Evidence map›Paper›PMID 38752002›Full record

ArticleClinical and experimental vaccine research2024

Immunoinformatics studies and design of a novel multi-epitope peptide vaccine against

Ali Dalir Ghaffari, Fardin Rahimi

Abstract read
In one paragraph

Article in Clinical and experimental vaccine research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Computational vaccine development against protozoa.Computational and structural biotechnology journal · 2025
    Review
  2. Sialic Acid-Binding Protein-1 (SABP1) ofJournal of parasitology research · 2025
    Article
  3. Article
  4. Evaluation ofRecent advances in inflammation & allergy drug discovery · 2025
    Article
  5. 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

2 authors.

Ali Dalir GhaffariDepartment of Parasitology and Mycology, Faculty of Medicine, Shahed University, Tehran, Iran.ORCID https://orcid.org/0000-0001-9635-2876
Fardin RahimiDepartment of Medical biotechnology, Faculty of Medicine, Shahed University, Tehran, Iran.ORCID https://orcid.org/0000-0002-4165-3417

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Infection by the intracellular apicomplexan parasite Materials and Methods: Top-ranked major histocompatibility complex (MHC)-I and MHC-II binding as well as shared, immunodominant linear B-cell epitopes were predicted and linked using appropriate linkers. Moreover, the 50S ribosomal protein L7/L12 (adjuvant) was mixed with the construct's N-terminal to increase the immunogenicity. Then, the vaccine's physicochemical characteristics, antigenicity, allergenicity, secondary and tertiary structure were predicted. Results: The finally-engineered chimeric vaccine had a length of 680 amino acids with a molecular weight of 74.66 kDa. Analyses of immunogenicity, allergenicity, and multiple physiochemical parameters indicated that the constructed vaccine candidate was soluble, non-allergenic, and immunogenic, making it compatible with humans and hence, a potentially viable and safe vaccine candidate against Conclusion:

Indexed as

CDPK1CDPK2CDPK3CDPK5ImmunoinformaticsIn silicoToxoplasma gondii

Identifiers

PMID38752002
PMCPMC11091428

What OpenQuestion holds

Textmetadata
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.