Novel biologics targeting the P2X7 ion channel

被引:35
作者
Koch-Nolte, Friedrich [1 ]
Eichhoff, Anna [1 ,2 ]
Pinto-Espinoza, Carolina [1 ]
Schwarz, Nicole [1 ]
Schaefer, Tobias [1 ]
Menzel, Stephan [1 ]
Haag, Friedrich [1 ]
Demeules, Melanie [2 ]
Gonde, Henri [2 ]
Adriouch, Sahil [1 ,2 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Inst Immunol, Hamburg, Germany
[2] Normandie Univ, UNIROUEN, Pathophysiol Autoimmun Neuromuscular Dis & Regene, INSERM,U1234, F-76000 Rouen, France
关键词
ANTIBODY GENE-TRANSFER; T-CELLS; RECEPTOR; NANOBODIES; BLOCKADE; INFLAMMATION; PROGRESSION; ACTIVATION; PROTEINS; EFFICACY;
D O I
10.1016/j.coph.2019.03.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Targeting the P2X7 ion channel, a danger sensor for extracellular nucleotides, improves outcomes in models of inflammation, cancer, and brain-diseases. Antibodies and nanobodies have been developed that antagonize or potentiate gating of P2X7. Their potential advantages over small-molecule drugs include high specificity, lower off-target effects, and tunable in vivo half-life. Genetic fusion of P2X7-specific biologics to binding modules may enable targeting of specific cell subsets. Besides directly modulating P2X7 function, antibodies can also initiate specific depletion of P2X7-expressing cells. Adeno-associated viral vectors (AAV) can be used to express P2X7-specific antibodies in vivo to achieve long-lasting biological effects. Furthermore, if successfully targeted to P2X7-expressing cells, AAVs may enable modulation of the function of P2X7-expressing immune cells via encoded transgenic RNA or proteins.
引用
收藏
页码:110 / 118
页数:9
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