Methods and compositions for coronavirus diagnostics and therapeutics

US2016238601A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016238601-A1
Application numberUS-201415029190-A
CountryUS
Kind codeA1
Filing dateOct 14, 2014
Priority dateOct 14, 2013
Publication dateAug 18, 2016
Grant date

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention provides methods and compositions for detecting a coronavirus in a sample and identifying the subgroup of the coronavirus in the sample.

First claim

Opening claim text (preview).

1 . A method of detecting the presence of a coronavirus in a sample and identifying the subgroup of the coronavirus in the sample, comprising: a) contacting a sample with a panel of proteins comprising: 1) one or more nucleocapsid proteins from a subgroup 2c coronavirus, 2) one or more nucleocapsid proteins from a subgroup 2b coronavirus, 3) one or more nucleocapsid proteins from a subgroup 2a coronavirus, 4) one or more nucleocapsid proteins from a subgroup 2d coronavirus, 5) one or more nucleocapsid proteins from a subgroup 1a coronavirus, 6) one or more nucleocapsid proteins from a subgroup 1b coronavirus, and 7) any combination of (1) through (6) above, under conditions whereby an antigen/antibody complex can form; and b) detecting formation of an antigen/antibody complex, whereby detection of formation of the antigen/antibody complex detects a coronavirus in the sample and whereby detection of formation of an antigen/antibody complex comprising the nucleocapsid protein(s) of (1) identifies the subgroup of the coronavirus in the sample as subgroup 2c; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (2) identifies the subgroup of the coronavirus in the sample as subgroup 2b; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (3) identifies the subgroup of the coronavirus in the sample as subgroup 2a; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (4) identifies the subgroup of the coronavirus in the sample as subgroup 2d; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (5) identifies the subgroup of the coronavirus in the sample as subgroup 1a; and detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (6) identifies the subgroup of the coronavirus in the sample as subgroup 1b. 2 . The method of claim 1 , further comprising contacting the sample with one or more nucleocapsid proteins from a subgroup 3 coronavirus, whereby detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of a subgroup 3 coronavirus identifies the subgroup of the coronavirus in the sample as a subgroup 3 coronavirus. 3 . A method of identifying a coronavirus spike protein for administration to elicit an immune response to coronavirus in a subject infected by a coronavirus and/or a subject at risk of coronavirus infection and/or to a subject for whom eliciting an immune response to a coronavirus is needed or desired, comprising: a) contacting a sample obtained from a subject infected with a coronavirus with a panel of proteins comprising: 1) one or more spike proteins from a subgroup 2c coronavirus, 2) one or more spike proteins from a subgroup 2b coronavirus, 3) one or more spike proteins from a subgroup 2a coronavirus, 4) one or more spike proteins from a subgroup 2d coronavirus, 5) one or more spike proteins from a subgroup 1a coronavirus, 6) one or more spike proteins from a subgroup 1b coronavirus, and 7) any combination of (1) through (6) above, under conditions whereby an antigen/antibody complex can form; and b) detecting formation of an antigen/antibody complex, whereby detection of formation of the antigen/antibody complex comprising the spike protein(s) of any of (1)-(6) identifies the presence of antibodies to a spike protein of the coronavirus that is infecting the subject of (a), thereby identifying a coronavirus spike protein for administration to the subject of (a) and/or to a subject infected with a coronavirus and/or to a subject at risk of coronavirus infection and/or to a subject for whom eliciting an immune response to a coronavirus is needed or desired. 4 . The method of claim 3 , further comprising contacting the sample with one or more spike proteins from a subgroup 3 coronavirus, whereby detection of an antigen/antibody complex comprising the spike protein(s) of a subgroup 3 coronavirus identifies the presence of antibodies to a spike protein of the coronavirus that is infecting the subject of (a), thereby identifying a coronavirus spike protein for administration to the subject of (a) and/or to a subject infected with a coronavirus and/or to a subject at risk of coronavirus infection and/or to a subject for whom eliciting an immune response to a coronavirus is needed or desired. 5 . The method of claim 3 , further comprising the step of administering the coronavirus spike protein identified according to the method to the subject of (a) and/or to a subject at risk of coronavirus infection and/or to a subject infected with a coronavirus and/or to a subject for whom eliciting an immune response to a coronavirus is needed or desired. 6 . The method of claim 5 , wherein the coronavirus spike protein is administered as part of an inactivated coronavirus. 7 . The method of claim 5 , wherein the coronavirus spike protein is administered as a VRP. 8 . A method of identifying a coronavirus spike protein for administration to elicit an immune response to coronavirus in a subject infected with a coronavirus and/or to a subject at risk of coronavirus infection and/or to a subject for whom eliciting an immune response to coronavirus is needed or desired, comprising: a) contacting a sample obtained from a subject known or suspected to be infected with a coronavirus with a panel of proteins comprising: 1) one or more nucleocapsid proteins from a subgroup 2c coronavirus, 2) one or more nucleocapsid proteins from a subgroup 2b coronavirus, 3) one or more nucleocapsid proteins from a subgroup 2a coronavirus, 4) one or more nucleocapsid proteins from a subgroup 2d coronavirus, 5) one or more nucleocapsid proteins from a subgroup 1a coronavirus, 6) one or more nucleocapsid proteins from a subgroup 1b coronavirus, and 7) any combination of (1) through (6) above, under conditions whereby an antigen/antibody complex can form; b) detecting formation of an antigen/antibody complex, whereby detection of formation of the antigen/antibody complex detects a coronavirus in the sample and whereby detection of formation of an antigen/antibody complex comprising the nucleocapsid protein(s) of (1) identifies the subgroup of the coronavirus in the sample as subgroup 2c; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (2) identifies the subgroup of the coronavirus in the sample as subgroup 2b; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (3) identifies the subgroup of the coronavirus in the sample as subgroup 2a; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (4) identifies the subgroup of the coronavirus in the sample as subgroup 2d; detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (5) identifies the subgroup of the coronavirus in the sample as subgroup 1a; and detection of an antigen/antibody complex comprising the nucleocapsid protein(s) of (6) identifies the subgroup of the coronavirus in the sample as subgroup 1b; c) contacting the sample from the subject with a panel of proteins comprising: 1) one or more spike proteins from a subgroup 2c coronavirus, 2) one or more spike proteins from a subgroup 2b coronavirus, 3) one or more spike proteins from a subgroup 2a coronavirus, 4) one or more spike proteins from a subgroup 2d coronavirus, 5) one or more spike proteins from a subgroup 1a coronavirus, 6) one or more spike proteins from a subgroup 1b coronavirus, and 7) any combination of (1) through (6) above, under conditions whereby an antigen/antibody complex can form; and d) detecting formation of an antigen/antibody complex, whereby detection of formation of the antigen/antibody complex comprising

Assignees

Inventors

Classifications

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US2016238601A1 cover?
The present invention provides methods and compositions for detecting a coronavirus in a sample and identifying the subgroup of the coronavirus in the sample.
Who is the assignee on this patent?
Univ North Carolina Chapel Hill
What technology area does this patent fall under?
Primary CPC classification G01N33/56983. Mapped technology areas include Physics.
When was this patent published?
Publication date Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).