Evidence map›Paper›PMID 42170000›Full record

ArticleJournal of human immunity2026

Expanding the scope of PI3K-δ inhibition: Leniolisib treatment in PRKCD deficiency.

Lorenzo Lodi, Valentina Guarnieri, Matilde Peri, Manuela Baronio, Silvia Ricci, Clementina Canessa, Francesca Lippi, Marta Voarino, Elisa Calistri, Laura Pisano and 6 more

Abstract read
In one paragraph

Article in Journal of human immunity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Lorenzo Lodi *Pediatric Immunology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0001-6902-544X
Valentina Guarnieri *Department of Health Sciences, University of Florence, Florence, Italy.ORCID https://orcid.org/0000-0002-5578-7002
Matilde PeriDepartment of Health Sciences, University of Florence, Florence, Italy.ORCID https://orcid.org/0009-0003-6798-207X
Manuela BaronioDepartment of Clinical and Experimental Sciences, Pediatrics Clinic, Azienda Socio-Sanitaria Territoriale Spedali Civili di Brescia, University of Brescia, Brescia, Italy.ORCID https://orcid.org/0009-0008-4692-378X
Silvia RicciPediatric Immunology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0001-7140-1694
Clementina CanessaPediatric Immunology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0003-1169-4039
Francesca LippiPediatric Immunology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0003-2533-1802
Marta VoarinoDepartment of Health Sciences, University of Florence, Florence, Italy.ORCID https://orcid.org/0009-0004-3376-9112
Elisa CalistriDepartment of Health Sciences, University of Florence, Florence, Italy.ORCID https://orcid.org/0000-0002-9560-4282
Laura PisanoUniversity of Florence, Florence, Italy.ORCID https://orcid.org/0000-0002-3999-7392
Anna PerronePediatric Radiology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0001-8108-7790
Grazia FenuPediatric Pulmonary Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0002-4360-8417
Giuseppe IndolfiUniversity of Florence, Florence, Italy.ORCID https://orcid.org/0000-0003-3830-9823
Vassilios LougarisDepartment of Clinical and Experimental Sciences, Pediatrics Clinic, Azienda Socio-Sanitaria Territoriale Spedali Civili di Brescia, University of Brescia, Brescia, Italy.ORCID https://orcid.org/0000-0003-2303-9533
Rebecca A MarshDivision of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID https://orcid.org/0000-0002-9645-0617
Chiara AzzariPediatric Immunology Unit, Meyer Children's Hospital IRCCS, Florence, Italy.ORCID https://orcid.org/0000-0001-7236-1655

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leniolisib, a selective phosphoinositide 3-kinase δ (PI3Kδ) inhibitor, is approved in several countries for the treatment of activated PI3Kδ syndrome (APDS) in patients 12 years of age and older. We report the first successful compassionate use of leniolisib in another inborn error of immunity, protein kinase C δ deficiency. In addition to infectious complications, the 14-year-old patient experienced lymphoproliferation in the form of splenomegaly, lymphadenopathy, and thymic hyperplasia; trilineage cytopenia; multiple forms of autoimmunity; and interstitial lung disease. Decision to initiate treatment with leniolisib was based on multiorgan-disease progression, lack of therapeutic alternatives, molecular evidence, overlap with APDS manifestations, and mammalian target of rapamycin hyperactivity. We observed improvement in lymphoproliferation, cytopenias, hepatic cytolysis, skin manifestations, pulmonary function, favorable changes in immunophenotypes, and no known drug-related adverse events. This experience supports expanding Leniolisib's potential indications to appropriately selected patients and conditions. Broader repurposing strategies for targeted therapies in diseases involving dysregulated PI3K signaling should be systematically evaluated in clinical trials.

Identifiers

PMID42170000
PMCPMC13177475

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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.