Replication-competent recombinant herpes simplex virus type 1 (HSV-1) comprising deletions in the ICP6 and IR regions

A recombinant herpes simplex virus type 1 (HSV-1), a recombinant HSV-1 vector, and a method of preparing the recombinant HSV-1, may enable easy genetic modification, as a relatively large foreign gene may be inserted or various foreign genes may be inserted simultaneously, as ICP6 and IR regions are simultaneously deleted. These may be used in cancer treatment as an oncolytic virus that is safe, while having an excellent effect in killing cancer cells.

1. 11. A recombinant herpes simplex virus type 1 (HSV-1) strain KOS, comprising: an HSV-1 genome, in which an infected-cell protein 6 (ICP6) region among genomic regions of HSV-1 is deleted, and the nucleotide sequence of SEQ ID NO:2 among nucleotide sequences of the internal repeat (IR) region between a unique long (UL) region and a unique short (US) region is deleted, wherein the recombinant HSV-1 is replication-competent and is an oncolytic virus that activates immune cells by exposing antigens of cancer cells by specifically killing cancer cells, wherein the simultaneous deletion of ICP6 and a nucleotide sequence of SEQ ID NO:2 enhances the ability to selectively kill cancer cells, and wherein the cancer is lung cancer or glioma.
2. 22. The recombinant HSV-1 of claim 1, comprising: a terminal repeat of a long (TRL) region; a UL region comprising a nucleotide sequence of at least one gene selected from the group consisting of UL1 to UL38 and UL40 to UL56; a US region comprising a nucleotide sequence of at least one gene selected from the group consisting of US1 to US12; a terminal repeat of a short (TRS) region, or a combination thereof, as a genomic region.
3. 33. The recombinant HSV-1 of claim 1, wherein the ICP6 region is a UL39 gene.
4. 44. The recombinant HSV-1 of claim 1, having a genome in which the nucleotide sequence of SEQ ID NO: 1 among nucleotide sequences of HSV-1 and ICP6 genes is deleted.
5. 55. The recombinant HSV-1 of claim 1, wherein the IR region comprises an internal repeat of a long (IRL) region and an internal repeat of a short (IRS) region.
6. 66. The recombinant HSV-1 of claim 1, wherein a part of a nucleotide sequence of a UL56 gene is additionally deleted, as a deleted part of the nucleotide sequence of the UL56 gene.
7. 77. The recombinant HSV-1 of claim 6, wherein the deleted part of the nucleotide sequence of the UL56 gene is the nucleotide sequence of SEQ ID NO: 3.
8. 88. The recombinant HSV-1 of claim 1, comprising: the nucleotide sequence of SEQ ID NO: 4.
9. 99. The recombinant HSV-1 of claim 1, exhibiting cancer cell or tumor cell specificity.
10. 1010. A recombinant HSV-1 vector, comprising: a genome nucleotide sequence of the recombinant HSV-1 of claim 1.
11. 1111. The 1 vector of claim 10, further comprising: a nucleotide sequence of a foreign gene.
12. 1212. A method of preparing a recombinant HSV-1 strain KOS, wherein the recombinant HSV-1 is replication-competent and is an oncolytic virus that activates immune cells by exposing antigens of cancer cells by specifically killing cancer cell, the method comprising: preparing a recombinant HSV-1 vector comprising a genome nucleotide sequence of HSV-1 strain KOS, in which an ICP6 region and the nucleotide sequence of SEQ ID NO:2 among nucleotide sequences of the IR region are deleted; and transfecting cells with the vector to obtain a recombinant HSV-1, wherein the simultaneous deletion of ICP6 and a nucleotide sequence of SEQ ID NO:2 enhances the ability to selectively kill cancer cells, and wherein the cancer is lung cancer or glioma.
13. 1313. The method of claim 12, wherein the recombinant HSV-1 vector comprises: a TRL region; a UL region comprising a nucleotide sequence of at least one gene selected from the group consisting of UL1 to UL38 and UL40 to UL56; a US region comprising a nucleotide sequence of at least one gene selected from the group consisting of US1 to US12; a TRS region, or a combination thereof.
14. 1414. A method of treating lung cancer or glioma, the method comprising: administering an effective amount of the recombinant HSV-1 of claim 1 to a subject in need thereof, thereby treating the lung cancer or glioma.
15. 1515. A method of treating lung cancer or glioma, the method comprising: administering an effective amount of the vector of claim 10 to a subject in need thereof, thereby treating the lung cancer or glioma.

SEQUENCE LISTING
The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Sep. 8, 2021, is named 535141USSL.txt and is 201,054 bytes in size.
TECHNICAL FIELD
The present disclosure relates to a recombinant herpes simplex virus type 1 (HSV-1), a recombinant HSV-1 vector, and a method of preparing the same.
BACKGROUND ART
Herpes simplex virus (Herpes Simplex Virus: HSV) is one type of virus that belongs to the herpes virus family and is categorized into HSV-type 1 and HSV-type 2, which are also known as human herpes virus type 1 and type 2, respectively. Nucleic acids are double stranded, linear DNA having a molecular weight of 96×106 Daltons.
As talimogene laherparepvec (T-VEC) was approved by the U.S. Food and Drug Administration (FDA) in 2015 and has been clinically used for the treatment of malignant melanoma, development of an oncolytic/anticancer virus based on the herpes virus is in progress. However, the use of most of the currently developed anticancer HSV-1 is limited by its low therapeutic efficacy because viral replication is limited due to the absence of genes required for viral replication. Also, HSV-1 is a DNA virus having a large genome size of 152 kb, which makes genetic modification of HSV-1 not easy.
Thus, a recombinant HSV-1 vector capable of facilitating genetic modification and having excellent cancer treatment effects needs to be developed.
DESCRIPTION OF EMBODIMENTS
Technical Problem
Provided is a recombinant herpes simplex virus type 1 (HSV-1) having an HSV-1 genome, in which an infected-cell protein 6 (ICP6) region and an internal repeat (IR) region are deleted among HSV-1 genomic regions.
Provided is a recombinant HSV-1 vector including a genomic nucleotide sequence of the recombinant HSV-1.
Provided is a method of preparing the recombinant HSV-1.
Provided is a pharmaceutical composition for preventing or treating cancer, the composition including the recombinant HSV-1 or recombinant HSV-1 vector.
Provided is a method of preventing or treating cancer, the method including administering an effective amount of the recombinant HSV-1 or recombinant HSV-1 vector to a subject in need thereof.
Provided is a use of the recombinant HSV-1 or recombinant HSV-1 vector in preparing an agent for preventing or treating cancer.
Solution to Problem
According to an aspect of the present disclosure, provided is a recombinant herpes simplex virus type 1 (HSV-1).
The recombinant HSV-1 according to an aspect of the present disclosure has an HSV-1 genome, in which an infected-cell protein 6 (ICP6) region and an internal repeat (IR) region between a unique long (UL) region and a unique short (US) region are deleted among HSV-1 genomic regions. A vector structure in which both the ICP6 and IR regions are simultaneously deleted among HSV genomic regions has not been reported yet, and thus the recombinant HSV-1 according to an embodiment of the present disclosure is a recombinant virus having a novel structure. Since about 20 kb of genes are missing due to the deletion of the ICP6 and IR regions, a relatively large foreign gene may be inserted or more than one various foreign genes may be simultaneously inserted to the recombinant HSV-1. ICP6, a ribonucleotide reductase, is an enzyme that is involved in the DNA biosynthesis of HSV-1 and is necessary for DNA replication of the virus when normal cells are infected with the virus. In recent years, a ribonucleotide reductase is known to be overexpressed in various cancer cells. Thus, when the ICP6 gene is removed, replication of a virus in normal cells is restricted, whereas a virus actively replicated in cancer cells may be prepared. Also, two copies of ICPO, ICP34.5, and ICP4 exist in HSV-1, and a virus may be replicated only with one copy thereof. Therefore, removing one copy of ICPO, ICP34.5, and ICP4 in the IR region allows insertion of therapeutic genes of various sizes and types without any influence on the viral replication. In addition, HSV-1 has an IR region, which makes a total of four isotype viruses, but when the IR region is removed, a relatively more stable virus, which is only one HSV-1 isotype, may be prepared. That is, cancer cell selectivity may be imparted by removing the ICP6 gene in the HSV-1 genomic region, and a space to insert the therapeutic gene as well as the structural stability of the HSV-1 oncolytic/anticancer virus may be secured by removing the IR region in the HSV-1 genomic region.
As used herein, the term “deletion” refers to removing of genes on the viral genome. For example, genes may be removed using a restriction enzyme. The entire gene or a part of the gene nucleotide sequence may be removed using a gene cloning method using a restriction enzyme Expression of the functional protein of the gene may not occur or may be inhibited by the gene deletion. Deletion of the ICP6 and IR regions corresponding to a size of about 20 kb may allow insertion of a foreign gene having a long nucleotide sequence.
The term “herpes simplex virus (HSV)” used herein refers to a virus that belongs to a herpesviridae family and is categorized into herpes simplex virus type 1 (HSV-1) and herpes simplex virus type 2 (HSV-2). HSV-1 is also referred to as a human herpes virus type 1 (HHV-1). A nucleic acid of HSV-1 is a double-stranded, linear DNA. Thus, the genome of HSV-1 may be composed of double-stranded, linear DNAs. The genome sequences of HSV-1 may include any genome sequence of an HSV-1 strain available in the art. Examples of the sequences of an HSV-1 genome are disclosed in NCBI GenBank Accession No. JQ673480.1. Unless otherwise indicated herein, “HSV-1” is used interchangeably with “wild-type HSV-1” and is distinguished from “recombinant HSV-1” according to the above aspect. An HSV-1 genomic region may include a terminal repeat of long (TRL) region, a unique long (UL) region, an internal repeat of long (IRL) region, an internal repeat of short (IRS) region, a unique short (US) region, and a terminal repeat of short (TRS) region. The UL region may include nucleotide sequences of UL1 to UL56 genes. The US region may include nucleotide sequences of US1 to US12 genes. Also, the HSV-1 genomic region may not include a TRL region and a TRS region. For example, the HSV-1 genomic region may include a UL region, an IRL region, an IRS region, and a US region.
In one embodiment, a recombinant HSV-1 may include at least one HSV-1 genomic region selected from the group consisting of a TRL region; a UL region including nucleotide sequences of at least one gene selected from UL1 to UL38 and UL40 to UL56; a US region including nucleotide sequences of at least one gene selected from US1 to US12; and a TRS region. In some embodiments, the recombinant HSV-1 may include a combination of HSV-1 genomic regions selected from the group consisting of a TRL region; a UL region including nucleotide sequences of at least one gene selected from UL1 to UL38 and UL40 to UL56; a US region including nucleotide sequences of at least one gene selected from US1 to US12; and a TRS region. In some embodiments, the recombinant HSV-1 may include a TRL region; a UL region including nucleotide sequences of at least one gene selected from UL1 to UL38 and UL40 to UL56; a US region including nucleotide sequences of at least one gene selected from US1 to US12; and a TRS region.
The “terminal repeat of long (TRL) region” may have a size of about 9.2 kb.
The “unique long (UL) region” may have a size of about 108 kb. The UL region of HSV-1 may include nucleotide sequences of UL1 to UL56 genes. The recombinant HSV-1 according to an embodiment of the present disclosure may include a UL region, and the UL region may include nucleotide sequences of at least one gene selected from UL1 to UL38 and UL40 to UL56.
The “infected-cell protein 6 (ICP6)” may be UL39 gene. A nucleotide sequence of the ICP6 may have a size of about 4.8 kb. Examples of the nucleotide sequences of the ICP6 gene may be nucleotide sequences 86,364 to 89,777 among the HSV-1 genomic sequences disclosed in NCBI GenBank Accession No. JQ673480.1. In one embodiment, a genome of the recombinant HSV-1 may be obtained by deleting the whole or a part of the ICP6 gene. In some embodiments, a genome of the recombinant HSV-1 may be obtained by deleting nucleotides 86,901 to 89,578 from the wild-type HSV-1 genomic sequence. For example, the genome of the recombinant HSV-1 may be obtained by deleting a nucleotide sequence of SEQ ID NO: 1 among nucleotide sequences of the ICP6 gene. Examples of amino acid sequences of the ICP6 protein are disclosed in NCBI GenBank Accession No. AFE62867.1.
In one embodiment, the deleted IR region may include at least one region selected from an internal repeat of long (IRL) region and an internal repeat of short (IRS) region. In some embodiments, the deleted IR region may include both an IRL region and an IRS region. The “IRL region” may have a size of about 9.2 kb. The “IRS region” may have a size of about 6.6 kb. Examples of nucleotide sequences of the IRL region may be nucleotide sequences 117,080 to 125,845 among the HSV-1 genomic sequences disclosed in NCBI GenBank Accession No. JQ673480.1. Examples of nucleotide sequences of the IRS region may be nucleotide sequences 126,241 to 132,463 among the HSV-1 genomic sequences disclosed in NCBI GenBank Accession No. JQ673480.1. In one embodiment, the genome of the recombinant HSV-1 may be obtained by deleting the whole or a part of the IR region. In some embodiments, the genome of the recombinant HSV-1 may be obtained by deleting nucleotides 117,080 to 131,261 from the wild-type HSV-1 genomic sequence. For example, the genome of the recombinant HSV-1 may be obtained by deleting a nucleotide sequence of SEQ ID NO: 2 nucleotide sequences of the IR region of HSV-1.
In one embodiment, the recombinant HSV-1 may be obtained by additionally deleting a part of the nucleotide sequence of the UL56 gene together with the deletion of the whole or a part of the IR region. Examples of nucleotide sequences of the UL56 gene may be nucleotide sequences 116, 142 to 116,846 among the HSV-1 genomic sequences disclosed in NCBI GenBank Accession No. JQ673480.1. In some embodiments, the genome of the recombinant HSV-1 may be obtained by deleting nucleotides 116,200 to 116,846 from the wild-type HSV-1 genomic sequence. For example, the deleted part of nucleotide sequence of the UL56 gene may be a nucleotide sequence of SEQ ID NO: 3. In some embodiments, the genome of the recombinant HSV-1 may be obtained by deleting nucleotides 116,200 to 131,261 from the wild-type HSV-1 genomic sequence.
The “US region” may have a size of about 13 kb. The US region of HSV-1 may include nucleotide sequences of US1 to US12 genes. According to an aspect of an embodiment, the recombinant HSV-1 may include a US region, and the US region may include nucleotide sequences of at least one gene selected from US1 to US12.
The “TRS region” may have a size of about 4 kb.
A genome of the recombinant HSV-1 may include a nucleotide sequence of SEQ ID NO: 4.
The recombinant HSV-1 may be an oncolytic virus. As used herein, the term “oncolytic virus” is interchangeably used with “oncolytic/anticancer virus”. An oncolytic virus may activate immune cells by exposing antigens of cancer cells by specifically killing cancer cells or tumor cells. In this regard, an oncolytic virus may be used by itself for anticancer purpose and may be used in combination with other anticancer agents to enhance the anticancer effects. Also, various therapeutic genes may be inserted into the oncolytic virus to enhance the anticancer effects.
The gene sequences are construed to include gene sequences that exhibit substantial identity or substantial similarity. The substantial identity refers to at least 80% homology, more preferably 90% homology, and most preferably 95% homology, when the sequence of the present invention is aligned with a sequence that is different from the sequence of the present invention to correspond each other as much as possible, and the aligned sequences are analyzed by algorithms commonly used in the art. The substantial similarity refers to all changes including a change in gene sequences such as deletion or insertion of one or more bases that do not affect the purpose of the present invention to minimize homologous recombination with recombinant viral vectors.
According to another aspect of an embodiment, provided is a recombinant HSV-1 vector including a genome nucleotide sequence of the recombinant HSV-1 according to an embodiment.
In particular, regarding a recombinant HSV-1 vector including a genome nucleotide sequence of HSV-1, the genome nucleotide sequence of HSV-1 provides a recombinant HSV-1 vector, in which ICP6 is deleted, and nucleotide sequences between a UL region and a US region are deleted.
The term “virus vector” refers to a virus-derived vector capable of delivering foreign or heterologous genetic information to a host.
The HSV-1, recombinant HSV-1, ICP6, IR region, and deletion may be defined the same as described above.
In one embodiment, the vector may include nucleotide sequences of at least one genome region of HSV-1 selected from the group consisting of a TRL region; a UL region including nucleotide sequences of at least one gene selected from UL1 to UL38 and UL40 to UL56; a US region including nucleotide sequences of at least one gene selected from US1 to US12; and a TRS region. In some embodiments, the vector may include a TRL region; a UL region including nucleotide sequences of at least one gene selected from UL1 to UL38 and UL40 to UL56; a US region including nucleotide sequences of at least one gene selected from US1 to US12; and a TRS region.
The recombinant HSV-1 vector may further include nucleotide sequences of a foreign gene. In one embodiment, a nucleotide sequence of the foreign gene may be inserted into the deleted ICP6 or IR regions. In some embodiments, when there are more than one foreign gene to be inserted, the nucleotide sequence of each foreign gene may be inserted into the ICP6 and IR regions, but embodiments are not limited thereto. The nucleotide sequence may be any nucleotide sequence of a foreign gene that may be carried by the vector. For example, the foreign gene that may be carried by the vector may be a gene having anticancer effects, but embodiments are not limited thereto.
The recombinant HSV-1 vector may sequentially include nucleotide sequences of a TRL region, a UL region, a US region, and a TRS region and may be characterized by deleted ICP6 and IR regions. In one embodiment, the recombinant HSV-1 vector may have a genetic map shown in FIG. 1C. The recombinant HSV-1 vector according to an embodiment including the genomic nucleotide sequence of HSV-1, in which the nucleotide sequences of the ICP6 and IR regions are deleted, is named “ΔICP6ΔIR HSV-1 vector”.
The recombinant HSV-1 vector may further include components that are generally included in a viral vector. For example, the recombinant HSV-1 vector may include a promoter that is operably linked to a foreign gene. The promoter may be of any type available in the art, and the type is not limited.
According to another aspect of an embodiment, provided is a method of preparing the recombinant HSV-1 according to the aspect above.
In particular, the method may include preparing a recombinant HSV-1 vector including genomic nucleotide sequences of HSV-1 having deleted ICP6 and IR regions; and transfecting cells with the vector to obtain a recombinant HSV-1.
The recombinant HSV-1 vector is defined the same as described above.
A method of transfecting cells with the vector may be performed using various methods available in the art. For example, cells may be transfected with the vector using methods such as microinjection (Capecchi, M. R., Cell, 22: 479 (1980); and Harland and Weintraub, J. Cell Biol. 101:1094-1099 (1985)), calcium phosphate precipitation (Graham, F. L. et al., Virology, 52: 456 (1973); and Chen and Okayama, Mol. Cell. Biol. 7:2745-2752 (1987)), electroporation (Neumann, E. et al., EMBO J., 1: 841 (1982); and Tur-Kaspa et al., Mol. Cell Biol., 6:716-718 (1986)), liposome-mediated transfection (Wong, T. K. et al., Gene, 10: 87 (1980); Nicolau and Sene, Biochim. Biophys. Acta, 721:185-190 (1982); and Nicolau et al., Methods Enzymol., 149:157-176 (1987)), DEAE-dextran treatment (Gopal, Mol. Cell Biol., 5:1188-1190 (1985)), and gene bombardment (Yang et al., Proc. Natl. Acad. Sci., 87:9568-9572 (1990)).
According to another aspect of an embodiment, provided is a pharmaceutical composition including the recombinant HSV-1 or recombinant HSV-1 vector.
According to another aspect of an embodiment, provided is a method of preventing or treating cancer, the method including administering an effective amount of the recombinant HSV-1 or recombinant HSV-1 vector to a subject in need thereof.
According to another aspect of an embodiment, provided is a use of the recombinant HSV-1 or recombinant HSV-1 vector in preparing an agent for preventing or treating cancer.
The recombinant HSV-1 and recombinant HSV-1 vector are defined the same as described above.
The pharmaceutical composition may be a pharmaceutical composition for anticancer.
A disease may be cancer or tumor.
The term “cancer” refers to diseases caused by cells having aggressive characteristics in which cells divide and grow ignoring normal cell growth limit, invasive characteristics in which cells penetrate the surrounding tissues, and metastatic characteristics in which cells spread to other areas inside and outside the body. The cancer may be used in the same meaning as a malignant tumor or a tumor and may include a solid tumor and a blood born tumor. A type of the cancer is not limited.
The pharmaceutical composition may be used in combination with an existing cancer treatment substance (e.g., anticancer agent) to improve the cancer treatment efficacy. Examples of the anticancer agent may include a metabolic antagonist, an alkylating agent, a topoisomerase antagonist, a microtubule antagonist, an anticancer antibiotic, a plant-derived alkaloid, or an antibody anticancer or a molecular target anticancer agent, and, more specifically, taxol, nitrogen mustard, imatinib, oxaliplatin, rituximab, erlotinib, trastuzumab, gefitinib, bortezomib, sunitinib, carboplatin, sorafenib, bevacizumab, cisplatin, cetuximab, viscum album, asparaginase, tretinoin, hydroxycarbamide, dasatinib, estramastine, gemtuzumab ozogamycin, ibritumomab tucetan, heptaplatin, methylaminolevulinic acid, amsacrine, alemtuzumab, procarbazine, alprostadil, holmium nitrate chitosan, gemcitabine, doxyfluridine, pemetrexed, tegapur, capecitabine, gimeracil, oteracil, azacitidine, methotrexate, uracil, cytarabine, fluorouracil, fludarabine, enocitabine, decitabine, mercaptopurine, thioguanine, cladribine, carmophor, raltitrexed, docetaxel, paclitaxel, irinotecan, velotecan, topotecan, vinorelbine, etoposide, vincristine, vinblastine, teniposide, doxorubicin, idarubicin, epirubicin, mitoxantrone, mitomycin, bleomycin, daunorubicin, dactinomycin, pyrarubicin, aclarubicin, peflomycin, temozolomide, busulfan, ifosfamide, cyclophosphamide, melphalan, altretamine, dacarbazine, thiotepa, nimustine, chlorambucil, mitoractol, lomustine and carmustine, imatinib, gefitinib, ertotinib, tristuzumab, rosiletinib, necitumumab, everolimus, ramucirumab, dacomitinib, foretinib, pembrolizumab, ipilimumab, nivolumab, dabrafenib, veliparib, seritinib, carmustine, cyclophosphamide, ifosfamide, ixabepilone, melphalan, mercaptopurine, mitoxantrone, or TS1, but embodiments are not limited thereto.
The composition may be administered simultaneously, separately, or sequentially in combination with an immune checkpoint inhibitor. The “immune checkpoint” refers to proteins involved in inducing stimulation or suppression signals of an immune response on the surface of immune cells, where cancer cells control the system through the immune checkpoint so that stimulus of the immune response and inhibition of the cancer cells according to the stimulus may not normally function and thus evade the surveillance network of the immune system, that is, neutralize the anti-tumor immune response. The immune checkpoint inhibitor may include at least one selected from PD-1 (programmed cell death-1), PD-L1 (programmed cell death-ligand 1), PD-L2 (programmed cell death-ligand 2), CD27 (cluster of differentiation 27), CD28 (cluster of differentiation 28), CD70 (cluster of differentiation 70), CD80 (cluster of differentiation 80; also known as B7-1), CD86 (cluster of differentiation 86; also known as B7-2), CD137 (cluster of differentiation 137), CD276 (cluster of differentiation 276), killer-cell immunoglobulin-like receptors (KIRs), lymphocyte-activation gene 3 (LAG3), tumor necrosis factor receptor superfamily, member 4 (TNFRSF4; also known as CD134), glucocorticoid-induced TNFR-related protein (GITR), glucocorticoid-induced TNFR-related protein ligand (GITRL), 4-1BB ligand (4-1BBL), and cytolytic T lymphocyte associated antign-4 (CTLA-4) antagonists, but embodiments are not limited thereto.
The pharmaceutical composition may further include a pharmaceutically acceptable carrier or diluent. The pharmaceutically acceptable carrier or diluent may be known in the art. Examples of the carrier or diluent may include lactose, dextrose, sucrose, sorbitol, mannitol, starch, acacia rubber, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water (e.g. saline and sterile water), syrup, methyl cellulose, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate, mineral oil, Ringer's solution, buffer, maltodextrin solution, glycerol, ethanol, dextran, albumin, and a combination thereof. The pharmaceutical composition may further include a lubricant, a wetting agent, a sweetener, a flavoring agent, an emulsifier, a suspending agent, or a preservative.
According to methods that are known in the art, the pharmaceutical composition may be formulated and prepared in the form of a unit dose using the pharmaceutically acceptable carrier and/or diluents, or may be introduced and prepared in a multi-dose container. Here, the pharmaceutical composition may be formulated as a solution, suspension, syrup, or an emulsion of an oil or aqueous solvent. In some embodiments, the pharmaceutical composition may be formulated as extracts, powders, powdered drugs, granules, tablets, or capsules. The pharmaceutical composition may further include a dispersant or a stabilizer. The aqueous solvent may include physiological saline or a phosphate buffer solution (PBS). The pharmaceutical composition according to an embodiment may be formulated into in the form of an oral or parenteral administration, preferably, in the form of a parenteral administration. In general, a sterile solution of an active ingredient is prepared and a buffer for adjusting the pH is added to the solution for intramuscular, intraperitoneal, transdermal, and intravenous administration. For the intravenous administration, an isotonic agent may further be added to a preparation for isotonicity.
A prescribed dosage (effective amount) of the pharmaceutical composition may vary according to various factors such as formulation method, administration route, age, weight, and gender of a patient, pathological conditions, diet, duration of administration, route of administration, excretion rate, and susceptibility to reaction, and the dosage may be appropriately adjusted by those or ordinary skill in the art in consideration of these factors. Available administration routes may include parenteral administration (e.g., subcutaneous, intramuscular, intra-arterial, intraperitoneal, transdermal, or intravenous administration), topical administration (including transdermal administration), and injection, or insertion of or a transplantable device or a substance. As a target animal for therapy according to an embodiment, a human and a mammal of interest may be exemplified. For example, the target may be a human being, a monkey, a mouse, a rat, a rabbit, sheep, a cow, a dog, a horse, or a pig.
According to another aspect of an embodiment, provided is a method of inhibiting viability of cancer cells or tumor cells, the method including administering an effective amount of the recombinant HSV-1 or recombinant HSV-1 vector or a pharmaceutical composition including the recombinant HSV-1 or recombinant HSV-1 vector to a subject. The method may be a cancer treatment method.
The term “treatment” refers to or includes alleviating, inhibiting the progress of, or preventing a disease, disorder, or condition, or at least one symptom thereof, and the term “active ingredient” or “pharmaceutically effective amount” refers to an amount of a composition used while performing a process according to the present disclosure sufficient to alleviate, inhibit the progress of, or prevent the disease, disorder, or condition, or at least one symptom thereof.
The terms “administering”, “introducing”, and “transplanting” are interchangeably used and may refer to placement of a composition according to an embodiment into an individual by a method or route which results in at least partial localization of the composition at a desired site. The composition according to an embodiment may be administered by any appropriate route that delivers an active ingredient of the composition to a desired position in a living individual. The cells may survive for a short time, e.g., several hours to 24 hours or for a long time, e.g., several days to several years after administration into the individual.
The terms “subject,” “individual,” and “patient” are used interchangeably herein to refer to a vertebrate, preferably a mammal, more preferably a human. Mammals include, but are not limited to, murines, simians, humans, farm animals, sport animals, and pets. Tissues, cells and their progeny of a biological entity obtained in vivo or cultured in vitro are also encompassed.
The term “effective amount” or “therapeutically effective amount” refers to the amount of an agent that is sufficient to effect beneficial or desired results. The therapeutically effective amount may vary depending upon one or more of: the subject and disease condition being treated, the weight and age of the subject, the severity of the disease condition, and the manner of administration, which may readily be determined by one of ordinary skill in the art. The term also applies to a dose that will provide an image for detection by any one of the imaging methods described herein. The specific dose may vary depending on one or more of: the particular agent chosen, the dosing regimen to be followed, whether it is administered in combination with other compounds, timing of administration, the tissue to be imaged, and the physical delivery system in which it is carried.
Advantageous Effects of Disclosure
Since a recombinant HSV-1 according to an embodiment is prepared by simultaneously deleting ICP6 and IR regions, a relatively large foreign gene may be inserted or various foreign genes may be simultaneously inserted into the virus and thus may facilitate the genetic modification. Also, the recombinant HSV-1 is an oncolytic/anticancer virus having safe and excellent effects for killing cancer cells and thus may be widely used in the cancer treatment field.



BRIEF DESCRIPTION OF DRAWINGS
FIG. 1A is a schematic diagram of the genome of a wild-type human simplex virus type 1 (HSV-1 WT);
FIG. 1B is a schematic diagram of an infected-cell protein 6 (ICP6)-deleted (ΔICP6) HSV-1 genome;
FIG. 1C is a schematic diagram of an ICP6 and internal repeat (IR) regions-deleted (ΔICP6ΔIR) HSV-1 genome;
FIG. 2 is a schematic diagram illustrating an rpsL-neo gene and positions of a UL56-rpsL-neo primer and a UsIR-rpsL-neo primer;
FIG. 3 is a schematic diagram of ΔICP6-ΔIR-rpsL-neo;
FIG. 4 shows results of performing polymerase chain reaction (PCR) performed using a UL55 S primer and a UsIR-rpsL neo AS primer to confirm insertion of rpsL-neo, wherein HSV-1 WT was used as a negative control, and ΔICP6-rpsL-neo was used as a positive control;
FIG. 5 shows results of PCR performed using an rpsL neo S primer and an rpsL neo AS primer to confirm insertion of rpsL-neo, wherein HSV-1 WT was used as a negative control, and ΔICP6-rpsL-neo was used as a positive control;
FIG. 6 shows results of PCR performed using a gC S primer and a gC AS primer that are used for detecting glycoprotein C to confirm insertion of rpsL-neo, wherein HSV-1 WT was used as a negative control, and ΔICP6-rpsL-neo was used as a positive control;
FIG. 7 shows results of PCR performed using a UL55 S primer and a AIR AS primer to confirm whether the IR region was well deleted from the ΔICP6ΔIR virus, wherein a AIR virus was used as a positive control;
FIG. 8 shows results of PCR performed using a rpsL-neo S primer and an rpsL-neo AS primer to confirm whether foreign gene rpsL-neo was well deleted from the ΔICP6ΔIR virus, wherein ΔICP6-ΔIR-rpsL-neo was used as a control;
FIG. 9 shows results of PCR performed using a UL55 S primer and an rpsL-neo S AS primer to confirm whether IR and rpsL-neo were well deleted from the ΔICP6ΔIR virus, wherein ΔICP6-ΔIR-rpsL-neo was used as a control; and
FIG. 10 shows graphs confirming anticancer effects and safety of the ΔICP6ΔIR virus,





    
    
        wherein FIG. 10A shows results confirmed from A549 cells; FIG. 10B shows results confirmed from U251N cells; FIG. 10C shows results confirmed from VERO cells; and FIG. 10D shows results confirmed from HswC cells.
    
    


MODE OF DISCLOSURE
Hereinafter, the present invention will be described in more detail with reference to Examples. However, these examples are for illustrative purposes only and the scope of the present invention is not limited to these examples.
Example 1: Construction of Recombinant HSV-1 (ΔICP6ΔIR HSV-1) in which ICP6 and IR Regions are Deleted
FIG. 1A is a schematic diagram of a genome of wild-type HSV-1. The HSV-1 genome is broadly categorized into a unique long (UL) region and a unique short (US) region. The UL region has a single replication origin; a and b composed of a terminal repeat (TP) and an internal repeat (IR) at the 5′ end; and a and b in the reverse direction at the 3′ end. The US region has two replication origins; a c sequence in the reverse direction at the 5′ end; forwarding c is repeated at the 3′ end; and a sequence is repeated once more at the 3′ end.
First, ΔICP6 HSV-1 in which a part of the ICP6 region is deleted is prepared from a genomic sequence of the HSV-1 WT. The nucleotides 86,364 to 89,777 in the wild-type HSV-1 genome sequence constitute a sequence encoding the ICP6 gene. The nucleotides 86,901 to 89,578, which are a part of the ICP6 gene, were deleted using a method known in the art, and this was names as “ΔICP6 HSV-1 virus.”
FIG. 1B is a schematic diagram of an ICP6-deleted (ΔICP6) HSV-1 genome.
Next, ΔICP6ΔIR virus from which the ICP6 and IR regions are deleted was constructed using the ΔICP6 HSV-1 virus as a template. In the wild-type HSV-1 genome sequence, the nucleotides 116,141 to 116,846 constituted a UL56 sequence, and the IR region was broadly composed of b′(117,080 to 125,845), a′(125,846 to 126,240), and c′(126,241 to 132,463). In this region, the nucleotides 116,200 to 131,261 corresponding to a partial region of UL56 gene to a partial region of IR region were deleted using a method known in the art. This was named “ΔICP6ΔIR HSV-1 virus.” FIG. 1C is a schematic diagram of an ICP6 and IR regions-deleted (ΔICP6ΔIR) HSV-1 genome.
Example 2: Construction of ΔICP6-ΔIR-rpsL-Neo to which Foreign Gene rpsL-Neo is Inserted
A foreign gene, 1319 bp, which is an rpsL-neo gene, was inserted to the ΔICP6ΔIR HSV-1 of Example 1, from which the ICP6 gene and the IR gene were simultaneously deleted, to construct a virus, and the insertion of the foreign gene of the virus was evaluated.
In particular, as shown in Table 1, a UL56-rpsL-neo primer having a sequence complementary to UL56 and rpsL-neo and a UsIR-rpsL-neo primer having a sequence complementary to UsIR and rpsL-neo were prepared. After adding a 2× green master mix (thermo scientific) reaction enzyme to 10 pmol of the UL56-rpsL-neo primer and the UsIR-rpsL-neo primer, PCR was performed with 200 ng of the rpsL-neo gene as a template. The PCR product was transformed into DH10b Escherichia coli together with the ΔICP6 total vector of Example 1 to induce homologous recombination to prepare ΔICP6-ΔIR-rpsL-neo expressing rpsL-neo.
FIG. 2 is a schematic diagram that shows positions of the rpsL-neo gene, the UL56-rpsL-neo primer, and the UsIR-rpsL-neo primer.
FIG. 3 is a schematic diagram of ΔICP6-ΔIR-rpsL-neo.









TABLE 1






SEQ



Primer 
ID



name
NO.
Sequence







UL56-
5
5′-


rpsL-

acaggaataccagaataatgaccaccacaatcgc


neo

gaccaccccaaatacaGGCCTGGTGATGATGGGG




GATCG-3′




(underline: sequence complementary 




to UL56, bold: sequence 




complementary to rpsL-neo)


 


UsIR-
6
5′-


rpsL-

cccgaggacgccccgatcgtccacacggagcgcg


neo

gctgccgacacggatcTCAGAAGAACTCGTCAAG




AAGGCG-3′




(bold: sequence complementary to 




rpsL-neo, underline: sequence 




complementary to UsIR)









PCRs were performed using the PCR primers in Table 2 to evaluate production of the homologous recombination. Conditions of each of the PCRs were as follows. After adding a 2× green master mix (thermo scientific) reaction enzyme to 10 pmol of the UL55 S primer and the UsIR-rpsL-neo AS primer, each of the PCRs was performed with 200 ng of the rpsL-neo gene as a template; and denaturing the resultant at 95° C. for 30 seconds, annealing at 58° C. for 30 seconds, and extending at 72° C. for 2 minutes in the PCR machine (Bio-rad). To confirm rpsL-neo and glycoprotein C, PCR was performed under conditions denaturing the resultant at 95° C. for 30 seconds, annealing at 58° C. for 30 seconds, and extending at 72° C. for 30 seconds at the same mixture ratio.









TABLE 2






SEQ ID



Primer name
NO.
Sequence (5′ → 3′)

















UL55 S
7
ACGCGTCGACtaaaaacaaaacatttcaa




acaaatcgcccca


 


UsIR-rpsL
8
cccgaggacgccccgatcgtccacacgga


neo AS

gcgcggctgccgacacggatcTCAGAAGA




ACTCGTCAAGAAGGCG


 


rpsL neo S
9
CGGCATCGCCCTAAAATTCGGCGTCCTC


 


rpsL neo AS
10
AAGAACCGGGCGCCCCTGCGCTGACAGC


 


gC S
11
CAGATCCGATGCCGGTTTCGGAATTCCAC




CCG


 


gC AS
12
CGGGTTAAACACCTGGCGGTCGTCCTCGA




AC


 


ICP6 R-rpsL-
13
GTTCCTGTCGCGACACACGGCGCCGCTCT


neo S

GCGGTATTCGGGGGGGAGGGGGGCCTGGT




GATGATGGCGGGATCG


 


ICP6 R-rpsL-
14
AGGGTCCCGTCCGCCTTCTCCGTGACATA


neo AS

CAGGGTCATGGATTGGCTATGTCAGAAGA




ACTCGTCAAGAAGGCG









FIG. 4 shows the results of PCR performed using a UL55 S primer and a UsIR-rpsL neo AS primer to confirm insertion of rpsL-neo. HSV-1 WT was used as a negative control, and ΔICP6-rpsL-neo was used as a positive control. After adding a 2× green master mix (thermo scientific) reaction enzyme to 10 pmol of an ICP6 R-rpsL-neo S primer and an ICP6 R-rpsL-neo AS primer, PCR was performed with 200 ng of ΔICP6-rpsL-neo as a template in the PCR machine (Bio-rad) under the conditions of denaturing the resultant at 95° C. for 30 seconds, annealing at 58° C. for 30 seconds, and extending at 72° C. for 1 minute and 30 seconds. The PCR products of rpsL-neo was transformed into DH10b E. coli together with the wild-type HSV-1 total vector to induce homologous recombinant to prepare ΔICP6-rpsL-neo. As a result, it was confirmed that the homologous recombinant was successfully achieved since a band of 2300 bp of the prepared ΔICP6-ΔIR-rpsL-neo was confirmed the same with that of the positive control. FIG. 5 shows the results of PCR performed using an rpsL neo S primer and an rpsL neo AS primer to confirm insertion of rpsL-neo. HSV-1 WT was used as a negative control, and ΔICP6-rpsL-neo was used as a positive control. As a result, it was confirmed that the homologous recombinant was successfully achieved since a band of 534 bp of the prepared ΔICP6-ΔIR-rpsL-neo was confirmed the same with that of the positive control.
FIG. 6 shows the results of PCR performed using a gC S primer and a gC AS primer for detecting glycoprotein C to confirm insertion of rpsL-neo. HSV-1 WT was used as a negative control, and ΔICP6-rpsL-neo was used as a positive control. As a result, it was confirmed that homologous recombination was successfully achieved since a band of 512 bp of the prepared ΔICP6-ΔIR-rpsL-neo was confirmed the same with that of the positive control.
Therefore, it was confirmed that the rpsL-neo gene, a foreign gene, was successfully inserted to the ΔICP6ΔIR virus.
Example 3: Construction of ΔICP6ΔIR Virus
The rpsL-neo gene, a foreign gene, was deleted from the ΔICP6-ΔIR-rpsL-neo prepared in Example 2 to prepare ΔICP6ΔIR virus.
In particular, after preparing the primers in Table 3, a primer annealing method was performed to prepare a two-stranded oligomer having a complementary sequence bound thereto. The prepared oligomer was transformed into DH10b E. coli together with the ΔICP6-ΔIR-rpsL-neo total vector of Example 2 to induce homologous recombination to prepare dICP6-dIR.









TABLE 3





Primer
SEQ ID



name
NO.
Sequence (5′ -> 3′)







ΔIR S
15
ACAGGAATACCAGAATAATGACCACCACAATCGCG




ACCACCCCAAATACAGATCCGTGTCGGCAGCCGCG




CTCCGTGTGGACGATCGGGGCGTCCTCG


 


ΔIR AS
16
CGAGGACGCCCCGATCGTCCACACGGAGCGCGGCT




GCCGACACGGATCTGTATTTGGGGTGGTCGCGATT




GTGGTGGTCATTATTCTGGTATTCCTGT









To confirm whether the ΔICP6ΔIR virus from which the foreign gene was deleted was successfully constructed or not, PCR was performed using the PCR primers above. After adding a 2× green master mix (thermo scientific) reaction enzyme to 10 pmol of a UL55 S primer and an AIR AS primer, PCR was performed with 200 ng of ΔICP6ΔIR as a template in the PCR machine (Bio-rad) under the conditions of denaturing the resultant at 95° C. for 30 seconds, annealing at 58° C. for 30 seconds, and extending at 72° C. for 1 minute. To confirm rpsL-neo, PCR was performed under conditions denaturing the resultant at 95° C. for 30 seconds, annealing at 58° C. for 30 seconds, and extending at 72° C. for 30 seconds at the same mixture ratio. FIG. 7 shows the results of PCR performed using a UL55 S primer and a AIR AS primer to confirm whether IR was well removed from the ΔICP6ΔIR virus. A AIR virus was used as a positive control. After adding a 2X green master mix (thermo scientific) reaction enzyme to 10 pmol of a UL56-rpsL-neo primer and a UsIR-rpsL-neo primer, PCR was performed with 200 ng of the AIR virus as a template in the PCR machine (Bio-rad) under the conditions of denaturing the resultant at 95° C. for 30 seconds, annealing at 58° C. for 30 seconds, and extending at 72° C. for 1 minute. The PCR products of rpsL-neo was transformed into DH10b E. coli together with a wild-type HSV-1 total vector to induce homologous recombination to prepare a AIR-rpsL-neo virus. Then, after performing primer annealing on the AIR S and AIR AS primers, the primers were transformed into DH10b E. coli together with a AIR-rpsL-neo total vector to induce homologous recombination to prepare a AIR virus.
As a result, it was confirmed that IR was successfully removed since a band of a size of 1 kb of the prepared ΔICP6ΔIR virus was confirmed the same with that of the positive control.
FIG. 8 shows the results of PCR to confirm whether a foreign gene, rpsL-neo, was well removed from an ICP6ΔIR virus by performing PCR using an rpsL-neo S primer and an rpsL-neo AS primer. The ΔICP6-ΔIR-rpsL-neo prepared in Example 2 was used as a control. As a result, unlike the control, ΔICP6-ΔIR-rpsL-neo, exhibited a band of about 500 bp, the ΔICP6ΔIR virus did not exhibit a band, and this confirms that the foreign gene, rpsL-neo, was successfully deleted.
FIG. 9 shows the results of PCR performed using a UL55 S primer and an rpsL-neo S AS primer to confirm whether IR and rpsL-neo were well removed from the ICP6ΔIR virus. The ΔICP6-ΔIR-rpsL-neo prepared in Example 2 was used as a control. As a result, unlike the control, ΔICP6-ΔIR-rpsL-neo, generated a band of about 1700 bp, the ΔICP6ΔIR virus did not generate a band, and this confirms that the IR and foreign gene were successfully deleted.
Thus, it confirms that the ΔICP6ΔIR virus with the foreign gene removed therefrom was successfully prepared.
Experimental Example 1: Confirmation of anticancer effects and safety of ΔICP6ΔIR virus of Example 3
A549 (human lung cancer, ATCC® CRM-CCL-185TM), U251N (human glioma, ATCC®), and VERO (monkey normal kidney, ATCC® CCL-81™) cells were divided into a 6-well plate at a density of 3.5×105 cells/well, and HswC (iXcells, 10HU-188) cells were divided at a density of 3×105 cells/well. After 24 hours, each of a wild-type HSV-1, a ΔICP6 virus from which only ICP6 is deleted, a AIR virus from which only IR is deleted, and a ΔICP6ΔIR virus from which both ICP6 and IR are deleted was infected with 0.1 MOI.
After 24 hours, 48 hours, 72 hours, and 120 hours, the cells and the supernatants were all collected and centrifuged at 4° C. for 10 minutes at 3000 rpm. Thus obtained pellets and the supernatants were separated, and the supernatants were remained at 4° C., and after freezing/thawing the pellets three times, the supernatants were added with the pellets, and the resultants were centrifuged once again at 4° C. for 10 minutes at 3000 rpm. Thereafter, only the supernatants were separated and a plaque assay was performed as follows.
VERO cells divided into a 12-well plate at a density of 1.5×105 were infected with the supernatants obtained as described above. After 8 hours, 1 ml of 1% methylcellulose was added to the cells. 3 days after the infection, the cells were dyed with 1% crystal violet staining solution to count the number of plaques.
As a result, it was confirmed that ΔICP6ΔIR showed cancer cell killing ability similar to that of wild-type virus HSV-1 and cancer cell killing ability higher than that of ΔICP6 or AIR. Also, progeny virus of low titer was produced in HswC cells, showing the characteristics of a vector that is safe for humans.