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Immunomodulatory interventions in myocardial infarction and heart failure: a systematic review of clinical trials and meta-analysis of IL-1 inhibition

机译:心肌梗死和心力衰竭的免疫调节干预:对系统试验和IL-1抑制的荟萃分析的系统评价

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摘要

Following a myocardial infarction (MI), the immune system helps to repair ischaemic damage and restore tissue integrity, but excessive inflammation has been implicated in adverse cardiac remodelling and development towards heart failure (HF). Pre-clinical studies suggest that timely resolution of inflammation may help prevent HF development and progression. Therapeutic attempts to prevent excessive post-MI inflammation in patients have included pharmacological interventions ranging from broad immunosuppression to immunomodulatory approaches targeting specific cell types or factors with the aim to maintain beneficial aspects of the early post-MI immune response. These include the blockade of early initiators of inflammation including reactive oxygen species and complement, inhibition of mast cell degranulation and leucocyte infiltration, blockade of inflammatory cytokines, and inhibition of adaptive B and T-lymphocytes. Herein, we provide a systematic review on post-MI immunomodulation trials and a meta-analysis of studies targeting the inflammatory cytokine Interleukin-1. Despite an enormous effort into a significant number of clinical trials on a variety of targets, a striking heterogeneity in study population, timing and type of treatment, and highly variable endpoints limits the possibility for meaningful meta-analyses. To conclude, we highlight critical considerations for future studies including (i) the therapeutic window of opportunity, (ii) immunological effects of routine post-MI medication, (iii) stratification of the highly diverse post-MI patient population, (iv) the potential benefits of combining immunomodulatory with regenerative therapies, and at last (v) the potential side effects of immunotherapies.
机译:心肌梗塞(MI)后,免疫系统有助于修复缺血性损伤并恢复组织完整性,但过度的炎症与不良的心脏重塑和发展为心力衰竭(HF)有关。临床前研究表明,炎症的及时解决可能有助于预防HF的发生和发展。预防患者发生MI后过度炎症的治疗尝试包括药理学干预措施,从广泛的免疫抑制到针对特定细胞类型或因素的免疫调节方法,目的是维持MI后早期免疫应答的有益方面。这些包括阻断包括活性氧和补体在内的早期炎症引发剂,抑制肥大细胞脱粒和白细胞浸润,阻断炎性细胞因子,以及抑制适应性B和T淋巴细胞。本文中,我们提供了针对MI后免疫调节试验的系统评价,以及针对炎性细胞因子Interleukin-1的研究的荟萃分析。尽管已针对各种目标进行了大量的临床试验,但研究人群,治疗的时机和类型以及显着的终点均存在显着的异质性,这限制了进行有意义的荟萃分析的可能性。总而言之,我们着重指出了未来研究的关键考虑因素,包括(i)机会性治疗窗口;(ii)MI后常规用药的免疫学作用;(iii)MI后高度多样化的患者群体的分层;(iv)免疫调节与再生疗法相结合的潜在好处,以及(v)免疫疗法的潜在副作用。

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