Antigen presenting cells from the cervical mucosa are thought to amplify incoming HIV-1 and spread infection systemically without being productively infected. Yet, the molecular mechanism at the cervical mucosa underlying this viral transmission pathway remains unknown. Here we identified a subset of HLA-DR CD14 CD11c cervical DCs at the lamina propria of the ectocervix and the endocervix that expressed the type-I interferon inducible lectin Siglec-1 (CD169), which promoted viral uptake. In the cervical biopsy of a viremic HIV-1 patient, Siglec-1 cells harbored HIV-1-containing compartments, demonstrating that , these cells trap viruses, a type-I interferon antiviral environment enhanced viral capture and -infection via Siglec-1. Nonetheless, HIV-1 transfer via cervical DCs was effectively prevented with antibodies against Siglec-1. Our findings contribute to decipher how cervical DCs may boost HIV-1 replication and promote systemic viral spread from the cervical mucosa, and highlight the importance of including inhibitors against Siglec-1 in microbicidal strategies.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503733 | PMC |
http://dx.doi.org/10.3389/fimmu.2019.00825 | DOI Listing |
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