Methods for preventing or treating coronavirus infections using immunomodulators and vaccine compositions comprising immunomodulators

Abstract

To provide a pharmaceutical composition comprising an immunomodulator for prophylaxis or treatment of coronavirus infection.SOLUTION: The invention provides a pharmaceutical composition comprising an immunomodulator for inducing IFNα production in epithelial cells. The immunomodulator is a detoxified Escherichia coli heat-labile toxin (LT), a Toll-Like Receptor (TLR) agonist or antagonist, Vaxfectin, or a pattern recognition receptor (PRR) agonist or antagonist. The epithelial cells are respiratory tract mucosal epithelial cells.SELECTED DRAWING: None

Description

[Technical field]

[0001]

[0002] The present invention relates to the treatment or prevention of coronavirus infection, and in particular to the treatment or prevention of coronavirus infection by administering an immunomodulatory agent. [Background technology]

[0002]

[0003] SARS-CoV, MERS-CoV, and SARS-CoV-2 are deadly coronavirus pathogens that have caused mass mortality in certain populations. In late 2019, SARS-CoV-2 began its assault on human hosts in Wuhan, Hubei province, People's Republic of China. The infection spread silently, with as many as 80% of infected individuals showing no significant symptoms of illness. However, the elderly and those with underlying conditions such as diabetes, hypertension, immunosuppression, etc. are particularly susceptible, with a mortality rate of over 15%. In China alone, SARS-CoV-2 infected over 80,000 people and claimed over 3,200 lives within three months.

[0003]

[0004] Current treatment options for SARS-CoV-2 are diverse and experimental, including antiviral drugs such as remdesivir, hydroxychloroquine, ritonavir / lopinavir, and ritonavir / lopinavir in combination with interferon beta. Remdesivir is an anti-infective drug for Ebola infection. In animal studies (SARS model) and a limited number of human subjects suffering from SARS-CoV-2, remdesivir has shown promising efficacy in inhibiting coronavirus and reducing fever. Hydroxychloroquine is believed to reduce infection in a significant number of patients. Nevertheless, its practical use is under debate due to lack of knowledge about its exact mechanism and adverse events derived from high dosage. The combination of hydroxychloroquine and azithromycin has been reported to be a game changer for SARS-CoV-2 treatment for its high efficacy, but has not been proven in studies. Ritonavir / lopinavir and ritonavir / lopinavir combined with interferon beta therapy are insufficient for the treatment of SARS-CoV-2.

[0004]

[0005] Bacillus Calmette-Guerin (BCG) has been proposed as a treatment option for SARS-CoV-2 due to its immunomodulatory properties. Apart from being an immunotherapeutic agent for SARS-CoV-2, BCG is a prophylactic vaccine for Mycobacterium tuberculosis. BCG is proposed to nonspecifically augment innate and adaptive immune responses via innate pattern recognition receptors, e.g., Toll-like receptors (TLRs) and C-type lectin receptors (CLRs), on dendritic cells (DCs), resulting in nonspecific / broad spectrum CD4 T cell activation. This immunological importance has given BCG a unique role in cancer immunotherapy (Nishida S et al., "Immune adjuvant therapy using Bacillus Calmette-Guerin cell wall skeleton (BCG-CWS) in advanced malignancies: A phase 1 study of safety and immunogenicity assessments," Medicine (Baltimore) 2019, 98(33):e16771).

[0005]

[0006] Other therapeutic drugs and preventive treatments for SARS-CoV-2 are currently under development by many academic societies or pharmaceutical companies. Vaccines are a typical preventive approach that encompasses the use of antigens, recombinant microorganisms, or nucleic acids encoding viral proteins to boost anti-SARS-CoV-2 immunity. Currently, the receptor binding domain (RBD) of SARS-CoV-2 is the most frequently tested antigenic target. Viral antigenic epitopes do not always promote the desired quantitative and qualitative immune response. To optimize vaccine efficacy, adjuvants can be incorporated. Adjuvants are often co-administered with vaccines to qualitatively or quantitatively boost antigen-specific immune responses via innate immune activation.

[0006]

[0007] Vaccines are key to stop the spread of SARS-CoV-2 infection. SARS-CoV-2 evolved from bats and pangolins before infecting humans via an unknown intermediate host. Currently, no promising treatments or vaccines are available for SARS-CoV-2 infection. Many vaccine strategies have been proposed for SARS CoV-2, including recombinant viral proteins, subunit vaccines, DNA or mRNA vaccines. Most SARS-CoV-2 vaccines in development use the viral spike protein (S protein) as the primary antigen and intramuscular (IM) injection as the route of administration. The S protein mediates the fusion of SARS-CoV-2 to host cells that have the angiotensin-converting enzyme 2 (ACE2) receptor, and the receptor-binding domain (RBD) of the S protein has been identified. Both human and animal studies have revealed that IgG titers against the S protein positively correlate with antibody-dependent enhancement of infection (ADE), which is a consequence of the immune response against the S protein and subsequent pathogenicity following the generation of non-RBD-inhibiting IgG. In a new epidemic or pandemic, pre-existing non-RBD-blocking IgG may bind to the S protein of various circulating strains of SARS-CoV-2 and enhance infection. Solutions to address ADE include altering the immunization pathway to induce mucosal sIgA, which has improved neutralizing capacity without the ADE burden.

[0007]

[0008] Mucous membranes cover the surfaces of body passages, such as the intestine, respiratory tract, and genitourinary tract. Mucous membranes are layers of epithelium coated with sIgA and antimicrobial molecules on the luminal side to protect the mucosa from infection. sIgA is a high molecular weight immunoglobulin and is the main defense molecule for adaptive mucosal immunity. The polymeric structure of IgA provides it with broader specificity than IgG against genetically drifted viral strains and improves its neutralizing capacity. IgA is also more resistant to host- or microbial-derived proteases than other Ig isotypes.

[0008]

[0009] Escherichia coli heat-labile toxin (LT) is useful as an adjuvant or immunomodulator for intranasal (IN) vaccination due to its ability to enhance immune mucosal responses to co-administered vaccines. Tamura S et al., "Intranasal Inactivated Influenza Vaccines: a Reasonable Approach to Improve the Efficacy of Influenza Vaccine?" Jpn J Infect Dis 2016, 69(3):165-179 reported that inactivated influenza vaccines combined with adjuvants via the intranasal route induced enhancement of both serum hemagglutination inhibition (HI) and secretory IgA (sIgA) antibodies. Some adverse events were reported, including fever, malaise, and headache; and local reactions, such as rhinitis, nasal congestion, and rhinorrhea, but were generally mild. Diarrhea and local inflammation are caused by ADP-ribosylase of the A subunit, which leads to water and electrolyte efflux from epithelial cells. Therefore, genetically detoxified LT with reduced or completely absent ADP-ribosylase activity was constructed to better support the unmet medical needs for mucosal adjuvants.

[0009]

[0010] Unlike wild-type LT, which induces secretion of proinflammatory cytokines such as IL-6 in cells of the neuronal phenotype SK-N-SH, and LTK63 developed by Chiron, LTh(αK) (also known as LTS61K (US Patent Application No. 13 / 097,218)) is unable to promote IL-6 secretion. In a clinical trial involving over 350 subjects, both healthy subjects aged 20-75 years and subjects with allergic rhinitis received multiple doses of LTh(αK) via the intranasal route, and none reported signs of facial nerve paralysis.

[0010]

[0011] Studies have supported that intranasal administration of LTB (a subunit of LT) alleviates autoimmune-induced inflammation. Both regulatory T cells and IL-10 are hallmarks of anti-inflammatory responses. Treatment with LTB may involve cross-linking the GM1 receptor complex involving TrkA or integrins, thereby triggering a signaling cascade that leads to regulatory T cell activation and IL-10 secretion.

[0011]

[0012] The type I IFN family is a multigene cytokine family that includes IFNα, IFNβ, and several less well-defined single gene products. IFNα and IFNβ are the best defined and most widely expressed type I IFNs. Type I IFNs are best known for inducing antiviral activity in both virus-infected and non-infected bystander cells by inducing host gene transcripts that interfere with viral replication by diverse mechanisms. Type I IFNs have various functions that regulate innate and adaptive immune responses against viral as well as bacterial pathogens. The outcome of IFNα / β responses during infection is highly context-dependent. Different tissue-specific conditions during infection affect when and where IFNα / β signals are delivered and the signaling pathways that are triggered downstream of the type I IFN receptor (IFNAR). This outcome determines the activation or repression of IFN-stimulated genes (ISGs). Overall, type I IFNs promote the initiation of immune responses.

[0012]

[0013] In light of the ongoing pandemic and high mutation rates of coronaviruses, particularly SARS-CoV, MERS-CoV, and SARS-CoV-2, there is a need for effective therapies for the treatment and / or prevention of coronavirus infections. Summary of the Invention

[0013]

[0014] In the present invention, it has surprisingly been found that immunomodulators, such as LTh(αK), can be used alone or as an adjuvant in combination with anti-coronavirus antigens to treat or prevent coronavirus infection. Thus, the present invention relates to the use of immunomodulators / adjuvants, such as LTh(αK), as therapeutic agents.

[0014]

[0015] The present disclosure relates to the discovery that immunomodulators, such as LTh(αK), can be used as therapeutic or prophylactic agents for the treatment or prevention of coronavirus infection in a subject. Accordingly, the present disclosure provides a method for treating or preventing coronavirus infection in a subject in need of or at risk of coronavirus infection, comprising administering to the subject a therapeutically effective amount of an immunomodulator.

[0015]

[0016] In one embodiment, the immunomodulator can signal through the mucosal epithelium. Preferably, the immunomodulator is a toxin or toxoid, more preferably, the immunomodulator is a toxin or toxoid of bacterial origin. In a preferred embodiment, the immunomodulator is detoxified LT, LTh(αK), Toll-like receptor (TLR) agonist or antagonist, Vaxfectin, or pattern recognition receptor (PRR) agonist or antagonist. In a further preferred embodiment, the immunomodulator does not induce cytokine IL6 production from cells, including epithelial cells, Langerhans cells, resident monocytes, and neuronal cells, upon contact. In another further preferred embodiment, the immunomodulator is LTh(αK). LTh(αK) corresponds to LTS61K disclosed in U.S. Patent Application Publication No. 2008 / 102078, which is an E. coli LT holotoxin that has been detoxified by lysine substitution at the position corresponding to position 61 of SEQ ID NO:5 disclosed in U.S. Patent Application Publication No. 2008 / 102078.

[0016]

[0017] In one embodiment, the coronavirus is a virus of the Orthocoronavirinae subfamily. In a preferred embodiment, the coronavirus is SARS-CoV, MERS-CoV, or SARS-CoV-2. In a more preferred embodiment, the coronavirus is SARS-CoV-2.

[0017]

[0018] In one embodiment, the immunomodulator is administered to the subject after the subject is challenged with a coronavirus. In another embodiment, the immunomodulator is administered to the subject before the subject is challenged with a coronavirus. In another embodiment, the immunomodulator is administered to the subject before and after the subject is challenged with a coronavirus. In another embodiment, the immunomodulator is administered to the subject one or more times before, after, or around the subject's challenge with a coronavirus. In a preferred embodiment, the immunomodulator is administered to the subject three times before the subject is challenged with a coronavirus. In another preferred embodiment, the immunomodulator is administered to the subject once after the subject is challenged with a coronavirus.

[0018]

[0019] In one embodiment, an immunomodulatory agent is administered to a subject in combination with an anti-coronavirus antigen.

[0019]

[0020] In one embodiment, the mucosal site may be any anatomical mucosa. In a preferred embodiment, the mucosal site is the sublingual mucosa, intranasal mucosa, airway mucosa, oral mucosa, vaginal mucosa, rectal mucosa, or other anatomical mucosa. In a further preferred embodiment, the antigen is administered to the sublingual mucosa. In another further preferred embodiment, the immunomodulatory agent may be administered to the intranasal mucosa and extend to the pharynx.

[0020]

[0021] In one embodiment, the immune response includes the production of antigen-specific IgG and subclasses thereof, antigen-specific IgA and subclasses thereof, antigen-specific IgM and subclasses thereof, and / or cell-mediated immunity. In another embodiment, the immune response includes upregulation of immune components. In another embodiment, the immune response includes downregulation of immune components. In another embodiment, the immune response includes production of immunoglobulins against the antigen. More preferably, the immune response provides a therapeutic benefit.

[0021]

[0022] The present disclosure further provides a vaccine composition for the treatment or prevention of a coronavirus infection comprising a pharma- ceutically acceptable amount of an immunomodulatory agent described herein.

[0022]

[0023] In one embodiment, the vaccine composition further comprises an anti-coronavirus antigen. In one embodiment, the anti-coronavirus antigen is an attenuated virus, an inactivated whole virus, a split coronavirus, a recombinant coronavirus, a coronavirus subunit, a coronavirus-derived peptide or protein, or a biological entity. In one embodiment, the anti-coronavirus antigen is an antigen originating from a virus of the Orthocoronavirus subfamily. In a preferred embodiment, the anti-coronavirus antigen is an antigen originating from SARS-CoV, MERS-CoV, or SARS-CoV-2. In a more preferred embodiment, the anti-coronavirus antigen is an antigen originating from SARS-CoV-2. In a more preferred embodiment, the anti-coronavirus antigen is an antigen originating from the SARS CoV-2 spike protein (S protein), SARS-CoV-2 spike recombinant (rA1), or the receptor binding domain (RBD) of SARS-CoV-2.

[0023]

[0024] The present disclosure further provides a method for treating or preventing a coronavirus infection in a subject in need of or at risk of a coronavirus infection, comprising administering to the subject a therapeutically effective amount of an immunomodulatory or vaccine composition described herein.

[0024]

[0025] The mechanism by which LTh(αK) achieves efficacy in treating or preventing coronavirus infection may be that following administration of LTh(αK) intranasally, LTh(αK) comes into direct contact with epithelial cells and binds to GM1 on the surface of epithelial cells. GM1 then signals the secretion of type 1 interferon (IFNα). IFNα activates DCs (pDCs and mDCs) to induce further cytokine activation. LTh(αK) can also induce DC activation by direct contact with the dendrites of intranasally exposed DCs or by utilizing transcytosis of AB5 through the epithelium. pDCs in the nasal associated lymphoid tissue (NALT) are the major source of IFNα, providing another wave of IFNα to regulate the immune response. DCs activated by LTh(αK) downregulate proinflammatory cytokines such as IL6 and IL5. IFNα produced by the mucosa drives IgA class switching to neutralize SARS-CoV-2. IgA class switching is TGFβ-dependent. TGFβ and IL10 upregulate Treg activity to attenuate inflammation.

[0025]

[0026] LTh(αK) promotes the secretion of antigen-specific IgA, which has the potential to block or neutralize infectious agents, such as SARS-CoV-2, before infection in the epithelium and not eliminate the potential for viral shedding. Furthermore, compared with IgG in the circulatory system, mucosal surfaces have much less contact with Fc receptor-expressing cells. This suggests a lower risk of ADE with virus-targeted IgA. Thus, LTh(αK) (alone or as an adjuvant co-administered with a candidate vaccine) can lower the risk of ADE development and may be useful in preventing or treating coronavirus infection.

[0026]

[0027] The present invention is described in detail in the following sections. Other features, objects, and advantages of the present invention can be readily found in the detailed description of the invention and in the claims. [Brief description of the drawings]

[0027] [Figure 1A] Figure 1A shows serum anti-RBD IgG titers after SARS CoV-2 vaccination with LTh(αK)-adjuvanted S1 via the IM route. The left bar corresponds to group 1 in Table 1, and the right bar corresponds to group 2. [Figure 1B] Figure 1B shows serum anti-RBD IgG titers after SARS CoV-2 vaccination with LTh(αK)-adjuvanted S1 via the IN route. The left bar corresponds to group 3 in Table 1, and the right bar corresponds to group 4. [Figure 1C] Figure 1C shows serum anti-RBD IgA titers after SARS CoV-2 vaccination with LTh(αK)-adjuvanted S1 via the IM route. The left bar corresponds to group 1 in Table 1, and the right bar corresponds to group 2. [Figure 1D] Figure 1D shows serum anti-RBD IgA titers after SARS CoV-2 vaccination with LTh(αK)-adjuvanted S1 via the IN route. The left bar corresponds to group 3 in Table 1, and the right bar corresponds to group 4. [Diagram 2] Figure 2 shows SARS-CoV-2 neutralizing IgG antibody titers after intranasal vaccination with LTh(αK)-adjuvanted recombinant RBD vaccine. [Diagram 3] Figure 3 shows SARS-CoV-2 spike recombinant (rA1)-specific IgA titers after intranasal vaccination with LTh(αK)-adjuvanted recombinant RBD vaccine. [Figure 4] FIG. 4 shows the histopathological scores of the lungs of SARS-CoV-2-infected Syrian golden hamsters with or without treatment with LTh(αK). [Figure 5A]Figure 5A shows the effect of LTh(αK) treatment on IFNα production. Figure 5B shows the phosphorylation of p65 induced by treatment of epithelial cells with LTh(αK). Figure 5C shows the inhibition of p65 phosphorylation by an inhibitor of NF-κB (pyrrolidine dithiocarbamate, PDTC). Figure 5D shows the results of a chromatin immunoprecipitation (ChIP) assay, which demonstrated the recruitment of p-p65 to the IFNα promoter in LTh(αK)-mediated epithelial activation. Figure 5E shows that treatment with PDTC blocked the production of IFNα by epithelial cells. [Figure 5B] Figure 5A shows the effect of LTh(αK) treatment on IFNα production. Figure 5B shows the phosphorylation of p65 induced by treatment of epithelial cells with LTh(αK). Figure 5C shows the inhibition of p65 phosphorylation by an inhibitor of NF-κB (pyrrolidine dithiocarbamate, PDTC). Figure 5D shows the results of a chromatin immunoprecipitation (ChIP) assay, which demonstrated the recruitment of p-p65 to the IFNα promoter in LTh(αK)-mediated epithelial activation. Figure 5E shows that treatment with PDTC blocked the production of IFNα by epithelial cells. [Figure 5C] Figure 5A shows the effect of LTh(αK) treatment on IFNα production. Figure 5B shows the phosphorylation of p65 induced by treatment of epithelial cells with LTh(αK). Figure 5C shows the inhibition of p65 phosphorylation by an inhibitor of NF-κB (pyrrolidine dithiocarbamate, PDTC). Figure 5D shows the results of a chromatin immunoprecipitation (ChIP) assay, which demonstrated the recruitment of p-p65 to the IFNα promoter in LTh(αK)-mediated epithelial activation. Figure 5E shows that treatment with PDTC blocked the production of IFNα by epithelial cells. [Figure 5D]Figure 5A shows the effect of LTh(αK) treatment on IFNα production. Figure 5B shows the phosphorylation of p65 induced by treatment of epithelial cells with LTh(αK). Figure 5C shows the inhibition of p65 phosphorylation by an inhibitor of NF-κB (pyrrolidine dithiocarbamate, PDTC). Figure 5D shows the results of a chromatin immunoprecipitation (ChIP) assay, which demonstrated the recruitment of p-p65 to the IFNα promoter in LTh(αK)-mediated epithelial activation. Figure 5E shows that treatment with PDTC blocked the production of IFNα by epithelial cells. [Figure 5E] Figure 5A shows the effect of LTh(αK) treatment on IFNα production. Figure 5B shows the phosphorylation of p65 induced by treatment of epithelial cells with LTh(αK). Figure 5C shows the inhibition of p65 phosphorylation by an inhibitor of NF-κB (pyrrolidine dithiocarbamate, PDTC). Figure 5D shows the results of a chromatin immunoprecipitation (ChIP) assay, which demonstrated the recruitment of p-p65 to the IFNα promoter in LTh(αK)-mediated epithelial activation. Figure 5E shows that treatment with PDTC blocked the production of IFNα by epithelial cells. [Figure 6] FIG. 6 shows the proposed mechanism of LTh(αK) in the treatment or prevention of coronavirus infection. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0028]

[0037] Unless otherwise defined herein, scientific and technical terms used in connection with the present invention shall have the meanings commonly understood by those skilled in the art. The meaning and scope of the terms should be clear; however, in the event of any potential ambiguity, the definitions set forth herein shall take precedence over any dictionary or external definitions.

[0029]

[0038] As utilized in accordance with the present disclosure, the following terms, unless otherwise indicated, shall be understood to have the following meanings:

[0030]

[0039] Throughout this specification, the word "comprise" or variations such as "comprises" or "comprising" will be understood to imply the inclusion of a specified integer (or component) or group of integers (or components) but not the exclusion of any other integer (or component) or group of integers (or components).

[0031]

[0040] The singular forms "a," "an," and "the" include plurals unless the context clearly dictates otherwise, and plural terms shall include the singular unless otherwise required by context.

[0032]

[0041] "Treatment" and "treating" and the like refer to an approach to obtain beneficial or desired results, including clinical results. For purposes of this disclosure, beneficial or desired results include, but are not limited to, inhibiting and / or suppressing the onset and / or progression of a condition or reducing the severity of such a condition, e.g., reducing the number and / or severity of symptoms associated with a condition, increasing the quality of life of people suffering from a condition, reducing the dosage of other medications needed to treat the condition, enhancing the effect of another medication the patient is taking for the condition, and / or prolonging the survival of a patient with the condition.

[0033]

[0042] "Prophylaxis," "prophylactic," "prevent," "preventing," and "prevention," and the like, refer to reducing the likelihood of developing a condition in a patient who is asymptomatic but at risk of developing a condition. A patient "at risk" may or may not have detectable symptoms, and may or may not exhibit detectable symptoms prior to the treatment methods disclosed herein.

[0034]

[0043] "Administering" a substance, compound, or agent to a subject, or "administration" of a substance, compound, or agent to a subject can be performed using one of a variety of methods known to those of skill in the art. For example, a compound or agent can be administered sublingually, intranasally, by inhalation into the lungs, or rectally. Administering can also be performed, for example, once, multiple times, and / or over one or more extended periods of time. In some embodiments, administration includes both direct administration (including self-administration) and indirect administration (including the act of prescribing a drug). For example, as used herein, a physician who instructs a patient to self-administer a drug or to have a drug administered by another person, and / or a physician who provides a patient with a prescription for a drug, administers the drug to the patient.

[0035]

[0044] As used herein, the terms "modulating" and "modulation" refer to the regulation of a condition, level, or amount. Modulation may be upregulation or downregulation.

[0036]

[0045] As used herein, the term "mucosal immune response" refers to an immune response induced at the mucosa, including, but not limited to, antigen-specific immunoglobulin G and its subclasses, immunoglobulin A and its subclasses, immunoglobulin M and its subclasses, and cell-mediated immunity against the immunized antigen.

[0037]

[0046] The term "mucosal site" as used herein refers to any anatomical mucosa that is covered with a mucosal epithelium. For example, a mucosal site may be the sublingual mucosa, nasal mucosa, respiratory tract mucosa, oral mucosa, vaginal mucosa, rectal mucosa, or other anatomical mucosa.

[0038]

[0047] The term "immunomodulator" as used herein refers to a drug or immune agent that modifies immunity and ultimately alters the immunogenic outcome to a specific antigen / allergen. For example, the immunomodulator can be a detoxified LT or Toll-like receptor (TLR) agonist.

[0039]

[0048] The terms "patient," "subject," or "individual" are used interchangeably and refer to either a human or non-human animal. The terms include mammals, such as humans, primates, farm animals (including cows, pigs), pets (e.g., dogs, cats), and rodents (e.g., mice and rats).

[0040]

[0049] "Effective amount" refers to the amount of a therapeutic agent or its pharma- ceutically acceptable salt that should be effective in a given treatment regimen, combining parameters of efficacy and toxicity potential, and based on the knowledge of the practicing medical professional. As is understood in the art, an effective amount can be administered in one or more doses.

[0041]

[0050] The present invention has surprisingly found that immunomodulators, such as LTh(αK), can achieve a protective immune response against coronavirus infection. The immunomodulators may be administered before, after, or both before and after coronavirus challenge. It has also been found that the immunomodulators, when used in combination with anti-coronavirus antigens as adjuvants, can induce the production of SARS CoV-2 neutralizing IgG and IgA. Furthermore, it has been found that the prior action of the immunomodulator involves activation of the p65 subunit of NF-κB and enhanced production of IFNα. The present invention provides a novel use of immunomodulators in the treatment or prevention of coronavirus infection to promote the development of novel therapeutic vaccines for coronavirus infection beyond conventional means.

[0042]

[0051] Having now generally described the present invention, the present invention may be more readily understood by reference to the following examples, which provide exemplary protocols for carrying out the methods of the present invention in treating or preventing coronavirus infection. The examples are provided for illustrative purposes only and are not intended to limit the scope of the present invention in any way. Efforts have been made to ensure accuracy with respect to numbers used (e.g., amounts, temperatures), but some experimental error and deviation should, of course, be allowed for. EXAMPLES

[0043]

[0052] Example 1 - Evaluation of the efficacy of LTh(αK) on serum anti-RBD IgG and IgA via intramuscular (IM) or intranasal (IN) routes S1 is a recombinant protein derived from the spike of SARS CoV-2. The animals used in the study were 8-week-old female Balb / c mice. The timing of administration and serum collection was performed according to the animal study protocol shown in Table 1 below. The serum samples were diluted as shown in Figure 1A to Figure 1D.

[0044] [Table 1]

[0045]

[0053] Example 2 - Evaluation of SARS-CoV-2 neutralizing IgG antibody titers after intranasal vaccination with LTh(αK)-adjuvanted recombinant RBD vaccine Balb / c mice received three 20 μg doses, 2 weeks apart, of Fc-conjugated SARS-CoV-2 spike recombinant (rA1) adjuvanted with 10 μg LTh(αK) via the intranasal route. Serum samples were collected at the end of the study (week 10) and serum neutralization titers against wild-type SARS-CoV-2 were analyzed as described by Manenti A et al., J Med Virol 2020, 92(10):2096-2104, with minor modifications. The results, shown in Figure 2, show that the intranasal vaccine induced 100%, 94%, 87%, and 65% virus neutralization at dilutions of 320, 640, 1280, and 2560, respectively.

[0046]

[0054] Example 3 - Evaluation of SARS-CoV-2 rA1-specific IgA titers following intranasal vaccination with LTh(αK)-adjuvanted recombinant RBD vaccine rA1-specific IgA titers from nasal washes or bronchoalveolar lavage fluid (BALF) were analyzed by ELISA. The results shown in Figure 3 indicate that rA1 intranasal vaccination induced rA1-, spike-1 (S1)-, and RBD-specific IgA antibodies from nasal washes and BALF. Nasal wash and BALF specimens were collected and measured by ELISA as described in Lin IP et al., PLoS One 2014, 9(3):e90293.

[0047]

[0055] Example 4 - Evaluation of the effect of LTh(αK) in the treatment and prevention of SARS-CoV-2-induced pneumonia Table 2 below shows a scheme for determining the efficacy of LTh(αK) in the treatment and prevention of SARS-CoV-2-induced pneumonia in Syrian golden hamsters. Hamsters in groups 1 and 2 were housed in a specific pathogen-free (SPF) environment and transferred to a biosafety level 3 (P3) facility on day 20. Hamsters in group 3 were kept in an SPF environment and prophylactically treated intranasally with LTh(αK) (10 μg / animal) on days 0, 7, and 14 before being transferred to the P3 facility on day 20 together with hamsters in groups 1 and 2. On day 21, all hamsters were immunized with SARS-CoV-2 virus (10 μg / animal) via the intranasal route. 5 On day 22, hamsters in group 1 received formulation buffer treatment via the intranasal route, while hamsters in groups 2 and 3 received LTh(αK) treatment (10 μg / animal) via the intranasal route. On day 24, all hamsters were sacrificed and tissues were collected for histopathological analysis.

[0048] [Table 2]

[0049]

[0056] Treatment with LTh(αK) reduced the histopathological score induced by SARS-CoV-2 in the lungs of Syrian golden hamsters (Figure 4). Hamsters in group 1 who received a placebo showed the most severe histopathological score (2.33). Hamsters in group 2 who received a single dose of LTh(αK) after challenge with SARS-CoV-2 (LTh(αK) single dose) showed an improved histopathological score (1.83). Hamsters in group 3 who received a combination of three prophylactic and one therapeutic treatments with LTh(αK) (LTh(αK)-3+1) showed a significant improvement (1.42) against SARS-CoV-2-induced pneumonia (p ≦ 0.05).

[0050]

[0057] Example 5 - Evaluation of the effect of LTh(αK) treatment on IFNα production and associated signaling pathways IFNα is a crucial player in inflammatory and anti-inflammatory responses during respiratory infection. During treatment of epithelial cells (BEAS-2B) with LTh(αK), an increase in IFNα protein was detected in the medium (Figure 5A). Treatment of epithelial cells with LTh(αK) also induced phosphorylation of p65 (Figure 5B). This phosphorylation was inhibited by pyrrolidine dithiocarbamate (PDTC), an inhibitor of NF-κB (Figure 5C), suggesting the involvement of the NF-κB pathway, rather than ERK. In chromatin immunoprecipitation (ChIP) assays (Figure 5D), recruitment of p-p65 to the IFNα promoter revealed a critical role for NF-κB in LTh(αK) to mediate epithelial activation. Furthermore, treatment with PDTC blocked the production of IFNα in the medium by epithelial cells (Figure 5E).

[0051]

[0058] Example 6 - Proposed Mode of Action From the examples described above, the mechanism of LTh(αK) in the treatment or prevention of coronavirus infection is proposed as shown in Figure 6. When LTh(αK) is administered intranasally, it directly contacts epithelial cells. GM1 on the surface of epithelial cells binds to LTh(αK) and signals the secretion of type 1 interferon (IFNα). IFNα is known to be able to regulate inflammatory pathways. Recent publications have revealed that crosstalk between inflammatory macrophages and CD8 cells in the alveoli of SARS-CoV-2-infected lungs sustains the inflammatory response. IFNα is also known to induce IL10 secretion in response to CD8, which can interrupt the crosstalk. IFNα is known to mediate the secretion of Ly6C loIt activates phenotypic monocytes to promote anti-inflammatory outcomes. IFNα then activates DCs (pDCs and mDCs) to induce further activity and cytokine activation. LTh(αK) can directly contact the dendrites of DCs exposed to the nasal cavity. Transcytosis of AB5 through the epithelium has also been reported. Transcytosis provides an additional pathway for LTh(αK)-induced DC activation. pDCs in the nasal-associated lymphoid tissue (NALT) are the major source of IFNα, providing another wave of IFNα to regulate immune responses. IFNα in an inflammatory environment promotes anti-inflammatory responses, as mentioned earlier. DCs activated by LTh(αK) downregulate proinflammatory cytokines, such as IL6 and IL5. IFNα produced by the mucosa drives IgA class switching to neutralize SARS-CoV-2. IgA class switching is TGFβ-dependent. TGFβ and IL10 upregulate Treg activity to attenuate inflammation.

[0052]

[0059] Interferon alpha (IFNα) plays an essential role in innate immunity against infections, including SARS-CoV-2. IFNα belongs to the type 1 interferon family and is secreted by many cell types at enhanced levels after infection. Treatment of nasal epithelial cells with LTh(αK) induced increased levels of IFNα, suggesting activation of the innate defense cascade after treatment. IFNα plays a crucial role in anti-inflammatory responses in addition to virus eradication. Hamsters challenged with SARS-CoV-2, tested in the examples, further proved this hypothesis. In conclusion, we propose that LTh(αK) is a potent immunomodulator and innate immune enhancer for the treatment of COVID-19 patients.

[0053] [Cross reference]

[0001] This application claims the benefit of U.S. Provisional Patent Application No. 63 / 022,017, filed May 8, 2020, which is incorporated herein by reference in its entirety.

[0054] A preferred embodiment of the present invention is as follows. [1] An immunomodulator for treating or preventing a coronavirus infection in a subject in need of or at risk of a coronavirus infection. [2] The immunomodulator according to [1], wherein the immunomodulator is a detoxified Escherichia coli heat-labile toxin (LT), a Toll-like receptor (TLR) agonist or antagonist, baxfectin, or a pattern recognition receptor (PRR) agonist or antagonist. [3] The immunomodulatory substance according to [2], wherein the LT is LTh(αK). [4] The immunomodulatory substance according to any one of [1] to [3], wherein the coronavirus is SARS-CoV, MERS-CoV, or SARS-CoV-2. [5] The immunoregulatory substance according to any one of [1] to [4], which is administered multiple times. [6] The immunomodulatory substance according to any one of [1] to [5], which is administered in combination with an anti-coronavirus antigen. [7] The immunomodulatory substance according to claim 6, wherein the anti-coronavirus antigen is an attenuated virus, an inactivated whole virus, a split coronavirus, a recombinant coronavirus, a coronavirus subunit, a coronavirus-derived peptide or protein, or a biological entity. [8] A vaccine composition comprising a medicamentously effective amount of the immunomodulatory substance according to any one of [1] to [4]. [9] The vaccine composition according to [8], further comprising an anti-coronavirus antigen.

[10] The vaccine composition according to claim 9, wherein the anti-coronavirus antigen is an attenuated virus, an inactivated whole virus, a split coronavirus, a recombinant coronavirus, a coronavirus subunit, a coronavirus-derived peptide or protein, or a biological entity.

[11] The vaccine composition according to any one of [8] to

[10] , for treating or preventing coronavirus infection in a subject in need thereof or at risk of coronavirus infection.

Claims

1. A pharmaceutical composition for inducing IFNα production in epithelial cells, comprising an immunomodulatory substance, wherein the immunomodulatory substance is a detoxified Escherichia coli heat-labile toxin (LT), and the LT is LTh(αK).

2. The pharmaceutical composition according to claim 1 , wherein the epithelial cells are airway mucosal epithelial cells.

3. An in vitro method of inducing IFNα production in epithelial cells comprising contacting the epithelial cells with an immunomodulatory agent, wherein the immunomodulatory agent is a detoxified Escherichia coli heat-labile toxin (LT), and the LT is LTh(αK).

4. The method according to claim 3 , wherein the epithelial cells are airway mucosal epithelial cells.

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