Evidence map›Paper›PMID 36528644›Full record

ArticleNPJ vaccines2022

Multivalent viral particles elicit safe and efficient immunoprotection against Nipah Hendra and Ebola viruses.

Duncan G Ithinji, David W Buchholz, Shahrzad Ezzatpour, I Abrrey Monreal, Yu Cong, Julie Sahler, Amandip Singh Bangar, Brian Imbiakha, Viraj Upadhye, Janie Liang and 15 more

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  8. CRISPR/Cas system and its application in the diagnosis of animal infectious diseases.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
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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

25 authors at 4 institutions in 2 countries.

Duncan G IthinjiSchool for Global Animal Health, Washington State University, Pullman, WA, USA.
David W Buchholz *Department of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0001-8874-6648
Shahrzad Ezzatpour *Department of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
I Abrrey Monreal *Department of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0003-0521-9063
Yu CongNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.ORCID http://orcid.org/0000-0001-5037-0729
Julie SahlerDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Amandip Singh BangarDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Brian ImbiakhaDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Viraj UpadhyeDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Janie LiangNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.
Andrew MaDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0002-6344-5950
Birgit Bradel-TrethewaySchool for Global Animal Health, Washington State University, Pullman, WA, USA.
Benjamin KazaDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Yao Yu YeoDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0002-7604-2296
Eun Jin ChoiDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Gunner P JohnstonDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Louis HuzellaNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.
Erin KollinsNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.
Saurabh DixitNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.
Shuiqing YuNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.
Elena PostnikovaNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.
Victoria OrtegaDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Avery AugustDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA.
Michael R HolbrookNational Institute of Allergy and Infectious Diseases (NIAID) Integrated Research Facility, Ft Detrick, Frederick, MD, 21702, USA.ORCID http://orcid.org/0000-0002-0824-2667
Hector C AguilarDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY, USA. ha363@cornell.edu.ORCID http://orcid.org/0000-0001-6879-8360
Cornell University · USNational Institute of Allergy and Infectious Diseases · USKenya Agricultural and Livestock Research Organization · KEWashington State University · US

Funding

Mechanisms of Nipah virus fusion and entryR01AI109022 · NIAID · WASHINGTON STATE UNIVERSITY · PI AGUILAR-CARRENO, HECTOR · 2014 to 2024
$4.3M
Identifying potent and broadly-neutralizing henipaviral antigens and epitopesR21AI142377 · NIAID · CORNELL UNIVERSITY · PI AGUILAR-CARRENO, HECTOR · 2019 to 2020
$416k
NIAID NIH HHS HHSN272201800013CNIAID NIH HHS R01 AI109022NIAID NIH HHS R21 AI142377
6 · The paper itself

Abstract

Experimental vaccines for the deadly zoonotic Nipah (NiV), Hendra (HeV), and Ebola (EBOV) viruses have focused on targeting individual viruses, although their geographical and bat reservoir host overlaps warrant creation of multivalent vaccines. Here we explored whether replication-incompetent pseudotyped vesicular stomatitis virus (VSV) virions or NiV-based virus-like particles (VLPs) were suitable multivalent vaccine platforms by co-incorporating multiple surface glycoproteins from NiV, HeV, and EBOV onto these virions. We then enhanced the vaccines' thermotolerance using carbohydrates to enhance applicability in global regions that lack cold-chain infrastructure. Excitingly, in a Syrian hamster model of disease, the VSV multivalent vaccine elicited safe, strong, and protective neutralizing antibody responses against challenge with NiV, HeV, or EBOV. Our study provides proof-of-principle evidence that replication-incompetent multivalent viral particle vaccines are sufficient to provide protection against multiple zoonotic deadly viruses with high pandemic potential.

Identifiers

PMID36528644
PMCPMC9759047
OpenAlexW4311718451

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.