Evidence map›Paper›PMID 34716460›Full record

ArticleApplied microbiology and biotechnology2021

Therapeutic efficacy of new botulinum toxin identified in CCUG 7968 strain.

Yeongduk An, Young-Je Kim, Chung-Sei Kim, Hyeona Yim, Myungseob Kim, Eui-Kyung Lee, Hyeon-Ji Oh, Jun-Hyeok Han, Eunseon Yoo, Sunghyun Kim and 4 more

Abstract read
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In one paragraph

Article in Applied microbiology and biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 4 institutions in 2 countries.

Yeongduk An *Department of Companion & Laboratory Animal Science, Experimental and Toxicologic Pathology, Kongju National University, 56 Gongju Daehak-ro, Chungnam, 32588, Republic of Korea.
Young-Je Kim *Research & Development Center, INIBIO Co., Ltd., Bucheon, Gyeonggi, 14445, Republic of Korea.
Chung-Sei KimResearch & Development Center, INIBIO Co., Ltd., Bucheon, Gyeonggi, 14445, Republic of Korea.
Hyeona YimResearch & Development Center, INIBIO Co., Ltd., Bucheon, Gyeonggi, 14445, Republic of Korea.
Myungseob KimSchool of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Eui-Kyung LeeSchool of Pharmacy, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Hyeon-Ji OhDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, 43 Jibong-ro, Wonmi-gu, Bucheon, Gyeonggi, 14662, Republic of Korea.
Jun-Hyeok HanDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, 43 Jibong-ro, Wonmi-gu, Bucheon, Gyeonggi, 14662, Republic of Korea.
Eunseon YooDepartment of Companion & Laboratory Animal Science, Experimental and Toxicologic Pathology, Kongju National University, 56 Gongju Daehak-ro, Chungnam, 32588, Republic of Korea.
Sunghyun KimDepartment of Companion & Laboratory Animal Science, Experimental and Toxicologic Pathology, Kongju National University, 56 Gongju Daehak-ro, Chungnam, 32588, Republic of Korea.
Joongseok WooDepartment of Companion & Laboratory Animal Science, Experimental and Toxicologic Pathology, Kongju National University, 56 Gongju Daehak-ro, Chungnam, 32588, Republic of Korea.
Edward R B MooreCulture Collection University of Gothenburg (CCUG), Sahlgrenska Academy of the University of Gothenburg, 41346, Gothenburg, Sweden.
Ji-Youn JungDepartment of Companion & Laboratory Animal Science, Experimental and Toxicologic Pathology, Kongju National University, 56 Gongju Daehak-ro, Chungnam, 32588, Republic of Korea. wangza@kongju.ac.kr.
Wooram ParkDepartment of Biomedical-Chemical Engineering, The Catholic University of Korea, 43 Jibong-ro, Wonmi-gu, Bucheon, Gyeonggi, 14662, Republic of Korea. wrpark@catholic.ac.kr.ORCID http://orcid.org/0000-0002-4614-0530
Kongju National University · KRCatholic University of Korea · KRSungkyunkwan University · KRUniversity of Gothenburg · SE

Funding

inibio co., ltd. INI101ministry of education, science and technology 2021R1A2C1010912
6 · The paper itself

Abstract

Botulinum neurotoxin type A (BoNT/A) induces muscle atrophy by cleaving synaptosomal-associated protein 25. Thus, BoNT/A has been actively utilized for the treatment of masseter and gastrocnemius hypertrophy. In this study, INI101 toxin was newly identified from the CCUG 7968 strain, and its therapeutic efficacy was evaluated both in vitro and in vivo. The INI101 toxin showed identical genetic sequence, amino acid sequence, and protein subunit composition to BoNT/A produced from strain Hall A. Electromyography (EMG), and immunofluorescence staining demonstrated that INI101 (at 2 ~ 8 U/rat) effectively blocked the neuromuscular junction with no toxicity in a rat model. The EMG results showed INI101 toxin-induced weight loss and volume reduction of the gastrocnemius, similar to the effects of Botox® (BTX). Histological and immunofluorescence staining was consistent with this EMG result, showing that INI101 toxin caused muscle fiber reduction in the gastrocnemius. Notably, INI101 toxin diffused less into adjacent muscle tissue than BTX, indicating that INI101 toxin may reduce potential side effects due to diffusion into normal tissues. INI101 toxin isolated from the novel strain CCUG 7968 is a newly identified meaningful biopharmaceutical comparable to the conventional BoNT/A in the medical field. KEY POINTS: • Botulinum neurotoxin type A (BoNT/A, INI101) was identified from the CCUG 7968 strain. • INI101 toxin showed similar safety and therapeutic efficacy comparable to conventional BoNT/A both in vitro and in vivo. • INI101 toxin is a meaningful biopharmaceutical comparable to the conventional BoNT/A in the medical field.

Indexed as

Botulinum Toxins, Type AAmino Acid SequenceAnimalsMuscle, SkeletalRatsBotulinum Toxins, Type AATCC19397Botulinum neurotoxin type ACCUG7968Compound muscle action potentialDystrophinMuscle contractionNeural cell adhesion moleculeNeuromuscular junction

Identifiers

PMID34716460
OpenAlexW3210574243

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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.