Evidence map›Paper›PMID 31941770›Full record

ArticleJournal of virology2020

Glycan Profiles of gp120 Protein Vaccines from Four Major HIV-1 Subtypes Produced from Different Host Cell Lines under Non-GMP or GMP Conditions.

Shixia Wang, Yegor Voronin, Peng Zhao, Mayumi Ishihara, Nickita Mehta, Mindy Porterfield, Yuxin Chen, Christopher Bartley, Guangnan Hu, Dong Han and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Shixia WangDepartment of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Yegor VoroninWorcester HIV Vaccine, Inc., Worcester, Massachusetts, USA.
Peng ZhaoComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.
Mayumi IshiharaComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.
Nickita MehtaComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.
Mindy PorterfieldComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.
Yuxin ChenDepartment of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Christopher BartleyWaisman Biomanufacturing, Madison, Wisconsin, USA.
Guangnan HuDepartment of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Dong HanDepartment of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Lance WellsComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.
Michael TiemeyerComplex Carbohydrate Research Center, University of Georgia, Athens, Georgia, USA.
Shan LuDepartment of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA shan.lu@umassmed.edu.
University of Georgia · USUniversity of Massachusetts Chan Medical School · US

Funding

Optimizing the immunogenicity of next generation polyvalent HIV vaccine formulatiU19AI082676 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LU, SHAN · 2009 to 2016
$15.8M
Variation in HIV-1 R5 Envs: Consequences for tropism, neutralization & vaccinesP01AI082274 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LU, SHAN · 2009 to 2013
$9.7M
Polyvalent DNA Plus Protein HIV VaccinesR01AI065250 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LU, SHAN · 2006 to 2010
$1.9M
Production of neutralizing mAbs from HIV vaccineesR33AI087191 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WANG, SHIXIA · 2012 to 2014
$1.4M
Production of neutralizing mAbs from HIV vaccineesR21AI087191 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WANG, SHIXIA · 2010 to 2011
$450k
NIAID NIH HHS P01 AI082274NIAID NIH HHS R01 AI065250NIAID NIH HHS R21 AI087191NIAID NIH HHS R33 AI087191NIAID NIH HHS U19 AI082676
6 · The paper itself

Abstract

Envelope (Env) glycoprotein of human immunodeficiency virus type 1 (HIV-1) is an important target for the development of an HIV vaccine. Extensive glycosylation of Env is an important feature that both protects the virus from antibody responses and serves as a target for some highly potent broadly neutralizing antibodies. Therefore, analysis of glycans on recombinant Env proteins is highly significant. Here, we present glycosylation profiles of recombinant gp120 proteins from four major clades of HIV-1 (A, B, C, and AE), produced either as research-grade material in 293 and CHO cells or as two independent lots of clinical material under good manufacturing practice (GMP) conditions. Almost all potential

Indexed as

AIDS VaccinesAnimalsAntibodies, MonoclonalAntibodies, NeutralizingCD4-Positive T-LymphocytesCHO CellsCricetulusEpitopesGlycosylationHEK293 CellsHIV-1HIV Envelope Protein gp120HumansImmunoglobulin GPolysaccharidesProtein DomainsAIDS VaccinesAntibodies, MonoclonalAntibodies, NeutralizingEpitopesHIV Envelope Protein gp120Immunoglobulin GPolysaccharidesRecombinant ProteinsEnv proteinglycosylationgp120HIV-1vaccine

Identifiers

PMID31941770
PMCPMC7081908
OpenAlexW2999267502

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.