Iriart Xavier, Blanchet Denis, Menard Sandie, Lavergne Rose-Anne, Chauvin Pamela, Adenis Antoine, Cassaing Sophie, Fillaux Judith, Magnaval Jean-François, Demar Magalie, Carme Bernard, Bessieres Marie-Hélène, Couppie Pierre, Nacher Mathieu, Berry Antoine, Aznar Christine
Service de Parasitologie-Mycologie, Centre Hospitalier Universitaire de Toulouse, Toulouse, France; INSERM UMR1043/CNRS UMR5282/Université de Toulouse UPS, Centre de Physiopathologie de Toulouse Purpan (CPTP), Toulouse F-31300, France.
Laboratoire Hospitalier et Universitaire Parasitologie Mycologie, Centre Hospitalier de Cayenne, BP 6006, 97300 Cayenne, French Guiana.
Int J Med Microbiol. 2014 Nov;304(8):1062-5. doi: 10.1016/j.ijmm.2014.07.016. Epub 2014 Aug 7.
In South America, disseminated histoplasmosis due to Histoplasma capsulatum var. capsulatum (H. capsulatum), is a severe and frequent opportunistic infection in AIDS patients. In areas outside the USA where specific-Histoplasma antigen detection is not available, the diagnosis is difficult. With the galactomannan antigen (GM) detection, a test commonly used for invasive aspergillosis diagnosis, there is a cross-reactivity with H. capsulatum that can be helpful for the diagnosis of histoplasmosis. The aim of this study was to evaluate the GM detection for the diagnosis of disseminated histoplasmosis in AIDS patients. The performance of the GM detection was evaluated with serum collected in French Guiana where H. capsulatum is highly endemic. Sera from AIDS patients with disseminated histoplasmosis occurring from 2002 to 2009 and from control HIV-positive patients without histoplasmosis were tested with the GM detection and Histoplasma-specific antibody detection (IEP). In 39 AIDS patients with proven disseminated histoplasmosis, the sensitivity of the Histoplasma IEP was only 35.9% and was linked to the TCD4+ lymphocyte level. For the GM detection, the sensitivity (Se) was 76.9% and specificity (Sp) was 100% with the recommended threshold for aspergillosis diagnosis (0.5). The test was more efficient with a threshold of 0.4 (Se: 0.82 [95% CI: 0.66-0.92], Sp: 1.00 [95% CI: 0.86-1.00], LR+: >10, LR-: 0.18). This study confirms that the GM detection can be a surrogate marker for the diagnosis of disseminated histoplasmosis in AIDS patients in endemic areas where Histoplasma EIA is not available.
在南美洲,由荚膜组织胞浆菌荚膜变种(荚膜组织胞浆菌)引起的播散性组织胞浆菌病,是艾滋病患者中一种严重且常见的机会性感染。在美国以外无法进行特定组织胞浆菌抗原检测的地区,诊断较为困难。使用常用于侵袭性曲霉病诊断的半乳甘露聚糖抗原(GM)检测,与荚膜组织胞浆菌存在交叉反应,这可能有助于组织胞浆菌病的诊断。本研究的目的是评估GM检测在艾滋病患者播散性组织胞浆菌病诊断中的作用。在荚膜组织胞浆菌高度流行的法属圭亚那收集血清,对GM检测的性能进行评估。对2002年至2009年发生播散性组织胞浆菌病的艾滋病患者血清以及无组织胞浆菌病的对照HIV阳性患者血清进行GM检测和组织胞浆菌特异性抗体检测(免疫电泳)。在39例确诊为播散性组织胞浆菌病的艾滋病患者中,组织胞浆菌免疫电泳的敏感性仅为35.9%,且与TCD4 +淋巴细胞水平相关。对于GM检测,按照曲霉病诊断的推荐阈值(0.5),敏感性(Se)为76.9%,特异性(Sp)为100%。当阈值为0.4时,该检测更有效(Se:0.82 [95%可信区间:0.66 - 0.92],Sp:1.00 [95%可信区间:0.86 - 1.00],阳性似然比:>10,阴性似然比:0.18)。本研究证实,在无法进行组织胞浆菌酶免疫分析的流行地区,GM检测可作为艾滋病患者播散性组织胞浆菌病诊断的替代标志物。