Emergence of neutralizing antibodies associates with clearance of SARS-CoV-2 during HIV-mediated immunosuppression

Author:

Karim Farina,Bernstein Mallory,Jule Zesuliwe,Lustig Gila,Upton Janine-Lee,Ganga Yashica,Khan Khadija,Reedoy Kajal,Mazibuko Matilda,Govender Katya,Thambu Kershnee,Ngcobo Nokuthula,Venter Elizabeth,Makhado Zanele,Hanekom Willem,von Gottberg Anne,Karim Quarraisha Abdool,Abdool Karim Salim S.,Manickchund Nithendra,Magula Nombulelo,Gosnell Bernadett I.,Moore Penny L.,Lessells Richard J.,de Oliveira TulioORCID,Moosa Mahomed-Yunus S.,Sigal AlexORCID

Abstract

To design effective vaccines and other immune interventions against a pathogen, it is necessary to know which aspect of immunity associates with protection. We investigated whether neutralizing antibodies associate with infection clearance in long-term SARS-CoV-2 infection during HIV-mediated immunosuppression. We monitored neutralizing antibody activity against SARS-CoV-2 over 1 to 2 years in five participants with advanced HIV disease and delayed control of HIV viremia. These participants had persistent SARS-CoV-2 infection ranging from 110 to 289 days which was associated with low or undetectable neutralizing antibody responses. SARS-CoV-2 clearance was associated with the emergence of neutralizing antibodies and occurred in two participants before suppression of HIV viremia, but after some CD4 T cell reconstitution. Vaccination only further increased neutralizing antibody levels in the advanced HIV disease participants who achieved HIV suppression pre-vaccination. During the prolonged SARS-CoV-2 infection we observed widespread evolution which was particularly pronounced in one Delta variant infection. This resulted in high-level escape from Delta-elicited neutralizing antibodies and a virus antigenically distinct from both ancestral SARS-CoV-2 and Omicron XBB in hamster experimental infections. The results offer new evidence that neutralizing antibodies associate with SARS-CoV-2 clearance and argue that successful management of HIV may be necessary to curtail long-term infection and evolution of co-infecting pathogens.

Publisher

Cold Spring Harbor Laboratory

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