Evidence map›Paper›PMID 26441930›Full record

ArticleFrontiers in microbiology2015

Pichia pastoris-expressed dengue 3 envelope-based virus-like particles elicit predominantly domain III-focused high titer neutralizing antibodies.

Lav Tripathi, Shailendra Mani, Rajendra Raut, Ankur Poddar, Poornima Tyagi, Upasana Arora, Aravinda de Silva, Sathyamangalam Swaminathan, Navin Khanna

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  5. Bioengineering (Basel, Switzerland) · 2021
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  17. Frontiers in microbiology · 2017
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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

9 authors.

Lav TripathiRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India.
Shailendra ManiRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India.
Rajendra RautRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India.
Ankur PoddarRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India.
Poornima TyagiRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India.
Upasana AroraRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India.
Aravinda de SilvaDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC USA.
Sathyamangalam SwaminathanDepartment of Biological Sciences, Birla Institute of Technology and Sciences, Hyderabad India.
Navin KhannaRecombinant Gene Products Group, International Centre for Genetic Engineering and Biotechnology, New Delhi India ; Translational Health Science and Technology Institute, NCR Biotech Science Cluster, Faridabad India ; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue poses a serious public health risk to nearly half the global population. It causes ~400 million infections annually and is considered to be one of the fastest spreading vector-borne diseases. Four distinct serotypes of dengue viruses (DENV-1, -2, -3, and -4) cause dengue disease, which may be either mild or extremely severe. Antibody-dependent enhancement (ADE), by pre-existing cross-reactive antibodies, is considered to be the major mechanism underlying severe disease. This mandates that a preventive vaccine must confer simultaneous and durable immunity to each of the four prevalent DENV serotypes. Recently, we used Pichia pastoris, to express recombinant DENV-2 E ectodomain, and found that it assembled into virus-like particles (VLPs), in the absence of prM, implicated in the elicitation of ADE-mediating antibodies. These VLPs elicited predominantly type-specific neutralizing antibodies that conferred significant protection against lethal DENV-2 challenge, in a mouse model. The current work is an extension of this approach to develop prM-lacking DENV-3 E VLPs. Our data reveal that P. pastoris-produced DENV-3 E VLPs not only preserve the antigenic integrity of the major neutralizing epitopes, but also elicit potent DENV-3 virus-neutralizing antibodies. Further, these neutralizing antibodies appear to be exclusively directed toward domain III of the DENV-3 E VLPs. Significantly, they also lack discernible ADE potential toward heterotypic DENVs. Taken together with the high productivity of the P. pastoris expression system, this approach could potentially pave the way toward developing a DENV E-based, inexpensive, safe, and efficacious tetravalent sub-unit vaccine, for use in resource-poor dengue endemic countries.

Indexed as

antibody-dependent enhancement (ADE)denguedengue envelopedengue vaccineneutralizing antibodyPichia pastorisvirus-like particle (VLP)

Identifiers

PMID26441930
PMCPMC4585145

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LicenceCC BY
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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.