Evidence map›Paper›PMID 31863125›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2020

Modification of the RANKL-RANK-binding site for the immunotherapeutic treatment of osteoporosis.

Y Ko, G Lee, B Kim, M Park, Y Jang, W Lim

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Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. The Role of Rosavin in the Pathophysiology of Bone Metabolism.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Inhibition of RANKL-Induced Osteoclastogenesis by Novel Mutant RANKL.International journal of molecular sciences · 2021
    Article
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

6 authors at 2 institutions in 1 country.

Y KoDepartment of Orthopaedic Surgery, Chosun University Hospital, Gwangju, 61453, South Korea.
G LeeDepartment of Orthopaedic Surgery, Chosun University Hospital, Gwangju, 61453, South Korea.
B KimDepartment of Orthopaedic Surgery, Chosun University Hospital, Gwangju, 61453, South Korea.
M ParkDepartment of Orthopaedic Surgery, Chosun University Hospital, Gwangju, 61453, South Korea.
Y JangDepartment of Orthopaedic Surgery, Chosun University Hospital, Gwangju, 61453, South Korea.
W LimDepartment of Orthopaedic Surgery, Chosun University Hospital, Gwangju, 61453, South Korea. wonbong@chosun.ac.kr.
Chosun University Hospital · KRChosun University · KR

Funding

The National Research Foundation of Korea (NRF) 2017R1D1A3B03031764The National Research Foundation of Korea (NRF) 2018R1D1A1B07047024
6 · The paper itself

Abstract

Here, we proposed the use of mutated RANKL as an immunogen for active immunization and to induce anti-cytokine antibodies for osteoporosis treatment.

introductionOsteoclasts are responsible for bone resorption in bone-related disorders. Anti-cytokine therapeutic antibodies such as denosumab are effective for the treatment of osteoporosis. However, problems with antibody manufacturing and the immunogenicity caused by multiple antibody doses have led to the use of auto-cytokines as immunogens to induce anti-cytokine antibodies.

methodsRANKL was point-mutated based on the crystal structure of the complex of RANKL and its receptor RANK.

resultsAs a proof of concept, immunization with RANKL produced high levels of specific antibodies and blocked osteoclast development in vitro and inhibited osteoporosis in RANKL-treated or ovariectomized mouse models.

conclusionsThe results demonstrate the successful use of mutated RANKL as an immunogen for the induction of anti-RANKL immune response. This strategy is useful in general anti-cytokine immunotherapy to avoid toxic side effects of osteoporosis treatment.

Indexed as

Bone ResorptionOsteoporosisAnimalsBinding SitesImmunotherapyMiceOsteoclastsRANK LigandRANK LigandImmune therapyMutated RANKLOsteoclastOsteoporosisRANK

Identifiers

PMID31863125
OpenAlexW2996215004

What OpenQuestion holds

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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.