Diagnosing Autoimmune Bullous Diseases-An Indian Perspective.

IF 1.9 Q3 DERMATOLOGY
Indian Dermatology Online Journal Pub Date : 2024-11-05 eCollection Date: 2025-05-01 DOI:10.4103/idoj.idoj_253_24
Adhyatm Bhandari, Dipankar De, Shikha Shah, Debajyoti Chatterjee, Vinod Kumar, Rahul Mahajan, Sanjeev Handa
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引用次数: 0

Abstract

Introduction: Autoimmune bullous diseases (AIBDs) are a group of illnesses characterized by autoantibodies targeting adhesion molecules in the skin and mucosa. Accurate diagnosis of the specific subtype of AIBD is crucial for effective management and predicting prognosis, especially in cases with an increased risk of malignancy. However, differentiating between subtypes can be challenging due to overlapping symptoms.

Overview of diagnostic tests: Direct immunofluorescence microscopy (DIF) detects in vivo bound antibodies in perilesional tissue biopsies and provides details about the probable site of autoantibody deposition within the skin/mucosae, immunoglobulin type, and pattern of antibody deposition. Indirect immunofluorescence (IIF) microscopy with organ substrate is a minimally invasive serological test that detects circulating autoantibodies. Enzyme-linked immunosorbent assay (ELISA) quantifies serum autoantibodies against specific autoantigens. Quantitative ELISA is useful for diagnosis, monitoring therapy, and assessing disease activity. Commercially available ELISA kits, including the multi-variant ones, can detect antibodies associated with AIBDs. BIOCHIP is a technique based on IIF that offers a sensitive and specific diagnostic alternative to ELISA. It uses microarrays with multiple antigenic substrates to simultaneously screen common AIBDs. The BIOCHIP slides contain different substrates, allowing the identification of multiple types of autoantibodies in a single test.

Indian context: While these diagnostic tests offer valuable insights into target antigens, antibody patterns, and disease subtypes, it is important to note that the availability of these tests is limited in most centers across India. This limitation can be attributed to factors such as the relatively higher cost of these investigations, challenges related to the stability of immuno-reactants, and a shortage of trained personnel capable of performing such tests.

Conclusion: This review discusses the diagnosis of AIBDs based on resources available in India, as of today. It also provides with practically applicable diagnostic algorithms for pragmatic diagnosis of AIBDs in Indian scenario.

诊断自身免疫性大疱性疾病——印度人的观点
自身免疫性大疱性疾病(aibd)是一组以自身抗体靶向皮肤和粘膜粘附分子为特征的疾病。准确诊断AIBD的特定亚型对于有效管理和预测预后至关重要,特别是在恶性肿瘤风险增加的病例中。然而,由于症状重叠,区分亚型可能具有挑战性。诊断试验概述:直接免疫荧光显微镜(DIF)在病灶周围组织活检中检测体内结合抗体,并提供皮肤/粘膜内自身抗体沉积的可能部位、免疫球蛋白类型和抗体沉积模式的详细信息。间接免疫荧光显微镜(IIF)与器官底物是一种微创血清学检测循环自身抗体。酶联免疫吸附试验(ELISA)定量血清针对特定自身抗原的自身抗体。定量ELISA是有用的诊断,监测治疗和评估疾病活动。市售的ELISA试剂盒,包括多变体试剂盒,可以检测与aibd相关的抗体。BIOCHIP是一种基于IIF的技术,为ELISA提供了一种敏感和特异性的诊断选择。它使用带有多种抗原底物的微阵列同时筛选常见的aibd。BIOCHIP载玻片包含不同的底物,允许在一次测试中识别多种类型的自身抗体。印度背景:虽然这些诊断测试对目标抗原、抗体模式和疾病亚型提供了有价值的见解,但重要的是要注意,在印度大多数中心,这些测试的可用性是有限的。这种限制可归因于这些调查的成本相对较高、与免疫反应物稳定性有关的挑战以及缺乏能够进行此类测试的训练有素的人员等因素。结论:这篇综述讨论了基于印度现有资源的aibd诊断。为印度情景下aibd的实用诊断提供了实际适用的诊断算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
11.80%
发文量
201
审稿时长
49 weeks
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