| Literature DB >> 34355765 |
Anna J Pietrobon1,2, Fábio S Y Yoshikawa1, Luana M Oliveira1, Natalli Z Pereira1, Tais Matozo2, Bruna C de Alencar2, Alberto J S Duarte1, Maria N Sato1.
Abstract
Vertical transmission is the main mechanism of human immunodeficiency virus type 1 (HIV-1) infection in infants, who may develop high viremia and rapidly progress to AIDS. Innate immunity agonists can control HIV-1 replication in vitro, but the protective effect in the neonatal period remains unknown. Herein, we evaluated the immunomodulatory and antiviral effects of type I interferon (IFN-I) adjuvants on cord blood monocyte-derived macrophages upon HIV-1 infection. Despite the phenotypic and transcriptional similarities between cord blood and adult macrophages, cord blood cells were prone to viral replication when infected with HIV-1. However, treatment with CL097 efficiently promoted the antiviral and inflammatory responses and inhibited HIV-1 replication in cord blood cells in an NF-κB and autophagy activation-independent manner. Our data suggest that cord blood macrophages are able to establish antiviral responses induced by IFN-I adjuvants similar to those of their adult counterparts, revealing a potential adjuvant candidate to enhance the neonatal immune response.Entities:
Keywords: HIV; TLR7/TLR8; macrophage; newborn
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Year: 2022 PMID: 34355765 DOI: 10.1093/infdis/jiab389
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226