Evidence map›Paper›PMID 16569867›Full record

ArticleAntimicrobial agents and chemotherapy2006

Sialidase fusion protein as a novel broad-spectrum inhibitor of influenza virus infection.

Michael P Malakhov, Laura M Aschenbrenner, Donald F Smee, Miles K Wandersee, Robert W Sidwell, Larisa V Gubareva, Vasiliy P Mishin, Frederick G Hayden, Do Hyong Kim, Alice Ing and 3 more

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
9.1field-weighted citation impact, top 2% 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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 231 citations in OpenAlex.

  1. Pooled it
  2. DAS181 Treatment of Severe Lower Respiratory Tract Parainfluenza Virus Infection in Immunocompromised Patients: A Phase 2 Randomized, Placebo-Controlled Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Acute and Subacute Toxicity of Sialidase FromVeterinary medicine international · 2025
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Journal of advanced veterinary and animal research · 2023
    Article
  19. Article
  20. Article

65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Michael P MalakhovNexBio, Inc., 6330 Nancy Ridge Dr., Suite 105, San Diego, CA 92121, USA.
Laura M Aschenbrenner
Donald F Smee
Miles K Wandersee
Robert W Sidwell
Larisa V Gubareva
Vasiliy P Mishin
Frederick G Hayden
Do Hyong Kim
Alice Ing
Erin R Campbell
Mang Yu
Fang Fang
University of Virginia · USUtah State University · US

Funding

T CELL MEMORY TO VIRUSESR01AI030048 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHMED, RAFI · 1990 to 2022
$5.2M
T CELL MEMORY TO VIRUSESR37AI030048 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI · 2001 to 2010
$3.9M
Broad-Spectrum Therapeutics for InfluenzaR43AI056786 · NIAID · NEXBIO, INC. · PI YU, MANG · 2003 to 2004
$918k
ANIMAL MODELS OF HUMAN VIRAL INFECTIONS FOR EVALUATION OF EXPERIMENTAL-266015435N01AI015435 · NIAID · UTAH STATE UNIVERSITY · 2004 to 2004
–
NIAID NIH HHS N01 AI015435NIAID NIH HHS N01 AI030048NIAID NIH HHS N01-AI-15435NIAID NIH HHS N01-AI-30048NIAID NIH HHS R43 AI056786NIAID NIH HHS R43AI056786
6 · The paper itself

Abstract

Influenza is a highly infectious disease characterized by recurrent annual epidemics and unpredictable major worldwide pandemics. Rapid spread of the highly pathogenic avian H5N1 strain and escalating human infections by the virus have set off the alarm for a global pandemic. To provide an urgently needed alternative treatment modality for influenza, we have generated a recombinant fusion protein composed of a sialidase catalytic domain derived from Actinomyces viscosus fused with a cell surface-anchoring sequence. The sialidase fusion protein is to be applied topically as an inhalant to remove the influenza viral receptors, sialic acids, from the airway epithelium. We demonstrate that a sialidase fusion construct, DAS181, effectively cleaves sialic acid receptors used by both human and avian influenza viruses. The treatment provides long-lasting effect and is nontoxic to the cells. DAS181 demonstrated potent antiviral and cell protective efficacies against a panel of laboratory strains and clinical isolates of IFV A and IFV B, with virus replication inhibition 50% effective concentrations in the range of 0.04 to 0.9 nM. Mouse and ferret studies confirmed significant in vivo efficacy of the sialidase fusion in both prophylactic and treatment modes.

Indexed as

AmphiregulinAnimalsAntiviral AgentsBacterial AdhesionCatalytic DomainCell LineDogsEGF Family of ProteinsFemaleFerretsGlycoproteinsHumansInfluenza, HumanIntercellular Signaling Peptides and ProteinsMiceMice, Inbred BALB CAmphiregulinAntiviral AgentsAREG protein, humanAreg protein, mouseEGF Family of ProteinsGlycoproteinsIntercellular Signaling Peptides and ProteinsNeuraminidasePeptide FragmentsRecombinant Fusion Proteins

Identifiers

PMID16569867
PMCPMC1426979
OpenAlexW2125902066

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.