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Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis

Respiratory Research volume 24, Article number: 112 (2023) Cite this article

Abstract

Background

Pulmonary fibrosis is an emerging complication of SARS-CoV-2 infection. In this study, we speculate that patients with COVID-19 and idiopathic pulmonary fibrosis (IPF) may share aberrant expressed microRNAs (miRNAs) associated to the progression of lung fibrosis.

Objective

To identify miRNAs presenting similar alteration in COVID-19 and IPF, and describe their impact on fibrogenesis.

Methods

A systematic review of the literature published between 2010 and January 2022 (PROSPERO, CRD42022341016) was conducted using the key words (COVID-19 OR SARS-CoV-2) AND (microRNA OR miRNA) or (idiopathic pulmonary fibrosis OR IPF) AND (microRNA OR miRNA) in Title/Abstract.

Results

Of the 1988 references considered, 70 original articles were appropriate for data extraction: 27 studies focused on miRNAs in COVID-19, and 43 on miRNAs in IPF. 34 miRNAs were overlapping in COVID-19 and IPF, 7 miRNAs presenting an upregulation (miR-19a-3p, miR-200c-3p, miR-21-5p, miR-145-5p, miR-199a-5p, miR-23b and miR-424) and 9 miRNAs a downregulation (miR-17-5p, miR-20a-5p, miR-92a-3p, miR-141-3p, miR-16-5p, miR-142-5p, miR-486-5p, miR-708-3p and miR-150-5p).

Conclusion

Several studies reported elevated levels of profibrotic miRNAs in COVID-19 context. In addition, the balance of antifibrotic miRNAs responsible of the modulation of fibrotic processes is impaired in COVID-19. This evidence suggests that the deregulation of fibrotic-related miRNAs participates in the development of fibrotic lesions in the lung of post-COVID-19 patients.

What is already known on this topic

An emerging complications of SARS-CoV-2 infection is pulmonary fibrosis. In this study, we speculate that patients with COVID-19 and idiopathic pulmonary fibrosis (IPF) may share aberrant expressed miRNAs associated to the progression of lung fibrosis.

What this study adds

This is the first review to identify miRNAs presenting similar alteration in COVID-19 and IPF. Interestingly, these miRNAs are key regulators of fibrosis processes. The deregulation of these fibrotic-related miRNAs may participate in the development of fibrotic lesions in the lung of post-COVID-19 patients.

How this study might affect research, practice or policy

The study of these miRNAs may help to decipher molecular pathways involved in the development of lung fibrosis in post-COVID-19 patients.

Introduction

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has infected more than 523 million persons and caused over 6.3 million deaths worldwide until May 2022 [1]. SARS-CoV-2 primarily affects the lungs, inducing a range of clinical manifestations, from asymptomatic to severe form characterized by acute respiratory distress syndrome (ARDS) and some immune-mediated lung complications, that require intensive care treatment and mechanical ventilation and can ultimately result in respiratory failure and death [2,3,4,5].

An emerging complication of SARS-CoV-2 infection is pulmonary fibrosis [6,7,8,9,10]. A recent meta-analysis study by Hama Amin et al. shows that a significant portion of recovered COVID-19 patients (44.9%) appear to have developed pulmonary fibrosis, which may persist over time [10]. The prevalence of post-COVID-19 fibrosis will become more apparent in time, but early analysis from patients with COVID-19 highlighted a high level of fibrotic lung function abnormalities [11,12,13,14,15]. In a recent study, McGroder et al. found that among survivors of severe COVID-19, 20% of non-mechanically ventilated and 72% of mechanically ventilated patients had fibrotic-like radiographic abnormalities 4 months after hospitalization, which correlates with loss of lung function and cough [12, 16]. Similarly, Aul et al. reported that patients who had severe COVID-19 infection, particularly those who were intubated and who have persistent breathlessness are at risk of developing post-COVID-19 pulmonary fibrosis [14]. In a recent study, they showed that up to 9.3% of post-COVID-19 patients with persistent respiratory symptoms present pulmonary fibrosis. In a multicentric observational study including 600 COVID-19 cases with lung involvement, Patil et al. observed lung fibrosis in 13.66% of post-COVID-19 pneumonia patients [15].

Idiopathic pulmonary fibrosis (IPF) is the archetypal progressive fibrosing interstitial lung disease, of unknown etiology and cure which leads to rapid death (2–3 years after diagnosis) [17,18,19,20,21]. IPF is characterized by progressive and irreversible destruction of the lung architecture caused by excessive extracellular matrix (ECM) deposition and remodeling, resulting in the formation of fibrotic scar that ultimately leads to organ destruction and death from respiratory failure [22, 23].microRNAs (miRNAs) are small noncoding RNA molecules (20–22 nucleotides) that post-transcriptionally modulate gene expression by blocking the translation or inducing degradation of target mRNAs [24,25,26,27,28]. Several studies reported the dysregulation of the levels of circulating miRNAs in lung diseases [29, 30]. Previously, we identified a unique signature of three sputum-derived miRNAs presenting an aberrant expression in IPF patients compared to healthy donors [29]. Besides their capacity as potential biomarkers of lung diseases, miRNAs are essential regulators of various cellular processes, including fibrosis [27, 31,32,33]. Several studies have shown that miRNAs also participate in SARS-CoV-2 infection and pathogenesis through different mechanisms [34, 35], such as: host cell miRNA expression interfering with SARS-CoV-2 cell entry [36, 37]; SARS-CoV-2-derived RNA transcripts acting as competitive endogenous RNAs that may attenuate host cell miRNA expression [38,39,40,41]; and host cell miRNA expression modulating SARS-CoV-2 replication [38, 42,43,44]. In addition, miRNAs have also been implicated in COVID-19 associated manifestations, including pulmonary fibrosis [45].

Because a portion of post-COVID-19 patients develops pulmonary fibrosis, we speculate that COVID-19 and IPF patients share aberrant expressed miRNAs that may be implicated in lung fibrosis. Therefore, the objective of this systematic review was to identify miRNAs presenting similar alterations in COVID-19 and IPF, and to present their impact on fibrogenesis.

Methods

Review question

The objective of this systematic review was to identify miRNAs presenting similar alterations in COVID-19 and IPF, and to present their impact on fibrogenesis.

Data sources and eligibility criteria

A systematic review of the literature was conducted to search for all articles reporting the deregulation of circulating or cellular miRNAs related to COVID-19 and IPF between 2010 and January 2022 according to PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines [46], with the relative flow diagram shown in Fig. 1. This study satisfied all the recommended items reported in the PRISMA 2020 checklist available (Additional file 1: Fig. S1). The protocol of this synthesis of the current literature has been registered in the International Prospective Register of Systematic Reviews (PROSPERO) database (CRD42022341016). The systematic review was conducted using a defined search strategy by two investigators (JG and MSN) using electronic databases (Pubmed, ScienceDirect, Scopus, EMBASE and Cochrane).

Fig. 1
figure 1

Flow diagram of the systematic research method for detecting matching miRNAs in COVID-19 and IPF

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Inclusion/exclusion criteria

The databases were searched using the keywords (COVID-19 OR SARS-CoV-2) AND (microRNA OR miRNA) or (idiopathic pulmonary fibrosis OR IPF) AND (microRNA OR miRNA) in Title/Abstract. We considered all studies that reported circulating miRNAs in either COVID-19/SARS-CoV-2 and/or IPF in human samples. Studies that are excluded in our meta-analysis met the following criteria: (1) reviews, letters, correspondence, expert opinion, and editorial; (2) animal or in vitro studies; (3) duplicate articles.

Data collection

Two independent reviewers (JG and MSN) performed the initial screening of study titles and abstracts, based on predefined inclusion and exclusion criteria, as mentioned above. After the selection of potential eligible papers using the title and the abstract, JG and MSN independently retrieved the full-text articles to assess the final eligibility. A third reviewer (MH) resolved disagreements. From a total of 1988 research articles that were obtained after an extensive database search, 70 original studies were selected for data extraction (Fig. 1).

Outcomes of interest and data extraction

After the selection of eligible papers, JG and MSN extracted the following information independently: name of the first author, year of publication, country of study, methodology (miRNA related and other relevant methods), sample source (biological material (patients’ samples and/or cell lines) and online databases), miRNAs analyzed, main results, and conclusions.

Results

The COVID-19 search identified 1188 articles and the IPF search 800 articles, for a total of 1988 articles. After the removal of 911 duplicates and 899 through the screening of titles and abstracts, we reviewed 178 full-text articles for eligibility and subsequently excluded 108. In the end, this resulted in a total of 70 articles related to deregulated miRNAs in COVID-19 and IPF: 27 studies focused on miRNAs in COVID-19, and 43 on miRNAs in IPF (Fig. 1).

Subsequent analysis revealed that 147 miRNAs were dysregulated in COVID-19 context (Additional file 2: Table S1), and 113 in IPF (Additional file 3: Table S2). A total of 34 miRNAs were overlapping in COVID-19 and IPF, 7 miRNAs presenting an upregulation in COVID-19 and IPF (miR-19a-3p, miR-200c-3p, miR-21-5p, miR-145-5p, miR-199a-5p, miR-23b, and miR-424) (Table 1), 9 miRNAs presenting a downregulation (miR-17-5p, miR-20a-5p, miR-92a-3p, miR-141-3p, miR-16-5p, miR-142-5p, miR-486-5p, miR-708-3p, and miR-150-5p) (Table 2), and 18 miRNAs presenting an opposite regulation in COVID-19 and IPF (Table 3).

Table 1 Overlapping upregulated miRNAs between COVID-19 and IPF
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Table 2 Overlapping downregulated miRNAs between COVID-19 and IPF
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Table 3 Overlapping miRNAs with opposite regulation between COVID-19 and IPF
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Overlapping miRNAs between COVID-19 and IPF: upregulated miRNAs

MiR-19a-3p in COVID-19 and IPF

M Fayyad-Kazan et al. have shown that eight miRNAs were differentially expressed in the plasma of COVID-19 patients versus healthy donors, among which miR-19a-3p being up-regulated whilst miR-17-5p being down-regulated in SARS-CoV-2-infected patients [47]. Similarly, Kadota et al. have shown that miR-19a-3p is upregulated in extracellular vesicles (EVs) derived from lung fibroblasts of IPF patients [48].

MiR-200c-3p in COVID-19 and IPF

MiR-200c-3p expression is upregulated in saliva [49] and serum [50] of COVID-19 patients, as well as serum of IPF patients [51]. Controversial results have been observed in the lung of IPF patients, with decreased expression of miR-200c-3p [52, 53].

MiR-21-5p in COVID-19 and IPF

The data collected on miR-21-5p demonstrate that its expression is upregulated in plasma [54] and serum [55] of COVID-19 patients, as well as in serum [51, 56, 57], serum-derived EVs [58] and alveolar epithelial cells (AECs) [52] of IPF patients compared to healthy controls.

MiR-145-5p in COVID-19 and IPF

MiR-145-5p is upregulated in COVID-19 patients [50, 59], particularly in EVs derived from the blood of patients with COVID-19 [50]. Similarly, this miRNA is upregulated in EVs generated in the IPF context [48]. Indeed, Kadota et al. found that lung fibroblast-derived EVs from IPF patients (n = 20) contain an elevated level of miR-145-5p compared to controls without IPF (n = 26) [48].

MiR-199a-5p in COVID-19 and IPF

MiR-199a-5p is upregulated in the blood of COVID-19 [60] and IPF patients [51] compared to healthy donors. In addition, Lino Cardenas et al. have shown that miR-199a-5p pulmonary expression was significantly increased in IPF patients [61].

MiR-23b and miR-424 in COVID-19 and IPF

MiR-23b is upregulated in plasma of COVID-19 patients [54] as well as in EVs derived from lung fibroblasts of IPF patients [48]. Similarly, the level of miR-424 is high in EVs from serum of COVID-19 [50] and lung fibroblasts of IPF patients [48].

Overlapping miRNAs between COVID-19 and IPF: downregulated miRNAs

MiR-17–92 cluster members in COVID-19 and IPF

M Fayyad-Kazan et al. have shown that miR-17-5p is down-regulated in SARS-CoV-2-infected patients [47]. The modulation of miR-17-5p in COVID-19 context was confirmed in another study by Demiray et al. Indeed, they highlighted the decrease of miR-17-5p in the serum of COVID-19 patients compared to healthy donors [62]. Similarly, miR-17-5p is downregulated in lung fibroblasts of IPF patients [63].

In addition, two other members of miR-17–92 cluster, miR-20a-5p and miR-92a-3p, are downregulated in both COVID-19 [60, 64] and IPF patients [63, 65].

miR-141-3p in COVID-19 and IPF

miR-141-3p is a member of the miR-200 family that has been associated with the regulation of the epithelial-mesenchymal transition (EMT) phenotype [66]. This miRNA is downregulated in COVID-19 peripheral blood mononuclear cells (PBMCs) [67] and IPF patients’ lungs [68, 69].

miR-16-5p in COVID-19 and IPF

miR-16-5p is downregulated in these two diseases [60, 70]. In a recent study, Gonzalo-Calvo et al. examined the plasma miRNA profile of hospitalized COVID-19 patients (n = 36) and identified several miRNAs dysregulated in ICU patients compared to ward patients (n = 43), among which miR-16-5p (downregulated) [60]. Lacedonia et al. also reported a reduction of the levels of miR-16-5p in the serum of a group of IPF patients (n = 61) compared to healthy controls (n = 15) [70].

miR-142-5p in COVID-19 and IPF

A study comparing patients affected by COVID-19 (n = 6) to healthy volunteers (n = 6) reported that the level of miR-142-5p being down-regulated [47]. In another study by Li et al. [64], whole-transcriptomic sequencing of blood samples from COVID-19 patients (n = 10) and healthy donors (n = 4) enabled to identified 23 differentially expressed miRNAs, among which an upregulation of miR-142-5p. In the IPF context, several studies reported a reduced level of miR-142-5p in serum [56] and lung tissues [69] of IPF patients compared to healthy controls.

miR-486-5p in COVID-19 and IPF

In the COVID-19 context, D de Gonzalo-Calvo et al. identified a signature of three miRNAs, among which miR-486-5p, that distinguishes between ICU and ward patients [60]. Similarly, miR-486-5p expression was decreased in serum samples from patients with silicosis, as well as the lung tissues of patients with either silicosis or IPF, compared with healthy donors [71].

MiR-708-3p in COVID-19 and IPF

miR-708-3p is downregulated in the PBMCs of COVID-19 [67] and IPF patients [63, 72] compared to healthy controls. In a recent study, Chen et al. have shown that the expression level of miR-708-3p is reduced between COVID-19 patients with mild and serious symptoms, and between COVID-19 patients and healthy controls [67]. Another study by Liu et al. showed that miR-708-3p expression was lower in the PBMCs of the patients with IPF than in those of the normal individuals [72].

MiR-150-5p in COVID-19 and IPF

MiR-150-5p is downregulated in the plasma of COVID-19 patients. Indeed, a study by D de Gonzalo-Calvo et al. reported a decrease of the level of miR-150-5p in critically ill COVID-19 patients [60]. Similarly, there is a reduction of the expression of miR-150-5p in the PBMCs of IPF patients according to disease severity [73].

Overlapping miRNAs between COVID-19 and IPF: miRNAs with opposite regulation

Several other overlapping miRNAs are of potential interest, but they present an opposite regulation in COVID-19 and IPF context (Table 3). Indeed, opposite regulation have been reported for miR-15a-5p [47, 50, 74], miR-31-5p [73, 75], miR-29c-3p [54, 76], miR-195-5p [69, 75], miR-27b-3p [60, 69], miR-15b-5p [74, 77] and miR-190a-5p [62, 63]: both are upregulated in COVID-19 and downregulated in IPF. For example, miR-15a-5p and miR-15b-5p are upregulated in blood of COVID-19 patients [47, 77], as well as in EVs derived from serum of COVID-19 patients for miR-15a-5p [50]. In contrast, the levels of these two miRNAs are decreased in the lung of IPF patients compared to healthy controls [74].

On the other hand, miR-142-3p [29, 33, 67, 77], miR-93-5p [62, 63], miR-96-5p [64, 78], miR-144-3p [64, 73], miR-34b [62, 79], miR-34c [67, 79], miR-192-5p [29, 67], and miR-1275 [73, 75] present a downregulation in COVID-19 and an upregulation in IPF (Table 3). Two studies reported a downregulation of miR-142-3p in blood [77] and PBMCs [67] of COVID-19 patients compared to controls, whereas two others showed an upregulation of miR-142-3p in exosomes derived from sputum [29] and plasma [33] of IPF patients compared to healthy controls. Njock et al. characterized for the first time the miRNA content of exosomes from the sputum of patients with IPF (n = 16) compared to healthy controls (n = 14) and identified a unique signature of three altered miRNAs: miR-142-3p, miR-33a-5p and let-7d-5p [29]. Interestingly, they found a negative correlation between miR-142-3p and diffusing capacity of the lungs for carbon monoxide/alveolar volume.

Other miRNAs present a controversial regulation in COVID-19 (Table 3). Two studies reported the upregulation of miR-29a-3p in the plasma [54] and PBMCs [80] of COVID-19 patients compared to healthy subjects, whereas two others reported its downregulation in the plasma [81] and serum [82] of COVID-19 patients. In IPF context, a study by Tsitoura et al. reported the reduction of the level of miR-29a-3p in BAL cells [83].

Discussion

It is well established that miRNAs are essential regulators of pulmonary fibrosis, by targeting several processes including ECM deposition and EMT. The miRNA balance which participates in the maintenance of physiological state in the lung is disrupted during IPF, participating in the progression of pulmonary fibrosis [84]. Similarly, we hypothesize that the miRNAs dysregulated in COVID-19 participate in the apparition of lung fibrogenesis by inducing collagen deposition and myofibroblast transformation. For this, we identified miRNAs similarly expressed in COVID-19 and IPF (Tables 1 and 2), and reported their implication in the pathogenesis of IPF (Fig. 2).

Fig. 2
figure 2

Overlapping of dysregulated miRNAs in COVID-19 and IPF: impact in the development of fibrotic lesions in the lung of post-COVID-19 patients

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Upregulated miRNAs during COVID-19: impact on fibrotic processes

The miR-200 family consisting of 5 members (miR-200a, miR-200b, miR-200c-3p, miR-141-3p and miR-429) has been shown to play crucial roles in the regulation of pulmonary fibrosis and is potentially important for the diagnosis and treatment of IPF [53]. Two members of the miR-200 family are dysregulated similarly in COVID-19 and IPF: miR-200c-3p (upregulated) and miR-141-3p (downregulated). Yang et al. have shown that miR-200 family members can reverse the fibrogenic activity of pulmonary fibroblasts from both bleomycin-treated mice and IPF patients [53]. Indeed, they have demonstrated that the introduction of miR-200c-3p diminishes bleomycin-induced pulmonary fibrosis in mice, suggesting that restoring miR-200c-3p may be a novel approach for treating lung fibrosis. In addition, the miR-200 family is also able to regulate the progression of pulmonary fibrosis by suppressing EMT of alveolar epithelial cells (AECs) [85].

Several studies demonstrated the profibrotic impact of miR-21-5p. Previously, Liu et al. have found an upregulation of miR-21-5p in the lungs of mice with bleomycin-induced fibrosis and also in the lungs of patients with IPF, primarily localized in myofibroblasts [86]. The overexpression of miR-21-5p in pulmonary fibroblasts increased the expression of profibrotic markers, such as fibronectin (FN) and α-smooth muscle actin (α-SMA) [86]. The authors have demonstrated that miR-21-5p induces fibrosis by interfering with SMAD7, a modulator of fibrotic pathway. MiR-21-5p inhibition suppressed morphological markers of pulmonary fibrosis in a mouse model of IPF and inversely regulates TGF-β1-induced ECM protein expression in human pulmonary fibroblast cell lines [87]. Another study by Yamada et al. has shown that miR-21-5p also facilitates EMT, one of the major processes underlying the dissemination of fibrotic injury [52].

Studies focusing on the functional properties of miR-145-5p in IPF context have been performed and highlighted its profibrotic property. Indeed, the overexpression of miR-145-5p in lung fibroblasts increased SMA-α expression, enhanced contractility, and promoted the formation of focal and fibrillar adhesions, and the depletion of miR-145-5p is protective against bleomycin-induced lung fibrosis [88]. It has been shown that miR-145-5p is also implicated in the induction of EMT process [89].

Lino Cardenas et al. have shown that miR-199a-5p pulmonary expression was significantly increased in IPF patients, and demonstrated that this miRNA behaves as a major mediator of lung fibrosis by promoting the pathogenic activation of pulmonary fibroblasts including proliferation, migration, invasion, and differentiation into myofibroblasts [61]. It has been shown that miR-199a-5p is also increased during liver fibrosis and that miR-199a-5p plays a role in hepatic stellate cell activation, promoting α-SMA production and fibrosis progression [90].

Kadota et al. highlighted that the expression of miR-23b and miR-424 are elevated in EVs derived from IPF lung fibroblasts compared to that in healthy controls [48]. These EVs are able to induce epithelial-cell senescence by targeting SIRT3, indeed acting as paracrine mediator in IPF pathogenesis. In addition, miR-424 induces the myofibroblast differentiation during EMT by potentiating the TGF-β signaling pathway [91, 92].

Downregulated miRNAs during COVID-19: impact on fibrotic processes

The polycistronic miR-17–92 cluster encodes six individual miRNAs: miR-17-5p, miR-18a-5p, miR-19a-3p, miR-19b-3p, miR-20a-5p and miR-92a-3p [93, 94]. Interestingly, three of them are downregulated in COVID-19 and IPF: miR-17-5p, miR-20a-5p, and miR-92a-3p (Table 2). Dakhlallah et al. have reported the reduction of miR-17∼92 cluster expression in lung tissue from IPF patients, and its re-expression leads to reduced fibrotic gene expression in vitro and in vivo [95]. In addition, several studies have shown that miR-17∼92 cluster members modulate the expression of matrix metalloproteinases implicated in IPF [96,97,98]. All these studies clearly demonstrated that the deregulation of miR-17∼92 cluster members are implicated in IPF development, and may participate in the progression of pulmonary fibrosis observed in post-COVID patients.

MiR-141-3p is a member of the miR-200 family that has been associated with the regulation of EMT phenotype [66]. A study by Huang et al. has shown that upregulation of miR-141-3p in tubular epithelial hindered EMT by enhancing E-cadherin and decreasing vimentin and fibroblast-specific protein 1 expression [99]. In another study, Qian et al. have shown that miR-141-3p inhibited EMT by targeting Zinc-finger E-box binding homeobox 1 (ZEB1) [68]. The decrease of miR-141-3p observed in COVID-19 patients could participate in the development of fibrotic lesions in the lung.

MiR-16-5p plays an important role in the regulation of EMT [100, 101]. The loss of expression of miR-16-5p observed during transdifferentiation of hepatic stellate cells (HSC) is correlated to the myofibroblast-specific phenotype [102]. The upregulation of miR-16-5p abrogates characteristic functions of myofibroblasts, including collagen and α-SMA expression, reversing myofibroblast phenotype to HSC-like cells [103, 104]. Interestingly, The overexpression of miR-16-5p in exosomes significantly suppressed the enhancing effects of TGF-β1 on proliferation, migration, and collagen (COL1A1) expression of fibroblasts, and attenuated bleomycin-induced skin fibrosis [105]. In an elegant study, Inomata et al. reported the antifibrotic properties of miR-16-5p and demonstrated that these effects occur via the mTORC2 pathway [101].miR-142-5p plays a pivotal role in tissue fibrogenesis, by regulating the switch of macrophage to profibrotic M2 phenotype. Indeed, the inhibition of miR-142-5p in vivo reduces bleomycin-induced lung fibrosis by modulating the polarization of macrophages to M2 phenotype and subsequent profibrotic activation [106].

MiR-486-5p and miR-708-3p also present antifibrotic properties. A study by Ji et al. revealed that the overexpression of miR-486-5p significantly decreased both the distribution and severity of lung lesions in silica-induced mouse model of pulmonary fibrosis compared to control group [71]. Another study by Liu et al. showed that the level of miR-708-3p decreased during fibrosis and inversely correlated with IPF [72]. Therefore, the decrease of these miRNAs might represent a primary pathogenic mechanism underlying the development of lung fibrosis in post-COVID-19 patients.

Interestingly, several downregulated miRNAs in COVID-19 context, but not in IPF, also possess antifibrotic properties, such as miR-142-3p [33] or miR-34c [107]. Guiot et al. have shown that the overexpression of miR-142-3p in alveolar epithelial cells and lung fibroblasts was able to reduce the expression of transforming growth factor β receptor 1 (TGFβ-R1) and profibrotic genes [33]. Furthermore, exosomes isolated from macrophages present antifibrotic properties due in part to the repression of TGFβ-R1 by miR-142-3p transfer in target cells. Following this, overexpression of miR-142-3p represses the expression of profibrotic genes in cardiomyocytes [108] and hepatic stellate cells [109].

Limitations

The main limitation is the heterogeneity of the individual studies. The differences can be biological, experimental, or variations in technique. For example, the difference in techniques, tissues and biofluids (blood/saliva, lung cells/exosomes), laboratory methods (RT-qPCR, sequencing) and various miRNA profiling platforms in selected studies. The effect of this limitation was reduced by collecting the results of these heterogeneous studies, evaluating their similarities and finding common differentially expressed miRNAs.

Conclusion

Several studies reported elevated levels of profibrotic miRNAs (miR-21-5p, miR-145-5p, miR-199a-5p, miR-23b and miR-424) in COVID-19 context. In addition, the balance of antifibrotic miRNAs responsible of the modulation of fibrotic processes (miR-17∼92 cluster members (miR-17-5p, miR-20a-5p, miR-92a-3p), miR-141-3p, miR-16-5p, miR-142-5p, miR-486-5p, miR-708-3p) is completely broken in COVID-19 (Fig. 2). All these evidences suggest that the deregulation of fibrotic-related miRNAs (upregulation of profibrotic miRNAs and downregulation of antifibrotic miRNAs) may participate in the development of fibrotic lesions in the lung of post-COVID-19 patients.

Availability of data and materials

The protocol of this synthesis of the current literature has been registered in the International Prospective Register of Systematic Reviews (PROSPERO) database (CRD42022341016). The data generated in this study may be available upon reasonable request from the corresponding author.

Abbreviations

ARDS:

Acute respiratory distress syndrome

BALF:

Bronchoalveolar lavage fluid

BLM:

Bleomycin

COVID-19:

Coronavirus disease 2019

ddPCR:

Droplet digital PCR

ECM:

Extracellular matrix

EMT:

Epithelial-mesenchymal transition

EVs:

Extracellular vesicles

EV-CATCHER:

Extracellular Vesicle Capture by AnTibody of CHoice and Enzymatic Release

HSC:

Hepatic stellate cells

ICU:

Intensive care unit

IPF:

Idiopathic pulmonary fibrosis

miRNA:

MicroRNA

PBMCs:

Peripheral blood mononuclear cells

qPCR:

Quantitative PCR

SARS-CoV-2:

Severe acute respiratory syndrome coronavirus 2

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Acknowledgements

Thank you to all co-authors for their contribution.

Funding

This study was supported by the Fonds d’Investissement de Recherche Scientifique du Centre Hospitalier Universitaire de Liège (FIRS) and the Centre Hospitalier Universitaire de Liège (CHU Liège).

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Authors and Affiliations

  1. Laboratory of Pneumology, GIGA Research Center, University of Liège, University Hospital of Liège, Liège, Belgium

    Julien Guiot, Monique Henket, Claire Remacle, Maureen Cambier, Marie Winandy, Catherine Moermans, Renaud Louis & Makon-Sébastien Njock

  2. Laboratory of Molecular Angiogenesis, GIGA Research Center, University of Liège, Liège, Belgium

    Claire Remacle, Maureen Cambier & Ingrid Struman

  3. Laboratory of Gastroenterology, GIGA Research Center, University of Liège, University Hospital of Liège, Liège, Belgium

    Edouard Louis

  4. Laboratory of Rheumatology, GIGA Research Center, University of Liège, University Hospital of Liège, Liège, Belgium

    Michel Malaise & Clio Ribbens

  5. Fibropole Research Group, University Hospital of Liège, Liège, Belgium

    Julien Guiot, Edouard Louis, Michel Malaise, Clio Ribbens, Renaud Louis & Makon-Sébastien Njock

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  1. Julien Guiot
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Contributions

The work presented here was carried out in collaboration between all authors. JG and M-SN developed the concept, designed the study, and carried out the literature research and study selection, data synthesis, and analysis. MH, CR, MC, and CM co-worked on the associated data collection. Disagreements were resolved by MH. JG and M-SN wrote the manuscript. JG, IS, MW, CM, EL, MM, RL, CR and MSN critically revised and provided important conceptual input. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Makon-Sébastien Njock.

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The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential competing interests.

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Supplementary Information

Additional file 1: Figure S1.

PRISMA 2020 checklist

Additional file 2: Table S1.

miRNA patterns in COVID-19

Additional file 3: Table S2.

miRNA patterns in IPF

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Guiot, J., Henket, M., Remacle, C. et al. Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis. Respir Res 24, 112 (2023). https://doi.org/10.1186/s12931-023-02413-6

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Keywords

Respiratory Research

ISSN: 1465-993X

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