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High frequency of HIV precursor-target-specific B cells in sub-Saharan populations

  • Flavio Matassoli*
  • , Alberto Cagigi
  • , Chen Hsiang Shen
  • , Amy R. Henry
  • , Timothy S. Johnston
  • , Chaim A. Schramm
  • , Christopher A. Cottrell
  • , Oleksandr Kalyuzhniy
  • , Abby Spangler
  • , Leigh Eller
  • , Merlin Robb
  • , Michael Eller
  • , Prossy Naluyima
  • , Peter D. Kwong
  • , Daniel C. Douek
  • , William R. Schief
  • , Sarah F. Andrews*
  • , Adrian B. McDermott
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

HIV gp120 engineered outer domain germline-targeting version 8 (eOD-GT8) was designed specifically to engage naive B cell precursors of VRC01-class antibodies. However, the frequency and affinity of naive B cell precursors able to recognize eOD-GT8 have been evaluated only in U.S. populations. HIV infection is disproportionally concentrated in sub-Saharan Africa, so we seek to characterize naive B cells able to recognize eOD-GT8 in sub-Saharan cohorts. We demonstrate that people from sub-Saharan Africa have a higher or equivalent frequency of naive B cells able to engage eOD-GT8 compared with people from the U.S. Genetically, the higher frequency of eOD-GT8-positive cells is accompanied by a higher level of naive B cells with gene signatures characteristic of the VRC01 class, as well as other CD4bs-directed antibodies. Our study demonstrates that vaccination with eOD-GT8 in sub-Saharan Africa could be successful at expanding and establishing a pool of CD4bs-directed memory B cells from naive precursors.

Original languageEnglish
Article number113450
JournalCell Reports
Volume42
Issue number12
DOIs
StatePublished - 26 Dec 2023

Keywords

  • B cell
  • CP: Immunology
  • CP: Microbiology
  • HIV
  • vaccine

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