4.8 Article

Functional HIV-1/HCV cross-reactive antibodies isolated from a chronically co-infected donor

Journal

CELL REPORTS
Volume 42, Issue 2, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2023.112044

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In a study of a chronically HIV-1/HCV co-infected individual, researchers identified five cross-reactive antibodies that show exceptional neutralization breadth and effector functions against both HIV-1 and HCV. One antibody also cross-reacts with influenza and coronaviruses, including SARS-CoV-2. The development of these antibodies is closely related to somatic hypermutation, providing potential directions for therapeutic and vaccine development against current and emerging infectious diseases. Chronic co-infection represents a complex immunological challenge that can provide insights into the fundamental rules of antibody-antigen specificity.
Despite prolific efforts to characterize the antibody response to human immunodeficiency virus type 1 (HIV-1) and hepatitis C virus (HCV) mono-infections, the response to chronic co-infection with these two ever-evolving viruses is poorly understood. Here, we investigate the antibody repertoire of a chronically HIV-1/HCV co -infected individual using linking B cell receptor to antigen specificity through sequencing (LIBRA-seq). We identify five HIV-1/HCV cross-reactive antibodies demonstrating binding and functional cross-reactivity between HIV-1 and HCV envelope glycoproteins. All five antibodies show exceptional HCV neutralization breadth and effector functions against both HIV-1 and HCV. One antibody, mAb688, also cross-reacts with influenza and coronaviruses, including severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We examine the development of these antibodies using next-generation sequencing analysis and lineage tracing and find that somatic hypermutation established and enhanced this reactivity. These antibodies provide a potential future direction for therapeutic and vaccine development against current and emerging infectious diseases. More broadly, chronic co-infection represents a complex immunological challenge that can provide insights into the fundamental rules that underly antibody-antigen specificity.

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