Evidence map›Paper›PMID 19567243›Full record

ArticleVaccine2009

Structural and immunogenicity studies of a cleaved, stabilized envelope trimer derived from subtype A HIV-1.

Yun Kenneth Kang, Sofija Andjelic, James M Binley, Emma T Crooks, Michael Franti, Sai Prasad N Iyer, Gerald P Donovan, Antu K Dey, Ping Zhu, Kenneth H Roux and 5 more

Abstract read
In one paragraph

Article in Vaccine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.5field-weighted citation impact, top 10% 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, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Innovations in HIV-1 Vaccine Design.Clinical therapeutics · 2020
    Review
  5. Article
  6. HIV-1 Consensus Envelope-Induced Broadly Binding Antibodies.AIDS research and human retroviruses · 2017
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. New approaches to HIV vaccine development.Current opinion in immunology · 2015
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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

15 authors at 5 institutions in 1 country.

Yun Kenneth KangProgenics Pharmaceuticals, Inc., Tarrytown, NY 10591, United States. kkang@progenics.com
Sofija Andjelic
James M Binley
Emma T Crooks
Michael Franti
Sai Prasad N Iyer
Gerald P Donovan
Antu K Dey
Ping Zhu
Kenneth H Roux
Robert J Durso
Thomas F Parsons
Paul J Maddon
John P Moore
William C Olson
Progenics Pharmaceuticals (United States) · USCornell University · USFlorida State University · USGeneral Atomics (United States) · USTorrey Pines Institute For Molecular Studies · US

Funding

Trimer Production and Immunogenicity TestingP01AI082362 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI WILSON, IAN A · 2009 to 2014
$16.0M
HIV VACCINE DESIGN AND DEVELOPMENT TEAMS (HVDDT)N01AI30030 · NIAID · PI , · 2007 to 2007
$5.2M
HIV VACCINE DESIGN AND DEVELOPMENT TEAMS (HVDDT)-266030030N01AI030030 · NIAID · PROGENICS PHARMACEUTICALS, INC · PI MADDON, PAUL J · 2003 to 2003
–
NIAID NIH HHS N01 AI030030NIAID NIH HHS N01 AI30030NIAID NIH HHS P01 AI082362
6 · The paper itself

Abstract

SOSIP gp140 trimers represent a soluble, stabilized, proteolytically cleaved form of the HIV-1 envelope (Env) glycoproteins. SOSIP gp140 derived from a subtype A HIV-1 isolate, KNH1144, forms exceptionally stable trimers that resemble virion-associated Env in antigenicity and topology. Here, we used electron microscopy to demonstrate that KNH1144 SOSIP gp140 trimers bound three soluble CD4 molecules in a symmetrical orientation similar to that seen for native Env. We compared the immunogenicities of KNH1144 SOSIP gp140 trimers and gp120 monomers in rabbits and found that the trimers were superior at eliciting neutralizing antibodies (NAbs) to homologous virus as well as neutralization-sensitive subtype B and C viruses. The NAb specificities for SOSIP antisera mapped in part to the CD4 binding site on gp120. We also observed adjuvant-dependent induction of antibodies to the residual levels of host cell proteins (HCPs) contained in the purified Env preparations. When present, HCP antibodies enhanced pseudovirus infection. Our findings are relevant for the further development of Env-based vaccines for HIV-1.

Indexed as

AnimalsAntibodies, MonoclonalAntigen-Antibody ComplexCD4 AntigensCell Lineenv Gene Products, Human Immunodeficiency VirusEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHIV-1HIV AntibodiesHIV Envelope Protein gp120HumansMicroscopy, ElectronModels, MolecularNeutralization TestsAntibodies, MonoclonalAntigen-Antibody ComplexCD4 Antigensenv Gene Products, Human Immunodeficiency Virusgp120 protein, Human immunodeficiency virus 1gp140 envelope protein, Human immunodeficiency virus 1HIV AntibodiesHIV Envelope Protein gp120

Identifiers

PMID19567243
PMCPMC4340663
OpenAlexW2124359177

What OpenQuestion holds

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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.