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经导管主动脉瓣置换术受者的炎症免疫反应。

Inflammatory immune response in recipients of transcatheter aortic valves.

作者信息

Veraar Cecilia, Koschutnik Matthias, Nitsche Christian, Laggner Maria, Polak Dominika, Bohle Barbara, Mangold Andreas, Moser Bernhard, Mascherbauer Julia, Ankersmit Hendrik J

机构信息

Division of Cardiothoracic and Vascular Anaesthesia and Intensive Care Medicine, Department of Anaesthesiology, General Intensive Care, and Pain Medicine, Medical University of Vienna, Vienna, Austria.

Laboratory for Cardiac and Thoracic Diagnosis, Regeneration and Applied Immunology, Medical University of Vienna, Vienna, Austria.

出版信息

JTCVS Open. 2021 Mar 12;6:85-96. doi: 10.1016/j.xjon.2021.02.012. eCollection 2021 Jun.

Abstract

OBJECTIVE

Transcatheter aortic valve implantation (TAVI) is rapidly replacing cardiac surgery due to its minimal invasiveness and practicality. Midterm immunological studies on the biocompatibility of galactose-alpha-1,3-galactose (α-Gal)-carrying bioprosthetic heart valves for TAVI are not available. In this study we investigated whether bioprosthetic heart valves employed for TAVI augment an α-Gal-specific antibody-dependent and antibody-independent immune response 3 months after TAVI implantation.

METHODS

This prospective observational study included 27 patients with severe aortic valve stenosis undergoing TAVI and 10 patients with severe mitral valve regurgitation treated with a transcatheter MitraClip (Abbott Laboratories, Abbott Park, Ill) procedure. Blood samples were drawn before and 90 days after treatment at a routine checkup. Serum samples were analyzed using enzyme-linked immunosorbent assay. Serum concentrations of α-Gal-specific immunoglobulin (Ig) G, IgG subclasses and IgE, complement factor 3a, NETosis-specific citrullinated H3, and the systemic inflammation markers soluble suppression of tumorigenicity and interleukin 33 were evaluated.

RESULTS

Three months after TAVI, we found significantly increased serum concentrations of α-Gal-specific IgG3, complement factor complement factor 3a, citrullinated H3 levels, and soluble suppression of tumorigenicity ( = .002,  = .001,  = .025, and  = .039, respectively). Sensitization of α-Gal-specific IgE antibodies occurred in 55% of all patients after TAVI.

CONCLUSIONS

Our results indicate that TAVI elicits a midterm, specific humoral immune response against α-Gal and causes an unspecific humoral inflammation compared with patients undergoing MitraClip implantation. This observation will lead to a better understanding of postintervention morbidity and the long-term durability of bioprostheses and indicates that caution is appropriate when designing implantation strategies for younger patients.

摘要

目的

经导管主动脉瓣植入术(TAVI)因其微创性和实用性正在迅速取代心脏手术。目前尚无关于用于TAVI的携带半乳糖-α-1,3-半乳糖(α-Gal)的生物人工心脏瓣膜生物相容性的中期免疫学研究。在本研究中,我们调查了用于TAVI的生物人工心脏瓣膜在植入TAVI 3个月后是否会增强α-Gal特异性抗体依赖性和抗体非依赖性免疫反应。

方法

这项前瞻性观察性研究包括27例接受TAVI的严重主动脉瓣狭窄患者和10例接受经导管二尖瓣夹合术(Abbott Laboratories,伊利诺伊州雅培公园)治疗的严重二尖瓣反流患者。在常规检查时于治疗前和治疗后90天采集血样。使用酶联免疫吸附测定法分析血清样本。评估血清中α-Gal特异性免疫球蛋白(Ig)G、IgG亚类和IgE、补体因子3a、中性粒细胞胞外陷阱形成特异性瓜氨酸化组蛋白H3以及全身炎症标志物可溶性肿瘤抑制因子和白细胞介素33的浓度。

结果

TAVI术后3个月,我们发现血清中α-Gal特异性IgG3、补体因子3a、瓜氨酸化组蛋白H3水平以及可溶性肿瘤抑制因子浓度显著升高(分别为P = 0.002、P = 0.001、P = 0.025和P = 0.039)。TAVI术后所有患者中有55%出现了α-Gal特异性IgE抗体致敏。

结论

我们的结果表明,与接受二尖瓣夹合术植入的患者相比,TAVI引发了针对α-Gal的中期特异性体液免疫反应,并导致非特异性体液炎症。这一观察结果将有助于更好地理解干预后发病率和生物假体的长期耐久性,并表明在为年轻患者设计植入策略时应谨慎行事。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/236f/9390500/28c277aa7d75/fx1.jpg

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