TY - JOUR
T1 - Would hemodialysis patients benefit from a Staphylococcus aureus vaccine?
AU - Connolly, Roisin
AU - Denton, Mark D.
AU - Humphreys, Hilary
AU - McLoughlin, Rachel M.
N1 - Publisher Copyright:
© 2019 International Society of Nephrology
PY - 2019/3
Y1 - 2019/3
N2 - 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.
AB - 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.
KW - cell-mediated immunity
KW - hemodialysis
KW - Staphylococcus aureus
UR - https://www.scopus.com/pages/publications/85060542046
U2 - 10.1016/j.kint.2018.10.023
DO - 10.1016/j.kint.2018.10.023
M3 - Review article
C2 - 30691691
AN - SCOPUS:85060542046
SN - 0085-2538
VL - 95
SP - 518
EP - 525
JO - Kidney International
JF - Kidney International
IS - 3
ER -