Evidence map›Paper›PMID 35909472›Full record

ArticleBioMed research international2022

Anti-Metalloprotease P-I Single-Domain Antibodies: Tools for Next-Generation Snakebite Antivenoms.

Marcela C S Silva, Soraya S Pereira, Marilia P Gouveia, Marcos B Luiz, Rosa M O Sousa, Anderson M Kayano, Aleff F Francisco, Nidiane D R Prado, Leandro S M Dill, Marcos R M Fontes and 5 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
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

15 authors at 3 institutions in 1 country.

Marcela C S SilvaFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0002-8238-4225
Soraya S PereiraFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0003-2116-7670
Marilia P GouveiaFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0001-6406-3914
Marcos B LuizFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0001-7879-6932
Rosa M O SousaFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0001-9754-6947
Anderson M KayanoFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0003-4418-7850
Aleff F FranciscoDepartamento de Biofísica e Farmacologia, Instituto de Biociências, UNESP, Botucatu, 18618-689 São Paulo, Brazil.ORCID https://orcid.org/0000-0002-6492-5729
Nidiane D R PradoFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0002-4771-6917
Leandro S M DillFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0003-2977-0001
Marcos R M FontesDepartamento de Biofísica e Farmacologia, Instituto de Biociências, UNESP, Botucatu, 18618-689 São Paulo, Brazil.ORCID https://orcid.org/0000-0002-4634-6221
Fernando B ZanchiFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0003-3386-0069
Rodrigo G StabeliPlataforma Bi-Institucional Fiocruz-USP, Ribeirão Preto, 14040-030 São Paulo, Brazil.ORCID https://orcid.org/0000-0002-0476-920X
Andreimar M SoaresFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0003-1032-2188
Juliana P ZulianiFundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, 76812-245 Rondônia, Brazil.ORCID https://orcid.org/0000-0001-9221-7749
Carla F C FernandesFundação Oswaldo Cruz, Fiocruz Ceará, Eusébio, 61760-000 Ceará, Brazil.ORCID https://orcid.org/0000-0001-8586-2782
Universidade Federal de Rondônia · BRUniversidade Estadual Paulista (Unesp) · BRFundação Oswaldo Cruz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to address the global antivenom crisis, novel antivenoms need to present high therapeutic efficacy, broad neutralization ability against systemic and local damage, sufficient safety, and cost-effectiveness. Due to biological characteristics of camelid single-domain antibodies (VHH) such as high affinity, their ability to penetrate dense tissues, and facility for genetic manipulation, their application in antivenoms has expanded considerably. VHHs that are active against the metalloprotease BjussuMP-II from the snake

Indexed as

BothropsCrotalid VenomsSingle-Domain AntibodiesSnake BitesAnimalsAntiveninsMetalloproteasesMolecular Docking SimulationNeutralization TestsAntiveninsCrotalid VenomsMetalloproteasesSingle-Domain Antibodies

Identifiers

PMID35909472
PMCPMC9325618
OpenAlexW4286213940

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.