Assay method of antibody
Disclosed is a method of for analyzing the relative potency of an antibody of interest using β-hexosaminidase degranulation in human cell line. This improved assay method is used to characterize functional assay of anti-IgE antibody with B-hexosaminidase.
1. An assay method comprising:
a) seeding RBL 2H3 hFCεRIa cells in an assay plate with a MEM media to form a cell suspension, wherein the RBL 2H3 hFCεRIa cells comprise an hFCεRIa receptor with an IgE or an NP IgE and an anti-IgE antibody;
b) optionally incubating the cell suspension with CO2,
c) sensitising and neutralizing the RBL 2H3 cells;
d) transferring the sensitized and neutralized RBL 2H3 cells obtained from step (c) to a pre-seeded assay plate;
e) incubating the pre-seeded assay plate;
f) washing the pre-seeded assay plate;
g) mixing an antigen into the pre-seeded assay plate and incubating the pre-seeded assay plate to obtain a supernatant;
h) transferring the supernatant obtained from the incubation in step (g) from the pre-seeded assay plate into a test assay plate;
i) incorporating a substrate into the test assay plate and incubating the test assay plate; and
j) measuring bioactivity of the anti-IgE antibody.
2. The assay method as claimed in claim 1 , wherein the concentration of the anti-IgE antibody in step (c) is varying.
3. The assay method as claimed in claim 2 , wherein the varying concentration of the anti-IgE antibody in step (c) is derived from the assay plate prepared with varying concentration from higher to lower concentration of the anti-IgE antibody with dilution in the MEM media.
4. The assay method as claimed in claim 1 , wherein the concentration of the NP-IgE is constant and selected from a group consisting of about 30 μl, about 40 μl, about 50 μl, and about 60 μl.
5. The assay method as claimed in claim 1 , wherein the anti-IgE antibody volume is constant in step (c) and is selected from the group consisting of about 30 μl, about 40 μl, about 50 μl, and about 60 μl.
6. The assay method as claimed in claim 1 , wherein the incubation is performed in step from 18 hours, 19 hours, 20 hours, 21 hours, 22 hours, 23 hours, and 24 hours.
7. The assay method as claimed in claim 1 , wherein temperature of the incubation in step (e) and/or step (g) is about 37° C.
8. The assay method as claimed in claim 1 , wherein the washing of step (f) is performed one or two times with a Tyrode's buffer containing 1% BSA, phosphate buffer, and carbonate citrate.
9. The assay method as claimed in claim 1 , wherein the antigen is selected from a group consisting of NP-BSA (bovine serum albumin) and anti-IgE antibody.
10. The assay method as claimed in claim 1 , wherein the substrate is M-NAG.
11. The assay method as claimed in claim 10 , wherein the M-NAG concentration is selected from a group consisting of about 0.5 mM, about 1 mM, about 1.5 mM, and about 2 mM.
12. The assay method as claimed in claim 1 , wherein the substrate is incubated for about 30 minutes to 40 minutes at 37° C.
13. The assay method as claimed in claim 1 , further comprising a quenching of the assay reaction post step (i) by using an ice cold sodium bicarbonate buffer.
14. The assay method as claimed in claim 1 , wherein the bioactivity of the anti-IgE antibody is measured within 2 days.
15. The assay method as claimed in claim 1 , wherein the bioactivity is measured by using an enzyme selected from a group consisting of prostaglandins, leukotrienes, kinins, ECF-A, PAF (platelet activating factor), histamine, and ß-hexosaminidase.
16. The assay method as claimed in claim 1 , wherein the bioactivity of the anti-IgE antibody is measured by the B-hexosaminidase degranulation takes less time than a histamine release degranulation.
17. The assay method as claimed in claim 1 , wherein the antigen in step (g) is incubated for at least 70 minutes.
18. The assay method as claimed in claim 12 , wherein the substrate is incubated for about 30 minutes at 37° C.
19. The assay method as claimed in claim 15 , wherein the bioactivity of the anti-IgE antibody is measured within 1.5 days.