Human neutrophil α‐defensin 4 inhibits HIV‐1 infection in vitro

Abstract
Human neutrophil α‐defensin 4 (HNP4) is more effective than HNP1–3 in protecting human peripheral blood mononuclear cells from infection by both X4 and R5 HIV‐1 strains. HNP4 binds to both CD4 and gp120 approximately two orders of magnitude weaker than does HNP1, and is less effectively sequestered by glycosylated serum proteins than HNP1. These results suggest that the HIV‐1 inhibition by HNP4 stems at least partially from a unique and lectin‐independent property of HNP4 with CD4 and/or gp120. Our finding identifies an anti‐HIV‐1 property of HNP4 and may have implications in the development of new antiviral agents for AIDS therapy.