Evidence map›Paper›PMID 34743292›Full record

ReviewMolecular neurobiology2022

Dendritic Cell-Targeted Therapies to Treat Neurological Disorders.

Asim Hussain, Hamza Rafeeq, Nimra Munir, Zara Jabeen, Nadia Afsheen, Khalil Ur Rehman, Muhammad Bilal, Hafiz M N Iqbal

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2022. 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
0.4field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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  6. 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

8 authors at 4 institutions in 3 countries.

Asim HussainDepartment of Biochemistry, Riphah International University, Faisalabad, 38040, Pakistan.
Hamza RafeeqDepartment of Biochemistry, Riphah International University, Faisalabad, 38040, Pakistan.
Nimra MunirDepartment of Biochemistry, University of Agriculture, Faisalabad, 38040, Pakistan.
Zara JabeenDepartment of Biochemistry, Riphah International University, Faisalabad, 38040, Pakistan.
Nadia AfsheenDepartment of Biochemistry, Riphah International University, Faisalabad, 38040, Pakistan.
Khalil Ur RehmanDepartment of Biochemistry, Riphah International University, Faisalabad, 38040, Pakistan.
Muhammad BilalSchool of Life Science and Food Engineering, Huaiyin Institute of Technology, Huaian, 223003, China. bilaluaf@hyit.edu.cn.
Hafiz M N IqbalTecnologico de Monterrey, School of Engineering and Sciences, 64849, Monterrey, Mexico. hafiz.iqbal@tec.mx.
Riphah International University · PKHuaiyin Institute of Technology · CNTecnológico de Monterrey · MXUniversity of Agriculture Faisalabad · PK

Funding

sistema nacional de investigadores CVU: 735340
6 · The paper itself

Abstract

Dendritic cells (DCs) are the immune system's highly specialized antigen-presenting cells. When DCs are sluggish and mature, self-antigen presentation results in tolerance; however, when pathogen-associated molecular patterns stimulate mature DCs, antigen presentation results in the development of antigen-specific immunity. DCs have been identified in various vital organs of mammals (e.g., the skin, heart, lungs, intestines, and spleen), but the brain has long been thought to be devoid of DCs in the absence of neuroinflammation. However, neuroinflammation is becoming more recognized as a factor in a variety of brain illnesses. DCs are present in the brain parenchyma in trace amounts under healthy circumstances, but their numbers rise during neuroinflammation. New therapeutics are being developed that can reduce dendritic cell immunogenicity by inhibiting pro-inflammatory cytokine production and T cell co-stimulatory pathways. Additionally, innovative ways of regulating dendritic cell growth and differentiation and harnessing their tolerogenic capability are being explored. Herein, we described the function of dendritic cells in neurological disorders and discussed the potential for future therapeutic techniques that target dendritic cells and dendritic cell-related targets in the treatment of neurological disorders.

Indexed as

Drug Delivery SystemsImmune ToleranceAnimalsDendritic CellsHumansNervous System DiseasesDendritic cellsDendritic cell–targeted therapiesDisease-specific therapiesDrug delivery systemsNeurological disorders

Identifiers

PMID34743292
OpenAlexW3211876787

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.