TY - JOUR
T1 - A scoping review on the importance of vaccination strategies targeting skin imprinting for arthropod-borne diseases
AU - Wouters, J
AU - Leal, ASD
AU - Adriaensen, W
N1 - FTX: (CC BY NC ND)
PY - 2025
Y1 - 2025
N2 - Tissue-resident memory T (TRM) cells in the skin play a critical role in early immune defense against pathogens entering via breaches such as arthropod bites. However, their specific induction through immunization strategies remains underexplored. We performed a scoping review following PRISMA guidelines to assess vaccination strategies capable of inducing skin TRM cells. Intradermal and skin scarification routes consistently induced skin TRM cells with 94–100% success rates, while viral vector, DNA-based, and live-attenuated vaccines were the most effective platforms, particularly when combined with adjuvants promoting local inflammation. CD69 and CD103 were the most frequently employed markers, despite significant methodological heterogeneity. Vaccine-induced TRM cells were shown to disseminate throughout the skin and confer durable protection, independent of circulating T cells. However, evidence is largely restricted to preclinical studies, underscoring the need for standardization of TRM cell identification and expanded human studies to translate these findings into clinical practice.
AB - Tissue-resident memory T (TRM) cells in the skin play a critical role in early immune defense against pathogens entering via breaches such as arthropod bites. However, their specific induction through immunization strategies remains underexplored. We performed a scoping review following PRISMA guidelines to assess vaccination strategies capable of inducing skin TRM cells. Intradermal and skin scarification routes consistently induced skin TRM cells with 94–100% success rates, while viral vector, DNA-based, and live-attenuated vaccines were the most effective platforms, particularly when combined with adjuvants promoting local inflammation. CD69 and CD103 were the most frequently employed markers, despite significant methodological heterogeneity. Vaccine-induced TRM cells were shown to disseminate throughout the skin and confer durable protection, independent of circulating T cells. However, evidence is largely restricted to preclinical studies, underscoring the need for standardization of TRM cell identification and expanded human studies to translate these findings into clinical practice.
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=itm_wosliteitg&SrcAuth=WosAPI&KeyUT=WOS:001521128500003&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1038/s41541-025-01189-8
DO - 10.1038/s41541-025-01189-8
M3 - Review
C2 - 40594008
SN - 2059-0105
VL - 10
JO - npj Vaccines
JF - npj Vaccines
M1 - 137
ER -