Evidence map›Paper›PMID 42287230›Full record

ReviewJournal of medicinal chemistry2026

Beyond α-GalCer: Medicinal Chemistry Insights Driving Structural Evolution of CD1d Ligands.

Emiliano Paradiso, Žiga Jakopin

Abstract readReview
In one paragraph

Review in Journal of medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Emiliano ParadisoFaculty of Pharmacy, University of Ljubljana, Ljubljana SI-1000, Slovenia.ORCID 0009-0002-8548-5520
Žiga JakopinFaculty of Pharmacy, University of Ljubljana, Ljubljana SI-1000, Slovenia.ORCID 0000-0001-9384-0858

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD1d-restricted glycolipids have emerged as a cornerstone in the development of next-generation immunotherapies. This perspective provides a comprehensive update on structure-activity relationships, specifically examining how modifications of the prototypical CD1d ligand α-galactosylceramide (α-GalCer) to the galactosyl headgroup, phytosphingosine base, and fatty acyl chain dictate the modulation of invariant natural killer T (iNKT) cell responses. We explore the key pharmacophores and receptor interactions that polarize subsequent immune response toward either a pro-inflammatory Th1 or an anti-inflammatory Th2 phenotype. Building upon the structural evolution of sophisticated chemotypes, we evaluate the potential of these agonists in synergistic combinations with other adjuvants. Furthermore, we highlight the emerging transition toward fully synthetic self-adjuvanting vaccines, which ensure cellular colocalization and coordinated activation by covalently integrating antigens with glycolipid agonists. Collectively, these advancements underscore the transformative potential of tailored glycolipid design in engineering specific and durable immunity against cancer and infectious diseases.

Indexed as

Antigens, CD1dGalactosylceramidesAnimalsChemistry, PharmaceuticalGlycolipidsHumansLigandsNatural Killer T-CellsStructure-Activity Relationshipalpha-galactosylceramideAntigens, CD1dGalactosylceramidesGlycolipidsLigands

Identifiers

PMID42287230
PMCPMC13312407

What OpenQuestion 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 OpenQuestion graph.