USE OF PLANT COMPOSITION, TRADITIONAL CHINESE MEDICINE COMPOSITION IN PREPARING MEDICINE FOR TREATING COVID-19

Abstract

The present invention relates to a method of treating moderate or severe symptoms of COVID-19 using a plant composition. The plant composition comprises Prepared Monkshood Daughter Root (Aconitum carmichaelii), Fragrant Solomonseal Rhizome (Polygonatum odoratum), Indian Bread (Poria cocos), Pinellia tuber (Pinellia ternata), Oriental Wormwood Herb (Artemisia scoparia), Scutellaria Root (Scutellaria baicalensis), Mongolian Snakegourd Fruit (Trichosanthes kirilowii), Magnolia Bark (Magnolia officinalis), Heartleaf Houttuynia Herb (Houttuynia cordata), and Baked Licorice Root and Rhizome (Glycyrrhiza glabra), which is used as a traditional Chinese medicine composition.

Claims

1. A method of treating moderate or severe symptoms of COVID-19 using a plant composition, wherein the plant composition comprises: Prepared Monkshood Daughter Root (Aconitum carmichaelii), Fragrant Solomonseal Rhizome (Polygonatum odoratum), Indian Bread (Poria cocos), Pinellia tuber (Pinellia ternata), Oriental Wormwood Herb (Artemisia scoparia), Scutellaria Root (Scutellaria baicalensis), Mongolian Snakegourd Fruit (Trichosanthes kirilowii), Magnolia Bark (Magnolia officinalis), Heartleaf Houttuynia Herb (Houttuynia cordata), and Baked Licorice Root and Rhizome (Glycyrrhiza glabra).

2. The method according to claim 1, wherein contents of each component of the plant composition is as follows: 1 part by weight of an aqueous extract of Prepared Monkshood Daughter Root (Aconitum carmichaelii), 1.5 parts by weight of an aqueous extract of Fragrant Solomonseal Rhizome (Polygonatum odoratum), 2.5 parts by weight of an aqueous extract of Indian Bread (Poria cocos), 1.5 part by weight of an aqueous extract of Pinellia tuber (Pinellia ternata), 2.5 parts by weight of an aqueous extract of Oriental Wormwood Herb (Artemisia scoparia), 1.5 parts by weight of an aqueous extract of Scutellaria Root (Scutellaria baicalensis), 2.5 parts by weight of an aqueous extract of Mongolian Snakegourd Fruit (Trichosanthes kirilowii), 1.5 parts by weight of an aqueous extract of Magnolia Bark (Magnolia officinalis), 5 parts by weight of an aqueous extract of Heartleaf Houttuynia Herb (Houttuynia cordata), and 1 part by weight of an aqueous extract of Baked Licorice Root and Rhizome (Glycyrrhiza glabra).

3. The method according to claim 1, wherein the plant composition inhibits binding of spike protein of coronavirus to type II angiotensin-converting enzyme (ACE2).

4. The method according to claim 1, wherein the plant composition inhibits an activity of viral 3CL protease.

5. A method of treating moderate or severe symptoms of COVID-19 using a traditional Chinese medicine composition, wherein the traditional Chinese medicine composition comprises: Prepared Monkshood Daughter Root (Aconitum carmichaelii), Fragrant Solomonseal Rhizome (Polygonatum odoratum), Indian Bread (Poria cocos), Pinellia tuber (Pinellia ternata), Oriental Wormwood Herb (Artemisia scoparia), Scutellaria Root (Scutellaria baicalensis), Mongolian Snakegourd Fruit (Trichosanthes kirilowii), Magnolia Bark (Magnolia officinalis), Heartleaf Houttuynia Herb (Houttuynia cordata), and Baked Licorice Root and Rhizome (Glycyrrhiza glabra).

6. The method according to claim 5, wherein contents of each component of the traditional Chinese medicine composition is as follows: 1 part by weight of an aqueous extract of Prepared Monkshood Daughter Root (Aconitum carmichaelii), 1.5 parts by weight of an aqueous extract of Fragrant Solomonseal Rhizome (Polygonatum odoratum), 2.5 parts by weight of an aqueous extract of Indian Bread (Poria cocos), 1.5 part by weight of an aqueous extract of Pinellia tuber (Pinellia ternata), 2.5 parts by weight of an aqueous extract of Oriental Wormwood Herb (Artemisia scoparia), 1.5 parts by weight of an aqueous extract of Scutellaria Root (Scutellaria baicalensis), 2.5 parts by weight of an aqueous extract of Mongolian Snakegourd Fruit (Trichosanthes kirilowii), 1.5 parts by weight of an aqueous extract of Magnolia Bark (Magnolia officinalis), 5 parts by weight of an aqueous extract of Heartleaf Houttuynia Herb (Houttuynia cordata), and 1 part by weight of an aqueous extract of Baked Licorice Root and Rhizome (Glycyrrhiza glabra).

7. The method according to claim 5, wherein the traditional Chinese medicine composition inhibits binding of spike protein of coronavirus to type II angiotensin-converting enzyme (ACE2).

8. The method according to claim 5, wherein the traditional Chinese medicine composition inhibits an activity of viral 3CL protease.

9. A method for preparing a traditional Chinese medicine composition for treating moderate or severe symptoms of COVID-19, comprising: mixing Prepared Monkshood Daughter Root (Aconitum carmichaelii), Fragrant Solomonseal Rhizome (Polygonatum odoratum), Indian Bread (Poria cocos), Pinellia tuber (Pinellia ternata), Oriental Wormwood Herb (Artemisia scoparia), Scutellaria Root (Scutellaria baicalensis), Mongolian Snakegourd Fruit (Trichosanthes kirilowii), Magnolia Bark (Magnolia officinalis), Heartleaf Houttuynia Herb (Houttuynia cordata), and Baked Licorice Root and Rhizome (Glycyrrhiza glabra), adding water therein, boiling and condensing the water to about ¼ volume to obtain a decoction which is the traditional Chinese medicine composition.

10. The method according to claim 9, wherein contents of each component of the traditional Chinese medicine composition is as follows: 1 part by weight of an aqueous extract of Prepared Monkshood Daughter Root (Aconitum carmichaelii), 1.5 parts by weight of an aqueous extract of Fragrant Solomonseal Rhizome (Polygonatum odoratum), 2.5 parts by weight of an aqueous extract of Indian Bread (Poria cocos), 1.5 part by weight of an aqueous extract of Pinellia tuber (Pinellia ternata), 2.5 parts by weight of an aqueous extract of Oriental Wormwood Herb (Artemisia scoparia), 1.5 parts by weight of an aqueous extract of Scutellaria Root (Scutellaria baicalensis), 2.5 parts by weight of an aqueous extract of Mongolian Snakegourd Fruit (Trichosanthes kirilowii), 1.5 parts by weight of an aqueous extract of Magnolia Bark (Magnolia officinalis), 5 parts by weight of an aqueous extract of Heartleaf Houttuynia Herb (Houttuynia cordata), and 1 part by weight of an aqueous extract of Baked Licorice Root and Rhizome (Glycyrrhiza glabra).

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0021] The detailed technical features, content and advantages of the present invention will now be described in more details hereinafter with reference to the accompanying drawings that show various embodiments of the invention as follows.

[0022] FIG. 1 is a schematic diagram of the potential pathway against SARS-CoV-2 infection and the method of the traditional Chinese medicine composition of the present invention to block viral infection;

[0023] FIG. 2 is a schematic diagram of the inhibitory effect of NRICM102 on the binding of the spike protein of SARS-CoV-2 to ACE2. FIG. 2A is analyzed by BioLayer Interferometry (BLI), and FIG. 2B is analyzed by enzyme linked immunosorbent assay (ELISA);

[0024] FIG. 3 is a schematic diagram of the inhibitory effect of NRICM102 on 3CL protease of SARS-CoV-2;

[0025] FIG. 4 is a schematic diagram of the therapeutic effect of NRICM102 on pulmonary embolism induced by SARS-CoV-2 spike protein and thrombin;

[0026] FIG. 5 is a schematic diagram of the therapeutic effect of NRICM102 on bleomycin-induced lung injury;

[0027] FIG. 6 is a schematic diagram of the effect of NRICM102 on the changes of spike protein and lung disease (72 hours) in K18-hACE2 mice induced by SARS-CoV-2 spike protein;

[0028] FIG. 7 is a schematic diagram of the effect of NRICM102 on pulmonary thrombosis, fibrotic factor expression and apoptosis induced by SARS-CoV-2 spike protein in K18-hACE2 mice;

[0029] FIG. 8 is a schematic diagram of the effect of NRICM102 on the expression of cytokines and chemokines induced by SARS-CoV-2 spike protein in human monocytes

[0030] FIG. 9 is a schematic diagram of the effect of NRICM102 on TGF-β-induced epithelial-mesenchymal transition (EMT) and fibroblast to myofibroblast transformation (FMT);

[0031] FIG. 10 is a schematic flow chart of the clinical study; and

[0032] FIG. 11 is a schematic diagram of the results analysis of the clinical study.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0033] The technical content of the present invention will become apparent by the detailed description of the following embodiments and the illustration of related drawings as follows. The main purpose of the drawings used herein is only for illustration and auxiliary description, and may not be of real scale and precise configuration in actual implementation of the present invention. Therefore, the scope of the present invention should not be interpreted or limited based on the ratio and configuration relationship of the attached drawings.

[0034] Unless otherwise defined, all the terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the present invention belongs. It will be further understood that terms such as those defined in commonly used dictionaries should be construed as having meanings consistent with the meanings in the context of the related art and the present invention, and are not to be construed as idealized or excessive formal meaning unless clearly defined herein.

[0035] All numerical values herein are understood to be modified by “about.” The term “about” as used herein means to encompass a variation of ±10%.

[0036] Materials and Methods:

[0037] Human bronchial epithelial cells (BEAS-2B) were purchased from Bioresource Collection and Research Center (BCRC, Taiwan); recombinant SARS-CoV-2 spike protein subunit 1 (S1) was purchased from GeneTex International Corporation (UK, product number GTX135817-pro); lipopolysaccharide (Escherichia coli, O55:B5) and bleomycin were purchased from Sigma (USA); the traditional Chinese medicine composition (NRICM102) was prepared by the Chinese Herbal Medicine Pharmacy in Taichung Veterans General Hospital.

[0038] Experimental animals were 6-8-week-old male C57BL/6 and ICR mice, purchased from the National Laboratory Animal Breeding and Research Center (Taipei, Taiwan); 14-16-week-old male K18-hACE2 transgenic mice were purchased from Jackson Laboratory and inbred at the Laboratory Animal Center of National Taiwan University College of Medicine. All experimental animals were treated with standard environmental and food conditions, namely 22±1° C., 55±5% humidity, and 12-hour light/dark cycle, with free access to food and water; all experimental animals were randomized into double-blind manner to reduce experimental bias.

Preparation Example 1

[0039] Traditional Chinese medicine composition and method for preparing the same

[0040] The traditional Chinese medicine composition of the present invention comprises Prepared Monkshood Daughter Root (Aconitum carmichaelii), Fragrant Solomonseal Rhizome (Polygonatum odoratum), Indian Bread (Poria cocos), Pinellia tuber (Pinellia ternata), Oriental Wormwood Herb (Artemisia scoparia), Scutellaria Root (Scutellaria baicalensis), Mongolian Snakegourd Fruit (Trichosanthes kirilowii), Magnolia Bark (Magnolia officinalis), Heartleaf Houttuynia Herb (Houttuynia cordata), and Baked Licorice Root and Rhizome (Glycyrrhiza glabra), which is the formula of Taiwan Chingguan Erhau (NRICM102). The dosages of the ten kinds of Chinese medicine are shown in Table 1 below (the grams (g) of each ingredient herein are exemplary, and the corresponding grams and the corresponding amount of decoction water can be adjusted according to the weight portion ratio).

TABLE-US-00001 TABLE 1 Ingredient of the traditional content (parts by weight Chinese medicine composition content(g) of an aqueous extract) Prepared Monkshood Daughter 7.50 1 Root (Aconitum carmichaelii) Fragrant Solomonseal Rhizome 11.25 1.5 (Polygonatum odoratum) Indian Bread (Poria cocos) 18.75 2.5 Pinellia tuber (Pinellia ternata) 11.25 1.5 Oriental Wormwood Herb 18.75 2.5 (Artemisia scoparia) Scutellaria Root (Scutellaria 11.25 1.5 baicalensis) Mongolian Snakegourd Fruit 18.75 2.5 (Trichosanthes kirilowii) Magnolia Bark (Magnolia 11.25 1.5 officinalis) Heartleaf Houttuynia Herb 37.50 5 (Houttuynia cordata) Baked Licorice Root and 7.50 1 Rhizome (Glycyrrhiza glabra)

[0041] The ten kinds of Chinese medicine described in Table 1 are mixed and put into a boiler, add 1.2 L of water for decoction, decocting to boiling point, and boil until the water is concentrated to 300 mL (that is, concentrated to about ¼ volume of water, and the concentrated water is about 40 parts by weight) to obtain a decoction, which is the traditional Chinese medicine composition (NRICM102, which will be used hereinafter).

Embodiment 1

[0042] ACE2-Spike Protein Binding and NRICM102 Binding Test:

[0043] Biolayer interferometric binding events were detected and monitored in real time using a FortéBio Octet Red 96e Biolayer Interferometer (Molecular Device). First, different variants of recombinant SARS-CoV-2 variant RBD proteins (purchased from Sino Biological) were immobilized on the HIS1K sensor tip at a concentration of 100 μg/mL in phosphate buffered saline (PBS) for 600 seconds, followed by blocking the sensor tip with 1% bovine serum albumin (BSA) for 5 minutes; NRICM102 was resuspended in kinetic buffer (PBST, NaCl adjusted to a concentration of 350 mM), and MRICM102 was 5-fold diluted. After that, each sample (recombinant SARS-CoV-2 variant RBD protein of different variants) was added, and the steps of baseline, association and dissociation were used to perform binding tests for 60 seconds, 300 seconds, and 600 seconds is performed in sequence respectively, the sensor tip generates atypical binding events to immobilized protein through non-specific binding effect; then, the correlation signals and curves were aligned to the test data with a 1:1 best fit model using FortéBio data analysis software. In addition, reference sensor subtraction was used to reduce the signal associated with atypical binding events, i.e., a set of blank sensors that were individually unloaded with protein were exposed to predetermined conditions.

[0044] Results.

[0045] Please refer to FIG. 2A, FIG. 2A is analyzed by BioLayer Interferometry (BLI). In the case of administering 5-fold dilution of NRICM102, NRICM102 can bind to the spike proteins of various SARS-CoV-2-related variants, among which NRICM102 has the highest binding activity for the Delta variant, followed by the Omicron variant, the Beta variant, the Gamma variant, Wild Type, and the Alpha variant.

Embodiment 2

[0046] ACE2-Spike Protein Inhibition Enzyme-Linked Immunosorbent Assay (ELISA)

[0047] Microplates were coated with recombinant SARS-CoV-2 variant RBD protein (0.1-2 μg/well), and after blocking with 1% bovine serum albumin (BSA) for 1 hour at 37° C., NRICM102 was serially diluted (1/10×, 1/50×, 1/100×, 1/150×, 1/300×, 1/600×, 1/900×, 1/1200×, 1/1500×, 1/2000×, 1/3000×, and 1/6000×) and added to the wells, reacted with recombinant SARS-CoV-2 variant RBD protein at 37° C. After the reaction was completed, hACE2 recombinant protein (0.2 μg/mL) was added to each well and incubated at 37° C. for 40 minutes, and then rabbit anti-human IgG-HRP (purchased from Immunology consultants laboratories, Inc.) was added to each well and incubated for 40 minutes. Then the HRP matrix 3,3′,5,5′-tetramethylbenzidine was added to each well for color development, and IN HCl was used to terminate the reaction after color development was completed, and the signal intensity was quantified at OD 450 nm using a spectrometer. The recombinant SARS-CoV-2 variant RBD spike proteins used include Alpha (B.1.1.7), Beta (B.1.351), Gamma (P.1), Delta (B.1.617.2), Omicron (B.1.1529) and the original wild-type coronavirus.

[0048] Results.

[0049] Please refer to FIG. 2B, FIG. 2B shows the effect of the administration of different dilution concentrations of NRICM102 on inhibiting the binding activity of SARS-CoV-2 spike protein and ACE2. As shown in the figure, the EC.sub.50 of NRICM102 for various SARS-CoV-2 related variants is as follows: 2090-fold dilution for Omicron variant, 1571-fold dilution for Gamma variant, 1151-fold dilution for Beta variant, 1117-fold dilution for Delta variant, 1068-fold dilution for Alpha variant, and 833.9-fold dilution for the wild type. From the results above, it can be seen that the antiviral properties of NRICM102 still have significant effects on different SARS-CoV-2 variants.

Embodiment 3

[0050] 3CL Protease Inhibition Assay:

[0051] Recombinant SARS-CoV-2 3CL protease (purchased from Pharmtekx, Taipei, Taiwan) was incubated with NRICM102 in reaction buffer (25 mM Tris, 100 mM NaCl, 1 mM EDTA, 1 mM DTT, pH 7.3) on ice for 30 min. A luciferase matrix peptide (Dabcyl-KTSAVLQSGFRKME(Edans)-OH, purchased from Kelowna International Scientific Inc., New Taipei City, Taiwan) was then added to induce a proteolytic reaction; Cytation 5 cell imaging multifunctional optical detector (BioTek, Vermont, USA) was used to excite the sample at 355 nm for 1 hour at 37° C., and the reaction was monitored at 538 nm, inhibition was calculated and graphed with GraphPad Prism graphing software.

[0052] Results:

[0053] Please refer to FIG. 3, FIG. 3 is a schematic diagram of the inhibitory effect of NRICM102 on the 3CL protease of SARS-CoV-2. As shown in the figure, NRICM102 has a significant inhibitory effect on 3CL protease, and its IC.sub.50 is 119-fold dilution; therefore, the results prove that NRICM102 has a significant inhibitory effect on 3CL protease activity.

Embodiment 4

[0054] Therapeutic test of recombinant SARS-CoV-2 spike protein subunit 1 (spike protein subunit 1, S1)-induced pulmonary embolism in K18-hACE2 mice and thrombin (Thrombin)-induced pulmonary embolism in ICR mice

[0055] Mice were anesthetized with intraperitoneal injection of xylazine (6 mg/kg) and ketamine (60 mg/kg). A small skin incision was created on the neck of each mouse. S1 (400 μg/kg in 2 mL/kg) was dissolved in sterile normal saline and instilled into the tracheal lumen. The incision was closed after instillation to allow the mice to recover. Mice treated as above were orally administered NRICM102 (1.5 g/kg or 3.0 g/kg) or vehicle (saline, as control group) daily for 3 consecutive days, then sacrificed the mice to collect lungs; the groups were as follows: Saline control group (Ctrl), S1+saline, S1+NRICM102 (1.5 g), and S1+NRICM102 (3.0 g).

[0056] Using lung perfusion detection, mice were perfused with 0.5 mL of 1% Evans blue through the right ventricle. The mouse lungs were then excised and photographed, and the degree of vascular occlusion was evaluated independently by detecting the optical density (OD, absorbance at 620 nm) of Evans blue, the percentage of hemoglobin bound with oxygen, was measured using an iSTAT G3+ detection kit (Abbott Point of Care Canada Limited, Canada).

[0057] Before sacrificing the mice, the distance traveled in a behavioral observation box (60×40×60 cm.sup.3) was tracked for 3 minutes to assess the movement activity of the mice, and thereafter an image tracking system (SMART v2.5.21, Panlab, Spain) was used to analyze the results; survival rate was calculated immediately (day 0) and 72 hours (day 3) after administration of S1.

[0058] The method for thrombin induced pulmonary embolism in ICR mice was by injection of α-thrombin (50 U/kg, bovine, Sigma-Aldrich, St. Louis, USA) through the inferior vena cava in 100 μL of sterile saline to induce acute pulmonary embolism in mice. The groups were as follows: saline control group (Ctrl), thrombin, and thrombin+NRICM102 group (3.0 g/kg/day, oral administration for 5 days). The analysis method is the same as the above-mentioned lung perfusion test, pulmonary blood oxygen saturation test and exercise observation; the survival rate is also calculated in the same manner as mentioned above.

[0059] Results.

[0060] Please refer to FIG. 4, FIG. 4 is a schematic diagram of the therapeutic effect of NRICM102 on pulmonary embolism induced by SARS-CoV-2 spike protein, and thrombin. From FIGS. 4A and 4C, it can be seen that the spike protein subunit 1 (S1) caused the lung perfusion to decrease by about 52%, from 3.59±0.13 (control group) to 1.72±0.14, and the pulmonary oxygen saturation decreased significantly from 96.5±0.6 to 83.6±3.7%; after 3 consecutive days of treatment with different doses of NRICM102, lung perfusion returned to 2.50±0.18 (1.5 g/kg of NRICM102) and 2.78±0.16 (3.0 g/kg of NRICM102), and the pulmonary oxygen saturation of both also recovered to greater than about 93%. Therefore, NRICM102 indeed significantly improve the pulmonary embolism induced by S1.

[0061] As shown in FIGS. 4B and 4D, thrombin also induced significant pulmonary embolism, killing 40% of the mice within 5 days and causing a decrease in lung perfusion by about 60% (from 3.54±0.04 to 1.38±0.18). After administration of 3.0 g/kg of NRICM102 for 5 consecutive days, the survival rate of mice was significantly improved to 100%, and the pulmonary perfusion recovered to 2.08±0.17 (p<0.05, with statistical significance). However, there were no significant differences in pulmonary oxygen saturation and animal mobility among the groups on day 5.

[0062] Therefore, the results prove that NRICM102 has significant therapeutic effect on pulmonary embolism caused by SARS-CoV-2 and thrombin.

Embodiment 5

[0063] Therapeutic Test of Bleomycin (BLM)-Induced Lung Injury in C57BL/6 Mice

[0064] Mice were anesthetized with intraperitoneal injection of xylazine (6 mg/kg) and ketamine (60 mg/kg). A small skin incision was made on the neck of each mouse. BLM (2 U/kg, purchased from Sigma) was dissolved in 40 μL of phosphate-buffered saline (PBS) and instilled into the tracheal lumen. After inoculation, the incision was closed, and the animal was allowed to recover. Mice treated as above were orally administered NRICM102 (1.5 g/kg or 3.0 g/kg) or vehicle (saline, as control group) daily for 20 consecutive days before sacrifice. During day 0 to day 21 after bleomycin administration, the mouse body weight and its survival rate were calculated (20% reduction of mouse body weight was selected as the end point of humane sacrifice), and the mouse lung function was measured by conventional plethysmography.

[0065] Results:

[0066] Please refer to FIG. 5, FIG. 5 is a schematic diagram of the therapeutic effect of NRICM102 on bleomycin-induced lung injury. As shown in FIG. 5A and FIG. 5B, compared with the control group, the mice administered bleomycin (BLM) showed significant weight loss on the 5th day, and the survival rate of the mice decreased significantly from the 7.sup.th day. The survival rate dropped to 0% on the 21.sup.st day. On the other hand, administration of NRICM102 significantly improved the phenomenon of BLM-induced weight loss, the survival rate of NRICM102 administration of 1.5 g/kg and 3.0 g/kg increased to 42.8% and 71.4%, respectively.

[0067] Lung tidal volume of mice was measured 3 days after bleomycin-induced lung injury. As shown in FIG. 5C, administration of NRICM102 (3.0 g) significantly reduced bleomycin-induced tidal volume. In addition, by staining with hematoxylin and eosin stain (H&E stain), FIG. 5D shows that the groups administered with NRICM102 have significantly improved the bleomycin-induced lung injury.

[0068] Therefore, the results prove that NRICM102 has significant therapeutic effect on pulmonary embolism caused by bleomycin.

Embodiment 6

[0069] Histopathological and Immunohistochemical Tests:

[0070] For immunohistochemical (IHC) staining, 15-20 consecutive sections (about 20-30 μm in thickness) of the same level of lung tissue were collected from different experimental groups for staining. All tissue sections were fixed, permeabilized and blocked and were randomly selected for specific marker staining with primary antibodies (diluted in PBS containing 3% albumin at 4° C. overnight).

[0071] Antibodies against S1 RBD (1:100) and citrulline histone H3 (CitH3, NET, 1:50), Ly6G (1:100), MPO (1:100), vWF (1:100), PAI-1 (1:100), PDPN (AT1, 1:100), SFTPC (AT2, 1:100), MIF (1:100) and TLR4 (1:100) were purchased from GeneTex (Irvine, Calif., USA); Antibodies against CD11b (1:50) and CD31 (also known as platelet endothelial cell adhesion molecule 1, PECAM-1) were purchased from Abcam (Cambridge, UK). SCF (1:50) and cCasp3 (1:50) antibodies were purchased from Santa Cruz (Santa Cruz Biotechnology, Inc., CA, USA); p-NFκB P65 antibody was purchased from BD Pharmingen (1:50, BD Pharmingen, San Diego, Calif., USA), and c-Kit antibody was purchased from Invitrogen (1:200, Invitrogen, Frederick, Md., USA).

[0072] After washing, all the sections were stained with secondary antibodies conjugated with Alexa Fluor® 488, Alexa Fluor® 555, or Alexa Fluor® 647 (all purchased from Cell Signaling Technology Inc., MA, USA). In order to counterstain the DNA in the nuclei, all sections on coverslips were mounted with medium containing 4′,6-diamidino-2-phenylindole (DAPI). All the properly stained sections on coverslips were examined using a laser-scanning confocal microscope (Zeiss LSM780, Carl Zeiss, Jena, Germany); imaging software (Zen 2011, black edition, Carl Zeiss MicroImaging GmbH, 1997-2011) and AlphaIase FC (Alpha Innotech, San Leandro, Calif., USA) across the entire image field of regions of interest sampled from each group under appropriate magnification (30ט100×) in 3 to 5 independent experiments. For tissue fibrosis detection, a Masson's trichrome staining protocol was followed. The above experiments were conducted to confirm whether administration of NRICM102 can reduce the effect of spike protein subunit 1 (S1) in lung tissue, thereby inhibiting neutrophil infiltration and inflammatory response; and to confirm whether administration of NRICM102 can reduce the expression of prothrombotic factors (vWF and PAI-1) and the formation of NET (CitH3) in lung tissue, thereby inhibiting pulmonary embolism.

[0073] Results:

[0074] Please refer to FIG. 6, FIG. 6 is a schematic diagram showing the effect of NRICM102 on the changes of spike protein and lung disease (72 hours) in K18-hACE2 mice with lung injury induced by SARS-CoV-2 spike protein. As shown in FIGS. 6A-6C, S1 accumulated to high levels in the bronchi and bronchioles, and the accumulation was accompanied by strong neutrophil and monocyte infiltration (CD11b and Ly6G) and strong inflammatory responses, including the expression of p-NFκB P65, MPO, TLR4 and IL-6; while in the NRICM102-administered group, the accumulation of S1 and the aforementioned inflammatory markers (S1, CD11b, Ly6G p-NFκB P65, MPO, TLR4 and IL-6) level was significantly reduced; in addition, the statistical summary of the selected labeled fluorescent staining (relative staining area or cell count (%)) was shown in FIG. 6D. Therefore, the above experimental results prove that NRICM102 can indeed inhibit neutrophil infiltration and inflammatory response.

[0075] Furthermore, please refer to FIG. 7, FIG. 7 is a schematic diagram showing the effect of NRICM102 on pulmonary thrombosis, fibrotic factor expression and apoptosis induced by SARS-CoV-2 spike protein in K18-hACE2 mice. It shown in FIG. 7A that after S1 induction, vWF and PAI-1 proteins are highly expressed in lung tissue, and from FIG. 7B and FIG. 7C, it can be seen that strong NET (CitH3) formation and neutrophil infiltration occurred in lung tissue; however, the expression levels of the aforementioned prothrombotic factors (vWF, PAI-1, and NET) were significantly reduced by administration of NRICM102.

[0076] Next, the loss of AT1 and AT2 alveolar cells in S1-induced mice was examined by inducing apoptosis; as shown in FIG. 7D, significant expression of cleaved caspase 3 and cCasp3 indicates that S1 induces strong apoptosis around lung tissue, while administration of NRICM102 significantly reduces apoptosis (cCasp3) and loss of AT1, AT2 alveolar cells.

[0077] Finally, examine whether the expression levels of fibrosis factors (c-Kit and stem cell factor (SCF)) in the lung tissue induced by S1 are increased: FIG. 7E shows that in the lung tissue induced by S1, fibrosis Factors (c-Kit and SCF) were strongly expressed in the peribronchioles, while administration of NRICM102 significantly reduced the expression levels of fibrotic factors. As shown in FIG. 7F and FIG. 7G, the statistical summary of the positive fluorescent staining (relative staining area or cell count (%)) of the selected markers was clearly observed in the S1+saline group. However, it was not observed in the control group (Ctrl) and S1+NRICM102 group. The results of Masson's trichrome staining for tissue fibrosis detection in FIG. 7H showed that typical tissue fibrosis (blue part) was clearly observed in the S1+saline group, but not in the Ctrl group, while the tissue fibrosis effect was significantly reduced in the S1+NRICM102 group. Therefore, the above results prove that NRICM102 can indeed treat pulmonary embolism and pulmonary fibrosis.

Embodiment 7

[0078] Monocyte Isolation and Cytokine Array Assay:

[0079] Peripheral blood mononuclear cells (PBMCs) are isolated from blood samples of healthy donors; that is, PBMCs are isolated from whole blood using Ficoll-Paque™ density gradient centrifugation, and monocytes (98% pure CD14.sup.+) were isolated from PBMCs by using a classical monocyte isolation kit (Miltenyi Biotec). The isolated monocytes were treated with S1 (100 □g/mL) and NRICM102 for 24 hours. The supernatant (ie, isolated monocytes) was then subjected to cytokine assays using the Human XL Cytokine Array Kit (Cytokine Array, R&D).

[0080] Results:

[0081] Please refer to FIG. 8, FIG. 8 is a schematic diagram showing the effect of NRICM102 on the expression of cytokines and chemokines induced by SARS-CoV-2 spike protein in human monocytes. As shown in FIG. 8, NRICM102 significantly inhibited the induced expression of various chemokines and cytokines which are factors related to cytokine storm, including TNF-α, CD31, RANTES, platelet factor 4 (PF4), IL-1α, IL-1β, IL-6, IL-8, macrophage inflammatory proteins-1α and 1β (MIP-1α, MIP-1β), MIP-3α, myeloperoxidase (MPO), macrophage migration inhibitory factor (MF), Granular Leukocyte Colony Stimulating Factor (G-CSF) and Angiopoietin-2.

Embodiment 8

[0082] Epithelial Mesenchymal Transition (EMT) and Fibroblast to Myofibroblast Transformation (FMT) Assay:

[0083] EMT of bronchial epithelial cells and fibroblast to myofibroblast transformation (FMT) are the key process in the development of pulmonary fibrosis. Epithelial cells which have undergone EMT which subsequently promotes the generation of FMT and fibrogenesis. TGF-β has been reported to induce EMT and FMT which are characterized by the expression of fibronectin (FN1) and alpha smooth muscle actin (α-SMA), respectively. Thus, when EMT occurs in bronchial epithelial cells exposed to TGF-β, fibronectin (FN1) and alpha smooth muscle actin (α-SMA) expression are considered the markers of TGF-β-induced EMT and FMT. In order to evaluate the effect of NRICM102 on EMT of human bronchial epithelial cells (BEAS-2B), the cells were treated with TGF-β or co-treated with TGF-β and NRICM102. And in order to evaluate the effect of NRICM102 on FMT of human fibroblast cells (HFL-1 cells), the cells were treated with TGF-β or co-treated with TGF-β and NRICM102, the processes are as follows:

[0084] For EMT assay, BEAS-2B cells were cultured in dishes coated with bovine serum albumin (BSA, purchased from Bionovas), native fibronectin human protein (purchased from Gibco) and bovine collagen I (purchased from Gibco). The cells were grown at 37° C. under 5% CO.sub.2 in bronchial epithelial cell growth basal medium (BEGM, purchased from Lonza). BEAS-2B cells (6×10.sup.3) were seeded in a 96-well black plate (purchased from Thermo Fisher Scientific) and incubated in BEGM for 24 hrs. Then, the cells were stimulated with 10 ng/mL TGF-0 (purchased from PeproTech) and incubated for 3 days.

[0085] For FMT assay, HFL-1 cells (6×10.sup.3) were seeded in a 96-well black plate (purchased from Thermo Fisher Scientific) and incubated in F-12K medium with 10% FBS for 24 hrs. The cells were washed 3 times with PBS buffer and starved in F-12K medium with 0.1% FBS for 24 h. Then, the cells were replaced with F-12K medium with 0.5% FBS containing 10 ng/mL TGF-β (purchased from PeproTech) and incubated for 3 days.

[0086] The BEAS-2B and HFL-1 cells were fixed with cold methanol (−20° C.) for 30 min at room temperature. Following fixation, permeabilization, and blocking, the BEAS-2B and HFL-1 cells were incubated with a fibronectin antibody (FN1, 1:800 dilution, Cell Signaling) or with alpha smooth muscle actin antibody (α-SMA, 1:800 dilution, Cell Signaling) overnight at 4° C., respectively. After washing, the cells were incubated with Alexa Fluor 488 anti-rabbit IgG (1:1000 dilution, Cell Signaling). The cells were incubated with DAPI (5 μg/mL, purchased from Thermo Fisher Scientific) for nuclear staining. Images were captured with a Cytation 5 Cell Imaging Multi-Optical Detector.

[0087] Data analysis was performed using GraphPad Prism software (version 9.0, GraphPad Software, San Diego, Calif.), and the results of the analysis are presented as mean±SEM (standard deviation). Statistical analysis involved one-way ANOVA, followed by S-N-K t-test analysis. Differences were considered statistically significant at p<0.05. In each figure, ** represents p<0.01.

[0088] Results:

[0089] Please refer to FIG. 9, FIG. 9 is a schematic diagram showing the effect of NRICM102 on TGF-β-induced epithelial-mesenchymal transition (EMT) and fibroblast to myofibroblast transformation (FMT). The results showed that TGF-β treatment significantly increased the expression of FN1 and α-SMA compared with that in the untreated cells. NRICM102 treatment significantly decreased the expression of FN1 and α-SMA in a dose-dependent manner compared with the expression in the TGF-β treated cells (FIGS. 9A and 9B). These results suggest that NRICM102 exhibited the capability to inhibit the TGF-βinduced transition of BEAS-2B cells from bronchial epithelial cells to a mesenchymal-like phenotype and formation of HFL-1 cells from fibroblast to myofibroblast.

Experimental Example 1

[0090] In order to determine the efficacy of NRICM102 (i.e. Taiwan Chingguan Erhau) on patients actually infected with COVID-19, experimental cooperation was carried out with several hospitals. According to the hypoxia symptoms of individual COVID-19 patients, the doctors used whether additional oxygen from an oxygen machine is required as the criteria for judging mild symptoms or moderate to severe symptoms. Patients who do not need additional oxygen supply (i.e., patients with mild symptoms) are prescribed NRICM101 (i.e., Taiwan Chingguan Yihau) for treatment, and patients who need oxygen supply (i.e., patients with moderate to severe symptoms) were prescribed NRICM102 for treatment, both traditional Chinese medicine composition were taken orally three times a day.

[0091] Please refer to FIG. 10, FIG. 10 is a schematic flow chart of the clinical study screening process. 840 patients with Covid-19 were admitted to the partnered hospitals between May 1 and Jul. 26, 2021. Among them, 121 patients were excluded from the base cohort for being under 20 years of age, previously treated elsewhere, admitted for other diseases, critically ill, or hospitalized for less than 2 days. The base cohort of 719 patients was initially divided into the mild-to-moderate group of 353 cases who required no oxygen therapy (non-oxygen group) and the severe-to-critical group of 366 cases who required oxygen therapy (oxygen group), with the former receiving NRICM101 or not and the latter receiving NRICM102 or not. After further excluding those who were vaccinated from the non-oxygen therapy group (not for the oxygen therapy group because vaccination was no longer a factor at this stage). Finally, 302 patients who did (151) and did not (151) receive NRICM101 as well as 246 patients who did (123) and did not (123) receive NRICM102 were included in the analysis. Among them, patients who did not receive NRICM101 and NRICM102 treatment only received usual care.

[0092] The patients who received treatment were those diagnosed as positive by PCR between May 1, 2021 and Jul. 26, 2021, and were continuously observed for 30 days. For the group without oxygen therapy, the primary endpoint was the subsequent need for intubation or ICU admission to the group with oxygen therapy, the primary endpoint was death. Patients were followed up from the time of hospital admission until one of the following events occurred: death, intubation, or 30 days of follow-up; those patients without a primary endpoint event had their data censored as of day 30 following hospital admission.

[0093] Results:

[0094] Please refer to FIG. 11, FIG. 11 is a schematic diagram of the analysis of clinical study results. Also, refer to Table 2 below, which present associations between the traditional Chinese medicine composition use and the endpoint.

TABLE-US-00002 TABLE 2 NRICM101 Intubation or NRICM102 Analysis ICU Admission Death No. of events/no. of patients at risk (%) TCM + Usual Care 0/164 (0.00) 7/126 (5.56) Usual Care 14/181 (7.73)  42/240 (17.50) Relative Risk (95% CI) —&{circumflex over ( )}    .sup.  40.80% (20.54%-81.12%){circumflex over ( )} Propensity score analyses - with matching TCM + Usual Care (%) 0/151 (0.00) 7/123 (5.69) Usual Care (%) 14/151 (9.27)  27/123 (21.95) Relative Risk (95% CI) —&*      .sup. 25.93% (11.73%-57.29%)* Hazard Ratio (95% CI) —$.sup.#     23.17% (10.36-51.82%).sup.# &is represented as Seriously underestimated relative risk (95% CI) = 15.8% (3.6%-68.3%) for unmatched data and 14.3% (3.3%-71.8%) for matched data when we included 2 censored cases as the endpoint. {circumflex over ( )}is represented as The chi-square test was used for unmatched data (p = 0.002 for death and p = 0.006 when we set 2 censored cases as intubation or ICU admission). *is represented as McNemar’s test compared the proportion of intubation or ICU admission (p = 0.003) and death (p < 0.001) for matched data. The power of McNemar’s test being larger than 0.852 for NRICM101 and 0.929 for NRICM102 indicates that the significance of both is not due to chance. $is represented as Seriously underestimated hazard ratio = 13.58% (3.40-54.21%) when we set 2 censored cases as the endpoint by the marginal Cox model. .sup.#is represented as Hazard ratio by marginal Cox regression and p < 0.001 by stratified log-rank test for both NRICM101 and NRICM102.

[0095] We present a seriously underestimated relative risk 15.8% (95% confidence interval [CI], 3.6%-68.3%) for unmatched data and 14.3% (95% CI, 3.3%-71.8%) for matched data when we set 2 censored cases as intubation or ICU admission. Additionally, the results of marginal Cox regression and log-rank tests for days of without intubation or transfer to ICU after matching indicated a significant association between NRICM101 use and usual care (hazard ratio, 13.58%; 95% CI, 3.40/6-54.21%). Patients who did not receive NRICM102 were more likely to have experienced a primary endpoint event than were patients who did (relative risk, 40.80%; 95% CI, 20.54%-81.12%) in the unmatched data analysis.

[0096] The results of marginal Cox regression, McNemar's test and log-rank tests after propensity score matching indicated a significant association between NRICM102 use and death (relative risk, 25.93%; 95% CI, 11.73%-57.29%; hazard ratio, 23.17%; 95% CI, 10.36/0-51.82%). Regarding the impact of potential confounders, the e-value was 7.1756 which is bigger than the RR of corticosteroids. Hence, the treatment effect of TCM was robust.

[0097] In conclusion, the traditional Chinese medicine composition NRICM102 (namely Taiwan Chingguan Erhau) according to the present invention can indeed treat patients with moderate or severe symptoms of COVID-19.

[0098] The present disclosure disclosed herein has been described by means of specific embodiments. However, numerous modifications, variations and enhancements can be made thereto without departing from the spirit and scope of the disclosure set forth in the claims.