Evidence map›Paper›PMID 37771574›Full record

ArticleFrontiers in bioengineering and biotechnology2023

VNAR development through antigen immunization of Japanese topeshark (

Hiroyuki Takeda, Tatsuhiko Ozawa, Hiroki Zenke, Yoh Ohnuki, Yuri Umeda, Wei Zhou, Honoka Tomoda, Akihiko Takechi, Kimiyoshi Narita, Takaaki Shimizu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 11 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 4 institutions in 1 country.

Hiroyuki Takeda *Proteo-Science Center, Ehime University, Matsuyama, Japan.
Tatsuhiko Ozawa *Department of Immunology, Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.
Hiroki ZenkeProteo-Science Center, Ehime University, Matsuyama, Japan.
Yoh OhnukiDepartment of Immunology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Yuri UmedaProteo-Science Center, Ehime University, Matsuyama, Japan.
Wei ZhouProteo-Science Center, Ehime University, Matsuyama, Japan.
Honoka TomodaFisheries Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Iyo, Japan.
Akihiko TakechiFisheries Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Iyo, Japan.
Kimiyoshi NaritaFisheries Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Iyo, Japan.
Takaaki ShimizuFisheries Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Iyo, Japan.
Takuya MiyakawaGraduate School of Biostudies, Kyoto University, Kyoto, Japan.
Yuji ItoGraduate School of Science and Engineering, Kagoshima University, Kagoshima, Japan.
Tatsuya SawasakiProteo-Science Center, Ehime University, Matsuyama, Japan.
Ehime University · JPUniversity of Toyama · JPKagoshima University · JPKyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The VNAR (Variable New Antigen Receptor) is the smallest single-domain antibody derived from the variable domain of IgNAR of cartilaginous fishes. Despite its biomedical and diagnostic potential, research on VNAR has been limited due to the difficulties in obtaining and maintaining immune animals and the lack of research tools. In this study, we investigated the Japanese topeshark as a promising immune animal for the development of VNAR. This shark is an underutilized fishery resource readily available in East Asia coastal waters and can be safely handled without sharp teeth or venomous stingers. The administration of Venus fluorescent protein to Japanese topesharks markedly increased antigen-specific IgM and IgNAR antibodies in the blood. Both the phage-display library and the yeast-display library were constructed using RNA from immunized shark splenocytes. Each library was enriched by biopanning, and multiple antigen-specific VNARs were acquired. The obtained antibodies had affinities of 1 × 10

Indexed as

biopanningdeep sequencingJapanese topesharkphage displayVNARyeast display

Identifiers

PMID37771574
PMCPMC10522858
OpenAlexW4386723793

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.