Method for analysis of subpopulations of cells
First Claim
1. In a method of identifying and enumerating two or more subpopulations of a population of cells of interest in a whole blood sample by means of flow cytometry, wherein the sample has been split into three aliquots, wherein the first aliquot is labeled with a first fluorescently labeled monoclonal antibody and a second fluorescently labeled monoclonal antibody that react differentially with all of populations of cells in such a manner as to separate the populations from one another when both antibodies are used, the second aliquot is labeled with a first fluorescently labeled irrelevant control and a second fluorescently labeled irrelevant control, and the third aliquot is labeled with a third fluorescently labeled monoclonal antibody and a fourth fluorescently labeled monoclonal antibody that are different from the first and second monoclonal antibodies and react differentially with the cells of the subpopulations of interest, and wherein the fluorescent label on the first antibody, first control and third antibody are the same and the fluorescent label on the second antibody, second control and fourth antibody are the same but which has an emission spectra different from the other fluorescent label, the improvement comprising the steps of:
- (a) establishing a cell population gate that will contain the maximum number of all cells in the population of interest with a minimum level of contamination from other cell populations by analyzing the first aliquot and selecting the gate based upon an analysis SSC and FL2 to set the SSC boundary and FSC and FL1 to set the FSC boundary and calculating the percentage of contamination of other populations of cells within the gate;
(b) establishing fluorescence markers for each of the fluorescence labels used by analyzing the second aliquot applying the gate from step (a) and selecting the markers based upon fluorescence emissions and calculating the percentage of non-specific staining in the sample; and
(c) analyzing the third aliquot using the gate and percent contamination from step (a) and the fluorescence markers and percent non-specific staining from step (b) to identify and enumerate cells in each subpopulation.
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Abstract
A method and kit for determination of subsets of leukocytes utilizing flow cytometry analysis techniques.
107 Citations
25 Claims
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1. In a method of identifying and enumerating two or more subpopulations of a population of cells of interest in a whole blood sample by means of flow cytometry, wherein the sample has been split into three aliquots, wherein the first aliquot is labeled with a first fluorescently labeled monoclonal antibody and a second fluorescently labeled monoclonal antibody that react differentially with all of populations of cells in such a manner as to separate the populations from one another when both antibodies are used, the second aliquot is labeled with a first fluorescently labeled irrelevant control and a second fluorescently labeled irrelevant control, and the third aliquot is labeled with a third fluorescently labeled monoclonal antibody and a fourth fluorescently labeled monoclonal antibody that are different from the first and second monoclonal antibodies and react differentially with the cells of the subpopulations of interest, and wherein the fluorescent label on the first antibody, first control and third antibody are the same and the fluorescent label on the second antibody, second control and fourth antibody are the same but which has an emission spectra different from the other fluorescent label, the improvement comprising the steps of:
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(a) establishing a cell population gate that will contain the maximum number of all cells in the population of interest with a minimum level of contamination from other cell populations by analyzing the first aliquot and selecting the gate based upon an analysis SSC and FL2 to set the SSC boundary and FSC and FL1 to set the FSC boundary and calculating the percentage of contamination of other populations of cells within the gate; (b) establishing fluorescence markers for each of the fluorescence labels used by analyzing the second aliquot applying the gate from step (a) and selecting the markers based upon fluorescence emissions and calculating the percentage of non-specific staining in the sample; and (c) analyzing the third aliquot using the gate and percent contamination from step (a) and the fluorescence markers and percent non-specific staining from step (b) to identify and enumerate cells in each subpopulation. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18)
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19. In a method of identifying and enumerating two or more subpopulations of lymphocytes in a whole blood sample, from which the erythrocytes have been removed, by means of flow cytometry, wherein the sample has been split into three aliquots, wherein the first aliquot is labeled with a first fluorescently labeled monoclonal antibody that reacts with substantially all leukocytes and a second fluorescently labeled monoclonal antibody that reacts with substantially all monocytes, the second aliquot is labeled with a first fluorescently labeled irrelevant control and a second fluorescently labeled irrelevant control, and the third aliquot is labeled with a third fluorescently labeled monoclonal antibody and a fourth fluorescently labeled monoclonal antibody that are different from the first and second monoclonal antibodies and react differentially with the subpopulations of lymphocytes, and wherein the fluorescent label on the first antibody, first control and third antibody are the same and the fluorescent label on the second antibody, second control and fourth antibody are the same but which has an emission spectra different from the other fluorescent label, the improvement comprising the steps of:
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(a) establishing a lymphocyte gate that will contain the maximum number of all lymphocytes with a minimum level of contamination from other cell populations and debris by analyzing the first aliquot and selecting the gate based upon an analysis of SSC and FL2 to set SSC limit and analysis of FSC and FL1 to set FSC limit and calculating the percentage of contamination of other populations of cells within the gate; (b) establishing fluorescence markers for each of the fluorescence labels used by analyzing the second aliquot applying the gate from step (a) and selecting the markers based upon fluorescence emissions and calculating the percentage of non-specific staining in the sample, and (c) analyzing the third aliquot using the gate and percent contamination from step (a) and the fluorescence markers and percent non-specific staining from step (b) to identify and enumerate cells in each subpopulation. - View Dependent Claims (20, 21, 22, 23, 24, 25)
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Specification