Opportunistic fungal infections are life-threatening especially in acute and chronic compromised patients. Early and accurate diagnosis is very important for the prompt onset of treatment and to reduce unnecessary use of antifungal drugs. Fungi are frequently recovered from lower airway samples of people with CF, yet the role of fungi in the progression of lung disease is debated. In a recent paper (Cuthbertson L et al, 2021) next generation sequencing of the ITS2 region was used to examine fungal community composition involving 42 cases of non-CF bronchiectasis and 134 patients with CF. Main results show the presence of Aspergillus in CF patients more frequently than in non bronchiectasis CF as expected, however other dominant members of the fungal airway microbiome as Candida have been documented, whose clinical effect is not still clear. Culture methods alone do not seem adequate for the clinical management of fungal disease.
In a recente review (Poore TS et al, 2021) it has been suggested that worsening of clinical outcomes may be associated with airway fungal detection, although most studies to date are retrospective or observational. Fungi can elicit a T helper cell type 2 (Th-2) mediated inflammatory reaction known as allergic bronchopulmonary aspergillosis (ABPA), particularly in those with a genetic atopic predisposition. In this review risk factors, the spectrum of fungal disease presentations, clinical outcomes after isolation of fungi from airway samples, the role of airway co-infections and the association between fungi and airway inflammation have been highlighted.
A Dutch epidemiological study prospectively analyzed respiratory samples of CF patients during a 3-year period, using a uniform fungal culture protocol, focusing on filamentous fungi and azole resistance in AF. Filamentous fungi were recovered from 699 patients from at least one respiratory sample, corresponding with 3787 cultured fungal species. A. fumigatus was cultured most often with a mean prevalence of 31.7%, followed by Penicillium species (12.6%), non-fumigatus Aspergillus species (5.6%), Scedosporium species (4.5%) and Exophiala dermatitidis and Cladosporium species (1.1% each). 107 different fungal species were identified, with 39 Penicillium species and 15 Aspergillus species (Engel TGP et al, 2019).
A recent review (Tracy MC and Moss RB, 2018) outlined potential risk factors for acquiring fungi, host-pathogen interactions that influence the role of fungi from bystander to pathogen, advances in the diagnostic approaches to isolating and identifying fungi in CF respiratory samples, challenges of classifying clinical phenotypes of CF patients with fungi, and current treatment approaches.
In general, the most common fungi in respiratory samples of patients with CF are Aspergillus fumigatus, Aspergillus terreus and Scedosporium species for filamentous fungi, and yeasts such as Candida albicans and Candida glabrata (Schwarz C et al, 2018).
Previous recommendations (Doring G, 2012) outlined that fungi may be either directly pathogenic or may increase the virulence of the most common bacteria in CF airways. Modifications of the tryptophan kynurenine pathway have been suggested as responsible of an ineffective airway inflammation response that fails to eradicate pathogenic fungi in CF patients (Iannitti RG et al, 2013). Recently (Kim SH et al, 2015) a combined clinical-genomic approach, including global analysis of the fungal microbiome from CF sputum samples, identified a genetic basis of pathogen adaptation associated to loss of function of transcriptional repressor Nrg1.
More recently (Hong G et al, 2019) the association between chronic inhaled antibiotics and Scedosporium isolation has been suggested including data from a retrospective cohort study of 19 023 subjects followed in the CF Foundation Patient Registry between January 1, 2010 and December 31, 2012, where the prevalence of Scedosporium spp was 615 (3.2%).
Efforts providing more rapid and more sensitive diagnosis of invasive fungal infections have been increasing in the last years. Real-time polymerase chain reaction (RT-PCR), galactomannan (GM) and 1,3-ß-D-Glucan (BG) tests performed both in sera and in BAL samples might aid to the early diagnosis and treatment of patients when invasive fungal infections are suspected in compromised patients (Sav H et al, 2012).
Therapeutic strategies depend on the detected fungus and the underlying clinical status of the patient. The antifungal therapy can range from a simple monotherapy up to a combination of three different drugs based on different clinical involvement ( Russo A et al, 2020) (Schwarz C et al, 2018)
A recent review (Staerck C, et al, 2017) outlines the potential role of antioxidant detoxifying enzymes against reactive oxygen species (ROS) and reactive nitrogen species (RNS) released by phagocytic cells during the colonization process of these emerging species, paving the way for future investigations on the role of these enzymes as new therapeutic targets.
Several recent studies reported experience in the treatment od Scedosporium.
In a multicentre study, including 12 centres from January 2008 to December 2014( Schwarz C et al, 2019) 31 patients with a lung infection caused by moulds of the genus Scedosporium/Lomentospora were treated with 36 courses of antifungal treatment Scedosporium apiospermum sensu stricto accounted for 48.4% of cases. A therapeutic response under antimycotics with a median duration 3.9 months was achieved in two/third of patients. Triple and double therapy were significantly more effective compared to monotherapy regarding FEV1, radiology, and symptoms.
A previous report indicated that colistin exhibits in vitro antifungal activity against filamentous ascomycetes occurring in CF patients either as single agent and in combination with other antifungals offering a novel therapeutic option (Schemuth H, 2012).
- To evaluate frequency of fungi beyond Aspergillus Fumigatus (AF) in CF
- to define potential risks factors
- to identify the role of more accurate diagnostic tools
- to inidicate the most efficacy treatment for uncommon fungi
What is known
1 CDSR (Francis NZ, 2022) on antifungal therapies for allergic bronchopulmonary aspergillosis in people with cystic fibrosis concluded that at present, there are no randomised controlled trials that evaluate the use of antifungal therapies for the treatment of ABPA in people with cystic fibrosis, although one trial is currently ongoing which can be eligible for a future update.
No CDSR is available on fungi spp beyond Aspergillus Fumigatus.
A previous review (Liu JC, 2013) focused on the role of Aspergillus spp. in the non-ABPA CF lung causing respiratory infection and worsening of lung disease in CF patients.
Changes in the airway microbiome over time, with Aspergillus spp. filling the empty seats, a changing milieu at the level of the airway surface but also frequency, type and administration route of antibiotics and increased exposure over time have all been suggested as potential factors in the increase of Aspergillus spp. colonisation with increasing age in CF.
Generally, the occurrence of other bacterial species beyond P. aeruginosa in CF airways may represent a target for therapy, as they are either directly pathogenic or may increase the virulence of other pathogens or inhibit antibiotics, thereby diluting their effects on P. aeruginosa (Doring G et al, 2012).
Diagnostic algorithms, radiological score and treatment options have been recently reported in a review as current approach of ABPA in children with CF (Sunman B et al, 2020).
An ongoing phase2/phase 3 trial (NCT04966234) is recruiting CF children and adolescents (age range: 8-17 years) with Aspergillus infection to determine the dosing regimen of Posaconazole at 100mg vs 40 mg.
Development and validation of biomarkers characteristic of different fungal clinical phenotypes, and controlled clinical trials of antifungal agents in well-characterized target populations remain goals to be achieved, as well as the need of more epidemiological studies on prevalence and clinical characteristics of fungi colonization out of AF in CF.