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. 2017 Jun 23;90(2):219–227.

Table 1. Studies on Microbial Agents and Antimicrobial Therapy in Pulmonary Fibrosis.

A. Microbial Agent implicated in Pulmonary Fibrosis
Viruses References
Hepatitis C Virus (HCV) [46-50]
Epstein-Barr Virus (EBV) [21,27,32-35,54]
Cytomegalovirus (CMV) [27,41,42]
Human Herpes Virus 1 (HHV-1) [43]
Human Herpes Virus 6 (HHV-6) [44]
Human Herpes Virus 7 (HHV-7) [27]
Human Herpes Virus 8 (HHV-8) [27]
Adenovirus [22,51,52]
Torque-Teno Virus (TTV) [53-56]
Murine gammaherpes virus type 68 (MHV-68) [29,36-38,67,95]
Parainfluenza Virus [54]
Parvovirus B19 [42]
Bacteria
Pseudomonas aeruginosa [58]
Streptococcus pneumonia [20,58]
Moraxella catarrhalis [58]
Proteus mirabilis [58]
Propionibacterium acnes [77]
Staphylococcus aureus [28]
Pneumocystis jirovecii [60]
Haemophilus influenza [19]
Mycobacteria [57]
Fungi
Aspergillus fumigatus [73]
Paracoccidiodes brasiliensis [69-71]
B. Antimicrobial Studies on infectious Agents involved in Pulmonary Fibrosis
Antivirals Findings
Ganciclovir 2-week course of ganciclovir may attenuate disease progression in a subgroup of advanced IPFa patients [26].
Valacyclovir Treatment with this antiviral led to a decrease in sputum viral load in lungs of patients with IPF [27].
Cidovir Antiviral treatment administered to symptomatic animals, improved survival from 20 to 80% compared with untreated symptomatic animals, but lung fibrosis persisted in 60% of the mice [96].
Antibiotics
Clarithromycin Antibiotic treatment with clarithromycin or amoxicillin led to significantly decreased lung hydroxyproline contents, thereby in blocking S. pneumoniae-induced fibrosis exacerbation in mice [20].
Amoxicillin Antibiotic treatment with clarithromycin or amoxicillin led to significantly decreased lung hydroxyproline contents, thereby in blocking S. pneumoniae-induced fibrosis exacerbation in mice [20].
Azithromycin This antibiotic showed a significant reduction in both fibrosis and restrictive lung function pattern in a bleomycin-induced PFb mouse model [25].
Co-trimoxazole Treating IPF patients with the addition of co-trimoxazole 960mg twice daily had no effect on lung function but resulted in improved quality of life and a reduction in mortality in those adhering to treatment [24].
Antifungals
Combined antifungal (Itraconazole) and immunomodulatory (Pentoxifylline) therapy A study conducted on the development of fibrosis in a model of experimental chronic pulmonary PCMc, employing a combined antifungal (Itraconazole) and immunomodulatory (Pentoxifylline) therapy resulted in a significant reduction of granulomatous inflammation and PF, when compared with the results of classical antifungal therapy using itraconazole alone [23].

aIPF: Idiopathic pulmonary fibrosis, bPF: Pulmonary fibrosis, cPCM: Paracoccidioidomycosis