Methods for identifying individuals with T cell immunity to specific infectious agents

Abstract

Methods, devices and kits for rapidly identifying individuals who have been previously infected with or vaccinated against a bacterial or viral pathogen, such as the SARS CoV-2 virus. [Solution] Pathogen-specific memory T cells, such as SARS CoV-2-specific memory T cells, when detected, provide an indication of past infection. Memory T cells are assayed by exposure to specific bacterial and / or viral antigens and then tested for activation by analysis of nucleotide content.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of U.S. Provisional Patent Application No. 63 / 211,398, filed June 16, 2021, which is incorporated by reference herein.

[0002] Sequence Listing

[0002] A "Sequence Listing" has been submitted with this application in the form of a text file named "0418961281SEQ.txt" (9,816 bytes) created on June 14, 2022, the contents of which are incorporated by reference in their entirety into this specification.

[0003] Technical Field The subject matter described herein relates to methods that can rapidly identify individuals who have been previously infected with bacterial and / or viral pathogens, such as the SARS CoV-2 virus. The methods provided herein detect antigen-specific memory T cells as an indicator of past infection, rather than the presence of pathogen-specific antibodies. [Background technology]

[0004] background

[0004] Memory T cells are an important part of the immune response against infectious pathogens and play several roles in protecting individuals against bacterial and viral infections. Memory T cells are found in certain tissues and body fluids, such as bone marrow, thymus tissue, and blood, and contain antibody-like receptors on their surface. When the memory T cell surface receptor comes into contact with a pathogenic antigen, such as a protein or peptide-based antigen, the cell becomes "activated," excretes immune effector proteins, and begins replicating.

[0005] Each unique subpopulation of memory T cells contains a different antibody-like surface receptor that is specific for a unique foreign antigen. When a memory T cell encounters its corresponding antigen, the antigen is bound by the antigen-specific cell surface receptor. Upon antigen-receptor binding, the memory T cell undergoes transformation, begins to excrete immune effector proteins such as cytokines, and begins rapid cell division. This transformation serves to expand the population of memory T cells primed to kill cells expressing the specific foreign antigen.

[0006]

[0006] An important aspect of memory T cell transformation in response to antigen detection and binding is the production of mRNA for expression of effector proteins such as cytokines and for cell division, which requires replication of the entire genome. This rapid and extensive change in the physiological state of the cell is amenable to specific detection methods directed at identifying the increased nucleic acid content present in activated memory T cells.

[0007] Severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is the virus strain that causes the respiratory illness coronavirus disease 2019 (COVID-19). Colloquially known as coronavirus, it was previously referred to by its provisional name 2019 novel coronavirus (2019-nCoV). SARS CoV-2 is a positive-sense single-stranded RNA virus. It is transmissible to humans, and the World Health Organization has designated the 2019 COVID-19 pandemic a Public Health Emergency of International Concern.

[0008]

[0008] Like other known coronaviruses, SARS CoV-2 is an enveloped virus that contains three outer structural proteins, namely membrane (M), envelope (E) and spike (S) proteins. The nucleocapsid (N) protein, together with the viral RNA genome, presumably forms a helical core located within the viral envelope. The SARS CoV-2 nucleocapsid (N) protein is a 423 amino acid predicted phosphoprotein of 46 kDa with little homology to other members of the coronavirus family. SARS CoV-2 uses its spike glycoprotein (S), the primary target of neutralizing antibodies, to bind to its receptor and mediate membrane fusion and viral entry. Each monomer of the trimeric S protein is approximately 180 kDa and contains two subunits, S1 and S2, that mediate attachment and membrane fusion, respectively.

[0009]

[0009] There is a need for methods, devices and kits to specifically and sensitively identify memory T cells that express surface receptors specific for a particular pathogen of interest, such as the SARS CoV-2 virus. Identification of such memory T cells provides valuable information regarding whether an individual has had previous exposure (either natural exposure or vaccination) and / or infection with the pathogen of interest. For example, exposure to, infection with and / or vaccination against certain bacteria and viruses, such as the SARS CoV-2 virus, can generate memory T cells specific for a particular pathogen.

[0010]

[0010] The above examples of the related art and limitations associated therewith are intended to be illustrative and not exhaustive. Other limitations of the related art will become apparent to those of ordinary skill in the art upon reading this specification and studying the drawings. Summary of the Invention [Means for solving the problem]

[0011] Quick Overview

[0011] The following aspects and embodiments thereof described and illustrated below are intended to be exemplary and explanatory and not limiting in scope.

[0012]

[0012] The technology disclosed herein relates to methods, devices and kits for detecting memory T cells that are activated after exposure to a specific bacterial and / or viral pathogenic antigen, such as a SARS CoV-2 viral antigen. The technology exposes memory T cells from a subject to a specific bacterial and / or viral antigen, such as a SARS CoV-2 viral antigen. The exposed memory T cells are then assayed for nucleotide content, and an increase in nucleotide content, such as an increase in RNA and / or DNA content, when compared to an inactive counterpart, indicates an activated memory T cell. Analysis of the cells with a reagent that detects total nucleotide content, such as an RNA and / or DNA dye, including a fluorescent dye, allows the technician to determine whether the memory T cell has an increase in nucleotide content, indicating that the cell has encountered its specific pathogenic antigen.

[0013] In one aspect, the technology described herein provides a method for determining the presence or absence of infectious agent-specific T cells in a sample from a subject. In another aspect, a method for confirming a subject's past exposure or vaccination to an infectious agent is provided. In some embodiments, the method includes exposing a biological sample containing memory T cells from the subject to one or more peptide antigens specific for the infectious agent. In some embodiments, the method further includes contacting the exposed memory T cells with an indicator compound associated with RNA, DNA, or both. In some aspects, the method further includes analyzing the memory T cells for the indicator compound.

[0014] In one aspect, the technology described herein provides a method for identifying SARS CoV-2 specific T cells in a sample from a subject. In another aspect, a method is provided for confirming a subject's past exposure to or vaccination against the SARS CoV-2 virus.

[0015] In some embodiments, the method includes exposing a biological sample containing memory T cells from a subject to one or more peptide antigens specific for SARS CoV-2. In some embodiments, the method further includes contacting the exposed memory T cells with an indicator compound associated with RNA, DNA, or both. In some aspects, the method further includes analyzing the memory T cells for the indicator compound.

[0016] In some embodiments, memory T cells are exposed to a peptide specific for SARS CoV-2 and simultaneously contacted with an indicator compound. In some embodiments, memory T cells are exposed to a peptide specific for SARS CoV-2 and subsequently contacted with an indicator compound.

[0017] In some aspects, the biological sample is a blood sample and / or a fraction of a blood sample. In some embodiments, the fraction of a blood sample is a buffy coat fraction or peripheral blood mononuclear cells (PBMCs) or a mixture of a buffy coat fraction and PBMCs.

[0018]

[0018] In some embodiments, exposing the biological sample to one or more peptide antigens specific to SARS CoV-2 includes exposure to a solution comprising one or more peptide antigens, an indicator compound and one or more of a buffer, a cellular energy source, and a balanced salt solution, whereby simultaneously with said exposure, the T cells are contacted with the indicator compound.

[0019] In some aspects, the method further comprises exposing the second biological sample comprising the memory T cells to a control reagent that (i) lacks one or more peptide antigens specific for SARS CoV-2 and (ii) comprises a control indicator compound associated with RNA, DNA, or both, thereby generating a control sample. In some embodiments, the second biological sample is from a subject, and the biological sample is from the same subject, or the second biological sample is a portion of a biological sample. In some embodiments, the indicator compound and the control indicator compound are the same. In other embodiments, the analysis comprises measuring a signal of an indicator compound associated with the memory T cells in the biological sample and measuring a signal of a control indicator compound associated with the memory T cells in the control sample. In some embodiments, the analysis comprises measuring a signal of an indicator compound associated with RNA in the biological sample and measuring a signal of a control indicator compound associated with RNA in the second biological sample. In other embodiments, the analysis includes measuring an RNA signal based on a signal of an indicator compound associated with the RNA, measuring a DNA signal based on a signal of an indicator compound associated with the DNA, and determining a ratio of the RNA signal to the DNA signal or the DNA signal to the RNA signal, In some embodiments, the indicator compound is a fluorescent dye that selectively stains RNA.

[0020]

[0020] In another embodiment, the exposed memory T cells are contacted with a first indicator compound that selectively stains RNA or DNA and a second indicator compound that non-specifically stains RNA and DNA.

[0021] In another embodiment, the indicator compound has an excitation between about 330-360 nm and an emission greater than between about 500-600 nm.

[0022] In some embodiments, the memory T cells are CD4+ and / or CD8+ T cells.

[0023] In some aspects, the method of any preceding claim further comprises incubating the biological sample for a period of time, e.g., about 10-60 minutes or about 10-30 minutes. In some embodiments, the incubation is performed after the sample has been exposed to the peptide antigen and contacted with the indicator reagent, but prior to analysis. In some embodiments, the sample is incubated at a temperature between about 25-40° C.

[0024] In another aspect, the one or more peptide antigens specific for SARS CoV-2 include between 2 and 20 SARS CoV-2 specific peptide antigens, or between 3 and 15 SARS CoV-2 specific peptide antigens. In some embodiments, the one or more peptide antigens specific for SARS CoV-2 include one or more of the peptides identified in SEQ ID NO:1 through SEQ ID NO:12. In some embodiments, the exposing step further includes exposing the biological sample to one or more peptide antigens non-specific for SARS CoV-2.

[0025]

[0025] In another aspect, the methods provided herein identify a subject's past exposure to an infectious pathogen. In some embodiments, the methods include exposing a biological sample containing memory T cells from the subject to one or more peptide antigens specific for the infectious pathogen. In some embodiments, the methods further include contacting the exposed memory T cells with an indicator compound associated with RNA, DNA, or both. In some aspects, the methods further include analyzing the memory T cells for the indicator compound.

[0026] In some embodiments, memory T cells are exposed to a peptide specific for an infectious pathogen and simultaneously contacted with an indicator compound. In some embodiments, memory T cells are exposed to a peptide specific for an infectious pathogen and subsequently contacted with an indicator compound.

[0027] In some embodiments, the infectious agent or pathogen is a viral pathogen, such as a respiratory syncytial virus or a human coronavirus, hi other embodiments, the pathogen is a bacterial pathogen, such as the Borrelia pathogen of Lyme disease.

[0028]

[0028] In addition to the exemplary aspects and embodiments described above, further aspects and embodiments will become apparent by reference to the drawings and by study of the following descriptions.

[0029]

[0029] Additional embodiments of the method and the like will be apparent from the following description, drawings, examples, and claims. As can be recognized from the above and following description, any feature described herein, and any combination of two or more of such features, is included within the scope of the present disclosure, provided that the features included in such combinations are not mutually inconsistent. In addition, any feature or combination of features may be specifically excluded from any embodiment of the present disclosure. Additional aspects and advantages of the present disclosure are set forth in the following description and claims, particularly when considered in conjunction with the accompanying examples and drawings.

[0030] [Table 1] DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0031] Detailed Description I. Definition Various aspects will now be described in more detail below. However, such aspects may be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey its scope to those skilled in the art.

[0032]

[0031] When a range of values ​​is provided, each intervening value between the upper and lower limits of the range, and any other stated or intervening values ​​within the stated range, are intended to be encompassed within the scope of the present disclosure. For example, when a range of 1 μm to 8 μm is stated, 2 μm, 3 μm, 4 μm, 5 μm, 6 μm, and 7 μm are expressly intended to be disclosed, as well as ranges of values ​​greater than or equal to 1 μm, and ranges of values ​​less than or equal to 8 μm.

[0033] The singular forms "a," "an," and "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to "a polymer" includes a single polymer as well as two or more of the same or different polymers, reference to "an excipient" includes a single excipient as well as two or more of the same or different excipients, etc.

[0034]

[0033] The word "about" when immediately preceding a numerical value means a range of plus or minus 10% of that value, unless the context of this disclosure indicates otherwise or contradicts such an interpretation, e.g., "about 50" means 45 to 55, "about 25,000" means 22,500 to 27,500, etc. For example, in a list of numerical values ​​such as "about 49, about 50, about 55", "about 50" means a range that extends to less than half the interval between the preceding and following values, e.g., a range greater than 49.5 and less than 52.5. Furthermore, the phrases "less than about a value" or "greater than about a value" should be understood in light of the definition of the term "about" provided herein.

[0035]

[0034] The term "about" is meant to encompass a deviation of plus or minus 5 percent, particularly with respect to a given amount.

[0036]

[0035] The compositions of the present disclosure can comprise, consist essentially of, or consist of the disclosed components.

[0037]

[0036] All percentages, parts and ratios are based on the total weight of the topical composition and all measurements are made at about 25°C unless otherwise specified.

[0038]

[0037] A "sample" is any material that is to be tested for the presence of a particular target memory T cell. Preferably, the sample is a fluid sample, preferably a liquid sample. Examples of liquid samples that can be tested using the testing device include bodily fluids, including blood, serum, plasma, saliva, urine, ocular fluid, semen, sputum, nasal fluid, and spinal fluid. For example, a sample for testing with the disclosed device can include liquid serum or plasma from a venous blood source, where the serum or plasma has been separated from whole blood by centrifugation. In other cases, the sample can be liquid plasma from a finger prick that has been separated from whole blood by a blood-plasma separator. Other sample examples include liquid plasma from a finger prick that has been separated from whole blood by a lateral flow device. In some embodiments, the sample includes a band that forms between red blood cells and plasma upon centrifugation of whole blood. In some cases, this band, also known as the "buffy coat," includes lymphocytes from whole blood and can be used as a sample to analyze for the presence of a particular population of memory T cells.

[0039]

[0038] "Peptide antigen" refers to a protein or peptide that binds to a specific receptor present on the cell surface of a specific population of memory T cells. Peptide sequences relevant to the present disclosure may include antigenic peptides or proteins from any pathogen of interest, such as bacterial or viral pathogens. In certain embodiments, the peptide antigen includes the SARS CoV-2 peptide antigens provided in Table 1. For example, the peptide antigen includes SARS CoV-2 proteins, peptides, such as the membrane (M), envelope (E), spike (including S, S1 and S2 subunits), and nucleocapsid (N) proteins of SARS CoV-2. The nucleocapsid (N) protein, together with the viral RNA genome, likely forms a helical core located within the viral envelope. The SARS CoV-2 nucleocapsid (N) protein is a 423 amino acid, predicted 46 kDa phosphoprotein with little homology to other members of the coronavirus family. SARS CoV-2 uses its spike glycoprotein (S), the primary target of neutralizing antibodies, to bind to its receptor and mediate membrane fusion and viral entry. Each monomer of the trimeric S protein is approximately 180 kDa and contains two subunits, S1 and S2, which mediate attachment and membrane fusion, respectively.

[0040] In some embodiments, the SARS CoV-2 peptide antigen comprises the full-length N protein and a specific epitope of the full-length N protein. Proteins and peptides can be selected as reaction partners based on sequences represented by the respective peptides and / or immunogenicity analysis. Peptides represented by the SARS CoV-2 N protein epitope map based on dividing the full-length N protein into segments of about 5-150, 7-130, 8-110, 10-100, 10-90, 10-80, 10-70, 10-75, 10-60, or 10-50 amino acid residues provide peptide antigens for use in the method. Other examples of peptide antigens include the full-length SARS CoV-2 S protein, sequences represented by the respective peptides and / or at least one specific epitope of the full-length SARS CoV-2 S protein based on immunogenicity analysis. Peptides represented by the SARS CoV-2 S protein epitope map based on dividing the full-length S protein into segments of about 5-150, 7-130, 8-110, 10-100, 10-90, 10-80, 10-70, 10-75, 10-60, or 10-50 amino acid residues provide peptide antigens for use in the method.

[0041]

[0040] Certain peptide antigens related to the SARS CoV-2 peptide antigen proteins are presented in Table 1. These peptides may contain antigens and / or epitopes for human memory T cell surface receptors specific for SARS CoV-2 and therefore can be used as components of the methods, devices and kits described herein for identifying such memory T cells.

[0042]

[0041] "Indicator compound" refers to a substance that indicates the level of nucleotides in a sample. For example, indicator compounds include dyes that label RNA, DNA, or both. In some cases, indicator compounds include fluorescent nucleotide dyes that exhibit excitation and emission wavelengths that are not blocked or absorbed by red blood cells.

[0043]

[0042] Less than the full scale of the disclosure may be claimed for any reason by reserving the right to proviso out or exclude any individual members of any such group, including any subranges or combinations of subranges within a group, which may be claimed according to a range or in any similar manner. Furthermore, less than the full scale of the disclosure may be claimed for any reason by reserving the right to proviso out or exclude any individual substituents, analogs, compounds, ligands, structures, or groups or any members thereof of any claimed group.

[0044]

[0043] Throughout this disclosure, various patents, patent applications and publications are referenced. The disclosures of these patents, patent applications and publications are incorporated by reference in their entirety into this disclosure to more fully describe the state of the art known to those skilled in the art as of the date of this disclosure. In the event of any inconsistency between the cited patents, patent applications and publications and this disclosure, this disclosure shall govern.

[0045]

[0044] For convenience, certain terms used in the present specification, examples, and claims are collected here. Unless otherwise defined, all technical and scientific terms used in this disclosure have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs.

[0046] II. Method In a first embodiment, a method is provided for identifying a subject's past exposure to an infectious pathogen. A subject's past exposure to a pathogen can occur by natural exposure or by vaccination against said pathogen. In some embodiments, the pathogen can be a virus, such as a syncytial virus or a human coronavirus. In some embodiments, the pathogen is a SARS CoV-2 virus. In other embodiments, the pathogen is a bacterial pathogen, such as the Borrelia pathogen of Lyme disease.

[0047]

[0046] In some embodiments, the methods described herein include obtaining a sample, such as blood, from a subject. For example, blood may be collected from a subject by finger prick or venipuncture. In some embodiments, the amount of blood collected is sufficient for analysis of memory T cells contained therein. For example, a blood sample in certain embodiments may include at least about 1.0 mL to about 10 mL of liquid whole blood. For example, a blood sample in certain embodiments may include about 1.0 mL, about 2.0 mL, about 3.0 mL, about 4.0 mL, about 5.0 mL, about 6.0 mL, about 7.0 mL, about 8.0 mL, about 9.0 mL, or about 10.0 mL of whole blood. In some embodiments, the blood is collected in a container containing appropriate storage components, buffers, and preservatives, including tubes containing heparin as an anticoagulant.

[0048] In some embodiments, the blood sample is centrifuged to separate the whole blood into separate layers containing plasma, red blood cells (RBCs), and lymphocytes. In some embodiments, the memory T cells are present in a band that forms between the plasma and RBCs upon centrifugation. This band contains lymphocytes, such as memory T cells, from the whole blood sample and is known as the "buffy coat."

[0049] In some embodiments, after centrifuging the whole blood sample to separate the plasma, RBCs, and buffy coat layer, about 30 μL to about 100 μL of the buffy coat layer containing lymphocytes, such as memory T cells, is removed. For example, certain embodiments may include removing about 30 μL, about 40 μL, about 50 μL, about 60 μL, about 70 μL, about 80 μL, about 90 μL, or about 100 μL of the buffy coat layer.

[0050] In some embodiments, about half of the removed buffy coat layer is added to a first well of a multi-well plate, such as a 96- or 384-well plate. For example, certain embodiments may include adding about 15 μL, about 20 μL, about 25 μL, about 30 μL, about 35 μL, about 40 μL, about 45 μL, or about 50 μL of the buffy coat layer to the first well of the multi-well plate. In some aspects, the amount of buffy coat sample added to the first well of the multi-well plate constitutes a test sample.

[0051] In some embodiments, the remaining half of the buffy coat layer is added to a second well of a multi-well plate, such as a 96- or 384-well plate. For example, certain embodiments may include adding about 15 μL, about 20 μL, about 25 μL, about 30 μL, about 35 μL, about 40 μL, about 45 μL, or about 50 μL of the buffy coat layer to the second well of the multi-well plate. In some aspects, the amount of buffy coat sample added to the second well of the multi-well plate constitutes a control sample.

[0052] In some embodiments, a suitable amount of test well solution is added to the test sample in the first well of the multi-well plate. In some embodiments, the test well solution contains a specific peptide antigen, such as a SARS CoV-2 peptide antigen, that corresponds to a surface receptor present on a target memory T cell, i.e., a memory T cell that expresses a surface receptor that can bind to the target peptide antigen. In some embodiments, the test well solution containing the specific target peptide antigen also contains a balanced salt solution, a buffer, and an energy source, such as glucose.

[0053] In some embodiments, the test well solution also includes a concentration of an indicator compound, such as a nucleotide dye, i.e., a fluorescent RNA and / or DNA dye. In some embodiments, the nucleotide dye is added simultaneously with the test sample solution. In other embodiments, the nucleotide dye is added sequentially, before or after the addition of the test well solution. In some embodiments, the nucleotide dye provides penetration of cell and nuclear membranes without affecting cellular function, and binds to all of the DNA, RNA, or both DNA and RNA molecules. In some embodiments, the nucleotide dye includes a fluorescent dye with excitation and emission wavelengths that are not absorbed and / or blocked by RBCs. For example, with excitation between about 330-360 nm and emission greater than between about 500-600 nm.

[0054]

[0053] In some embodiments, about 50 μL to about 150 μL of test well solution is added to the test sample in the first well of the multi-well plate. For example, in some embodiments, about 50 μL, about 60 μL, about 70 μL, about 80 μL, about 90 μL, about 100 μL, about 110 μL, about 120 μL, about 130 μL, about 140 μL, or about 150 μL of test well solution is added to the test sample in the first well of the multi-well plate.

[0055] In some embodiments, an appropriate amount of control well solution is added to the control sample in the second well of the multi-well plate. In some embodiments, the control well solution contains all of the same components as the test well solution, except that it lacks a specific peptide antigen, such as a SARS CoV-2 peptide antigen. For example, in some embodiments, the control well solution contains a balanced salt solution, a buffer, and an energy source, such as glucose.

[0056] In some embodiments, the control well solution also contains a concentration of an indicator compound, such as a nucleotide dye, i.e., a fluorescent RNA and / or DNA dye. In some embodiments, the nucleotide dye is added simultaneously with the control sample solution. In other embodiments, the nucleotide dye is added sequentially, before or after the addition of the control well solution.

[0057] In some embodiments, about 50 μL to about 150 μL of control well solution is added to the control sample in the second well of the multi-well plate.For example, in some embodiments, about 50 μL, about 60 μL, about 70 μL, about 80 μL, about 90 μL, about 100 μL, about 110 μL, about 120 μL, about 130 μL, about 140 μL, or about 150 μL of control well solution is added to the control sample in the second well of the multi-well plate.

[0058] In some embodiments, the test sample and control sample including the buffy coat and the additional test sample and control sample solutions are incubated at a temperature of about 25° C. to about 40° C. for about 10 minutes to about 60 minutes. For example, in some embodiments, the test sample and control sample are incubated at a temperature of about 25° C., about 30° C., about 35° C., or about 40° C. for about 10 minutes, about 20 minutes, about 30 minutes, about 40 minutes, or about 50 minutes. In some embodiments, the test sample and control sample are incubated at about 37° C. for about 30 minutes. In some embodiments, the test sample and control sample may be incubated at about 37° C. for a longer period, for example, about 2 hours, about 4 hours, about 6 hours, about 12 hours, about 18 hours, or about 24 hours, before reading the test result.

[0059] In some embodiments, after incubation, the first well containing the test sample and the second well containing the control sample are analyzed to ascertain the total amount of labeled nucleotides present in each well. In some embodiments, the analysis may include visual inspection. In other embodiments, the analysis may include analysis by a plate reader. In other embodiments, the analysis may include fluorescence analysis, such as scanning the test and control wells with a fluorometer. In other embodiments, the analysis may include spectroscopic analysis of the test and control samples using electromagnetic radiation, such as, but not limited to, absorbance spectroscopy (ultraviolet, visible, or infrared), including reflectance or transmittance spectroscopy, or emission spectroscopy, including fluorescence and luminescence spectroscopy, Raman spectroscopy, and any type of radiation scattering.

[0060]

[0059] In one embodiment, the indicator compound is a fluorescent compound such as a fluorescent dye having an excitation between about 300 and 400 nm, or between about 320 and 380 nm, or between 330 and 360 nm, and an emission greater than about 600 nm, or greater than 600 nm and less than about 1000 nm.

[0061] In some embodiments, after the analysis of the test sample and the control sample is completed, the amount of nucleotides present in each sample is compared. If the test sample shows higher nucleotide expression, this indicates that the test sample, i.e., the buffy coat sample, contains memory T cells that express surface receptors specific for peptide antigens, such as SARS CoV-2 peptide antigens, that were present in the test well solution. Specifically, the surface receptors present on the memory T cells from the buffy coat sample interact with the peptide antigens in the test well solution, causing the transformation of the memory T cells, which is characterized by increased RNA and / or DNA expression for increased expression of immune effector proteins and replication of the entire genome for rapid cell division.

[0062]

[0061] Thus, if a test sample exhibits increased RNA and / or DNA expression compared to a control sample, this indicates that the sample is from an individual who has experienced previous exposure, vaccination, and / or infection with a pathogen, such as the SARS CoV-2 virus, associated with a peptide antigen, such as the SARS CoV-2 peptide antigen, present in the test well solution.

[0063]

[0062] Furthermore, if the test sample and control sample exhibit similar levels of RNA and / or DNA expression, this indicates that the sample is from an individual who has not experienced previous exposure, vaccination, and / or infection with a pathogen associated with the peptide antigen present in the test well solution.

[0064] A. Peptide Antigens In some aspects, the peptide antigen comprises a protein or peptide that binds to a specific receptor present on the cell surface of a specific population of memory T cells. The peptide antigen may comprise any antigenic peptide or protein from a pathogen of interest. In some embodiments, the peptide antigen is an antigen from a specific bacterial and / or viral pathogen.

[0065] In some embodiments, the peptide antigens are highly specific bacterial and / or viral peptide antigens. In some embodiments, the bacterial and / or viral peptide antigens are specific for the antigen of interest and have little to no measurable cross-reactivity with related bacterial or viral antigens. For example, seasonal coronavirus infections lead to mild cold or flu-like illnesses to which many people have had past exposure. Such individuals express memory T cells that correspond to seasonal cold and influenza coronavirus strains. In one embodiment, the peptide antigens used in the method have little or no binding to seasonal cold and / or influenza (influenza a and / or b) coronavirus strains.

[0066]

[0065] Thus, the peptide antigens for use in the methods described herein are specific for memory T cells against a particular infectious agent, such as SARS CoV-2, RSV, and / or Lyme disease. Thus, the peptide antigens will exhibit little, if any, non-specific cross-reactivity with seasonal cold and flu specific memory T cells, and will react only with appropriate specific target memory T cells, such as, for example, SARS CoV-2 memory T cells, Lyme disease specific T cells, and RSV specific memory T cells.

[0067] In some embodiments, the method provides multiple antigenic peptides specific for SARS CoV-2 that do not cross-react with any of the seasonal coronavirus subtypes in common / seasonal cold and flu circulation. In some embodiments, the method includes at least 3 to about 15 different peptide antigens specific for SARS CoV-2 virus without exhibiting cross-reactivity with seasonal coronavirus strains.

[0068] In certain embodiments, peptide antigens comprising SARS CoV-2 antigenic peptide sequences for memory T cell assays are based on the nucleocapsid (N), spike (S), and M protein sequences provided in Table 1. In some embodiments, the antigenic peptides are chemically synthesized with an N-terminal biotin and a miniPEG linker.

[0069] B. Indicator compound In some embodiments, the method provides specific and sensitive indicator compounds for detecting and indicating the expression level of nucleotides such as RNA and / or DNA in a given sample. In some embodiments, the indicator compounds include several different types of fluorescent dyes. In some embodiments, the indicator compounds bind only to RNA. In other embodiments, the indicator compounds may bind only to DNA. In still other embodiments, the indicator compounds may bind to both RNA and DNA.

[0070] In some embodiments, the indicator compound is a fluorescent compound. In some embodiments, the fluorescent indicator compound exhibits a fluorescent signal upon binding of a nucleotide that is at least about 15 to about 20 times greater than the unbound indicator.

[0071] In some embodiments, the indicator compound is capable of rapid diffusion through both the cell membrane and the nuclear membrane, hi some embodiments, the indicator compound is non-toxic and does not affect cellular processes upon binding to nucleic acids.

[0072] In some aspects, current technology provides for the use of separate RNA-specific indicator compounds along with specific DNA-specific indicator compounds to ascertain RNA and DNA expression separately. In some embodiments, the ratio of RNA expression to DNA expression can provide useful calculations related to determining assay results such as the amplitude, timing and sequencing of memory T cell transformation responses to antigens.

[0073] In some aspects, the indicator compounds exhibit distinct excitation and emission wavelengths for the specific dyes used for separate analysis of RNA and DNA, so that RNA and DNA can be analyzed separately based on the distinct excitation and emission wavelengths of each indicator compound. In other embodiments, current technology provides the same indicator compounds for both RNA and DNA analysis.

[0074] In some embodiments, the indicator compound can be a fluorescent compound, dye, or stain selective for RNA. For example, the indicator can be SYTO TMThe indicator compound may be a cell-permeant nucleic acid stain that selectively stains intracellular RNA, such as the 13 green fluorescent nucleic acid stain. In some embodiments, the stain is essentially non-fluorescent in the absence of nucleic acid and exhibits bright green fluorescence when bound to RNA. In some embodiments, the indicator compound exhibits an absorption / emission maximum of about 490 nm to about 530 nm. In some embodiments, the indicator exhibits a strong signal when bound to RNA and a weak fluorescent signal when bound to DNA.

[0075] In another embodiment, the indicator compound can be a fluorescent compound, dye, or stain that is non-selective for either RNA or DNA, but is capable of staining both RNA and DNA. TM There are cell-permeant fluorescent nucleic acid stains that exhibit fluorescence when bound to nucleic acids, such as those sold by Hoechst, Inc. Another exemplary indicator compound is a dye compound that is non-toxic to cells and non-toxic to nucleic acids, such as the Hoechst stains identified as Hoechst stains 33342 and 34580. Both stains are excited by ultraviolet light at about 350 nm, and both emit blue-cyan fluorescence at about 461 nm. A Stokes shift of about 100 nm between the excitation and emission spectra is beneficial. These dyes bind to the minor groove of double-stranded DNA.

[0076] In another embodiment, the method utilizes two indicator compounds, a first indicator compound that selectively stains RNA or DNA and a second indicator compound that non-specifically stains RNA and DNA. In one embodiment, the indicator compound(s) have an absorption between about 300-400 nm, about 320-380 nm, or about 330-360 nm, and an emission greater than about 500 nm to about 600 nm. In an embodiment in which two indicator compounds are used, the first indicator compound has a first absorption / emission profile that is different from the second absorption / emission profile of the second indicator compound.

[0077] III. Devices and Kits Severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is a viral strain that causes the respiratory disease coronavirus disease 2019 (COVID-19). The methods described herein provide a sensitive and specific method for the detection of memory T cells specific for a particular pathogenic peptide antigen, such as memory T cells specific for SARS CoV-2 viral peptide antigens. The methods provide for identifying whether an individual has been previously exposed to or infected with SARS CoV-2. In addition, in some embodiments, the methods, kits and devices provided herein provide valuable knowledge regarding whether an individual is protected from future infections, such as SARS CoV-2 infection, through the immune response provided by SARS CoV-2-specific memory T cells. Thus, the high volume and rapid screening provided by the methods, devices and kits provided herein for assaying subjects previously infected with SARS CoV-2 provides important epidemiological data about the COVID-19 status of each subject and the local population status regarding the spread of the virus. Also provided are devices and kits for carrying out one or more of the methods provided herein, along with instructions for using the devices and kits in the provided methods of detecting memory T cells specific for a particular pathogen, such as the SARS CoV-2 virus. EXAMPLES

[0078] IV. Working Examples

[0077] The following examples are illustrative in nature and are not intended to be limiting in any way.

[0079] Example 1 Method for detecting SARS COV-2 specific memory T cells

[0078] 5-10 mL of blood is drawn from the subject by venipuncture into a tube containing heparin as an anticoagulant. The tube is centrifuged to separate the RBCs from the plasma. During centrifugation, lymphocytes form a buffy coat band between the red blood cells and the plasma. 100 μL of buffy coat cells are removed from the plasma / RBC interface of the centrifuged sample tube. Half of the buffy coat volume (50 μL) is added to one well of a 96-well plate to create a test well. The remaining half of the buffy coat sample is added to a second well to create a control well.

[0080]

[0079] 100 μL of test solution containing SARS CoV-2 specific peptide antigen, balanced salt solution, buffer, glucose as an energy source, and a predetermined concentration of fluorescent nucleotide dye is added to the test well.

[0081]

[0080] 100 μL of a control solution containing a balanced salt solution, a buffer, glucose as an energy source, and a predetermined concentration of a fluorescent nucleotide dye is added to the control wells. The control solution is the same as the test solution without the SARS CoV-2 specific peptide antigen.

[0082]

[0081] The 96-well plate is incubated at 37°C for 30 minutes. After incubation, the two wells are scanned using a fluorometer and the signals of the two wells are compared. If the signal from the test well is higher than the control well, the buffy coat sample is indicated to be positive for the presence of memory T cells specific for the SARS CoV-2 viral peptide antigen. This indicates that the subject has had a past exposure to the SARS CoV-2 virus, which results in the activation of memory T cells and the rapid production of new RNA and DNA during the test, resulting in an increased fluorescent signal in the test sample compared to the control sample.

[0083] Example 2 Point-of-care test for SARS COV-2-specific memory T cells

[0082] 50 μl of blood is collected from the subject by finger prick into a tube containing heparin as an anticoagulant. The tube is centrifuged to separate the RBCs from the plasma. During centrifugation, lymphocytes form a buffy coat band between the red blood cells and the plasma. 5 μL of buffy coat cells are removed from the plasma / RBC interface of the centrifuged sample tube. Half of the buffy coat volume (2.5 μL) is added to one well of a 96-well plate to create a test well. The remaining half of the buffy coat sample is added to a second well to create a control well.

[0084]

[0083] 5 μL of test solution containing SARS CoV-2-specific peptide antigen, balanced salt solution, buffer, glucose as an energy source, and a predetermined concentration of fluorescent nucleotide dye is added to the test well.

[0085]

[0084] 5 μL of a control solution containing a balanced salt solution, a buffer, glucose as an energy source, and a predetermined concentration of a fluorescent nucleotide dye is added to the control wells. The control solution is the same as the test solution without the SARS CoV-2 specific peptide antigen.

[0086]

[0085] The 96-well plate is incubated at 37°C for 10 minutes. After incubation, the two wells are scanned using a fluorometer and the signals of the two wells are compared. If the signal from the test well is higher than the control well, the buffy coat sample is indicated to be positive for the presence of memory T cells specific for the SARS CoV-2 viral peptide antigen. This indicates that the subject has had a past exposure to the SARS CoV-2 virus, which results in the activation of memory T cells and the rapid production of new RNA and DNA during the test, resulting in an increased fluorescent signal in the test sample compared to the control sample.

[0087]

[0086] While several exemplary aspects and embodiments have been discussed above, those skilled in the art will recognize certain modifications, permutations, additions, and subcombinations thereof. Accordingly, it is intended that the following appended claims and the claims introduced below be construed to include all such modifications, permutations, additions, and subcombinations that are within their true spirit and scope.

Claims

1. A method for identifying the presence of SARS-CoV-2-specific T cells in a sample from a subject to confirm past exposure to the SARS-CoV-2 virus or vaccination with the SARS-CoV-2 virus, comprising: exposing a biological sample containing memory T cells from the subject to one or more peptide antigens specific for SARS-CoV-2; contacting the exposed memory T cells with an indicator compound associated with RNA, DNA, or both, wherein the contacting is simultaneous with the exposure or subsequent to the exposure; analyzing the memory T cells for the indicator compound; and a method comprising the above steps.

2. The method according to claim 1, wherein the biological sample is a blood sample.

3. The method according to claim 2, wherein the biological sample is a fraction of the blood sample.

4. The method according to claim 3, wherein the fraction of the blood sample is a buffy coat fraction or peripheral blood mononuclear cells (PBMCs) or a mixture of a buffy coat fraction and PBMCs.

5. The exposure to one or more peptide antigens specific for SARS-CoV-2 comprises exposure to a solution comprising one or more of the one or more peptide antigens, the indicator compound, a buffer, an energy source for the cells, and a balanced salt solution, whereby the T cells are contacted with the indicator compound simultaneously with the exposure. The method according to claim 1.

6. The method further comprises exposing a second biological sample containing memory T cells to a control reagent that (i) lacks one or more peptide antigens specific for SARS-CoV-2 and (ii) contains a control indicator compound associated with RNA, DNA, or both, thereby generating a control sample. The method according to claim 1.

7. The method according to claim 6, wherein the second biological sample is from the same subject as the biological sample, or the second biological sample is part of the biological sample.

8. The method according to claim 6, wherein the indicator compound and the control indicator compound are the same.

9. The analysis according to claim 6 comprises measuring a signal of the indicator compound associated with memory T cells in the biological sample and measuring a signal of the control indicator compound associated with memory T cells in the control sample.

10. The method according to claim 6, wherein the analysis includes measuring a signal of an indicator compound associated with RNA in the biological sample and measuring a signal of a control indicator compound associated with RNA in the second biological sample.

11. The method according to claim 1, wherein the analysis includes measuring an RNA signal based on a signal of an indicator compound associated with RNA, measuring a DNA signal based on a signal of an indicator compound associated with DNA, and determining a ratio of the RNA signal to the DNA signal or a ratio of the DNA signal to the RNA signal.

12. The method according to claim 1, wherein the indicator compound is a fluorescent dye that selectively stains RNA.

13. The method according to claim 1, wherein the contacting includes contacting the exposed memory T cells with a first indicator compound that selectively stains RNA or DNA, and a second indicator compound that non-specifically stains RNA and DNA.

14. The method according to claim 1, wherein the indicator compound has an excitation between about 330 and 360 nm and an emission greater than between about 500 and 600 nm.

15. The method according to claim 1, wherein the memory T cells are CD4+ and / or CD8+ T cells.

16. The method according to claim 1, further including incubating for a certain period after the contacting and before the analysis.

17. The method according to claim 16, wherein the incubating is at a temperature between about 25 and 40 °C.

18. The method according to claim 16, wherein the period is between about 10 and 60 minutes, or between about 10 and 30 minutes.

19. The method according to claim 1, wherein the one or more peptide antigens specific for SARS-CoV-2 include peptide antigens specific for SARS-CoV-2 between 2 and 20, or peptide antigens specific for SARS-CoV-2 between 3 and 15.

20. The method according to claim 1, wherein the exposing further includes exposing the biological sample to one or more peptide antigens non-specific for SARS-CoV-2.

21. The method according to claim 1, wherein the one or more peptide antigens specific for SARS-CoV-2 include one or more of the peptides specified by SEQ ID NO: 1 to SEQ ID NO:

12.

22. A method for confirming a subject's past exposure to an infectious pathogen, comprising: exposing a biological sample containing memory T cells from the subject to one or more peptide antigens specific for the pathogen; contacting the exposed memory T cells with an indicator compound related to RNA, DNA, or both, wherein the contact is simultaneous with the exposure or subsequent to the exposure; analyzing the memory T cells for the indicator compound; and a method comprising the steps of:

23. The method according to claim 22, wherein the pathogen is a viral pathogen such as respiratory syncytial virus or human coronavirus.

24. The method according to claim 22, wherein the pathogen is a bacterial pathogen such as the Borrelia pathogen of Lyme disease.

25. The method according to claim 22, wherein the biological sample is a blood sample.

26. The method according to claim 25, wherein the biological sample is a fraction of the blood sample.

27. The method according to claim 26, wherein the fraction of the blood sample is a buffy coat fraction or peripheral blood mononuclear cells (PBMCs) or a mixture of the buffy coat fraction and PBMCs.

28. The exposure to one or more peptide antigens specific for the pathogen comprises exposure to a solution containing one or more of the one or more peptide antigens, the indicator compound, and a buffer, an energy source for the cells, and a balanced salt solution, whereby the T cells are contacted with the indicator compound simultaneously with the exposure. The method according to claim 22.

29. The method further comprises exposing a second biological sample containing memory T cells to a control reagent that (i) lacks one or more peptide antigens specific for the pathogen and (ii) contains a control indicator compound related to RNA, DNA, or both, thereby generating a control sample. The method according to claim 22.

30. The method according to claim 29, wherein the second biological sample is from the subject, the biological sample is from the same subject, or the second biological sample is a part of the biological sample.

31. The method according to claim 29, wherein the indicator compound and the control indicator compound are the same.

32. The method according to claim 29, wherein the analysis comprises measuring a signal of an indicator compound associated with memory T cells in the biological sample and measuring a signal of a control indicator compound associated with memory T cells in the control sample.

33. The method according to claim 29, wherein the analysis comprises measuring a signal of an indicator compound associated with RNA in the biological sample and measuring a signal of a control indicator compound associated with RNA in the second biological sample.

34. The method according to claim 22, wherein the analysis comprises measuring an RNA signal based on a signal of an indicator compound associated with RNA, measuring a DNA signal based on a signal of an indicator compound associated with DNA, and determining a ratio of the RNA signal to the DNA signal or a ratio of the DNA signal to the RNA signal.

35. The method according to claim 22, wherein the indicator compound is a fluorescent dye that selectively stains RNA.

36. The method according to claim 22, wherein the contacting comprises contacting the exposed memory T cells with a first indicator compound that selectively stains RNA or DNA, and a second indicator compound that non-specifically stains RNA and DNA.

37. The method according to claim 22, wherein the indicator compound has an excitation between about 330 and 360 nm and an emission greater than between about 500 and 600 nm.

38. The method according to claim 22, wherein the memory T cells are CD4+ and / or CD8+ T cells.

39. The method according to claim 22, further comprising incubating for a certain period after the contacting and before the analysis.

40. The method according to claim 39, wherein the incubating is at a temperature between about 25 and 40 °C.

41. The method according to claim 39, wherein the period is between about 10 and 60 minutes, or between about 10 and 30 minutes.

42. The method according to claim 22, wherein the one or more peptide antigens specific for the pathogen comprise between 2 and 20 peptide antigens specific for the pathogen, or between 3 and 15 peptide antigens specific for the pathogen.

43. The method according to claim 22, wherein the exposing further comprises exposing the biological sample to one or more peptide antigens non-specific for the pathogen.

44. A method for identifying the presence of infectious agent-specific T cells in a sample from a subject and confirming past exposure to the infectious agent or vaccination with the infectious agent, comprising: exposing a biological sample containing memory T cells from the subject to one or more peptide antigens specific for the infectious agent; contacting the exposed memory T cells with an indicator compound related to RNA, DNA, or both, wherein the contacting is simultaneous with or subsequent to the exposure; analyzing the memory T cells for the indicator compound; and a method comprising the steps of:

45. The method according to claim 1, wherein the indicator compound is not cell-permeable.

46. The method according to claim 1, wherein the indicator compound is a Hoechst stain.

47. The method according to claim 46, wherein the indicator compound is Hoechst stain 33342 or Hoechst stain 34580.

48. The method according to claim 22, wherein the indicator compound is not cell-permeable.

49. The method according to claim 22, wherein the indicator compound is a Hoechst stain.

50. The method according to claim 49, wherein the indicator compound is Hoechst stain 33342 or Hoechst stain 34580.

51. The method according to claim 44, wherein the indicator compound is not cell-permeable.

52. The method according to claim 44, wherein the indicator compound is a Hoechst stain.

53. The method according to claim 52, wherein the indicator compound is Hoechst stain 33342 or Hoechst stain 34580.