Target intelligence / Profile preview

Protein phosphatase 3 catalytic subunit alpha (PPP3CA) (PPP3CA)

Target
PPP3CA
Molecular classification
Enzyme, Serine/threonine-protein phosphatase
01

Overview

Calcineurin A, specifically the alpha isoform (PPP3CA), is the catalytic subunit of the calcium-dependent serine/threonine phosphatase calcineurin (UniProt: P16298). It plays a pivotal role in the immune system by dephosphorylating the Nuclear Factor of Activated T-cells (NFAT), which then translocates to the nucleus to induce the transcription of cytokines like interleukin-2 (IL-2) (PubMed: 23160471). In the context of engineered EBV-specific T cells, Calcineurin A is a primary target for modification to confer resistance to calcineurin inhibitors (CNIs) such as tacrolimus and cyclosporine (PubMed: 28814475). This engineering is crucial for patients undergoing hematopoietic stem cell or solid organ transplantation who require CNIs to prevent graft-versus-host disease or organ rejection but also need functional EBV-specific T cells to combat EBV-driven lymphoproliferative disorders. By introducing mutations like CNA12 or using gene-editing techniques, these T cells can maintain their effector functions despite the presence of systemic immunosuppression (PubMed: 23160471). Consequently, Calcineurin A serves as both a traditional drug target for immunosuppression and a strategic site for genetic enhancement in adoptive immunotherapy.

Other names
Calcineurin APPP3CACALNACALNA1CNA1Protein phosphatase 2B catalytic subunit alpha
02

Mechanism of action

Calcineurin inhibitors (CNIs) bind to intracellular immunophilins (FKBP12 for tacrolimus; cyclophilin for cyclosporine) to form a complex that inhibits the phosphatase activity of Calcineurin A, thereby preventing the dephosphorylation of NFAT and subsequent T-cell activation (PubMed: 23160471).

03

Biological functions

Signal transductionImmune responseT-cell activationProtein dephosphorylationCalcium signaling
04

Disease associations

Post-transplant lymphoproliferative disorderEpstein-Barr virus infectionGraft-versus-host diseaseCancerOrgan transplant rejection
05

Safety considerations

NephrotoxicityNeurotoxicityIncreased risk of opportunistic infectionsPotential for engineered T-cell exhaustionRisk of graft-versus-host disease if T-cell specificity is not strictly maintained
06

Interacting drugs

Tacrolimus

3 more in the full profile.

07

Biomarkers

NFAT nuclear translocationInterleukin-2 (IL-2) levelsEBV viral loadT-cell proliferation

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