Evidence map›Paper›PMID 36656048›Full record

ArticleHuman vaccines & immunotherapeutics2023

Epitope-based precision immunotherapy of Type 1 diabetes.

Rebuma Firdessa Fite, Camillo Bechi Genzano, Roberto Mallone, Remi J Creusot

Open access · goldAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2023. 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
4.1field-weighted citation impact, top 6% 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, 13 citations in OpenAlex.

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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 2 institutions in 2 countries.

Rebuma Firdessa FiteColumbia Center for Translational Immunology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Camillo Bechi GenzanoColumbia Center for Translational Immunology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Roberto MalloneUniversité Paris Cité, Institut Cochin, CNRS, INSERM, Paris, France.
Remi J CreusotColumbia Center for Translational Immunology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-8328-8155
Columbia University Irving Medical Center · USCentre National de la Recherche Scientifique · FR

Funding

In vivo development and reactivity of human autoreactive T cellsR01AI142428 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CREUSOT, REMI J · 2019 to 2023
$2.0M
Tissue-engineered lymph node stroma to study peripheral tolerance in autoimmune diabetesR56AI151217 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TOMEI, ALICE · 2021 to 2021
$433k
Unraveling the tolerogenic potential of lymph node fibroblastic reticular networks in autoimmune diabetesR56DK131087 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CREUSOT, REMI J, TOMEI, ALICE · 2022 to 2023
$332k
NIAID NIH HHS R01 AI142428NIAID NIH HHS R56 AI151217NIDDK NIH HHS R56 DK131087
6 · The paper itself

Abstract

Antigen-specific immunotherapies (ASITs) address important clinical needs in treating autoimmune diseases. However, Type 1 diabetes is a heterogeneous disease wherein patient characteristics influence responsiveness to ASITs. Targeting not only disease-relevant T cell populations, but also specific groups of patients using precision medicine is a new goal toward achieving effective treatment. HLA-restricted peptides provide advantages over protein as antigens, however, methods for profiling antigen-specific T cells need to improve in sensitivity, depth, and throughput to facilitate epitope selection. Delivery approaches are highly diverse, illustrating the many ways relevant antigen-presenting cell populations and anatomical locations can be targeted for tolerance induction. The role of persistence of antigen presentation in promoting durable antigen-specific tolerance requires further investigation. Based on the outcome of ASIT trials, the field is moving toward using patient-specific variations to improve efficacy, but challenges still lie on the path to delivering more effective and safer treatment to the T1D patient population.

Indexed as

Autoimmune DiseasesDiabetes Mellitus, Type 1AntigensEpitopesHumansImmunotherapyAntigensEpitopesantigen-specific therapyantigen-specific toleranceendotypeepitopeprecision medicineType 1 diabetes

Identifiers

PMID36656048
PMCPMC9980607
OpenAlexW4317434159

What OpenQuestion holds

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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.