Multi-Donor Longitudinal Antibody Repertoire Sequencing Reveals the Existence of Public Antibody Clonotypes in HIV-1 Infection

Ian Setliff(Vanderbilt University Medical Center), Wyatt J. McDonnell(Vanderbilt University Medical Center), Nagarajan Raju(Vanderbilt University Medical Center), Robin Bombardi(Vanderbilt University Medical Center), Amyn A. Murji(Vanderbilt University Medical Center), Cathrine Scheepers(National Health Laboratory Service), Rutendo Ziki(National Institute for Communicable Diseases), Charissa Mynhardt(National Institute for Communicable Diseases), Bryan E. Shepherd(Vanderbilt University), Alusha A. Mamchak, Nigel Garrett(Centre for the AIDS Programme of Research in South Africa), Salim S. Abdool Karim(Centre for the AIDS Programme of Research in South Africa), S. Mallal(Murdoch University), James E. Crowe(Vanderbilt University Medical Center), Lynn Morris(University of the Witwatersrand), Ivelin S. Georgiev(Vanderbilt University)
Cell Host & Microbe
June 1, 2018
Cited by 128Open Access
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Abstract

Characterization of single antibody lineages within infected individuals has provided insights into the development of Env-specific antibodies. However, a systems-level understanding of the humoral response against HIV-1 is limited. Here, we interrogated the antibody repertoires of multiple HIV-infected donors from an infection-naive state through acute and chronic infection using next-generation sequencing. This analysis revealed the existence of "public" antibody clonotypes that were shared among multiple HIV-infected individuals. The HIV-1 reactivity for representative antibodies from an identified public clonotype shared by three donors was confirmed. Furthermore, a meta-analysis of publicly available antibody repertoire sequencing datasets revealed antibodies with high sequence identity to known HIV-reactive antibodies, even in repertoires that were reported to be HIV naive. The discovery of public antibody clonotypes in HIV-infected individuals represents an avenue of significant potential for better understanding antibody responses to HIV-1 infection, as well as for clonotype-specific vaccine development.


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