Evidence map›Paper›PMID 36629456›Full record

ReviewExpert opinion on drug delivery2023

Drug delivery targets and strategies to address mast cell diseases.

Clayton H Rische, Ariel N Thames, Rebecca A Krier-Burris, Jeremy A O'Sullivan, Bruce S Bochner, Evan A Scott

Abstract readReview
In one paragraph

Review in Expert opinion on drug delivery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

6 authors.

Clayton H RischeDepartment of Biomedical Engineering, Northwestern University McCormick School of Engineering, Evanston, IL, USA.
Ariel N ThamesMedical Scientist Training Program, Northwestern University, Feinberg School of Medicine, Chicago, USA.ORCID 0000-0001-5418-6048
Rebecca A Krier-BurrisDivision of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Jeremy A O'SullivanDivision of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Bruce S BochnerDivision of Allergy and Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Evan A ScottDepartment of Biomedical Engineering, Northwestern University McCormick School of Engineering, Evanston, IL, USA.ORCID 0000-0002-8945-2892

Funding

Exploiting Siglec-6 for targeted anti-allergy drug delivery into human mast cellsR21AI159586 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BOCHNER, BRUCE S, SCOTT, EVAN ALEXANDER · 2021 to 2022
$417k
NIAID NIH HHS R21 AI159586
6 · The paper itself

Abstract

introductionCurrent and developing mast cell therapeutics are reliant on small molecule drugs and biologics, but few are truly selective for mast cells. Most have cellular and disease-specific limitations that require innovation to overcome longstanding challenges to selectively targeting and modulating mast cell behavior. This review is designed to serve as a frame of reference for new approaches that utilize nanotechnology or combine different drugs to increase mast cell selectivity and therapeutic efficacy. AREAS COVERED: Mast cell diseases include allergy and related conditions as well as malignancies. Here, we discuss the targets of existing and developing therapies used to treat these disease pathologies, classifying them into cell surface, intracellular, and extracellular categories. For each target discussed, we discuss drugs that are either the current standard of care, under development, or have indications for potential use. Finally, we discuss how novel technologies and tools can be used to take existing therapeutics to a new level of selectivity and potency against mast cells. EXPERT OPINION: There are many broadly and very few selectively targeted therapeutics for mast cells in allergy and malignant disease. Combining existing targeting strategies with technology like nanoparticles will provide novel platforms to treat mast cell disease more selectively.

Indexed as

Biological ProductsHypersensitivityMast Cell Activation DisordersNeoplasmsDrug Delivery SystemsHumansMast CellsBiological Productsallergycancercell targetingMast cellsmastocytosisnanoparticles

Identifiers

PMID36629456
PMCPMC9928520

What OpenQuestion holds

Textmetadata
LicenceTDM
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.