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抗CD40和抗CD40L抗体联合应用作为临床前心脏异种移植中共刺激阻断的方法

Combination of Anti-CD40 and Anti-CD40L Antibodies as Co-Stimulation Blockade in Preclinical Cardiac Xenotransplantation.

作者信息

Bender Martin, Abicht Jan-Michael, Reichart Bruno, Neumann Elisabeth, Radan Julia, Mokelke Maren, Buttgereit Ines, Leuschen Maria, Wall Felicia, Michel Sebastian, Ellgass Reinhard, Steen Stig, Paskevicius Audrius, Lange Andreas, Kessler Barbara, Kemter Elisabeth, Klymiuk Nikolai, Denner Joachim, Godehardt Antonia W, Tönjes Ralf R, Burgmann Jonathan M, Figueiredo Constança, Milusev Anastasia, Zollet Valentina, Salimi-Afjani Neda, Despont Alain, Rieben Robert, Ledderose Stephan, Walz Christoph, Hagl Christian, Ayares David, Wolf Eckhard, Schmoeckel Michael, Brenner Paolo, Binder Uli, Gebauer Michaela, Skerra Arne, Längin Matthias

机构信息

Department of Anaesthesiology, University Hospital, LMU Munich, 81377 Munich, Germany.

Transregional Collaborative Research Center 127, Walter Brendel Centre of Experimental Medicine, LMU Munich, 81377 Munich, Germany.

出版信息

Biomedicines. 2024 Aug 22;12(8):1927. doi: 10.3390/biomedicines12081927.

Abstract

The blockade of the CD40/CD40L immune checkpoint is considered essential for cardiac xenotransplantation. However, it is still unclear which single antibody directed against CD40 or CD40L (CD154), or which combination of antibodies, is better at preventing organ rejection. For example, the high doses of antibody administered in previous experiments might not be feasible for the treatment of humans, while thrombotic side effects were described for first-generation anti-CD40L antibodies. To address these issues, we conducted six orthotopic pig-to-baboon cardiac xenotransplantation experiments, combining a chimeric anti-CD40 antibody with an investigational long-acting PASylated anti-CD40L Fab fragment. The combination therapy effectively resulted in animal survival with a rate comparable to a previous study that utilized anti-CD40 monotherapy. Importantly, no incidence of thromboembolic events associated with the administration of the anti-CD40L PAS-Fab was observed. Two experiments failed early because of technical reasons, two were terminated deliberately after 90 days with the baboons in excellent condition and two were extended to 120 and 170 days, respectively. Unexpectedly, and despite the absence of any clinical signs, histopathology revealed fungal infections in all four recipients. This study provides, for the first time, insights into a combination therapy with anti-CD40/anti-CD40L antibodies to block this immune checkpoint.

摘要

CD40/CD40L免疫检查点的阻断被认为是心脏异种移植的关键。然而,目前仍不清楚哪种针对CD40或CD40L(CD154)的单克隆抗体,或哪种抗体组合在预防器官排斥方面效果更佳。例如,先前实验中使用的高剂量抗体可能不适用于人类治疗,同时第一代抗CD40L抗体存在血栓形成的副作用。为解决这些问题,我们进行了6次猪到狒狒的原位心脏异种移植实验,将嵌合抗CD40抗体与一种研究性的长效聚唾液酸化抗CD40L Fab片段相结合。联合治疗有效地提高了动物存活率,其存活率与先前使用抗CD40单药治疗的研究相当。重要的是,未观察到与抗CD40L PAS - Fab给药相关的血栓栓塞事件。2次实验因技术原因早期失败,2次在90天后故意终止,此时狒狒状态良好,另外2次分别延长至120天和170天。出乎意料的是,尽管没有任何临床症状,但组织病理学检查显示所有4只受体均有真菌感染。本研究首次深入探讨了使用抗CD40/抗CD40L抗体联合治疗来阻断该免疫检查点的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04cd/11351779/906656d0d403/biomedicines-12-01927-g001.jpg

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