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APRIL (protein)

Protein-coding gene in the species Homo sapiens

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A proliferation-inducing ligand (APRIL), also known as tumor necrosis factor ligand superfamily member 13 (TNFSF13), is a protein of the TNF superfamily recognized by the cell surface receptor TACI. It is encoded by the TNFSF13 gene.

01Nomenclature

In the cluster of differentiation terminology, APRIL is designated CD256. TNFSF13 is the HUGO standard gene name, but APRIL is more commonly used in medical literature.

02Function

The protein encoded by this gene is a member of the tumor necrosis factor ligand (TNF) ligand family. This protein is a ligand for TNFRSF17/BCMA, a member of the TNF receptor family. This protein and its receptor are both found to be important for B cell development. In vivo experiments suggest an important role for APRIL in the long-term survival of plasma cells in the bone marrow. Mice deficient in APRIL have normal immune system development. However, APRIL-deficient mice have also been reported to possess a reduced ability to support plasma cell survival. In vitro experiments suggested that this protein may be able to induce apoptosis through its interaction with other TNF receptor family proteins such as TNFRSF6/FAS and TNFRSF14/HVEM. Three alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported.

03Interactions

TNFSF13 has been shown to interact with TNFRSF13B and B-cell activating factor.

04Clinical significance

APRIL is being explored as a target for autoimmune diseases and B cell malignancies. At least one anti-APRIL monoclonal antibody (mAb) has been announced to enter phase I clinical trials for multiple myeloma.

APRIL is also a target for IgA nephropathy. At least one anti-APRIL mAb has finished phase 3 trials for this indication. APRIL is believed to contribute to the disease process by causing B cells to produce excessive galactose-deficient IgA1.

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Sources and credits

This article is adapted from the Wikipedia article APRIL (protein), written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.

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