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Update on non-infectious uveitis treatment: anti-TNF-alpha and beyond. 非感染性葡萄膜炎治疗的最新进展:抗肿瘤坏死因子-α及其他。
Pub Date : 2024-08-02 eCollection Date: 2024-01-01 DOI: 10.3389/fopht.2024.1412930
Khushboo Chauhan, Mudit Tyagi

Non-infectious uveitis (NIU) encompasses a range of conditions marked by inflammation within various layers of the eye. NIU is a significant contributor to irreversible vision loss among the working-age population in developed countries. The aim of treating uveitis is to manage inflammation, prevent its recurrences and to restore or salvage vision. Presently, the standard treatment protocol for NIU involves initiating corticosteroids as the primary therapeutic agents, although more aggressive approaches and steroid sparing agent may be necessary in certain cases. These advanced treatments option include synthetic immunosuppressants like antimetabolites, calcineurin inhibitors and alkylating agents. For patients who exhibit an intolerance or resistance to corticosteroids and conventional immunosuppressive therapies, biologic agents have emerged as a promising alternative. Notably, among the biologic treatments evaluated, TNF-α inhibitors, anti-CD20 therapy and alkylating agents have shown considerable efficacy. In this review, we delve into the latest evidence surrounding the effectiveness of biologic therapy and introduce novel therapeutic strategies targeting immune components as potential avenues for advancing treatment of NIU.

非感染性葡萄膜炎(NIU)包括一系列以眼球各层发炎为特征的疾病。在发达国家,非传染性葡萄膜炎是造成工作年龄人口视力不可逆转下降的重要原因。治疗葡萄膜炎的目的是控制炎症,防止复发,恢复或挽救视力。目前,NIU 的标准治疗方案包括使用皮质类固醇作为主要治疗药物,但在某些情况下可能需要使用更积极的方法和类固醇替代药物。这些先进的治疗方法包括合成免疫抑制剂,如抗代谢药物、钙调磷酸酶抑制剂和烷化剂。对于那些对皮质类固醇和传统免疫抑制剂疗法不耐受或产生抗药性的患者,生物制剂已成为一种很有前途的替代疗法。值得注意的是,在已评估的生物疗法中,TNF-α抑制剂、抗CD20疗法和烷化剂已显示出相当大的疗效。在这篇综述中,我们将深入探讨有关生物疗法有效性的最新证据,并介绍针对免疫成分的新型治疗策略,以此作为推进 NIU 治疗的潜在途径。
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引用次数: 0
High-throughput ultrastructural analysis of macular telangiectasia type 2. 2 型黄斑毛细血管扩张症的高通量超微结构分析
Pub Date : 2024-07-30 eCollection Date: 2024-01-01 DOI: 10.3389/fopht.2024.1428777
Charles L Zucker, Paul S Bernstein, Richard L Schalek, Jeff W Lichtman, John E Dowling

Introduction: Macular Telangiectasia type 2 (MacTel), is an uncommon form of late-onset, slowly-progressive macular degeneration. Associated with regional Müller glial cell loss in the retina and the amino acid serine synthesized by Müller cells, the disease is functionally confined to a central retinal region - the MacTel zone.

Methods: We have used high-throughput multi-resolution electron microscopy techniques, optimized for disease analysis, to study the retinas from two women, mother and daughter, aged 79 and 48 years respectively, suffering from MacTel.

Results: In both eyes, the principal observations made were changes specific to mitochondrial structure both outside and within the MacTel zone in all retinal cell types, with the exception of those in the retinal pigment epithelium (RPE). The lesion areas, which are a hallmark of MacTel, extend from Bruch's membrane and the choriocapillaris, through all depths of the retina, and include cells from the RPE, retinal vascular elements, and extensive hypertrophic basement membrane material. Where the Müller glial cells are lost, we have identified a significant population of microglial cells, exclusively within the Henle fiber layer, which appear to ensheathe the Henle fibers, similar to that seen normally by Müller cells.

Discussion: Since Müller cells synthesize retinal serine, whereas retinal neurons do not, we propose that serine deficiency, required for normal mitochondrial function, may relate to mitochondrial changes that underlie the development of MacTel. With mitochondrial changes occurring retina-wide, the question remains as to why the Müller cells are uniquely susceptible within the MacTel zone.

简介2型黄斑部远端血管扩张症(MacTel)是一种不常见的晚发性、缓慢进展性黄斑变性。该病与视网膜中区域性Müller胶质细胞缺失和Müller细胞合成的氨基酸丝氨酸有关,在功能上局限于视网膜中央区域--MacTel区:方法:我们使用高通量多分辨率电子显微镜技术,并针对疾病分析进行了优化,研究了患有MacTel的两位女性(母亲和女儿,年龄分别为79岁和48岁)的视网膜:在两只眼睛中,观察到的主要现象是所有视网膜细胞类型(视网膜色素上皮细胞(RPE)除外)的线粒体结构在 MacTel 区内外都发生了特殊变化。病变区是 MacTel 的标志,它从布鲁赫膜和绒毛膜延伸到视网膜的各个深度,包括来自 RPE 的细胞、视网膜血管元件和广泛的肥厚基底膜物质。在Müller神经胶质细胞消失的地方,我们发现了大量的小胶质细胞,它们只存在于Henle纤维层中,似乎在保护Henle纤维,这与Müller细胞正常情况下的保护作用类似:由于Müller细胞能合成视网膜丝氨酸,而视网膜神经元不能,我们认为丝氨酸缺乏是线粒体正常功能所必需的,可能与线粒体变化有关,而线粒体变化是MacTel发病的基础。线粒体的变化发生在整个视网膜上,问题仍然是为什么在 MacTel 区域内 Müller 细胞是唯一易受影响的细胞。
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引用次数: 0
Retinal vascular reactivity in carriers of X-linked inherited retinal disease – a study using optical coherence tomography angiography X 连锁遗传性视网膜疾病携带者的视网膜血管反应性--利用光学相干断层血管造影术进行的研究
Pub Date : 2024-07-09 DOI: 10.3389/fopht.2024.1415393
S. Gocuk, X. Hadoux, Charmaine Catipon, Elise Cichello, Himeesh Kumar, J. Jolly, Peter van Wijngaarden, Thomas Llewelyn Edwards, L. Ayton, David Cordeiro Sousa
Female carriers of X-linked inherited retinal diseases (IRDs) can show highly variable phenotypes and disease progression. Vascular reactivity, a potential disease biomarker, has not been investigated in female IRD carriers. In this study, functional optical coherence tomography angiography (OCT-A) was used to dynamically assess the retinal microvasculature of X-linked IRD carriers.Genetically confirmed female carriers of IRDs (choroideremia or X-linked retinitis pigmentosa), and healthy women were recruited. Macular angiograms (3x3mm, Zeiss Plex Elite 9000) were obtained in 36 eyes of 15 X-linked IRD female carriers and 21 age-matched control women. Two tests were applied to test vascular reactivity: (i) mild hypoxia and (ii) handgrip test, to induce a vasodilatory or vasoconstrictive response, respectively. Changes to vessel density (VD) and vessel length density (VLD) were independently evaluated during each of the tests for both the superficial and deep capillary plexuses.In the control group, the superficial and deep VD decreased during the handgrip test (p<0.001 and p=0.037, respectively). Mean superficial VLD also decreased during the handgrip test (p=0.025), while the deep plexus did not change significantly (p=0.108). During hypoxia, VD and VLD increased in the deep plexus (p=0.027 and p=0.052, respectively) but not in the superficial plexus. In carriers, the physiologic vascular responses seen in controls were not observed in either plexus during either test, with no difference in VD or VLD noted (all p>0.05).Functional OCT-A is a useful tool to assess dynamic retinal microvascular changes. Subclinical impairment of the physiological vascular responses seen in carriers of X-linked IRDs may serve as a valuable clinical biomarker.
X 连锁遗传性视网膜疾病(IRD)的女性携带者可表现出高度多变的表型和疾病进展。血管反应性作为一种潜在的疾病生物标志物,尚未在女性IRD携带者中进行过研究。本研究采用功能性光学相干断层血管造影术(OCT-A)来动态评估X连锁IRD携带者的视网膜微血管情况。研究人员招募了经基因证实的女性IRD(脉络膜血症或X连锁视网膜色素变性)携带者和健康女性。对 15 名 X 连锁 IRD 女性携带者和 21 名年龄匹配的对照女性的 36 只眼睛进行了黄斑血管造影(3x3mm,Zeiss Plex Elite 9000)。对血管反应性进行了两种测试:(i) 轻度缺氧;(ii) 手握试验,分别诱导血管扩张或血管收缩反应。在每项测试中,都对浅层和深层毛细血管丛的血管密度(VD)和血管长度密度(VLD)的变化进行了独立评估。功能性 OCT-A 是评估动态视网膜微血管变化的有用工具,X 连锁 IRD 携带者的亚临床生理血管反应损伤可作为一种有价值的临床生物标志物。
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引用次数: 0
The use of rh-NGF in the management of neurotrophic keratopathy 在神经营养性角膜病的治疗中使用 rh-NGF
Pub Date : 2024-07-08 DOI: 10.3389/fopht.2024.1408587
Anna M Roszkowska, R. Spinella, Alessandro Calderone, Marianna Sindoni, Bogumił H. Wowra, Maciej Kozak, Katarzyna Sajak-Hydzik, Jorge Aliò
Neurotrophic keratitis or keratopathy (NK) is a degenerative corneal disease induced by impairment of the trigeminal nerve function. This condition may lead to persistent epithelial defects, corneal ulceration, and perforation. The diagnosis of NK requires a careful investigation of any ocular and systemic condition associated with the disease and ocular surface and corneal sensitivity examinations. In the past, several medical and surgical procedures were used to treat this condition with different clinical effectiveness. Cenegermin is a recombinant human nerve growth factor (rh-NGF) that supports corneal reinnervation. Different clinical trials have demonstrated the safety and efficacy of topical cenegermin in patients with moderate to severe neurotrophic keratitis. In this review, we report the literature on clinical results regarding the treatment of NK with cenegermin since its approval by the European Medicines Agency (EMA) and the Food and Drug Administration (FDA) in 2017 and 2018, respectively.
神经营养性角膜炎或角膜病(NK)是一种因三叉神经功能受损而诱发的角膜变性疾病。这种疾病可能导致持续性上皮缺损、角膜溃疡和穿孔。诊断 NK 需要仔细检查与该病相关的任何眼部和全身状况,并进行眼表和角膜敏感性检查。过去,曾有几种药物和手术方法用于治疗这种疾病,但临床效果不一。Cenegermin 是一种重组人神经生长因子(rh-NGF),可支持角膜神经再支配。不同的临床试验已证明,中重度神经营养性角膜炎患者局部使用塞内格尔明具有安全性和有效性。在这篇综述中,我们报告了自欧洲药品管理局(EMA)和美国食品和药物管理局(FDA)分别于 2017 年和 2018 年批准使用 cenegermin 治疗 NK 后的临床结果文献。
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引用次数: 0
Updates on protein-prenylation and associated inherited retinopathies 蛋白质异戊烯化及相关遗传性视网膜病变的最新进展
Pub Date : 2024-07-04 DOI: 10.3389/fopht.2024.1410874
Sudhat Ashok, Sriganesh Ramachandra Rao
Membrane-anchored proteins play critical roles in cell signaling, cellular architecture, and membrane biology. Hydrophilic proteins are post-translationally modified by a diverse range of lipid molecules such as phospholipids, glycosylphosphatidylinositol, and isoprenes, which allows their partition and anchorage to the cell membrane. In this review article, we discuss the biochemical basis of isoprenoid synthesis, the mechanisms of isoprene conjugation to proteins, and the functions of prenylated proteins in the neural retina. Recent discovery of novel prenyltransferases, prenylated protein chaperones, non-canonical prenylation-target motifs, and reversible prenylation is expected to increase the number of inherited systemic and blinding diseases with aberrant protein prenylation. Recent important investigations have also demonstrated the role of several unexpected regulators (such as protein charge, sequence/protein-chaperone interaction, light exposure history) in the photoreceptor trafficking of prenylated proteins. Technical advances in the investigation of the prenylated proteome and its application in vision research are discussed. Clinical updates and technical insights into known and putative prenylation-associated retinopathies are provided herein. Characterization of non-canonical prenylation mechanisms in the retina and retina-specific prenylated proteome is fundamental to the understanding of the pathogenesis of protein prenylation-associated inherited blinding disorders.
膜锚定蛋白质在细胞信号、细胞结构和膜生物学中发挥着关键作用。亲水性蛋白质在翻译后会受到多种脂质分子(如磷脂、糖基磷脂酰肌醇和异戊二烯)的修饰,从而被分隔并锚定在细胞膜上。在这篇综述文章中,我们将讨论异戊二烯合成的生化基础、异戊二烯与蛋白质结合的机制以及神经视网膜中前酰化蛋白质的功能。最近发现的新型预炔基转移酶、预炔基蛋白伴侣、非典型预炔基化目标基团和可逆预炔基化预计将增加蛋白质预炔基化异常的遗传性系统疾病和致盲疾病的数量。最近的重要研究还表明,一些意想不到的调节因素(如蛋白质电荷、序列/蛋白质伴侣相互作用、光照历史)在预酰化蛋白质的感光器贩运过程中发挥了作用。本文讨论了前炔化蛋白质组研究的技术进展及其在视觉研究中的应用。本文还提供了已知和推测的前酰化相关视网膜病变的临床最新进展和技术见解。表征视网膜和视网膜特异性前酰化蛋白质组的非经典前酰化机制是了解蛋白质前酰化相关遗传性致盲疾病发病机制的基础。
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引用次数: 0
Prevalence of limbal stem cell deficiency at an academic referral center over a two-year period. 一家学术转诊中心两年内患瓣膜干细胞缺乏症的比例。
Pub Date : 2024-06-24 eCollection Date: 2024-01-01 DOI: 10.3389/fopht.2024.1392106
Jason S Goldberg, Daniel J Fraser, Joshua H Hou

Aim: To evaluate the prevalence and clinical characteristics of limbal stem cell deficiency (LSCD) in the setting of a tertiary referral cornea practice at an academic center.

Patient and methods: A retrospective chart review was performed to identify all unique medical record numbers (MRNs) presenting to a single cornea specialist (JHH) at the University of Minnesota during calendar years 2019 and 2020. Records were queried and confirmed for a diagnosis of LSCD. Clinical characteristics of identified patients, including demographics, etiology of LSCD, severity of LSCD, treatment, and best corrected visual acuity (BCVA) at final follow-up, were documented.

Results: In total 1436 unique MRNs were identified over the study period. There were 61 individuals (91 eyes) diagnosed with LSCD, resulting in a prevalence of 4.25% (95% CI, 3.33-5.42). Of 91 eyes, 60 eyes were bilateral (65.9%). Among all eyes, ocular surface burns were the most common etiology (18.7%) followed by iatrogenic or medicamentosa (15.4%). There were 51 eyes (56.0%) that underwent some form of transplantation. The median BCVA at final follow-up was Snellen 20/80 (range 20/20 to no light perception).

Conclusions: The prevalence of LSCD found at a cornea subspecialty tertiary referral center in our study was much higher than previously reported prevalence rates. This may reflect referral bias and potential underdiagnosis of LSCD in practices outside of subspecialty referral centers. The high prevalence rate in our study also suggests that LSCD patients are concentrated in subspecialty referral practices, with many having high morbidity disease. This constitutes a major health burden for these practices.

目的:评估学术中心角膜病三级转诊诊所中角膜缘干细胞缺乏症(LSCD)的发病率和临床特征:对病历进行回顾性审查,以确定2019年和2020年期间向明尼苏达大学的一位角膜病专家(JHH)就诊的所有唯一病历号(MRN)。对记录进行了查询并确诊为 LSCD。记录了已确诊患者的临床特征,包括人口统计学、LSCD 的病因、LSCD 的严重程度、治疗和最终随访时的最佳矫正视力 (BCVA):研究期间共发现了 1436 个独特的 MRN。有 61 人(91 只眼)被诊断为 LSCD,患病率为 4.25%(95% CI,3.33-5.42)。在 91 只眼睛中,60 只为双眼(65.9%)。在所有眼睛中,眼表烧伤是最常见的病因(18.7%),其次是先天性或药物性(15.4%)。51只眼睛(56.0%)接受了某种形式的移植手术。最后随访时的 BCVA 中位数为斯奈伦 20/80(范围从 20/20 到无光感):结论:在我们的研究中,角膜亚专科三级转诊中心发现的 LSCD 患病率远高于之前报道的患病率。这可能反映了转诊偏差以及亚专科转诊中心以外的医疗机构对 LSCD 的潜在诊断不足。我们研究中的高患病率还表明,LSCD 患者主要集中在亚专科转诊诊所,其中许多人患有高发病率疾病。这给这些诊疗机构带来了沉重的健康负担。
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引用次数: 0
Intensity-based optoretinography reveals sub-clinical deficits in cone function in retinitis pigmentosa 基于强度的视网膜成像显示视网膜色素变性患者视锥功能的亚临床缺陷
Pub Date : 2024-06-04 DOI: 10.3389/fopht.2024.1373549
Mina Gaffney, Thomas B. Connor, Robert F. Cooper
Clinical tools have been widely used in the diagnosis, description, and monitoring the progression of retinitis pigmentosa (RP); however, many of these methods have inherently low sensitivity and specificity, and significant photoreceptor disruption can occur before RP progression has clinically manifest. Adaptive optics scanning light ophthalmoscopy (AOSLO) has shown promise as a powerful tool for assessing photoreceptor disruption both structurally and functionally due to its increased resolution.Here we assess photoreceptor structure and function at the cellular level through AOSLO by acquiring intensity based optoretinography (iORG) in 15 individuals with no reported retinal pathology and 7 individuals with a prior clinical diagnosis of RP. Photoreceptor structure was quantified by calculating cone nearest neighbor distance (NND) across different retinal eccentricities from the AOSLO images. Cone outer segment length was measured across different retinal eccentricities using optical coherence tomography (OCT) derived longitudinal reflectivity profiles (LRPs). Finally, iORG measures of photoreceptor function were compared to retinal sensitivity as measured using the macular integrity assessment (MAIA) microperimeter.Broadly, participants with RP exhibited increasing cone nearest neighbor distances and decreasing cone outer segment length as a function of retinal eccentricity, consistent with prior reports for both controls and individuals with RP. Nearly all individuals with RP had reduced iORG amplitudes for all retinal eccentricities when compared to the control cohort, and the reduction was greater in eccentricities further from the fovea. Comparing iORG amplitudes to MAIA retinal sensitivity, we found that the iORG was more sensitive to early changes in photoreceptor function whereas MAIA was more sensitive to later stages of disease.This highlights the utility of iORG as a method to detect sub-clinical deficits in cone function in all stages of disease progression and supports the future use of iORG for identifying cells that are candidates for cellular based therapies.
临床工具已被广泛应用于视网膜色素变性(RP)的诊断、描述和进展监测;然而,其中许多方法本身的灵敏度和特异性都很低,而且在RP进展出现临床表现之前,就可能发生严重的感光受体破坏。在这里,我们通过自适应光学扫描光视网膜镜(AOSLO)对 15 名未报告视网膜病变的患者和 7 名先前临床诊断为 RP 的患者进行了基于强度的视网膜成像(iORG),从而在细胞水平上评估了感光器的结构和功能。通过计算 AOSLO 图像中不同视网膜偏心率的视锥近邻距离 (NND),对感光细胞结构进行量化。利用光学相干断层扫描(OCT)得出的纵向反射率曲线(LRP)测量不同视网膜偏心的锥体外节长度。最后,光感受器功能的 iORG 测量结果与使用黄斑完整性评估(MAIA)微压计测量的视网膜灵敏度进行了比较。总体而言,RP 患者的视锥近邻距离增加,视锥外节长度减少,这与之前关于对照组和 RP 患者的报告一致。与对照组相比,几乎所有RP患者在所有视网膜偏心率下的iORG振幅都有所减小,而在离眼窝更远的偏心率下,减小的幅度更大。将 iORG 振幅与 MAIA 视网膜灵敏度进行比较后,我们发现 iORG 对感光细胞功能的早期变化更为敏感,而 MAIA 对疾病的后期阶段更为敏感。
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引用次数: 0
Spatial-temporal comparison of Eph/Ephrin gene expression in ocular lenses from aging and knockout mice 老化小鼠和基因敲除小鼠眼球晶状体中 Eph/Ephrin 基因表达的时空比较
Pub Date : 2024-06-04 DOI: 10.3389/fopht.2024.1410860
Peter N. Huynh, Catherine Cheng
Cataracts, defined as any opacity in the transparent ocular lens, remain the leading cause of blindness and visual impairment in the world; however, the etiology of this pathology is not fully understood. Studies in mice and humans have found that the EphA2 receptor and the ephrin-A5 ligand play important roles in maintaining lens homeostasis and transparency. However, due to the diversity of the family of Eph receptors and ephrin ligands and their promiscuous binding, identifying functional interacting partners remains a challenge. Previously, 12 of the 14 Ephs and 8 of 8 ephrins in mice were characterized to be expressed in the mouse lens. To further narrow down possible genes of interest in life-long lens homeostasis, we collected and separated the lens epithelium from the fiber cell mass and isolated RNA from each compartment in samples from young adult and middle-aged mice that were either wild-type, EphA2–/– (knockout), or ephrin-A5–/–. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) was implemented to compare transcript levels of 33 Eph and ephrin gene variants in each tissue compartment. Our results show that, of the Eph and ephrin variants screened, 5 of 33 showed age-related changes, and 2 of 33 showed genotype-related changes in lens epithelium. In the isolated fibers, more dynamic gene expression changes were observed, in which 12 of 33 variants showed age-related changes, and 6 of 33 showed genotype-related changes. These data allow for a more informed decision in determining mechanistic leads in Eph-ephrin-mediated signaling in the lens.
白内障(定义为透明眼球晶状体的任何混浊)仍然是世界上失明和视力受损的主要原因;然而,这种病症的病因尚未完全明了。对小鼠和人类的研究发现,EphA2 受体和 ephrin-A5 配体在维持晶状体平衡和透明度方面发挥着重要作用。然而,由于Eph受体和ephrin配体家族的多样性及其杂乱的结合,确定功能性相互作用伙伴仍然是一个挑战。此前,小鼠的 14 种 Ephs 和 8 种ephrins 中,有 12 种在小鼠晶状体中表达。为了进一步缩小晶状体终身稳态中可能存在的相关基因的范围,我们收集并分离了晶状体上皮细胞和纤维细胞团,并从野生型、EphA2-/-(基因敲除)或ephrin-A5-/-的年轻成年小鼠和中年小鼠的样本中分离出了各区室的 RNA。我们采用逆转录定量聚合酶链反应(RT-qPCR)来比较各组织区系中 33 种 Eph 和 ephrin 基因变体的转录水平。我们的研究结果表明,在筛选出的 Eph 和 ephrin 变体中,33 个变体中有 5 个表现出与年龄相关的变化,33 个变体中有 2 个在晶状体上皮细胞中表现出与基因型相关的变化。在离体纤维中,我们观察到了更为动态的基因表达变化,33 个变体中有 12 个出现了与年龄相关的变化,33 个变体中有 6 个出现了与基因型相关的变化。这些数据有助于在确定 Eph-ephrin 介导的晶状体信号转导机制线索时做出更明智的决定。
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引用次数: 0
High salt diet alleviates disease severity in native experimental autoimmune uveitis. 高盐饮食可减轻原生实验性自身免疫性葡萄膜炎的病情严重程度。
Pub Date : 2024-05-31 eCollection Date: 2024-01-01 DOI: 10.3389/fopht.2024.1370374
Naomi Derluyn, Vincent Foucart, Marko Verce, Rami Abdo, Louis Vaudoisey, Deborah Lipski, Véronique Flamand, Amandine Everard, Catherine Bruyns, François Willermain

Background: Recent studies reported a link between high salt diet (HSD) and clinical exacerbation in mouse models of autoimmune diseases, mainly through the induction of pathogenic Th17 cells and/or HSD-induced dysbiosis. However, the topic remains controversial and not fully understood.

Purpose: In this study, we investigated the effects of HSD on the development of experimental autoimmune uveitis (EAU) in C57BL/6J mice.

Methods and results: Unexpectedly, our data showed a significant attenuating effect of HSD on disease severity of native EAU, induced by direct immunization with IRBP peptide. That said, HSD had no effect on EAU disease severity induced by adoptive transfer of semi-purified auto-reactive IRBP-specific T lymphocytes. Accordingly, HSD did not affect IRBP-specific systemic afferent immune response as attested by no HSD-linked changes in T lymphocytes proliferation, cytokine production and Treg proportion. Gut microbiota analysis from cecal samples in naïve and EAU mice demonstrated that HSD affected differentially α-diversity between groups, whereas β-diversity was significantly modified in all groups. Unknown Tannerellaceae was the only taxon associated to HSD exposure in all treatment groups. Interestingly, a significantly higher abundance of unknown Gastranaerophilales, with potential anti-inflammatory properties, appeared in HSD-fed native EAU mice, only.

Discussion: In conclusion, our study suggests a possible impact of HSD on gut microbiota composition and consequently on development and clinical severity of EAU. Further studies are required to investigate the potential beneficial role of Gastranaerophilales in EAU.

背景:最近的研究报道了高盐饮食(HSD)与自身免疫性疾病小鼠模型临床恶化之间的联系,主要是通过诱导致病性Th17细胞和/或HSD诱导的菌群失调。目的:在这项研究中,我们调查了 HSD 对 C57BL/6J 小鼠实验性自身免疫性葡萄膜炎(EAU)发病的影响:出乎意料的是,我们的数据显示,HSD对IRBP肽直接免疫诱导的原发性EAU的疾病严重程度有显著的抑制作用。尽管如此,HSD对通过收养性转移半纯化的自身反应性IRBP特异性T淋巴细胞诱导的EAU疾病严重程度没有影响。因此,HSD不会影响IRBP特异性的全身传入性免疫反应,T淋巴细胞的增殖、细胞因子的产生和Treg比例没有发生与HSD相关的变化就证明了这一点。对天真小鼠和 EAU 小鼠盲肠样本进行的肠道微生物群分析表明,HSD 对不同组间的α-多样性有不同影响,而β-多样性在所有组中都有显著变化。在所有处理组中,未知丹顶鹤科是唯一与接触 HSD 相关的分类群。有趣的是,仅在喂食 HSD 的本地 EAU 小鼠中,具有潜在抗炎特性的未知嗜胃肠菌的丰度明显更高:总之,我们的研究表明 HSD 可能会影响肠道微生物群的组成,进而影响 EAU 的发展和临床严重程度。还需要进一步研究嗜胃肠球菌对 EAU 的潜在有益作用。
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引用次数: 0
Case report: Inferior valved for non-valved glaucoma drainage device exchange for glaucoma control and cosmesis. 病例报告:下阀式青光眼引流装置与无阀式青光眼引流装置互换,以控制青光眼并改善外观。
Pub Date : 2024-05-31 eCollection Date: 2024-01-01 DOI: 10.3389/fopht.2024.1361898
Abdullah M Khan, Maram E A Abdalla Elsayed, Rizwan Malik

Introduction: While the exchange of a superior valved glaucoma drainage device (GDD) for a non-valved GDD has been reported for achieving glaucoma control, inferior GDD exchange for improving the cosmetic appearance of the eyes due to poor appearance caused by encapsulated GDDs has not been previously documented. Here, we report on two patients with inferior valved GDDs who underwent an exchange for non-valved devices for glaucoma control and cosmetic improvement.

Case description: We report on the case of a 23-year-old gentleman and that of an 8-year-old girl, both of whom had inferior valved GDDs with uncontrolled intraocular pressure and unsightly appearance due to encapsulated GDD plates within the palpebral aperture. Both patients were unhappy about the appearance of their eyes. In each case, improvements in both glaucoma control and cosmesis were achieved by exchanging the valved GDDs for non-valved ones.

Conclusion: Exchanging a valved for a non-valved GDD might help improve the cosmetic appearance of the eyes, in addition to providing glaucoma control.

导言:将上瓣膜青光眼引流装置(GDD)换成无瓣膜 GDD 以达到控制青光眼的目的已有报道,但将下瓣膜青光眼引流装置换成无瓣膜 GDD 以改善包膜 GDD 造成的外观不佳而导致的眼部外观不佳的情况还未见报道。在此,我们报告了两名患有下瓣膜 GDD 的患者,他们接受了无瓣膜装置的交换手术,从而控制了青光眼并改善了外观:我们报告了一名 23 岁男性和一名 8 岁女孩的病例,这两名患者都患有下瓣膜 GDD,眼压无法控制,而且由于 GDD 板被包裹在睑板孔内,外观难看。这两名患者都对自己的眼睛外观不满意。通过将带阀 GDD 换成无阀 GDD,两例患者的青光眼控制和外观都得到了改善:结论:将有瓣膜的 GDD 换成无瓣膜的,除了能控制青光眼外,还有助于改善眼睛的外观。
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Frontiers in ophthalmology
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