHerpesvirus 8, HumanHumansImmunotoxinsMolecular Sequence DataRecombinant ProteinsVero CellsViral ProteinsAntibodies, ViralAntiviral AgentsDNA, ViralGlycoproteinsImmunotoxinsK8.1 protein, Human herpesvirus 8Recombinant ProteinsViral Proteinsganciclovirhuman herpesvirus-8KSHV lytic infectionKSHV surface glycoproteinmulticentric Castleman diseasePseudomonas exotoxin Areciprocal drug potentiationtargeted cytotoxic proteins

Identifiers

PMID22377676
PMCPMC3361659
OpenAlexW2077582150

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.