# CD8+ T cell aging is associated with macular neovascularization area change in neovascular age-related macular degeneration: a prospective cohort study

**Authors:** Alexander Kai Thomsen, Maria Abildgaard Steffensen, Kathrine Gotfredsen, Henrik Vorum, Bent Honoré, Mogens Holst Nissen, Torben Lykke Sørensen

PMC · DOI: 10.1186/s12886-025-04570-2 · BMC Ophthalmology · 2026-01-10

## TL;DR

This study finds that the aging of CD8+ T cells is linked to changes in macular neovascularization in patients with neovascular age-related macular degeneration.

## Contribution

The novel finding is the association between CD8+ T cell aging markers and treatment response in neovascular AMD patients.

## Key findings

- A reduction in MNV area was significantly associated with lower proportions of CD8+CD27- and CD8+CD28- T cells.
- A non-significant trend suggested higher CD8+ naïve T cells correlated with greater MNV area reduction.
- Aging T cell profiles may influence treatment outcomes in nAMD patients.

## Abstract

Neovascular age-related macular degeneration (nAMD) is characterized by formation of macular neovascularization (MNV). The aging immune system plays an important role in nAMD pathogenesis. Loss of the costimulatory markers CD27 and CD28 on T cells and increased T cell differentiation is associated with immunosenescence and proinflammatory T cell activation. In this study we investigate the association between MNV area change following anti-VEGF treatment and the aging T cell profile in nAMD patients.

This prospective cohort study included treatment-naïve nAMD patients. Participants were examined with optical coherence tomography angiography at time of diagnosis and following loading dose to assess the MNV area change. A blood sample was analyzed for circulating aging T cell profile with flow cytometry for the costimulatory markers CD27, CD28, and CD56, as well as T cell differentiation (naïve, central memory, and effector memory) of CD4+ and CD8+ T cells.

54 eyes of 54 patients were included. A significant association was found between a reduction of MNV area and a reduction of the CD8+CD27- T cell proportion (β, 0.71; 95% CI, 0.17 to 1.26; P = 0.035), as well as CD8+CD28- T cell proportion (β, 0.72; 95% CI, 0.20 to 1.23; P = 0.035). A non-significant negative trend was observed between MNV area change and CD8 + naïve T cells (P = 0.099).

Our results suggest that a less advanced aging T cell profile characterized by lower levels of CD8+CD27- and CD8+CD28- T cells is associated with a greater reduction of MNV area following anti-VEGF treatment in treatment-naïve nAMD patients.

The online version contains supplementary material available at 10.1186/s12886-025-04570-2.

## Linked entities

- **Proteins:** CD27 (CD27 molecule), CD28 (CD28 molecule), NCAM1 (neural cell adhesion molecule 1)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** age-related macular degeneration (MESH:D008268), neovascular (MESH:D016510)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12882413/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12882413/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12882413/full.md

---
Source: https://tomesphere.com/paper/PMC12882413