Evidence map›Paper›PMID 25972551›Full record

ArticleJournal of virology2015

Comparable Antigenicity and Immunogenicity of Oligomeric Forms of a Novel, Acute HIV-1 Subtype C gp145 Envelope for Use in Preclinical and Clinical Vaccine Research.

Lindsay Wieczorek, Shelly J Krebs, Vaniambadi Kalyanaraman, Stephen Whitney, Sodsai Tovanabutra, Carlos G Moscoso, Eric Sanders-Buell, Constance Williams, Bonnie Slike, Sebastian Molnar and 22 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Stable, high yield expression of gp145 Env glycoprotein from HIV-1 in mammalian cells.Biologicals : journal of the International Association of Biological Standardization · 2021
    Article
  10. Article
  11. A reversed phase HPLC method for the quantification of HIV gp145 glycoprotein levels from cell culture supernatants.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2021
    Article
  12. Liposome Formulations as Adjuvants for Vaccines.Current topics in microbiology and immunology · 2021
    Article
  13. HIV vaccinology: 2021 update.Seminars in immunology · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

32 authors at 9 institutions in 3 countries.

Lindsay WieczorekMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Shelly J KrebsMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Vaniambadi KalyanaramanAdvanced Biosciences Laboratories, Inc., Rockville, Maryland, USA.
Stephen WhitneyAdvanced Biosciences Laboratories, Inc., Rockville, Maryland, USA.
Sodsai TovanabutraMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Carlos G MoscosoUniversity of California, Davis, California, USA.
Eric Sanders-BuellMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Constance WilliamsNew York University School of Medicine and Veterans Affairs Medical Center, New York, New York, USA.
Bonnie SlikeMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Sebastian MolnarMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Vincent DussuptMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
S Munir AlamDuke University, Durham, North Carolina, USA.
Agnes-Laurence ChenineMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Tina TongHJF-DAIDS, Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Edgar L HillHJF-DAIDS, Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Hua-Xin LiaoDuke University, Durham, North Carolina, USA.
Michael HoelscherKlinikum of the University of Munich, Department of Infectious Diseases and Tropical Medicine, Munich, Germany German Center for Infection Research (DZIF), Munich, Germany.
Leonard MabokoNational Institute for Medical Research-Mbeya Medical Research Center, Mbeya, Tanzania.
Susan Zolla-PaznerNew York University School of Medicine and Veterans Affairs Medical Center, New York, New York, USA.
Barton F HaynesDuke University, Durham, North Carolina, USA.
Michael PensieroDivision of AIDS, NIH, Bethesda, Maryland, USA.
Francine McCutchanMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Shawyon Malek-SalehiUniversity of California, Davis, California, USA.
R Holland ChengUniversity of California, Davis, California, USA.
Merlin L RobbMilitary HIV Research Program, Bethesda, Maryland, USA Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Thomas VanCottAdvanced Biosciences Laboratories, Inc., Rockville, Maryland, USA.
Nelson L MichaelMilitary HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Mary A MarovichMilitary HIV Research Program, Bethesda, Maryland, USA Division of AIDS, NIH, Bethesda, Maryland, USA.
Carl R AlvingMilitary HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Gary R MatyasMilitary HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Mangala RaoMilitary HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Victoria R PolonisMilitary HIV Research Program, Bethesda, Maryland, USA Walter Reed Army Institute of Research, Silver Spring, Maryland, USA vpolonis@hivresearch.org.
Henry M. Jackson Foundation · USWalter Reed Army Institute of Research · USDuke University · USUniversity of California, Davis · USOffice of AIDS Research · USGerman Center for Infection Research · DENational Institute for Medical Research · TZNew York University · USVeterans Health Administration · US

Funding

PROTECTIVE HUMAN MONOCLONAL ANTIBODIES TO HIV1R01HL059725 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ZOLLA-PAZNER, SUSAN B · 1997 to 2014
$8.8M
Present Homologous and Heterologous Antigen with Hepatitis E VirusR56AI095382 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CHENG, R.HOLLAND · 2012 to 2012
$385k
NHLBI NIH HHS HL59725NHLBI NIH HHS R01 HL059725NIAID NIH HHS HHSN272200800014CNIAID NIH HHS R56 AI095382PHS HHS HHSN272200800014C
6 · The paper itself

Abstract

unlabelledEliciting broadly reactive functional antibodies remains a challenge in human immunodeficiency virus type 1 (HIV-1) vaccine development that is complicated by variations in envelope (Env) subtype and structure. The majority of new global HIV-1 infections are subtype C, and novel antigenic properties have been described for subtype C Env proteins. Thus, an HIV-1 subtype C Env protein (CO6980v0c22) from an infected person in the acute phase (Fiebig stage I/II) was developed as a research reagent and candidate immunogen. The gp145 envelope is a novel immunogen with a fully intact membrane-proximal external region (MPER), extended by a polylysine tail. Soluble gp145 was enriched for trimers that yielded the expected "fan blade" motifs when visualized by cryoelectron microscopy. CO6980v0c22 gp145 reacts with the 4E10, PG9, PG16, and VRC01 HIV-1 neutralizing monoclonal antibodies (MAbs), as well as the V1/V2-specific PGT121, 697, 2158, and 2297 MAbs. Different gp145 oligomers were tested for immunogenicity in rabbits, and purified dimers, trimers, and larger multimers elicited similar levels of cross-subtype binding and neutralizing antibodies to tier 1 and some tier 2 viruses. Immunized rabbit sera did not neutralize the highly resistant CO6980v0c22 pseudovirus but did inhibit the homologous infectious molecular clone in a peripheral blood mononuclear cell (PBMC) assay. This Env is currently in good manufacturing practice (GMP) production to be made available for use as a clinical research tool and further evaluation as a candidate vaccine. IMPORTANCE: At present, the product pipeline for HIV vaccines is insufficient and is limited by inadequate capacity to produce large quantities of vaccine to standards required for human clinical trials. Such products are required to evaluate critical questions of vaccine formulation, route, dosing, and schedule, as well as to establish vaccine efficacy. The gp145 Env protein presented in this study forms physical trimers, binds to many of the well-characterized broad neutralizing MAbs that target conserved Env epitopes, and induce cross-subtype neutralizing antibodies as measured in both cell line and primary cell assays. This subtype C Env gp145 protein is currently undergoing good manufacturing practice production for use as a reagent for preclinical studies and for human clinical research. This product will serve as a reagent for comparative studies and may represent a next-generation candidate HIV immunogen.

Indexed as

AIDS VaccinesAnimalsDrug Evaluation, Preclinicalenv Gene Products, Human Immunodeficiency VirusHIV-1HIV AntibodiesHIV InfectionsHumansLeukocytes, MononuclearMolecular Sequence DataNeutralization TestsRabbitsVaccinationAIDS Vaccinesenv Gene Products, Human Immunodeficiency VirusHIV Antibodies

Identifiers

PMID25972551
PMCPMC4505676
OpenAlexW2104197131

What OpenQuestion holds

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Registered trials

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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.