Evidence map›Paper›PMID 24945244›Full record

ArticlePLoS pathogens2014

Protective efficacy of passive immunization with monoclonal antibodies in animal models of H5N1 highly pathogenic avian influenza virus infection.

Yasushi Itoh, Reiko Yoshida, Shintaro Shichinohe, Megumi Higuchi, Hirohito Ishigaki, Misako Nakayama, Van Loi Pham, Hideaki Ishida, Mitsutaka Kitano, Masahiko Arikata and 16 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. 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
3.2field-weighted citation impact, top 8% 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, 32 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

26 authors at 5 institutions in 3 countries.

Yasushi ItohDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Reiko YoshidaDivision of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Shintaro ShichinoheLaboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Megumi HiguchiDivision of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Hirohito IshigakiDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Misako NakayamaDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Van Loi PhamDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Hideaki IshidaDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Mitsutaka KitanoDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan; Infectious Diseases, Medicinal Research Laboratories, Shionogi & Co., Ltd., Toyonaka, Osaka, Japan.
Masahiko ArikataDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Naoko KitagawaDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Yachiyo MitsuishiDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Kazumasa OgasawaraDepartment of Pathology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Hideaki TsuchiyaResearch Center for Animal Life Science, Shiga University of Medical Science, Otsu, Shiga, Japan.
Takahiro HionoLaboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Masatoshi OkamatsuLaboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Yoshihiro SakodaLaboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Hiroshi KidaLaboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Mutsumi ItoDivision of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Le Quynh MaiNational Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Yoshihiro KawaokaDivision of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan; Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin, United States of America.
Hiroko MiyamotoDivision of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Mari IshijimaDivision of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Manabu IgarashiDivision of Bioinformatics, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Yasuhiko SuzukiDivision of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Ayato TakadaDivision of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Japan.
Hokkaido University · JPShiga University of Medical Science · JPNational Institute Of Hygiene And Epidemiology · VNShionogi (Japan) · JPUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Highly pathogenic avian influenza (HPAI) viruses of the H5N1 subtype often cause severe pneumonia and multiple organ failure in humans, with reported case fatality rates of more than 60%. To develop a clinical antibody therapy, we generated a human-mouse chimeric monoclonal antibody (MAb) ch61 that showed strong neutralizing activity against H5N1 HPAI viruses isolated from humans and evaluated its protective potential in mouse and nonhuman primate models of H5N1 HPAI virus infections. Passive immunization with MAb ch61 one day before or after challenge with a lethal dose of the virus completely protected mice, and partial protection was achieved when mice were treated 3 days after the challenge. In a cynomolgus macaque model, reduced viral loads and partial protection against lethal infection were observed in macaques treated with MAb ch61 intravenously one and three days after challenge. Protective effects were also noted in macaques under immunosuppression. Though mutant viruses escaping from neutralization by MAb ch61 were recovered from macaques treated with this MAb alone, combined treatment with MAb ch61 and peramivir reduced the emergence of escape mutants. Our results indicate that antibody therapy might be beneficial in reducing viral loads and delaying disease progression during H5N1 HPAI virus infection in clinical cases and combined treatment with other antiviral compounds should improve the protective effects of antibody therapy against H5N1 HPAI virus infection.

Indexed as

Acids, CarbocyclicAnimalsAntibodies, Monoclonal, HumanizedAntibodies, Monoclonal, Murine-DerivedAntibodies, NeutralizingAntibodies, ViralAntiviral AgentsCell LineCyclopentanesDogsDrug Therapy, CombinationFemaleGuanidinesImmunization, PassiveImmunocompromised HostInfluenza A Virus, H5N1 SubtypeAcids, CarbocyclicAntibodies, Monoclonal, HumanizedAntibodies, Monoclonal, Murine-DerivedAntibodies, NeutralizingAntibodies, ViralAntiviral AgentsCyclopentanesGuanidinesInterleukin-6Neuraminidaseperamivir

Identifiers

PMID24945244
PMCPMC4055766
OpenAlexW2120666666

What OpenQuestion holds

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LicenceCC BY
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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.