WO2022149717A1 - In vitro analysis method for risk of virus infection on basis of pharyngeal airway tissue-derived cell - Google Patents

Abstract

The present invention relates to an in vitro analysis method for the risk of virus infection on the basis of a pharyngeal airway tissue-derived cell and, specifically, the present invention relates to: a method, for analyzing whether or not there is virus infection on the basis of a pharyngeal airway tissue-derived cell, comprising a step of using a primary cell isolated from a human pharyngeal airway tissue discarded after a surgery; and a method for screening an antiviral agent on the basis of a pharyngeal tissue-derived cell using the primary cell. In the method for analyzing whether or not there is virus infection using a primary cell isolated from a human pharyngeal airway tissue, a human body-derived primary cell is used in place of an immortalized cell line used in an existing virus infection study. Therefore, the method has the advantages of obtaining more accurate results and economic advantages, reducing unnecessary animal experiments, and efficiently reducing time and cost required for discovery and effectiveness assessment of an antiviral agent. Therefore, the method for analyzing whether or not there is virus infection and screening an antiviral agent using a primary cell isolated from a human pharyngeal airway tissue can be utilized as a platform for verifying effectiveness and safety in developing a therapeutic agent against virus infection diseases having increased attack rates worldwide.

Description

In vitro analysis method for risk of viral infection based on cells derived from upper respiratory tract tissue

The present invention relates to an in vitro assay method for viral infection risk based on cells derived from upper respiratory tract tissue.

Among the basic epidemiologic factors affecting disease development, including etiology, host, and environment, etiology can be subdivided into biological, physico-chemical, and social factors, which are major factors in disease occurrence. Common entry routes of pathogens are the respiratory tract, gastrointestinal tract, and skin, and most microorganisms are inhaled mainly through the respiratory tract. Among them, viruses are infectious microorganisms that are much smaller than fungi or bacteria and penetrate living cells. The virus attaches to and penetrates the cell and releases genetic material into the cell to control the cell and cause the virus to replicate. Eventually, the virus prevents the infecting cell from functioning normally and causes it to die, and when it dies, the cell releases a new virus that will infect other cells.

Respiratory viral infection mainly appears as upper respiratory tract infection and is easily spread through contact with an infected person or respiratory droplets. The upper respiratory tract is the upper part of the airway and is the most invasive part of the human respiratory system. The upper respiratory tract infection caused by these viruses is clinically very high. In the United States, it is reported that acute respiratory infections account for 53% of all acute diseases, and that 36% of school absences are due to respiratory infections. Acute respiratory infection is the most common disease in Korea and occurs even in healthy adults without underlying diseases. In particular, after the first outbreak of COVID-19 in Wuhan, China in 2019, the WHO declared a pandemic on March 11, 2020, and a global pandemic is underway. In response, each country is taking countermeasures, and domestic and foreign pharmaceutical and bio companies are concentrating on developing therapeutics and vaccines. In particular, in a difficult situation caused by the spread of COVID-19, the discovery of antiviral substances is an essential response strategy for virus control.

Therefore, it is necessary to develop a technology capable of rapidly diagnosing and evaluating cellular infection caused by external substances such as bacteria and viruses, but a technology for rapid diagnosis of infection and discovery and evaluation of drugs has not yet been developed. .

Accordingly, the present inventors developed an in vitro evaluation platform for viral infection using an upper respiratory tract-derived cell culture system, and completed the present invention by confirming that it can be used for discovery of antiviral candidates and therapeutic agents, and confirmation of efficacy and safety.

Accordingly, it is an object of the present invention to provide a method for analyzing viral infection based on cells derived from upper respiratory tract tissue, comprising the step of using primary cells isolated from human upper respiratory tract tissue discarded after surgery.

Another object of the present invention is to provide a screening method for an antiviral agent based on cells derived from upper respiratory tract tissue using primary cells isolated from human upper respiratory tract tissue discarded after surgery.

In order to achieve the object of the present invention as described above, the present invention provides a method for analyzing viral infection based on cells derived from upper respiratory tract tissue, comprising the step of using primary cells isolated from human upper respiratory tract tissue discarded after surgery. provides

In one embodiment of the present invention, the primary cells may be tonsil-derived mesenchymal stem cells (Tonsil-derived mesenchymal stem cells, TMSC).

In one embodiment of the present invention, the primary cells may be cells isolated from the human upper respiratory tract tissue discarded after the operation by processing collagenase I and DNase I and centrifugation.

In one embodiment of the present invention, the primary cells may have the form of a cell population formed in the form of spheroids through three-dimensional co-culture using a polydimethylsiloxane (PDMS) mold.

In one embodiment of the present invention, the virus may be a coronavirus (Coronavirus) or a reovirus (Reovirus).

In one embodiment of the present invention, the virus infection may be performed by in vitro RT-PCR analysis, immunofluorescence staining analysis or microscopic analysis using primary cells isolated from the human upper respiratory tract tissue.

The present invention also provides a screening method for an antiviral agent based on cells derived from upper respiratory tract tissue using primary cells isolated from human upper respiratory tract tissue discarded after surgery.

In one embodiment of the present invention, after treating the antiviral candidate material before or after infecting the primary cells with the virus, it may be to analyze the changes in the primary cells according to the virus infection.

In one embodiment of the present invention, the analysis of the changes in the primary cells may be performed by RT-PCR analysis, immunofluorescence staining analysis or microscopic analysis.

The method for analyzing virus infection using primary cells isolated from human upper respiratory tract tissue according to the present invention replaces the immortalized cell line used in the conventional virus infection study and uses human-derived primary cells to obtain more accurate results and economic effects. It can be obtained, and unnecessary animal experiments can be reduced, and there is an effect that can effectively reduce the time and cost required for the discovery and efficacy evaluation of the antiviral agent. Therefore, the method for analyzing viral infection and screening for antiviral agents using primary cells isolated from human upper respiratory tract tissue according to the present invention is a platform for validation of efficacy and stability in the development of therapeutic agents for viral infectious diseases, which are increasing in incidence worldwide can be usefully used as

1 shows a photograph of a site with human upper respiratory tract tissue and a photograph of microscopic observation of the morphology of primary cells isolated and cultured from human upper respiratory tract tissue discarded after surgery.

2 is a photograph showing the result of forming a spheroid-type cell population through three-dimensional co-culture by varying the number of primary cells isolated and cultured from human upper respiratory tract tissue discarded after surgery in an embodiment of the present invention. .

3 is a result of confirming the cytopathic effect (CPE) for the group infected with human coronavirus NL63 and the non-infected group for primary cells isolated and cultured from human upper respiratory tract tissue discarded after surgery in an embodiment of the present invention; (A), and shows the result of confirming the presence of virus infection by performing immunofluorescence staining using a human coronavirus NL63-specific antibody (B).

Figure 4 is a reovirus-infected group and non-infected group of primary cells isolated and cultured from human upper respiratory tract tissue discarded after surgery in an embodiment of the present invention. Shows the result of confirming the virus infection through RT-PCR analysis using the primer set (A), and shows the result of confirming the degree of apoptosis through electron microscopy analysis (B).

5 is a virus infection using the LIVE/DEAD assay kit for the group infected with reovirus and the non-infected group targeting primary cells isolated and cultured from human upper respiratory tract tissue discarded after surgery in an embodiment of the present invention. After visualizing whether or not the cells survived, the observed photograph (A) and the graph show the results of comparative analysis of the degree of cell survival (B).

The present invention is characterized by providing an in vitro analysis method for viral infection risk based on cells derived from upper respiratory tract tissue, and specifically, the present invention includes using primary cells isolated from human upper respiratory tract tissue discarded after surgery, upper respiratory tract tissue It is characterized by providing a method for analyzing whether or not virus infection is based on derived cells.

Currently, infectious diseases are increasing worldwide, and infectious diseases with high mortality such as Spanish flu and bird flu are also increasing every year. It is urgent.

Therefore, the present inventors were researching to develop a platform capable of rapidly and accurately discovering viral infection and antiviral agents in vitro, and used primary cells isolated from human upper respiratory tract tissue discarded after surgery to determine whether viral infection and antiviral in vitro. A method for screening for viral agents has been established.

In particular, in the present invention, primary cells isolated from human upper respiratory tract tissue discarded after surgery were used, and in the case of various respiratory viruses such as COVID-19, the upper respiratory tract tissue or cells are primarily infected during human infection. If the throat is swollen and painful, there is a high probability that the throat tissue is infected with a virus or a causative organism. In this case, the probability that the virus is the cause is about 85%. Therefore, when an antiviral agent screening platform is invented using primary cells derived from pharyngeal tissue, tissue-specific immune responses can be confirmed than when cells derived from other tissues or previously sold cell lines are used. In particular, the tonsils are a part of the lymphatic system, and are very suitable as a platform for investigating the cellular biological mechanism of immune response to airborne and ingested infectious agents and the efficacy and possibility of side effects in the human body when developing therapeutic substances, or methods of suppressing side effects. It is indispensable to establish and utilize human-derived cells directly related to external infection as a platform. Therefore, in the present invention, for this reason, primary cells were isolated from the upper respiratory tract tissue and used.

In the present invention, the “primary cell” is also called a “primary cell”, and refers to a normal cell directly obtained from a living organism as a cell directly cultured from an animal tissue or organ. When these cells are cultured, they grow while dividing to a certain extent, but when passage is continued, they have a limitation in aging. Despite these limitations, primary cells have the advantage of being similar to the actual reaction of an organism, so they are used in the production of biologics.

The primary cells of the present invention may include any primary cells isolated from upper respiratory tract tissue, specifically human upper respiratory tract tissue, but are not limited thereto, but tonsil-derived mesenchymal stem cells (Tonsil-derived mesenchymal stem cells, TMSC), tonsil-derived fibroblasts, immune cells and dendritic cells (Tonsil-derived Dendritic cells).

In addition, the primary cells are treated and reacted with collagenase I and DNase I to human upper respiratory tract tissue discarded after surgery, and then centrifuged to use primary cells isolated from the tissue. The centrifugation may be performed at 1800 to 3000 RPM at 25° C. for 5 minutes.

In addition, the primary cells that can be used in the present invention can use a cell population of spheroids through three-dimensional co-culture.

In this case, the three-dimensional co-culture is performed using a polydimethylsiloxane (PDMS) mold.

In the present invention, the "spheroid" refers to a spherical cell mass having a 3D three-dimensional structure, can be prepared from tissue or stem cells, and can be cultured in three dimensions due to self-renewal and differentiation ability. can It can also have an environment that allows it to interact with the surrounding environment during the growth process of the cell. Accordingly, it is possible to almost similarly or completely mimic the organs or cells that are actually interacting in vivo, and it can be an excellent model for observing the development of therapeutic agents for diseases and the like.

Furthermore, the present inventors confirmed whether virus infection can be analyzed using primary cells isolated and cultured from the human upper respiratory tract discarded after surgery according to the present invention. According to an embodiment of the present invention, the primary cells are inoculated with a virus. After infection, it was confirmed that the primary cells according to the present invention can be used as a cell platform capable of analyzing virus infection in vitro through analysis with a control group not inoculated with the virus.

Therefore, the primary cells according to the present invention can be usefully used to analyze whether or not viral infection based on cells derived from the upper respiratory tract tissue.

In addition, the primary cell according to the present invention can be used as a cell platform for screening antiviral agents. Specifically, after treating the antiviral candidate before or after infecting the primary cell of the present invention with a virus, Antiviral agents can be screened by comparing and analyzing changes in primary cells following virus infection with a control group not infected with the virus.

In this case, the analysis of the primary cells is not limited thereto, but may be performed by RT-PCR analysis, immunofluorescence staining analysis, or microscopic analysis.

In addition, the virus that can be analyzed for infection in the present invention may include any virus that mainly causes respiratory diseases, and is not specifically limited thereto, but coronavirus (Coronavirus), reovirus (Reovirus), influenza Influenza Virus, Parainfluenza Virus, Respiratory Syncytial Virus (RSV), Rhinovirus, Adenovirus, Metapneumovirus, Bocavirus or enteroviruses.

The method for analyzing viral infection using primary cells isolated from human upper respiratory tract tissue discarded after surgery provided by the present invention and the method for screening antiviral agents can replace the immortalized cell line used in conventional viral infection research. In addition, more accurate results can be obtained than immortalized cell lines and economically advantageous effects can be obtained.

In particular, immortalized cells can proliferate close to infinity, but instead lose their original function and have characteristics of cells different from those existing in the living body. It may be different from the results of

In addition, the method using the primary cells of the present invention has the advantage of reducing unnecessary animal experiments, and can reduce the time and expense required for the discovery and efficacy evaluation of antiviral agents, so that in the process of developing therapeutic agents for viral infections It can be used as a new analytical platform for validation of efficacy and stability.

Hereinafter, the present invention will be described in more detail through examples. These Examples are for illustrating the present invention in more detail, and the scope of the present invention is not limited to these Examples.

<Example 1>

Isolation and culture of primary cells from human upper respiratory tract

Tissue discarded after tonsillectomy was obtained, and primary cells, tonsil-derived mesenchymal stem cells (TMSC), were isolated and cultured from the tissue as follows. After the tissue immediately after surgery was refrigerated, it was treated with collagenase I and DNase I to facilitate the separation of cells from the tissue, and then the tissue was sectioned. Thereafter, the mesenchymal stem cells were isolated by centrifugation at 2000 rpm at 25° C. for 5 minutes using a centrifuge for separation from other cells. The isolated cells were cultured in an incubator in which 10% FBS and 1% AA were added DMEM (Dulbecco's modified Eagle's medium) culture medium at a temperature of 37°C and 5% CO2 was preserved, and the cells isolated from each tissue were mixed. Instead, the cells were separated and the characteristics of each cell were analyzed.

As a result of the analysis, FIG. 1 shows a photograph of the human larynx, which is the site from which the primary cells were separated, and a photograph of the cell morphology of the primary cells isolated by the above method observed under a microscope.

<Example 2>

Preparation of spheroids using human upper respiratory tract-derived primary cells

The present inventors constructed an environment in which spheroids can be produced through three-dimensional culture of primary cells (tonsillium-derived mesenchymal stem cells) isolated and cultured from the human upper respiratory tract according to Example 1. To this end, the number of cells of the primary cells was varied and regulated, and a polydimethylsiloxane (PDMS) mold was used to form a spheroid-type cell population through a three-dimensional co-culture system. Specifically, the culture through the three-dimensional co-culture system is performed in a hemispherical microwell in which a liquid polymer of polydimethylsiloxane (PDMS) that forms a meniscus by surface tension is cured into a hemispherical micro-form. In the example, the amygdala-derived mesenchymal stem cell suspension was added and left for 3 days to spontaneously form a spherical culture form. In addition, for the formation of a spheroid-shaped cell mass, spheroids were prepared using a StemFIT 3D (microFIT company) product, and a certain number of cells were dispensed into the StemFIT 3D product in consideration of the size of the spheroid to be manufactured, Incubated at 37°C and 5% Co2 incubator for 2 days. At this time, as a medium for culture, a DMEM medium supplemented with 10% FBS and 1% AA was used.

As a result, as shown in FIG. 1, it was confirmed that spheroids were formed in the culture conditions with different cell numbers through the above method, and the basic width of the spheroids generated even in culture with different cell numbers was average It was confirmed that it was generated in an almost uniform size from 100um to 150um.

<Example 3>

Confirmation of cell degeneration due to human coronavirus infection using human upper respiratory tract-derived primary cells according to the present invention

Primary cells isolated and cultured from the human upper respiratory tract according to the method of Example 1 were inoculated into the primary cells using human coronavirus NL63 (human coronavirus NL63), then cultured for 2 hours, and then the denaturing effect of the cells ( CPE: cytopathic effect) was analyzed.

As a result, as shown in FIG. 3, it was found that the cytopathic effect occurred in the primary cells infected with the human coronavirus NL63, and the cytopathic effect did not appear in the control group not infected with the virus (Fig. 3a). In addition, through immunofluorescence staining analysis using a specific antibody against human coronavirus NL63, it was confirmed that the cells were actually infected by human coronavirus NL63 in the virus-infected cell group (Fig. 3b).

<Example 4>

Confirmation of Reo virus infection using human upper respiratory tract-derived primary cells according to the present invention

Primary cells isolated and cultured from the human upper respiratory tract by the method of Example 1 were each infected with orthoreovirus, and then used in the following experiments. In this case, a group not infected with the virus was used as a control group.

<4-1> RT-PCR analysis

After freezing and thawing the virus-infected cells twice, the supernatant was obtained through centrifugation, and RNA was extracted from the supernatant using an RNA extraction kit used in the art, and the following Orthoreovirus detection RT-PCR was performed using the primer set.

L1 segment lambda-3 protein (Primer target size: 415bp)

L1-F Primer: 5'-GCATCCATTGTAAATGACGAGTCTG-3' (SEQ ID NO: 1)

L1-R Primer: 5'-CTTGAGATTAGCTCTAGCATCTTCTG-3' (SEQ ID NO: 2)

As a result of the analysis, as shown in FIG. 4a, in the group infected with 5 virus stocks in the primary cells isolated and cultured from the upper respiratory tract of 3 patients, infection with orthoreovirus could be confirmed through RT-PCR. On the other hand, the reaction product of RT-PCR was not detected in the control group not infected with the virus.

From these results, the present inventors found that, when using the human upper respiratory tract-derived primary cells established in the present invention, virus infection can be accurately diagnosed and detected in vitro.

<4-2> Optical microscope analysis

For primary cells and control cells derived from human upper respiratory tract infected with orthoreovirus, apoptosis according to virus infection time was observed through an electron microscope.

As a result, as shown in Figure 4b, it was confirmed that the cytopathic effect appears in some infected cells from 5 days after orthoreovirus infection. Through this, the present inventors found that, when using the human upper respiratory tract-derived primary cells established by the method of the present invention, virus infection can be confirmed even through light microscopic analysis.

<4-3> Confirmation of survival of cells due to virus infection

Furthermore, the present inventors analyzed whether it is possible to determine whether or not the cells survive virus infection using primary cells isolated and cultured from the human upper respiratory tract according to the present invention. For this purpose, for the cells infected with orthoreovirus and the control cells not infected with the virus used in <4-2>, the viability of the cells on the 6th day after infection was measured using a LIVE/DEAD® assay kit (Invitrogen). analyzed. At this time, living cells are labeled with green fluorescence, and dead cells are labeled with red fluorescence, so that the survival of the cells can be visualized and observed.

As a result of the analysis, as shown in FIG. 5A , the virus-infected cells showed that the dead cells were stained red, whereas the control cells not infected with the virus showed all green live cells.

In addition, as a result of quantifying the labeled fluorescence intensity and confirming it graphically, it was confirmed that the virus-infected group reduced the number of live cells by 21.5% (compared to 0.8 ± 0.9 control) due to the effect of virus infection, and the number of dead cells increased by 54.2% (2.2 ± 0.1 compared to the control group) was confirmed.

Through these results, the present inventors found that the problem with the immortalized cell line, which is a host cell essential for the existing virus infection research and development of infection treatment drugs, was that it was not a cell in the human body, and that it was It was found that the present invention can solve the fact that it takes a lot of time and money. In particular, the present invention can provide an upper respiratory tract cell-based platform that can verify the effectiveness and safety of virus infection and antiviral drug discovery by using actual human-derived primary cells.

So far, with respect to the present invention, the preferred embodiments have been looked at. Those of ordinary skill in the art to which the present invention pertains will understand that the present invention may be implemented in a modified form without departing from the essential characteristics of the present invention. Therefore, the disclosed embodiments are to be considered in an illustrative rather than a restrictive sense. The scope of the present invention is indicated in the claims rather than the foregoing description, and all differences within the scope equivalent thereto should be construed as being included in the present invention.

Claims (9)

1. Using primary cells isolated from human upper respiratory tract tissue discarded after surgery,

   A method for analyzing viral infection based on cells derived from upper respiratory tract tissue.
2. The method of claim 1,

   The primary cells are tonsil-derived mesenchymal stem cells (Tonsil-derived mesenchymal stem cells, TMSC), tonsil-derived fibroblasts (Tonsil-derived Fibroblasts), immune cells or dendritic cells (Tonsil-derived Dendritic cells) characterized in that, A method for analyzing viral infection based on cells derived from upper respiratory tract tissue.
3. The method of claim 1,

   The primary cell is a virus infection based on cells derived from upper respiratory tract tissue, characterized in that the cells isolated from the tissue by processing collagenase I and DNase I and centrifugation in the human upper respiratory tract tissue discarded after the operation how to analyze it.
4. According to claim 1,

   The method of analyzing whether the primary cells are virus-infected based on cells derived from upper respiratory tract tissue, characterized in that they have the form of a cell population formed in the form of spheroids through three-dimensional co-culture using a polydimethylsiloxane (PDMS) mold.
5. The method of claim 1,

   The virus is Coronavirus, Reovirus, Influenza Virus, Parainfluenza Virus, Respiratory Syncytial Virus (RSV), Rhinovirus, adenovirus. (Adenovirus), metapneumovirus (Metapneumovirus), bocavirus (Bocavirus) or enterovirus (Enterovirus), characterized in that the virus infection based on cells derived from the upper respiratory tract tissue.
6. According to claim 1,

   Whether the virus is infected is a virus based on cells derived from upper respiratory tract tissue, characterized in that it is performed by RT-PCR analysis, immunofluorescence staining or microscopic analysis in vitro using primary cells isolated from the human upper respiratory tract tissue. How to analyze for infection.
7. A screening method for antiviral agents based on cells derived from upper respiratory tract tissue using primary cells isolated from human upper respiratory tract tissue discarded after surgery.
8. 8. The method of claim 7,

   Screening of antiviral agents based on cells derived from upper respiratory tract tissue, characterized in that after treating the antiviral candidate material before or after infecting the primary cells with the virus, and analyzing the changes in the primary cells according to the virus infection Way.
9. 9. The method of claim 8,

   Analyzing the changes in the primary cells is a screening method for antiviral agents based on cells derived from upper respiratory tract tissue, characterized in that performed by RT-PCR analysis, immunofluorescence staining analysis or microscopic analysis.

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