锁孔血蓝蛋白
免疫系统
抗体
免疫学
血蓝蛋白
生物
免疫
抗体效价
体液免疫
效价
T细胞
作者
Ornella Binazon,Mario Cocco,Daniel Thwaites,Christopher B. Cooper,Mahan Moshir,Peter Vanhoenacker,Dieter Defever,A. Van de Sompel,Sophie Steeland,Gwenda Pynaert,Peter Ulrichts,Judith Baumeister
标识
DOI:10.1080/1547691x.2025.2459934
摘要
Efgartigimod is a human IgG1 antibody Fc fragment that reduces IgG levels through neonatal Fc receptor blockade. This study evaluated whether efgartigimod affects the generation of T-cell-dependent antibodies and cellular immune responses to keyhole limpet hemocyanin (KLH) immunization in non-human primates. Cynomolgus monkeys received efgartigimod or vehicle control intravenously for 11 wk, followed by a recovery phase. KLH challenges occurred during both the dosing phase and the recovery phase. No statistically significant differences emerged in anti-KLH IgM levels between the efgartigimod and control groups. Likewise, comparable KLH-specific T cell responses were observed between groups. Anti-KLH IgG titers were lower in efgartigimod-treated animals compared with controls only after the first boost of KLH, coinciding with decreases in total IgG titers in efgartigimod-treated animals, and returned to baseline levels by the end of the recovery phase. Taken together, these results indicate that efgartigimod does not suppress T-cell-dependent antibody responses or antibody class-switching. The findings of this study are consistent with efgartigimod's pharmacological mechanism of action and suggest that efgartigimod does not impair the generation of effective immune responses.
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