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免疫复合物而非新生Fc受体在小鼠单次注射后抗TNF-α抗体免疫中的关键作用

Crucial Role for Immune Complexes but Not FcRn in Immunization against Anti-TNF-α Antibodies after a Single Injection in Mice.

作者信息

Arnoult Christophe, Brachet Guillaume, Cadena Castaneda Diana, Azzopardi Nicolas, Passot Christophe, Desvignes Celine, Paintaud Gilles, Heuzé-Vourc'h Nathalie, Watier Hervé, Gouilleux-Gruart Valérie

机构信息

Université François Rabelais de Tours, CNRS, UMR 7292, F-37032 Tours, France.

Laboratoire d'Immunologie, Centre Hospitalier Régional Universitaire de Tours, F-37032 Tours, France.

出版信息

J Immunol. 2017 Jul 15;199(2):418-424. doi: 10.4049/jimmunol.1601246. Epub 2017 Jun 5.

Abstract

The immunogenicity of infliximab and adalimumab is a major concern because patients may develop Abs also called antidrug Abs (ADA), directed against these anti-TNF-α Abs after just a few weeks of treatment. These ADAs can lead to a decrease in biologic concentration, which is associated with lower treatment efficacy. Our aim was to study the involvement of immune complexes and neonatal Fc receptor (FcRn) in the emergence of ADAs in the case of anti-TNF-α Abs. Wild type and FcRn knockout mice were injected once with either infliximab or adalimumab, alone or preincubated with TNF-α. Adalimumab cross-reacts with murine TNF-α whereas infliximab is species specific. When injected alone, only adalimumab elicited a humoral response. By preforming immune complexes with TNF-α, an anti-infliximab response was elicited. Surprisingly, both wild type and FcRn knockout mice were able to mount an immune response against anti-TNF-α Abs, suggesting that immune complexes are a major determinant of this immunization.

摘要

英夫利昔单抗和阿达木单抗的免疫原性是一个主要问题,因为患者在治疗仅几周后就可能产生针对这些抗TNF-α抗体的抗体,也称为抗药物抗体(ADA)。这些ADA会导致生物制剂浓度降低,这与较低的治疗效果相关。我们的目的是研究免疫复合物和新生儿Fc受体(FcRn)在抗TNF-α抗体情况下ADA出现过程中的作用。野生型和FcRn基因敲除小鼠分别单次注射英夫利昔单抗或阿达木单抗,单独注射或与TNF-α预孵育。阿达木单抗与小鼠TNF-α交叉反应,而英夫利昔单抗具有物种特异性。单独注射时,只有阿达木单抗引发了体液反应。通过与TNF-α形成免疫复合物,引发了抗英夫利昔单抗反应。令人惊讶的是,野生型和FcRn基因敲除小鼠都能够对抗TNF-α抗体产生免疫反应,这表明免疫复合物是这种免疫反应的主要决定因素。

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