Author:
Marichannegowda Manukumar Honnayakanahalli,Setua Saini,Bose Meera,Sanders-Buell Eric,King David,Zemil Michelle,Wieczorek Lindsay,Diaz-Mendez Felisa,Chomont Nicolas,Thomas Rasmi,Francisco Leilani,Eller Leigh Anne,Polonis Victoria R.,Tovanabutra Sodsai,Tagaya Yutaka,Michael Nelson L.,Robb Merlin L.,Song Hongshuo
Abstract
AbstractNearly all transmitted/founder (T/F) HIV-1 are CCR5 (R5)-tropic. While previous evidence suggested that CXCR4 (X4)-tropic HIV-1 are transmissible, detection was not at the earliest stages of acute infection. Here, we identified an X4-tropic T/F HIV-1 in a participant in acute infection cohort. Coreceptor assays demonstrated that this T/F virus is strictly CXCR4 tropic. The participant experienced significantly faster CD4 depletion compared with R5 virus infected participants in the same cohort. Naïve and central memory CD4 subsets declined faster than effector and transitional memory subsets. All CD4 subsets, including naïve, were productively infected. Increased CD4+T cell activation was observed over time. This X4-tropic T/F virus is resistant to broadly neutralizing antibodies (bNAbs) targeting V1/V2 and V3 regions. These findings demonstrate that X4-tropic HIV-1 is transmissible through the mucosal route in people with the wild-type CCR5 genotype and have implications for understanding the transmissibility and immunopathogenesis of X4-tropic HIV-1.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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