# Leniolisib reduced lymphoproliferative disease in murine autoimmune lymphoproliferative syndrome

**Authors:** Chopie Hassan, Yolanda Ponstein, Robert Hanssen, Kevin S. Thorneloe, Rebecca A. Marsh, V. Koneti Rao

PMC · DOI: 10.70962/jhi.20250125 · Journal of Human Immunity · 2025-11-17

## TL;DR

Leniolisib, a PI3Kδ inhibitor, reduced lymphoproliferation and disease markers in a mouse model of autoimmune lymphoproliferative syndrome.

## Contribution

Leniolisib's efficacy in reducing ALPS features in a murine model is demonstrated for the first time.

## Key findings

- Leniolisib reduced lymphadenopathy and splenomegaly in a dose-dependent manner.
- Treatment decreased elevated double-negative T cells in ALPS mice.
- Results support clinical evaluation of leniolisib for ALPS patients.

## Abstract

Treating patients with ALPS can be challenging. This article examines the efficacy of leniolisib, a selective PI3Kδ inhibitor, in a murine model of ALPS, illustrating a reduction in lymphoproliferation and disease-associated biomarkers such as elevated double-negative T cells.

Autoimmune lymphoproliferative syndrome (ALPS) is an inborn error of immunity (IEI) characterized by abnormal FAS-mediated apoptosis of lymphocytes that leads to lymphoproliferation and expansion of CD4−/CD8− double-negative T cells (DNTs). In patients with ALPS-FAS, DNTs have been reported to exhibit increased activity in the phosphoinositide 3-kinase δ (PI3Kδ)/mammalian target of rapamycin (mTOR) pathway. Although mTOR inhibition with sirolimus has improved autoimmune cytopenias and organomegaly in patients with ALPS, it requires monitoring of serum levels, and common adverse events frequently hamper long-term use. As leniolisib, a selective PI3Kδ inhibitor, reduced lymphoproliferation in another IEI known as activated PI3Kδ syndrome, efficacy was examined in a murine model of ALPS. Changes in organ weight and key immune subsets in MRL/lpr−/− mice receiving vehicle or leniolisib (40 or 80 mg/kg/day) by oral gavage were assessed. Leniolisib limited the canonical features of ALPS, including lymphadenopathy, splenomegaly, and elevated DNTs, in a dose-dependent manner. These results support the evaluation of leniolisib in patients with ALPS (NCT06549114).

## Linked entities

- **Proteins:** FAS (Fas cell surface death receptor), MTOR (mechanistic target of rapamycin kinase)
- **Chemicals:** leniolisib (PubChem CID 57495353), sirolimus (PubChem CID 5284616)
- **Diseases:** Autoimmune lymphoproliferative syndrome (MONDO:0011158)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, PIK3CD (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta) [NCBI Gene 5293] {aka APDS, IMD14, IMD14A, IMD14B, P110DELTA, PI3K}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}
- **Diseases:** lymphadenopathy (MESH:D008206), IEI (MESH:D007154), ALPS (MESH:D056735), PI3Kdelta syndrome (MESH:D003699), splenomegaly (MESH:D013163), organomegaly (MESH:D016878), lymphoproliferative disease (MESH:D008232), autoimmune cytopenias (MESH:D001327)
- **Chemicals:** Leniolisib (MESH:C000625376), sirolimus (MESH:D020123)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12829769/full.md

## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829769/full.md

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Source: https://tomesphere.com/paper/PMC12829769