Antibody Isotype Switching as a Mechanism to Counter HIV Neutralization Escape
Cathrine Scheepers, Valerie Bekker, Colin Anthony, Simone I. Richardson, Brent Oosthuysen, Thandeka Moyo-Gwete, Prudence Kgagudi, Dale Kitchin, Molati Nonyane, Talita York, Dieter Mielke, Batsirai Mabvakure, Zizhang Sheng, Bronwen E. Lambson, Arshad Ismail, Nigel Garrett, Salim S. Abdool Karim, Lawrence Shapiro, Carolyn Williamson, Lynn Morris, Penny L. Moore
Abstract
Neutralizing antibodies (nAbs) to highly variable viral pathogens show remarkable diversification during infection, resulting in an "arms race" between virus and host. Studies of nAb lineages have shown how somatic hypermutation (SHM) in immunoglobulin (Ig)-variable regions enables maturing antibodies to neutralize emerging viral escape variants. However, the Ig-constant region (which determines isotype) can also influence epitope recognition. Here, we use longitudinal deep sequencing of an HIV-directed nAb lineage, CAP88-CH06, and identify several co-circulating isotypes (IgG3, IgG1, IgA1, IgG2, and IgA2), some of which share identical variable regions. First, we show that IgG3 and IgA1 isotypes are better able to neutralize longitudinal autologous viruses and epitope mutants than can IgG1. Second, detrimental class-switch recombination (CSR) events that resulted in reduced neutralization can be rescued by further CSR, which we term "switch redemption." Thus, CSR represents an additional immunological mechanism to counter viral escape from HIV-specific antibody responses.