IP Library › Granted Patent US 12,539,328
Granted Patent B2
US 12,539,328 · App. 18/608,668 · Granted Feb 3, 2026

Oral vaccine via dental bacteria and emitted peptides to prevent COVID-19 infection

Inventor: David Kotlyar (Sterling, VA)
A61K39/215A61K2039/522A61K2039/523A61K2039/542A61K2039/543
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Quick Facts
Patent No.
US 12,539,328
App. No.
18/608,668
Granted
Feb 3, 2026
Kind
B2
Abstract

Disclosed is a pharmaceutical composition to prevent transmission of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the pharmaceutical composition comprising: genetically modified bacteria; sequences of small peptides; and pharmaceutical excipients, wherein the genetically modified oral bacteria are modified to translate, produce, and emit the sequences of small peptides which neutralize SARS-CoV-2 against COVID-19, wherein transgenic technology is used to modify the genetically modified oral bacteria to add genes in genetically modified oral bacteria that are transcribed to produce small peptides from the sequences of small peptides so added, wherein the sequences of small peptides show extreme binding and neutralization to SARS-CoV-2 but not to host proteins or processes, and wherein the pharmaceutical excipients aid the oral and/or nasal administration of the pharmaceutical composition.

Claims (23)

1 . A pharmaceutical composition to prevent transmission of a pathogen, the pharmaceutical composition comprising:

a) genetically modified commensal bacteria capable of colonizing an oral and/or nasal mucosa of a subject;

and

b) pharmaceutical excipients,

wherein the genetically modified commensal bacteria are from mouth and/or nose commensal bacteria modified by transgenic technology to comprise genes encoding small peptides, such that the bacteria transcribe, translate, produce, and secrete the small peptides expressed in situ at the oral and/or nasal mucosa of the subject and which neutralize the pathogen,

wherein the small peptides are selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8, SEQ ID NO: 9, and SEQ ID NO: 10,

wherein the transgenic technology is used to modify commensal bacteria to produce transgenic bacteria to obtain the genetically modified commensal bacteria by introducing a recombinant vector into the commensal bacteria, the recombinant vector comprising genes encoding the small peptides inserted into a vector to add said genes that are transcribed and translated for recombinant expression in the genetically modified commensal bacteria to produce and secrete the small peptides from the genetically modified commensal bacteria in situ at the oral and/or nasal mucosa,

wherein the genetically modified commensal bacteria deliver the small peptides in situ at the oral and/or nasal mucosa of the subject,

wherein the subject is a mammal,

wherein the pathogen is a coronavirus,

wherein the coronavirus comprises severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2),

wherein the pharmaceutical excipients comprise stabilizers, buffers, cryoprotectants, or other agents formulated to aid the oral and/or nasal administration of the pharmaceutical composition, and

wherein the genetically modified commensal bacteria carrying the added genes encoding the small peptides provide an effective and easy administration by means of an easy-to-administer pharmaceutical composition for neutralization of the pathogen to prevent transmission of the pathogen in situ at the oral and/or nasal mucosa of the subject.

2 . The pharmaceutical composition of claim 1 , wherein the genetically modified commensal bacteria are obtained from Staphylococcus lugdunensis , genetically modified with the use of transgenic technology.

3 . The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated as an oral vaccine to prevent transmission of the pathogen in situ at the oral mucosa of the subject, or a nasal spray vaccine to prevent transmission of the pathogen in situ at the nasal mucosa of the subject.

4 . The pharmaceutical composition of claim 1 , wherein one or more of the small peptides are modified with extra n-glycosylation sites to improve half-life.

5 . A method of treating or preventing infection of a pathogen in a subject, the method comprising the step of administering a therapeutically effective amount of the pharmaceutical composition of claim 1 to the subject.

6 . The method of claim 5 , wherein the the pharmaceutical composition of claim 1 is administered as an oral vaccine to prevent transmission of the pathogen or a nasal spray vaccine to prevent transmission of the pathogen.

7 . The method of claim 5 , wherein the subject is a mammal.

8 . A method of blocking entry of a pathogen in a subject comprising the step of administering a therapeutically effective amount of the pharmaceutical composition of claim 1 to the subject.

9 . The method of claim 8 , wherein the the pharmaceutical composition of claim 1 is administered as an oral vaccine to prevent transmission of the pathogen or a nasal spray vaccine to prevent transmission of the pathogen.

10 . The method of claim 8 , wherein the subject is a mammal.

11 . The pharmaceutical composition of claim 1 , wherein the small peptides disrupt and/or block the interaction and binding of the pathogen and/or proteins of the pathogen with host receptors at the oral and/or nasal mucosal surface of the subject owing to the production and secretion of the small peptides in situ in the mouth and nose of the subject to prevent pathogen attachment and entry into the host cells to prevent the transmission of the pathogen at the initial stage of interaction at the mouth and/or nose of the subject exposed to the pathogen, and this leads to prevention of acquisition of infection, prevention of morbidities caused by infection from the pathogen, and prevention of death caused by said infection.

Continuity (3)
Continuation PCTUS2022076681 · Sep 19, 2022
Provisional Application 63245553 · Sep 17, 2021
Related Publication 20240226281A1 · Jul 11, 2024
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