Anti COVID-19 Therapies targeting nucleocapsid and spike proteins
Disclosed herein are methods for inducing immunity against a virus such as a coronavirus in the mucosal tissue of a patient, include administering a vaccine composition to the patient by oral administration (e.g., nasal injection, nasal inhalation, oral inhalation, and/or oral ingestion). Also disclosed are compositions for assaying the presence of anti-viral antibodies induced by the administered vaccine or the presence of viral proteins in a saliva sample include a stabilizing solution and may also include the use of aragonite particle beads. Compositions and methods are presented for prevention and/or treatment of a coronavirus disease wherein the composition comprises comprises a recombinant entity. The recombinant entity is bivalent, comprising a nucleic acid encoding a coronavirus 2 nucleocapsid protein CoV2 nucleocapsid protein fused to an endosomal targeting sequence, and a nucleic acid encoding a CoV2 spike protein sequence optimized for cell surface expression.
1 . A nucleic acid encoding a chimeric protein comprising 1) a CoV2 nucleocapsid (N) protein having the amino acid sequence of SEQ ID NO: 1 and 2) an endosomal targeting sequence (ETSD) having the amino acid sequence of SEQ ID NO: 2.
2 . The nucleic acid of claim 1 , wherein the nucleic acid portion has a nucleotide sequence of SEQ ID NO:3.
3 . The nucleic acid of claim 1 , wherein the nucleic acid further comprises a co-stimulatory molecule and/or an immune stimulatory cytokine.
4 . The nucleic acid of claim 3 , wherein the co-stimulatory molecule is selected from the group consisting of CD80, CD86, CD30, CD40, CD30L, CD40L, ICOS-L, B7-H3, B7-H4, CD70, OX40L, 4-IBBL, GITR-L, TIM-3, TIM-4, CD48, CD58, TLIA, ICAM-1, and LFA3.
5 . The nucleic acid of claim 3 , wherein the immune stimulatory cytokine is selected from the group consisting of IL-2, IL-12, IL-15, nogapendekin alfa-imbakicept, IL-21, IPSI, and LMP1.
6 . A vaccine composition comprising the nucleic acid of claim 1 , wherein the composition is formulated for injection.
7 . A method for inducing immunity against CoV2 in a patient in need thereof, the method comprising administering to the patient the vaccine composition of claim 6 .
8 . A replication defective adenovirus, wherein the adenovirus comprises:
a. an E1 gene region deletion;
b. an E2b gene region deletion; and
c. the nucleic acid of claim 1 .
9 . A yeast or lysate thereof, wherein the yeast comprises the nucleic acid of claim 1 .
10 . A replication defective adenoviral vector comprising the following components: an E1 gene region deletion; an E2b gene region deletion; and a nucleic acid portion that encodes a chimeric protein comprising a SARS-CoV-2 N protein and an endosomal targeting sequence.
11 . The replication defective adenoviral vector of claim 10 , wherein the nucleic acid portion that encodes the chimeric protein is depicted by SEQ ID NO:3.
12 . The replication defective adenoviral vector of claim 10 , further comprising a trafficking sequence, a co-stimulatory molecule, and/or an immune stimulatory cytokine.
13 . The replication defective adenoviral vector of claim 10 , wherein the co-stimulatory molecule is selected from the group consisting of CD80, CD86, CD30, CD40, CD30L, CD40L, ICOS-L, B7-H3, B7-H4, CD70, OX40L, 4-IBBL, GITR-L, TIM-3, TIM-4, CD48, CD58, TLIA, ICAM-1, and LFA3.
14 . The replication defective adenoviral vector of claim 10 , wherein the immune stimulatory cytokine is selected from the group consisting of IL-2, IL-12, IL-15, nogapendekin alfa-imbakicept, IL-21, IPSI, and LMP1.
15 . A method for inducing immunity against a coronavirus in a patient in need thereof, the method comprising administering to the subject an immunotherapy composition comprising a recombinant entity, wherein the recombinant entity comprises a nucleic acid that encodes a nucleocapsid protein of coronavirus 2 (CoV2) and an endosomal targeting sequence.
16 . The method of claim 15 , wherein the recombinant entity comprises a replication defective adenoviral vector comprising an E1 gene region deletion and an E2b gene region deletion.
17 . The method of claim 15 , wherein an immune stimulatory cytokine is administered.
18 . The method of claim 17 , wherein the immune stimulatory cytokine is selected from the group consisting of IL-2, IL-12, IL-15, IL-15 super agonist (N803), IL-21, IPS 1, and LMP 1.
19 . The method of claim 15 , wherein the coronavirus is SARS-CoV-2.
20 . The method of claim 15 , wherein the coronavirus is not SARS-CoV-2.