Methods and kits for detecting IgE-expressing B cells

Patent metadata

Field	Value
Publication number	US-9823248-B2
Application number	US-201114358287-A
Country	US
Kind code	B2
Filing date	Nov 15, 2011
Priority date	Nov 15, 2011
Publication date	Nov 21, 2017
Grant date	Nov 21, 2017

Abstract

The invention relates to the field of medical diagnostics. In particular, it relates method and kits for identification and classification of IgE-related diseases, e.g. Type I hypersensitivity, as well as for monitoring of treatment efficacy, for instance anti-IgE therapy. Provided is a multi-color flow cytometric method for analyzing memory B cell and plasma cell subsets in a biological sample, comprising staining the sample with a panel of fluorochrome-conjugated antibodies comprising antibodies against IgM, IgA, IgG, IgD and IgE; an antibody against a B cell marker and an antibody against the CD38 antigen; subjecting the sample to flow cytometry and gating for lymphocytes based on forward scatter and side scatter pattern; gating the lymphocytes for expression of the B cell specific marker and CD38 to discriminate between CD38 dim memory B cells and CD38 hi plasma cells; and quantitating the IgE+ cells within the memory B cell population and/or the plasma cell population by the negative selection of cells expressing IgM, IgA, IgG and/or IgD and the positive selection of IgE expressing cells.

First claim

The invention claimed is:

1. A multi-color flow cytometric method for analyzing memory B cell and plasma cell subsets in a biological sample from a subject, comprising the steps of:
(i) staining the sample with an antibody cocktail comprising fluorochrome-conjugated antibodies, said antibody cocktail comprising antibodies against IgM, IgA, IgG, IgD and IgE, an antibody against a B cell marker and an antibody against the CD38 antigen, wherein each of said antibodies in said antibody cocktail is conjugated to a different fluorochrome than the other antibodies, or wherein antibodies selected from the group consisting of anti-IgA, anti-IgE and anti-IgG are conjugated with a total of two fluorochromes, wherein a first antibody selected from the group consisting of anti-IgA, anti-IgE and anti-IgG is conjugated to a first fluorochrome, a second antibody selected from the group consisting of anti-IgA, anti-IgE and anti-IgG is conjugated to a second, distinct fluorochrome and the third antibody selected from the group consisting of anti-IgA, anti-IgE and anti-IgG is conjugated simultaneously to the first and second fluorochrome;
(ii) subjecting the sample to multicolor flow cytometry and gating for lymphocytes based on forward scatter and side scatter pattern;
(iii) gating the lymphocytes for expression of the B cell specific marker to identify B cells, and for expression of CD38 to identify a memory B cell population having diminished CD38(CD38 dim ) expression and a plasma cell population having high CD38 (CD38 hi );
(iv) determining surface expression of IgM, IgA, IgG, IgD and IgE on the cells in said identified memory B cell population and/or said plasma cell population; and
(v) detecting and quantitating the IgE+ cells within the memory B cell population and/or the plasma cell population by the negative selection of cells expressing IgM, cells expressing IgA, cells expressing IgG and cells expressing IgD, and the positive selection of IgE expressing cells.

2. The method according to claim 1 , wherein the B cell marker is CD19, CD20, CD79a or CD22 antigen.

3. The method according to claim 1 , wherein the panel of fluorochrome-conjugated antibodies comprises, in addition to said B cell marker, at least one further fluorochrome-conjugated antibody reactive with a B cell antigen.

4. The method according to claim 3 , wherein the further B cell antigen is a marker for characterization of memory B cells.

5. The method according to claim 3 , wherein the further B cell antigen is a marker for characterization of plasma B cells.

6. The method according to claim 3 , wherein the B cell antigen is a marker selected from the group consisting of CD23, CD40, CD80, CD86, CD180, transmembrane activator and CAML interactor (TACI), CD200, CD73, T-cell leukemia/lymphoma protein-1 (TCL1) and CD62L.

7. The method according to claim 3 , wherein the further B cell antigen is a marker for characterization of plasma B cells and is CD20 or CD138 antigen.

8. The method according to claim 1 , wherein the biological sample is blood, bone marrow, lymphoid tissue, tears, cerebrospinal fluid, saliva or fluid from skin vesicles.

9. The method according to claim 1 , further comprising at least one step of characterizing the IgE+ memory B cell population and/or the IgE+ plasma cell population.

10. The method according to claim 9 , wherein characterizing comprises staining the cells with an anti-CD27 antibody and detecting within the IgE+ memory B cell population the CD27+ and CD27− memory B cell subsets.

11. The method according to claim 9 , wherein characterizing comprises determining the antigen specificity of the IgE+ memory B cell population and/or the IgE+ plasma cell population by contacting the cells with a fluorochrome-conjugated antigen of interest.

12. The method according to claim 9 , wherein the antigen of interest is an allergen.

13. The method according to claim 1 , wherein the B cell marker is CD19 antigen.

14. The method according to claim 1 , wherein said two fluorochromes are fluorescein isothiocyante (FITC) and phycoerythrin (PE).

15. A method to diagnose and/or classify a disease or condition associated with altered IgE levels and IgE specificity, comprising analyzing memory B cell and plasma cell subsets in a biological sample isolated from a subject according to the method of claim 1 , further comprising the step of correlating the amount of IgE+ plasma and/or IgE+ memory B cells with the disease diagnosis and/or classification, wherein an increased number of IgE+ memory B cells and/or plasma cells as compared to healthy controls without disease or conditions associated with altered IgE levels and IgE specificity is indicative of the subject suffering from the disease.

16. The method according to claim 15 , wherein the disease is selected from the group consisting of type 1 hypersensitivity, an immune disease with suspected involvement of IgE antibodies.

17. The method according to claim 15 , wherein said type 1 hypersensitivity is selected from the group consisting of asthma, hay fever (rhinitis), food allergy, and atopic dermatitis, wherein said immune disease with suspected involvement of IgE antibodies is selected from the group consisting of rheumatoid arthritis (RA), mastocytosis, Graves disease and systemic lupus erythematosis (SLE), and wherein said parasitic infection is a helminth infection.

Assignees

• Van Zelm Menno Cornelis
• Van Dongen Jacobus Johannes Maria
• Orfao De Matos Correia E Vale José Alberto
• Univ Erasmus Med Ct Rotterdam
• Uniersidad De Salamanca

Inventors

• Van Zelm Menno Cornelis
• Van Dongen Jacobus Johannes Maria
• Orfao De Matos Correia E Vale José Alberto

Classifications

• G01N33/582

  with fluorescent label · CPC title

• G01N33/6854

  Immunoglobulins · CPC title

• G01N33/564

  for pre-existing immune complex or autoimmune disease {, i.e. systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, rheumatoid factors or complement components C1-C9} · CPC title

• G01N33/56972 Primary

  White blood cells · CPC title

• G01N2800/24

  Immunology or allergic disorders · CPC title