Facultad de Farmacia y Bioquímica, CONICET, Instituto de Nanobiotecnología (NANOBIOTEC), Universidad de Buenos Aires, Buenos Aires, Argentina.
CONICET, Instituto de Investigaciones en Microbiología y Parasitología Médica (IMPaM), Universidad de Buenos Aires, Buenos Aires, Argentina.
Appl Microbiol Biotechnol. 2021 Mar;105(5):1837-1859. doi: 10.1007/s00253-021-11170-9. Epub 2021 Feb 15.
Histoplasmosis is a worldwide-distributed systemic mycosis caused by the dimorphic fungus Histoplasma capsulatum. Its clinical manifestations range from subclinical or mild respiratory illness to progressive disseminated histoplasmosis (PDH), a life-threatening disease, whose accurate diagnosis is still challenging and limited in many countries, where this disease is highly endemic. In this regard, Histoplasma antigen testing is now included in the WHO Essential Diagnostics List. The final diagnosis of histoplasmosis is established by culture and/or visualization of the yeast cells by cytology or histopathology using specific stains. However, both procedures have limited sensitivity to detect the disease and cultures are time-consuming. Antibody detection assays are effective for the subacute and chronic clinical forms of histoplasmosis. However, their sensitivity is low in the immunocompromised host. Several molecular "in-house" tests were also developed and showed promising results, but none of these tests are commercially available and their standardization and validation are still pending. Antigen detection assays have high sensitivity in PDH cases and are of great value for the follow-up of patients with histoplasmosis; however, cross-reactivity with other related fungi are common. In addition, this assay is expensive and only performed in few laboratories. Novel protein antigen candidates have been recently identified and produced by DNA-recombinant techniques in order to obtain standardized and specific reagents for the diagnosis of histoplasmosis, as opposed to the unspecific antigens or crude extracts currently used. This review describes the currently available assays, highlighting their strengths and limitations and reports the latest approaches to achieve reliable and rapid diagnostic tests for histoplasmosis. KEY POINTS: • PDH causes thousands of deaths per year globally. • Rapid accurate diagnosis of PDH is unfeasible in many regions. • Fast, accurate, and low-cost diagnostic alternatives are currently under development.
组织胞浆菌病是一种由双相真菌荚膜组织胞浆菌引起的世界性分布的系统性真菌病。其临床表现从亚临床或轻度呼吸道疾病到进行性播散性组织胞浆菌病(PDH)不等,PDH 是一种危及生命的疾病,在许多疾病高度流行的国家,其准确诊断仍然具有挑战性且受到限制。在这方面,组织胞浆菌抗原检测现已被纳入世卫组织基本诊断检测清单。通过使用特定染色剂通过细胞学或组织病理学对酵母细胞进行培养和/或可视化,建立组织胞浆菌病的最终诊断。然而,这两种方法对检测疾病的敏感性都有限,且培养过程耗时。抗体检测试验对于组织胞浆菌病的亚急性和慢性临床形式是有效的。然而,在免疫功能低下的宿主中,其敏感性较低。还开发了几种分子“内部”检测方法,并且显示出有希望的结果,但这些检测方法均未上市,其标准化和验证仍在进行中。抗原检测在 PDH 病例中具有很高的敏感性,对组织胞浆菌病患者的随访非常有价值;然而,与其他相关真菌的交叉反应很常见。此外,该检测昂贵,仅在少数实验室进行。最近通过 DNA 重组技术鉴定并生产了新型蛋白抗原候选物,以便获得用于组织胞浆菌病诊断的标准化和特异性试剂,而不是目前使用的非特异性抗原或粗提物。本综述描述了目前可用的检测方法,强调了它们的优势和局限性,并报告了用于实现组织胞浆菌病可靠和快速诊断检测的最新方法。关键点: • PDH 每年在全球造成数千人死亡。 • 在许多地区,快速准确诊断 PDH 是不可行的。 • 目前正在开发快速、准确和低成本的诊断替代方法。