EBioMedicine (Mar 2016)

Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8+ and CD4+ T Cells

  • Wenjie Yin,
  • Laurent Gorvel,
  • Sandra Zurawski,
  • Dapeng Li,
  • Ling Ni,
  • Dorothée Duluc,
  • Katherine Upchurch,
  • JongRok Kim,
  • Chao Gu,
  • Richard Ouedraogo,
  • Zhiqing Wang,
  • Yaming Xue,
  • HyeMee Joo,
  • Jean-Pierre Gorvel,
  • Gerard Zurawski,
  • SangKon Oh

DOI
https://doi.org/10.1016/j.ebiom.2016.01.029
Journal volume & issue
Vol. 5, no. C
pp. 46 – 58

Abstract

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Dendritic cells (DCs) are major antigen-presenting cells that can efficiently prime and cross-prime antigen-specific T cells. Delivering antigen to DCs via surface receptors is thus an appealing strategy to evoke cellular immunity. Nonetheless, which DC surface receptor to target to yield the optimal CD8+ and CD4+ T cell responses remains elusive. Herein, we report the superiority of CD40 over 9 different lectins and scavenger receptors at evoking antigen-specific CD8+ T cell responses. However, lectins (e.g., LOX-1 and Dectin-1) were more efficient than CD40 at eliciting CD4+ T cell responses. Common and distinct patterns of subcellular and intracellular localization of receptor-bound αCD40, αLOX-1 and αDectin-1 further support their functional specialization at enhancing antigen presentation to either CD8+ or CD4+ T cells. Lastly, we demonstrate that antigen targeting to CD40 can evoke potent antigen-specific CD8+ T cell responses in human CD40 transgenic mice. This study provides fundamental information for the rational design of vaccines against cancers and viral infections.

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