Evidence map›Paper›PMID 30071025›Full record

ArticlePloS one2018

Robotic selection for the rapid development of stable CHO cell lines for HIV vaccine production.

Sara M O'Rourke, Gabriel Byrne, Gwen Tatsuno, Meredith Wright, Bin Yu, Kathryn A Mesa, Rachel C Doran, David Alexander, Phillip W Berman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  6. Article
  7. 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
  8. Article
  9. Rapid and sensitive detection of SARS-CoV-2 antibodies by biolayer interferometry.medRxiv : the preprint server for health sciences · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Development of a Stable MGAT1Frontiers in immunology · 2018
    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

9 authors at 1 institution in 1 country.

Sara M O'RourkeDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0001-8624-0483
Gabriel ByrneDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0003-4369-8739
Gwen TatsunoDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.
Meredith WrightDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.
Bin YuDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0002-3705-0453
Kathryn A MesaDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.
Rachel C DoranDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.
David AlexanderDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.
Phillip W BermanDepartment of Biomolecular Engineering, The University of California at Santa Cruz, Santa Cruz, California, United States of America.
University of California, Santa Cruz · US

Funding

Re-engineering gp120 to include glycan-dependent epitopesR01AI113893 · NIAID · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BERMAN, PHILLIP WAYNE · 2014 to 2017
$4.2M
NIAID NIH HHS R01 AI113893
6 · The paper itself

Abstract

The production of envelope glycoproteins (Envs) for use as HIV vaccines is challenging. The yield of Envs expressed in stable Chinese Hamster Ovary (CHO) cell lines is typically 10-100 fold lower than other glycoproteins of pharmaceutical interest. Moreover, Envs produced in CHO cells are typically enriched for sialic acid containing glycans compared to virus associated Envs that possess mainly high-mannose carbohydrates. This difference alters the net charge and biophysical properties of Envs and impacts their antigenic structure. Here we employ a novel robotic cell line selection strategy to address the problems of low expression. Additionally, we employed a novel gene-edited CHO cell line (MGAT1- CHO) to address the problems of high sialic acid content, and poor antigenic structure. We demonstrate that stable cell lines expressing high levels of gp120, potentially suitable for biopharmaceutical production can be created using the MGAT1- CHO cell line. Finally, we describe a MGAT1- CHO cell line expressing A244-rgp120 that exhibits improved binding of three major families of bN-mAbs compared to Envs produced in normal CHO cells. The new strategy described has the potential to eliminate the bottleneck in HIV vaccine development that has limited the field for more than 25 years.

Indexed as

Antibody FormationHigh-Throughput Screening AssaysRoboticsAIDS VaccinesAnimalsAntibodies, NeutralizingAutomation, LaboratoryCHO CellsCricetinaeCricetulusHEK293 CellsHIV-1HIV AntibodiesHumansAIDS VaccinesAntibodies, NeutralizingHIV Antibodies

Identifiers

PMID30071025
PMCPMC6071959
OpenAlexW2951570670

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.