Evidence mapPaperPMID 35336018Full record

ReviewPharmaceutics2022

Nanotechnology in Immunotherapy for Type 1 Diabetes: Promising Innovations and Future Advances.

Saumya Nigam, Jack Owen Bishop, Hanaan Hayat, Tahnia Quadri, Hasaan Hayat, Ping Wang

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

6 authors at 1 institution in 1 country.

Saumya NigamPrecision Health Program, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0003-1845-5049
Jack Owen BishopPrecision Health Program, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0001-9068-1986
Hanaan HayatPrecision Health Program, Michigan State University, East Lansing, MI 48824, USA.
Tahnia QuadriPrecision Health Program, Michigan State University, East Lansing, MI 48824, USA.
Hasaan HayatPrecision Health Program, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0001-9294-1016
Ping WangPrecision Health Program, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0001-6712-8939
Michigan State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes is a chronic condition which affects the glucose metabolism in the body. In lieu of any clinical "cure," the condition is managed through the administration of pharmacological aids, insulin supplements, diet restrictions, exercise, and the like. The conventional clinical prescriptions are limited by their life-long dependency and diminished potency, which in turn hinder the patient's recovery. This necessitated an alteration in approach and has instigated several investigations into other strategies. As Type 1 diabetes (T1D) is known to be an autoimmune disorder, targeting the immune system in activation and/or suppression has shown promise in reducing beta cell loss and improving insulin levels in response to hyperglycemia. Another strategy currently being explored is the use of nanoparticles in the delivery of immunomodulators, insulin, or engineered vaccines to endogenous immune cells. Nanoparticle-assisted targeting of immune cells holds substantial potential for enhanced patient care within T1D clinical settings. Herein, we summarize the knowledge of etiology, clinical scenarios, and the current state of nanoparticle-based immunotherapeutic approaches for Type 1 diabetes. We also discuss the feasibility of translating this approach to clinical practice.

Indexed as

autoimmunityB cellsbeta cellscell therapyimmune checkpoint moleculesimmunotherapymicroRNAnanoparticlesstem cellsT cellstype 1 diabetes

Identifiers

PMID35336018
PMCPMC8955746
OpenAlexW4221011747

What Socratic 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 Socratic graph.