# SEC61: a potential therapeutic target in transplantation

**Authors:** Maria Laura Saiz, Cristian Ruiz Bernet, Carlos Lopez-Larrea, Beatriz Suarez-Alvarez

PMC · DOI: 10.3389/fimmu.2026.1787920 · Frontiers in Immunology · 2026-03-18

## TL;DR

This paper explores SEC61 as a promising target in kidney transplantation, linking it to immune regulation, calcium balance, and potential therapeutic benefits.

## Contribution

The paper highlights SEC61's multifunctional roles and proposes it as a novel immunomodulatory target in kidney transplantation.

## Key findings

- SEC61 regulates antigen cross-presentation and cytokine secretion in transplant immunobiology.
- Pharmacological inhibition of SEC61 may reduce ER stress and tubular injury during ischemia–reperfusion.
- Phase I oncology data suggest feasibility of SEC61 modulation, though transplant-specific validation is needed.

## Abstract

The SEC61 translocon complex has emerged as a multifunctional therapeutic target linking protein secretion, calcium homeostasis, and immune regulation in kidney transplantation. Beyond canonical protein translocation, SEC61 regulates antigen cross-presentation, cytokine secretion (IL-2, IFN-γ, TNF-α), surface activation molecules (CD62L), and functions as an endoplasmic reticulum calcium-leak channel that modulates unfolded protein response activation under specific physiological and stress conditions. During ischemia–reperfusion injury, ATP depletion impairs SERCA-mediated calcium reuptake while SEC61-mediated calcium efflux persists, triggering ER stress and tubular injury. Selective pharmacological SEC61 inhibition has been proposed to confer multiple immunomodulatory and cytoprotective effects - including reduced antigen cross-presentation, suppression of high-burden secretory lymphocytes, limited T cell migration, and intrinsic antiviral activity through blockade of envelope glycoprotein biogenesis—based on mechanistic and preclinical evidence, although these effects remain to be validated in transplant-specific models. Emerging phase I oncology data with client-selective inhibitors demonstrate the feasibility of pharmacologic SEC61 modulation in humans, although the safety, dosing, and patient population in transplantation may differ substantially from oncology settings. This review examines SEC61’s multifaceted roles in transplant immunobiology and its therapeutic potential as a novel immunomodulatory target in kidney transplantation.

## Linked entities

- **Genes:** SEC61A1 (SEC61 translocon subunit alpha 1) [NCBI Gene 29927]
- **Proteins:** IL2 (interleukin 2), IFNG (interferon gamma), TNF (tumor necrosis factor), SELL (selectin L)
- **Diseases:** ischemia–reperfusion injury (MONDO:0005203)

## Full-text entities

- **Genes:** ERVK-20 (endogenous retrovirus group K member 20) [NCBI Gene 100616444] {aka c11_B, env}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, SELL (selectin L) [NCBI Gene 6402] {aka CD62L, LAM1, LECAM1, LEU8, LNHR, LSEL}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SEC61A1 (SEC61 translocon subunit alpha 1) [NCBI Gene 29927] {aka ADTKD5, CVID15, HNFJ4, HSEC61, SEC61, SEC61A}
- **Diseases:** tubular injury (MESH:D000230), ischemia (MESH:D007511), reperfusion injury (MESH:D015427)
- **Chemicals:** calcium (MESH:D002118), ATP (MESH:D000255)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13038442/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038442/full.md

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Source: https://tomesphere.com/paper/PMC13038442