Department for Oral Health & Medicine, UZB University Centre for Dental Medicine Basel, University of Basel, Basel, Switzerland.
Department of Pathology, University of Helsinki and Helsinki University Hospital, HUS, Diagnostiikkakeskus, Patologia, PL 400, 00029 HUS, Helsinki, Finland.
Support Care Cancer. 2024 Feb 23;32(3):185. doi: 10.1007/s00520-024-08396-4.
Allogeneic hematopoietic stem cell transplant (HSCT) recipients receiving long-term and high-dose immunosuppressive medications suffer commonly from oral candida infections. This prospective cohort study examined oral fungal carriage in HSCT recipients and screened the susceptibility against commonly used antifungal agents. An increasing oral occurrence of Candida spp. and the development of resistance against clinically administered fluconazole were hypothesized.
Two hundred HSCT recipients were included and followed up for 2 years post-HSCT. Oral microbiological specimens were analyzed with matrix-assisted laser desorption/ionization-time of flight mass spectrometry assays (MALDI-TOF). The colorimetric method was applied for the susceptibility testing by commercially available Sensititre YeastOne (SYO®, TREK Diagnostics Systems, Thermo-Fisher, UK).
The prevalence of oral Candida spp. carriage increased statistically significantly after a year post-HSCT being 30, 26, 35, 44, and 47%, pre-HSCT, 3, 6, 12, and 24 months post-HSCT, respectively. Altogether, 169 clinical oral Candida strains were isolated. Fourteen Candida spp. were identified, and C. albicans was predominant in 74% of the isolates pre-HSCT with a descending prevalence down to 44% 2 years post-HSCT. An increasing relative proportion of non-albicans species post-HSCT was evident. No development of resistance of C. albicans against fluconazole was found. Instead, a shift from C. albicans towards non-albicans species, especially C. dubliensis, C. glabrata, and relatively seldom found C. krusei, was observed.
Oral Candida carriage increases after HSCT. Instead of the expected development of resistance of C. albicans against fluconazole, the relative proportion of non-albicans strains with innate resistance against azole-group antifungals increased.
接受长期和大剂量免疫抑制药物治疗的异基因造血干细胞移植(HSCT)受者通常患有口腔念珠菌感染。本前瞻性队列研究检查了 HSCT 受者的口腔真菌携带情况,并筛查了对常用抗真菌药物的敏感性。假设 HSCT 后,口腔念珠菌属的发生率增加,以及对临床给予的氟康唑的耐药性发展。
纳入 200 例 HSCT 受者,并在 HSCT 后随访 2 年。通过基质辅助激光解吸/电离飞行时间质谱分析(MALDI-TOF)对口腔微生物标本进行分析。采用比色法对市售 Sensititre YeastOne(SYO®,TREK 诊断系统,Thermo-Fisher,英国)进行药敏试验。
HSCT 后 1 年,口腔念珠菌属携带率呈统计学显著增加,分别为 30%、26%、35%、44%和 47%,分别为 HSCT 前、HSCT 后 3 个月、6 个月、12 个月和 24 个月。共分离出 169 株临床口腔念珠菌株。鉴定出 14 种念珠菌,HSCT 前以白色念珠菌为主,占 74%,2 年后降至 44%。HSCT 后,非白色念珠菌的相对比例增加。未发现白色念珠菌对氟康唑的耐药性。相反,观察到从白色念珠菌向非白色念珠菌的转变,特别是杜氏念珠菌、光滑念珠菌和相对少见的克柔念珠菌。
HSCT 后口腔念珠菌携带增加。没有发现白色念珠菌对氟康唑的耐药性发展,而是具有内在抗唑类抗真菌药物耐药性的非白色念珠菌菌株的相对比例增加。