Evidence map›Paper›PMID 36839774›Full record

ReviewPharmaceutics2023

Peptide Vaccines in Melanoma: Chemical Approaches towards Improved Immunotherapeutic Efficacy.

Beáta Biri-Kovács, Zoltán Bánóczi, Anitha Tummalapally, Ildikó Szabó

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Peptide vaccines get an OS update.Nature chemical biology · 2024
    Article
  9. 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

4 authors at 1 institution in 1 country.

Beáta Biri-KovácsELKH-ELTE Research Group of Peptide Chemistry, 1117 Budapest, Hungary.
Zoltán BánócziELKH-ELTE Research Group of Peptide Chemistry, 1117 Budapest, Hungary.ORCID 0000-0003-1880-4042
Anitha TummalapallyELKH-ELTE Research Group of Peptide Chemistry, 1117 Budapest, Hungary.
Ildikó SzabóELKH-ELTE Research Group of Peptide Chemistry, 1117 Budapest, Hungary.
Eötvös Loránd University · HU

Funding

János Bolyai research grant of the Hungarian Academy of Sciences BO/00381/22Lendület (Momentum) Programme of the Hungarian Academy of Sciences LENDULET_2021-28New National Excellence Program Bolyai+ ÚNKP-22-5-ELTE-1157
6 · The paper itself

Abstract

Cancer of the skin is by far the most common of all cancers. Although the incidence of melanoma is relatively low among skin cancers, it can account for a high number of skin cancer deaths. Since the start of deeper insight into the mechanisms of melanoma tumorigenesis and their strong interaction with the immune system, the development of new therapeutical strategies has been continuously rising. The high number of melanoma cell mutations provides a diverse set of antigens that the immune system can recognize and use to distinguish tumor cells from normal cells. Peptide-based synthetic anti-tumor vaccines are based on tumor antigens that elicit an immune response due to antigen-presenting cells (APCs). Although targeting APCs with peptide antigens is the most important assumption for vaccine development, peptide antigens alone are poorly immunogenic. The immunogenicity of peptide antigens can be improved not only by synthetic modifications but also by the assistance of adjuvants and/or delivery systems. The current review summarizes the different chemical approaches for the development of effective peptide-based vaccines for the immunotherapeutic treatment of advanced melanoma.

Indexed as

adjuvantsimmunotherapymelanomananoparticlespeptide antigenspeptide-based vaccines

Identifiers

PMID36839774
PMCPMC9963291
OpenAlexW4318480244

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.