Evidence map›Paper›PMID 38720922›Full record

ReviewADMET & DMPK2024

Understanding yeast shells: structure, properties and applications.

Larissa Silva de Macêdo, Samara Sousa de Pinho, Anna Jéssica Duarte Silva, Ingrid Andrêssa de Moura, Benigno Cristofer Flores Espinoza, Maria da Conceição Viana Invenção, Pedro Vinícius Silva Novis, Marco Antonio Turiah Machado da Gama, Matheus do Nascimento Carvalho, Lígia Rosa Sales Leal and 4 more

Abstract readReview
In one paragraph

Review in ADMET & DMPK, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Vaccines · 2024
    Article
  6. 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

14 authors.

Larissa Silva de MacêdoLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Samara Sousa de PinhoLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Anna Jéssica Duarte SilvaLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Ingrid Andrêssa de MouraLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Benigno Cristofer Flores EspinozaLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Maria da Conceição Viana InvençãoLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Pedro Vinícius Silva NovisLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Marco Antonio Turiah Machado da GamaLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Matheus do Nascimento CarvalhoLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Lígia Rosa Sales LealLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Bruna Isabel Santos CruzLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Beatriz Mendonça Alves BandeiraLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Vanessa Emanuelle Pereira SantosLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.
Antonio Carlos de FreitasLaboratory of Molecular Studies and Experimental Therapy - LEMTE; Department of Genetics, Biosciences Center, Federal University of Pernambuco; Pernambuco - Recife 50670-901, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: The employment of yeasts for biomedical purposes has become increasingly frequent for the delivery of prophylactic and therapeutic products. Its structural components, such as β-glucans, mannan, and chitin, can be explored as immunostimulators that show safety and low toxicity. Besides, this system minimizes antigen degradation after administration, facilitating the delivery to the target cells. Review approach: This review sought to present molecules derived from yeast, called yeast shells (YS), and their applications as carrier vehicles for drugs, proteins, and nucleic acids for immunotherapy purposes. Furthermore, due to the diversity of information regarding the production and immunostimulation of these compounds, a survey of the protocols and immune response profiles generated was presented. Key results: The use of YS has allowed the development of strategies that combine efficiency and effectiveness in antigen delivery. The capsular structure can be recognized and phagocytized by dendritic cells and macrophages. In addition, the combination with different molecules, such as nanoparticles or even additional adjuvants, improves the cargo loading, enhancing the system. Activation by specific immune pathways can also be achieved by different administration routes. Conclusion: Yeast derivatives combined in different ways can increase immunostimulation, enhancing the delivery of medicines and vaccine antigens. These aspects, combined with the simplicity of the production steps, make these strategies more accessible to be applied in the prevention and treatment of various diseases.

Indexed as

delivery vehicleencapsulationimmunostimulatorNanocapsulesβ-glucans

Identifiers

PMID38720922
PMCPMC11075163

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.