Shenoy Aniruddh, Marwaha Pavan Kaur, Worku Dominic Adam
Haematology, Christie Hospital, Manchester M20 4BX, UK.
Faculty of Medicine, University of Southampton, Southampton SO17 1BJ, UK.
J Clin Med. 2023 Jan 18;12(3):770. doi: 10.3390/jcm12030770.
Encephalitis is a life-threatening neurological condition with multiple causes in the setting of Human Immunodeficiency Virus (HIV). CD8 Encephalitis (CD8E) is a newly recognised condition which can present in an acute manner, with pertinent features including classical radiological findings with an intense brain parenchymal infiltration of CD8+ T cells. This review attempted to clarify the symptomatology, distribution and determinants of this condition, as well as to examine its vast unknowns.
A literature review was undertaken in July 2022, utilising the PubMed and Google Scholar databases. Papers published between 2006-2022 were reviewed. Eighteen papers, totalling 57 patients, were found and analysed. Statistical analysis was undertaken using Chi-squared and Wilcoxon rank-sum tests as appropriate, with < 0.05 deemed significant.
In this review, 57 patients were identified, with a female (61%, 34/56) and Black African (70%, 40/57) preponderance. Females were more likely to present with headache ( = 0.006), and headache was more likely to be present in those who died ( = 0.02). There was no statistically significant association between baseline CD4 count ( = 0.079) and viral load ( = 0.72) with disease outcome. Overall, 77% (41/53) of patients had classical imaging findings, including bilateral gadolinium-enhancing punctate and perivascular white matter lesions. However, many patients (23/57) required a brain biopsy as part of their diagnostic workup. Corticosteroid treatment was commonly prescribed in patients (64%, 35/55) and had a mortality benefit, with an overall survival in this group of 71% ( = 0.0008). In those who died, median survival was 5.5 months. In rare instances, recurrence of the disease was noted, which responded poorly to treatment.
CD8E represents a new and complex condition with few risk factors identified for its occurrence. The presenting symptoms are broad, but headache appears to be more common in females and more significantly associated with death. Though rare, CD8E is likely under-diagnosed, possibly due to overlapping features with other illnesses and lack of physician experience in its recognition and management. Corticosteroids demonstrate a clear mortality benefit, but more studies are required to determine their optimal dosing and duration, as well as the use of steroid-sparing agents. Further reviews should help to better determine the risk factors for the condition, as well as non-invasive biomarkers, to aid in diagnosis and help to predict poor prognosis and disease recurrence.
脑炎是一种危及生命的神经系统疾病,在人类免疫缺陷病毒(HIV)感染的情况下有多种病因。CD8 脑炎(CD8E)是一种新认识的疾病,可急性起病,其相关特征包括典型的影像学表现以及 CD8+T 细胞对脑实质的强烈浸润。本综述试图阐明该疾病的症状、分布和决定因素,并探讨其诸多未知之处。
2022 年 7 月进行了文献综述,利用 PubMed 和谷歌学术数据库。对 2006 年至 2022 年发表的论文进行了回顾。共找到并分析了 18 篇论文,涉及 57 例患者。根据情况适当使用卡方检验和 Wilcoxon 秩和检验进行统计分析,P<0.05 被认为具有统计学意义。
在本综述中,共纳入 57 例患者,以女性(61%,34/56)和非洲黑人(70%,40/57)居多。女性更易出现头痛(P = 0.006),且死亡患者中头痛更为常见(P = 0.02)。基线 CD4 计数(P = 0.079)和病毒载量(P = 0.72)与疾病转归之间无统计学显著关联。总体而言,77%(41/53)的患者有典型的影像学表现,包括双侧钆增强点状和血管周围白质病变。然而,许多患者(23/57)在诊断检查中需要进行脑活检。皮质类固醇治疗在患者中常用(64%,35/55),且有降低死亡率的益处,该组患者的总体生存率为 71%(P = 0.0008)。在死亡患者中,中位生存期为 5.5 个月。在罕见情况下,会出现疾病复发,且对治疗反应不佳。
CD8E 是一种新的复杂疾病,其发生的危险因素较少。呈现的症状多种多样,但头痛在女性中似乎更常见,且与死亡的关联更为显著。尽管罕见,但 CD8E 可能诊断不足,可能是由于与其他疾病特征重叠以及医生对其识别和管理缺乏经验。皮质类固醇显示出明显的降低死亡率的益处,但需要更多研究来确定其最佳剂量和疗程,以及类固醇替代药物的使用。进一步的综述应有助于更好地确定该疾病的危险因素以及非侵入性生物标志物,以辅助诊断并帮助预测不良预后和疾病复发。