Superinfection Drives HIV Neutralizing Antibody Responses from Several B Cell Lineages that Contribute to a Polyclonal Repertoire
Katherine L. Williams,
Bingjie Wang,
Dana Arenz,
James A. Williams,
Adam S. Dingens,
Valerie Cortez,
Cassandra A. Simonich,
Stephanie Rainwater,
Dara A. Lehman,
Kelly K. Lee,
Julie Overbaugh
Affiliations
Katherine L. Williams
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA
Bingjie Wang
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA; Medical Scientist Training Program, University of Washington School of Medicine, Seattle, WA 98195, USA
Dana Arenz
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA
James A. Williams
Department of Medicinal Chemistry, University of Washington, Seattle, WA 98195, USA
Adam S. Dingens
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA; Program in Molecular and Cellular Biology, University of Washington, Seattle, WA 98195, USA
Valerie Cortez
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA; Program in Molecular and Cellular Biology, University of Washington, Seattle, WA 98195, USA
Cassandra A. Simonich
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA; Medical Scientist Training Program, University of Washington School of Medicine, Seattle, WA 98195, USA
Stephanie Rainwater
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA
Dara A. Lehman
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA
Kelly K. Lee
Department of Medicinal Chemistry, University of Washington, Seattle, WA 98195, USA
Julie Overbaugh
Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98195, USA; Corresponding author
Summary: Eliciting broad and potent HIV-specific neutralizing antibody responses represents the holy grail of HIV vaccine efforts. Data from singly infected individuals with broad and potent plasma neutralizing activity targeting one epitope have guided our understanding of how these responses develop. However, far less is known about responses developed by superinfected individuals who acquire two distinct HIV strains. Here, we isolated HIV-specific mAbs from a superinfected individual with a broad plasma response. In this superinfection case, neutralizing activity resulted from multiple distinct B cell lineages that arose in response to either the initial or the superinfecting virus, including an antibody that targets the N332 supersite. This nAb, QA013.2, was specific to the superinfecting virus and was associated with eventual reemergence of the initial infecting virus. The complex dynamic between viruses in superinfection may drive development of a unique collection of polyclonal nAbs that present a higher barrier to escape than monoclonal responses. : Superinfection occurs when an HIV-infected person acquires a second infection with a genetically distinct HIV virus. Williams et al. isolate HIV-specific mAbs from a superinfected individual with a broad plasma response. In this superinfection case, neutralizing activity resulted from multiple distinct B cell lineages that arose in response to the initial or superinfecting virus, including an antibody that targets the N332 supersite. Keywords: HIV, antibody, broadly neutralizing antibody, HIV viral escape