Abstract
Staphylococcus aureus bloodstream infection can have potentially catastrophic consequences for patients on hemodialysis. Consequently, an effective vaccine to prevent S aureus infection would have a significant influence on morbidity and mortality in this group. To date, however, efforts to develop a vaccine have been unsuccessful. Previous antibody-inducing vaccine candidates did not prevent or attenuate S aureus infection in clinical trials. Recent advances have helped to elucidate the role of specific T-cell subsets, notably T-helper cell 1 and T-helper cell 17, in the immune response to S aureus. These cells are essential for coordinating an effective phagocytic response via cytokine production, indirectly leading to destruction of the organism. It is now widely accepted that next-generation S aureus vaccines must also induce effective T-cell–mediated immunity. However, there remains a gap in our knowledge: how will an S aureus vaccine drive these responses in those patients most at risk? Given that patients on hemodialysis are an immunocompromised population, in particular with specific T-cell defects, including defects in T-helper cell subsets, this is likely to affect their ability to respond to an S aureus vaccine. We urgently need a better understanding of T-cell–mediated immunity in this cohort if an efficacious vaccine is ever to be realized for these patients.
| Original language | English |
|---|---|
| Pages (from-to) | 518-525 |
| Number of pages | 8 |
| Journal | Kidney International |
| Volume | 95 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 2019 |
| Externally published | Yes |
Keywords
- cell-mediated immunity
- hemodialysis
- Staphylococcus aureus
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