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内脏亲嗜性的免疫应答:全面综述。

Immune response to viscerotropic : a comprehensive review.

机构信息

Department of Health Sciences, University of Florence, Florence, Italy.

Immunology Unit, Department of Pediatrics, Meyer Children's Hospital IRCCS, Florence, Italy.

出版信息

Front Immunol. 2024 Sep 18;15:1402539. doi: 10.3389/fimmu.2024.1402539. eCollection 2024.

Abstract

and infections are associated with a broad clinical spectrum, ranging from asymptomatic cases to visceral leishmaniasis (VL) with high mortality rates. Clinical manifestations such as post-kala-azar dermal leishmaniasis (PKDL) and visceral leishmaniasis-associated hemophagocytic lymphohistiocytosis-mimic (VL-associated HLH-mimic) further contribute to the diversity of clinical manifestations. These clinical variations are intricately influenced by the complex interplay between the host's immune response and the parasite's escape mechanisms. This narrative review aims to elucidate the underlying immunological mechanisms associated with each clinical manifestation, drawing from published literature within the last 5 years. Specific attention is directed toward viscerotropic sinfection in patients with inborn errors of immunity and acquired immunodeficiencies. In VL, parasites exploit various immune evasion mechanisms, including immune checkpoints, leading to a predominantly anti-inflammatory environment that favors parasite survival. Conversely, nearly 70% of individuals are capable of mounting an effective pro-inflammatory immune response, forming granulomas that contain the parasites. Despite this, some patients may experience reactivation of the disease upon immunosuppression, challenging current understandings of parasite eradication. Individuals living with HIV and those with inborn errors of immunity present a more severe course of infection, often with higher relapse rates. Therefore, it is crucial to exclude both primary and acquired immune deficiencies in patients presenting disease relapse and VL-associated HLH-mimic. The distinction between VL and HLH can be challenging due to clinical similarities, suggesting that the nosological entity known as VL-associated HLH may represent a severe presentation of symptomatic VL and it should be considered more accurate referring to this condition as VL-associated HLH-mimic. Consequently, excluding VL in patients presenting with HLH is essential, as appropriate antimicrobial therapy can reverse immune dysregulation. A comprehensive understanding of the immune-host interaction underlying infection is crucial for formulating effective treatment and preventive strategies to mitigate the disease burden.

摘要

并且感染与广泛的临床谱相关,从无症状病例到死亡率高的内脏利什曼病(VL)不等。临床表现,如黑热病后皮肤利什曼病(PKDL)和内脏利什曼病相关噬血细胞性淋巴组织细胞增多症模拟(VL 相关 HLH 模拟),进一步导致临床表现的多样性。这些临床变化受到宿主免疫反应和寄生虫逃避机制之间复杂相互作用的复杂影响。本综述旨在阐明与每种临床表现相关的潜在免疫学机制,取材于过去 5 年发表的文献。特别关注免疫缺陷患者的内脏嗜性感染。在 VL 中,寄生虫利用各种免疫逃避机制,包括免疫检查点,导致主要的抗炎环境,有利于寄生虫的存活。相反,近 70%的人能够产生有效的促炎免疫反应,形成含有寄生虫的肉芽肿。尽管如此,一些患者在免疫抑制时可能会重新激活疾病,这对当前对寄生虫根除的理解提出了挑战。艾滋病毒感染者和免疫缺陷患者的感染病程更为严重,经常出现更高的复发率。因此,在疾病复发和 VL 相关 HLH 模拟的患者中,排除原发性和获得性免疫缺陷至关重要。由于临床相似性,VL 和 HLH 之间的区别具有挑战性,这表明所谓的 VL 相关 HLH 的病名实体可能代表有症状 VL 的严重表现,更准确地称其为 VL 相关 HLH 模拟。因此,在出现 HLH 的患者中排除 VL 至关重要,因为适当的抗菌治疗可以逆转免疫失调。深入了解感染背后的免疫宿主相互作用对于制定有效的治疗和预防策略以减轻疾病负担至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be08/11445144/b5804e2dfc7d/fimmu-15-1402539-g001.jpg

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