| Literature DB >> 32060507 |
Ryota Sato1,2, Chieko Makino-Okamura1, Quingshun Lin1, Muying Wang3, Jason E Shoemaker3,4,5, Tomohiro Kurosaki1,6, Hidehiro Fukuyama1,2,7.
Abstract
Aluminum precipitates have long been used as adjuvants for human vaccines, but there is a clear need for safer and more effective adjuvants. Here we report in a mouse model that the psoriasis drug Oxarol ointment is a highly effective vaccine adjuvant. By applying Oxarol ointment onto skin, humoral responses and germinal center (GC) reactions were augmented, and the treated mice were protected from death caused by influenza virus infection. Keratinocyte-specific vitamin D3 receptor (Vdr) gene expression was required for these responses through induction of the thymic stromal lymphopoietin (Tslp) gene. Experiments involving administration of recombinant TSLP or, conversely, anti-TSLP antibody demonstrated that TSLP plays a key role in the GC reactions. Furthermore, cell-type-specific Tslpr gene deletion or diphtheria toxin-mediated deletion of specific cell types revealed that CD11c+ cells excluding Langerhans cells were responsible for the Oxarol-mediated GC reactions. These results indicate that active vitamin D3 is able to enhance the humoral response via Tslp induction in the skin and serves as a new vaccine adjuvant. © The Japanese Society for Immunology. 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: TSLP; adjuvant; keratinocytes; vitamin D3
Year: 2020 PMID: 32060507 DOI: 10.1093/intimm/dxaa012
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823