HIV-1 ENTRY INTO CD4(-CKR-5() CELLS IS MEDIATED BY THE CHEMOKINE RECEPTOR CC)

The beta-chemokines MIP-1 alpha, MIP-1 beta and RANTES inhibit infecti on of CD4(+) T cells by primary, non-syncytium-inducing (NSI) HIV-1 st rains at the virus entry stage, and also block env-mediated cell-cell membrane fusion. CD4(+) T cells from some HIV-1-exposed uninfected ind ividuals cannot fuse with NSI HIV-1 strains and secrete high levels of beta-chemokines. Expression of the beta-chemokine receptor CC-CKR-5 i n CD4(+), non-permissive human and non-human cells renders them suscep tible to infection by NSI strains, and allows env-mediated membrane fu sion. CC-CKR-5 is a second receptor for NSI primary viruses.