Abstract
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.
| Original language | English |
|---|---|
| Article number | 137 |
| Journal | npj Vaccines |
| Volume | 10 |
| Issue number | 1 |
| Number of pages | 15 |
| ISSN | 2059-0105 |
| DOIs | |
| Publication status | Published - 1-Jul-2025 |
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