Protein antigen conjugated with cholesteryl amino-pullulan nanogel shows delayed degradation in dendritic cells and augmented immunogenicity

Vaccine ◽  
2021 ◽  
Author(s):  
Wang Long ◽  
Shinji Kunitake ◽  
Shin-ichi Sawada ◽  
Kazunari Akiyoshi ◽  
Takeshi Tsubata
2018 ◽  
Vol 520 ◽  
pp. 101-111 ◽  
Author(s):  
Chalathan Saengruengrit ◽  
Patcharee Ritprajak ◽  
Supason Wanichwecharungruang ◽  
Apoorva Sharma ◽  
Georgeta Salvan ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Mareike Rentzsch ◽  
Robert Wawrzinek ◽  
Claudia Zelle-Rieser ◽  
Helen Strandt ◽  
Lydia Bellmann ◽  
...  

Immune modulating therapies and vaccines are in high demand, not least to the recent global spread of SARS-CoV2. To achieve efficient activation of the immune system, professional antigen presenting cells have proven to be key coordinators of such responses. Especially targeted approaches, actively directing antigens to specialized dendritic cells, promise to be more effective and accompanied by reduced payload due to less off-target effects. Although antibody and glycan-based targeting of receptors on dendritic cells have been employed, these are often expensive and time-consuming to manufacture or lack sufficient specificity. Thus, we applied a small-molecule ligand that specifically binds Langerin, a hallmark receptor on Langerhans cells, conjugated to a model protein antigen. Via microneedle injection, this construct was intradermally administered into intact human skin explants, selectively loading Langerhans cells in the epidermis. The ligand-mediated cellular uptake outpaces protein degradation resulting in intact antigen delivery. Due to the pivotal role of Langerhans cells in induction of immune responses, this approach of antigen-targeting of tissue-resident immune cells offers a novel way to deliver highly effective vaccines with minimally invasive administration.


Vaccine ◽  
2019 ◽  
Vol 37 (35) ◽  
pp. 4963-4974 ◽  
Author(s):  
Julia Volckmar ◽  
Laura Knop ◽  
Sabine Stegemann-Koniszewski ◽  
Kai Schulze ◽  
Thomas Ebensen ◽  
...  

Biomaterials ◽  
2009 ◽  
Vol 30 (5) ◽  
pp. 910-918 ◽  
Author(s):  
Michael J. Heffernan ◽  
Sudhir P. Kasturi ◽  
Stephen C. Yang ◽  
Bali Pulendran ◽  
Niren Murthy

Immunobiology ◽  
2000 ◽  
Vol 201 (5) ◽  
pp. 568-582 ◽  
Author(s):  
Helga Bernhard ◽  
Eric S. Huseby ◽  
Susan L. Hand ◽  
Matthias Lohmann ◽  
Wendy Y. Batten ◽  
...  

Blood ◽  
1996 ◽  
Vol 88 (9) ◽  
pp. 3508-3512 ◽  
Author(s):  
K Garrigan ◽  
P Moroni-Rawson ◽  
C McMurray ◽  
I Hermans ◽  
N Abernethy ◽  
...  

We have compared dendritic cells (DC) isolated from mouse spleen, or generated in vitro from bone marrow (BM) precursors cultured in granulocyte macrophage-colony stimulating factor (GM-CSF) and interleukin-4 (IL-4), for the ability to process and present soluble antigen and stimulate major histocompatibility complex (MHC) Class II-restricted T cells. DC from spleen or BM cultures were equally able to stimulate the in vitro proliferation of allogeneic T cells or of antigen-specific T-cell receptor (TCR)-transgenic T cells. Both DC populations also induced comparable levels of IL-2 secretion by a T-cell hybridoma. Therefore, splenic and BM-derived DC express comparable levels of (Antigen + MHC Class II) ligands and/or costimulatory molecules and have comparable ability to stimulate T-cell responses. When presentation of a native protein antigen, rather than peptide, was evaluated, BM-derived DC were at least 50 times better than splenic DC at stimulating the proliferation of TCR-transgenic T cells. The antigen processing ability of the two populations was similar only when splenic DC were used immediately ex vivo. Therefore, unlike spleen DC, BM-derived DC maintain the capacity to process protein antigen for MHC Class II presentation during in vitro culture. Due to these characteristics, BM-derived DC may represent a useful tool in immunotherapy studies, as they combine high T-cell stimulatory properties with the capacity to process and present native antigen.


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