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
Affiliations
Wenjie Yin
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Laurent Gorvel
Unité de Recherche sur les Maladies Infectieuses, Tropicales Emergentes, IRD 198, CNRS UMR7278, INSERM U1095, 27 bd Jean Moulin, 13385 Cedex 05, Marseille, France
Sandra Zurawski
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Dapeng Li
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Ling Ni
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Dorothée Duluc
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Katherine Upchurch
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
JongRok Kim
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Chao Gu
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Richard Ouedraogo
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Zhiqing Wang
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Yaming Xue
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
HyeMee Joo
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
Jean-Pierre Gorvel
CIML, Aix Marseille Université, CNRS UMR 7280, INSERM U1104, parc scientifique de Luminy, Case 906, Marseille, France
Gerard Zurawski
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
SangKon Oh
Baylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA
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.