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Envelope protein-specific B cell receptors direct lentiviral vector tropism in vivo

Authors
  • Takano, Kari-Ann
  • Wong, Anita AL
  • Brown, Rebecca
  • Situ, Kathy
  • Chua, Bernadette Anne
  • Abu, Angel Elma
  • Pham, Truc T
  • Reyes, Glania Carel
  • Ramachandran, Sangeetha
  • Kamata, Masakazu
  • Li, Melody MH
  • Wu, Ting-Ting
  • Rao, Dinesh S
  • Arumugaswami, Vaithilingaraja
  • Dorshkind, Kenneth
  • Cole, Steve
  • Morizono, Kouki
Publication Date
May 01, 2024
Source
eScholarship - University of California
Keywords
License
Unknown
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Abstract

While studying transgene expression after systemic administration of lentiviral vectors, we found that splenic B cells are robustly transduced, regardless of the types of pseudotyped envelope proteins. However, the administration of two different pseudotypes resulted in transduction of two distinct B cell populations, suggesting that each pseudotype uses unique and specific receptors for its attachment and entry into splenic B cells. Single-cell RNA sequencing analysis of the transduced cells demonstrated that different pseudotypes transduce distinct B cell subpopulations characterized by specific B cell receptor (BCR) genotypes. Functional analysis of the BCRs of the transduced cells demonstrated that BCRs specific to the pseudotyping envelope proteins mediate viral entry, enabling the vectors to selectively transduce the B cell populations that are capable of producing antibodies specific to their envelope proteins. Lentiviral vector entry via the BCR activated the transduced B cells and induced proliferation and differentiation into mature effectors, such as memory B and plasma cells. BCR-mediated viral entry into clonally specific B cell subpopulations raises new concepts for understanding the biodistribution of transgene expression after systemic administration of lentiviral vectors and offers new opportunities for BCR-targeted gene delivery by pseudotyped lentiviral vectors.

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