FLOW BASED ASSAYS FOR THERAPEUTICS

Abstract

This invention provides methods to evaluate therapeutic efficacy of therapeutic monoclonal antibodies.

Claims

1. A method of analyzing a response to therapeutic antibodies, the method comprising: exposing a first aliquot of whole blood sample to a first therapeutic antibody and a second aliquot of whole blood sample to a second therapeutic antibody; combining exposed blood cells from the whole blood sample with a panel of labeled reporters, the panel of labeled reporters comprising at least two labeled reporters selected from the group consisting of a labeled reporter directed against a target cell depletion surface marker, a labeled reporter directed against a target cell activation surface marker expressed on white blood cell populations, and a labeled reporter directed against cytokine production by white blood cells to thereby simultaneously produce assay signals generated by each for the at least two labeled reporters; subjecting the whole blood cell sample mixtures to flow cytometry and measuring signals generated by each of the plurality of labeled cells of each aliquot in a flow cytometer; and combining the measured signals into an assay output for flow cytometric multiparameter analysis to determine a cellular response to the first therapeutic antibody and to the second therapeutic antibody and provide simultaneous differentiation between signals associated with one or more of target cell depletion, activation of white cell subpopulations, and cytokine production by white cells.

2. The method of claim 1, wherein at least one of the first therapeutic antibody and the second therapeutic antibody are in dry form.

3. The method of claim 1, wherein at least one of the panel of labeled reporters are in dry form.

4. The method of claim 1, wherein the target cell is a B cell.

5. The method of claim 1, wherein the first therapeutic antibody and the second therapeutic antibody independently binds to at least one antigen selected from the group consisting of CD20, CD38, CD19, PDL1, and PD1.

6. The method of claim 1, wherein the white cell subpopulations include NK cells.

7. The method of claim 1, wherein the therapeutic antibody binds a cytokine.

8. The method of claim 7, wherein the cytokine is TNF

9. The method of claim 1, wherein the plurality of labeled reporters includes a cell surface marker and a cytokine.

10. The method of claim 1, wherein the plurality of labeled reporters includes antibodies to CD137 and to CD69.

11. The method of claim 1, wherein the plurality of labeled reporters includes antibodies to INF-7 and to IL8.

12. The method of claim 1, wherein the plurality of labeled reporters includes antibodies to CD66b and CD11c.

13. The method of claim 1, wherein the plurality of labeled reporters includes antibodies to CD203c, CD63, CD3, CRTH2, and CD45.

14. The method of claim 1, wherein: the therapeutic antibody binds to at least one antigen to generate a signal associated with target cell depletion, the at least one antigen comprising CD19, CD38, tumor necrosis factor alpha (TNF), PD-1, PD-L1, CRTH2, or a mixture thereof, the therapeutic antibody binds to at least one antigen to generate a signal associated with activation of white blood cell subpopulations, the at least one antigen comprising CD69, CD107a, CD54, CD137, CD66b, CD11b, CD11c, TNF, CD203c, CD16, CRTH2, or a mixture thereof; the therapeutic antibody binds to at least one antigen to generate a signal associated with cytokine production by white blood cells, the at least one antigen comprising IFN, TNF, IL-6, IL-8, IL-10, or a mixture thereof, or a mixture thereof.

15. The method of claim 1, wherein the at least two labeled reporters are independently in wet or dry form.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0026] FIG. 1 is a summary that highlights (in colored boxes) the markers that produced good results in the assays of the invention.

[0027] FIG. 2 illustrates steps of performing methods of the invention showing a short and simple user operations.

[0028] FIG. 3 shows variations of expression of CD16 on NK cells from various donors with and without treatment by Obinituzumab.

[0029] FIG. 4 shows variations of KIR positivity between NK cells from the same set of donors with and without treatment by Obinituzumab using the extracellular panel used in FIG. 3.

[0030] FIGS. 5A-5J show the ability of the methods of the invention to assess the function of an anti-CD20mAb. The top panel (FIGS. 5A, 5B, 5E, 5F, and 5G) shows the results of assays in the absence of mAb and the bottom panel (FIGS. 5C, 5D, 5H, 5I, and 5J) shows the results of assays in the presence of mAb.

[0031] FIGS. 6A-6L show ability of the methods of the invention to compare different mAbs. Specifically they show the results of assays in the absence of mAb, panel shows the results of assays in the presence of Rituximab in the presence of Obinutuzumab. The results show the same magnitude of B cell depletion with both mAbs. OBI however is shown to be more potent in engaging NK cells.

[0032] FIG. 7 shows the mechanisms of actions mediated by soluble (sTNF) and membrane-bound (tmTNF).

[0033] FIG. 8 shows the results of assays of the invention using the extracellular panel for three different anti-TNF biologics-infliximab (IFX), adalimumab (ADA) and etanercept (ETA) used to block soluble TNF.

[0034] FIG. 9 shows the results of assays of the invention using the extracellular panel for three different anti-TNF mAbs-IFX, ADA and ETA used to block membrane bound TNF.

[0035] FIGS. 10A-10J show the results of assays to monitor ADCC using the extracellular panel for three different anti-TNF mAbs-IFX, ADA and ETA The top panels (FIGS. 10A, 10B, 10C, 10G, and 10H) are the results from 4 hours after addition of one of the therapeutic antibodies (IFX, ADA, or ETA), showing the depletion of soluble TNF. The lower panel (FIGS. 10D, 10E, 10F, 10I, and 10J) are the results from 4 hours after addition of one of therapeutic antibodies, showing ADCC response in the lower right quadrant.

DETAILED DESCRIPTION

[0036] The present invention provides an approach based on the use of dry and room temperature stable reagents that enable whole blood sample analysis. In particular, the invention provides a ready-to-use approach for studying by flow cytometry the effect or function of a given therapeutic mAb (or any other biologics) on a given whole blood sample. In one embodiment, both staining reagents (fluorochrome conjugated antibodies) and therapeutic agents (therapeutic mAb or any other biologic) are provided in a dry, room temperature stable and ready-to-use format. In this case, only whole blood needs to be added in the dry reagent tube/container, which makes the assays of the invention very simple and highly standardizable, and therefore highly desirable in clinical research settings. The invention can be of interest in various situations, whether it deals with mAb characterization or patient stratification.

Anti-CD20 Antibodies

[0037] To illustrate the use and interest of the invention, the case of anti-CD20 therapeutic mAbs is considered here. One skilled in the art would readily appreciate that the method and composition disclosed herein can be used to study the effect or function of any therapeutic antibody or agent. Non-limiting examples of such therapeutic antibodies and agents include Anti-CD38, anti-CD19, anti-PDL1, and anti-PD1 antibody. It is a relevant study case as there is today a lot of activity around this category of mAbs. Anti-CD20 mAbs are currently used to treat various pathologies, from B-cell lymphoma to auto-immune diseases and have been commercialized for more than 15 years.

[0038] Different challenges are currently encountered in the field of anti-CD20 therapies. The first challenge is that biosimilars to rituximab, the first anti-CD20 therapeutic mAb to be approved in 1997, can now be commercialized once developed, tested, and approved. Several companies may attempt to develop biosimilars to this molecule, because Rituximab annual revenues are very large (greater than $7B). The availability of tools that would enable a fine comparison between several molecules is thus crucial A second challenge is related to patient stratification and treatment personalization. Several therapeutic mAbs targeting the CD20 antigen are on the market and more molecules (biosimilars, biobetters or other originators) are in their later phases of development. Thus more than one anti-CD20 molecule could be chosen to treat a given patient. Putting aside biosimilars that should behave similarly, a doctor must best determine the anti-CD20 therapeutic mAb to be used for a given patient. Indeed, as a function of the mAb chosen, not only the success of the therapy can vary but also the magnitude and the potential gravity of the side effects. A particular side effect is called infusion related reactions (IRR). It occurs for some patients while treated with Rituximab and much more frequently (>10%) when Obinituzumab is being used. These IRRs may be very violent, potentially fatal, side reactions and may include anaphylactic shock or cytokine release syndrome (CRS). CRS is caused by a large, rapid release of cytokines into the blood from immune cells affected by the immunotherapy. Signs and symptoms of cytokine release syndrome include fever, nausea, headache, rash, rapid heartbeat, low blood pressure, and trouble breathing. It is of the great importance to be able to predict the occurrence of such reaction for a given individual so that the treatment can be modified to limit the risk as much as possible.

[0039] While the capability to predict success, failure, or side effects is crucial for patient stratification and treatment personalization, it is also very important in the context of biopharmaceutical development.

[0040] The present invention has been developed to potentially answer the previously described questions. Schematically, it has been developed so that what could happen in via could be mimicked in vitro while only relying on a very simple and straightforward experimental procedure. These objectives could be leveraged for both patient stratification and therapeutic mAb comparability assessment.

[0041] We have prepared several cytometry panels to address different

TABLE-US-00001 TABLE 1 Extracellular panel Violet Laser (405 nm) Blue Laser (488 nm) Red laser (638 nm) PB KrO FITC PE ECD PECy5 PECy7 APC APC- APC- A700 A750 CD107a CD45 CD54 Mix of CD16 CD19 CD69 CD314 CD56 CD3 + KIRs CD14

[0042] The above extracellular panel (Table 1) enables the concomitant monitoring of B cell depletion as well as NK cell activation upon a stimulation with (for example) an anti-CD20 therapeutic antibody. In the present format, both the staining reagents and the therapeutics are ready to be used in the sample vials as dry reagents and blood simply needs to be added before incubation at 37 C. to start the assay.

[0043] Labeled reporters (typically fluorescently-labeled antibodies) directed against cellular components CD45, CD19, CD56, CD3, CD14, and a Mix of killer immunoglobulin-like receptors (KIRs), are gating reagents while labeled reporters directed against CD107a, CD69, and CD54 help characterize the activation status of both NK cells and monocytes (CD69 and CD54). The first row of the above panel shows a laser used to excite the fluorescent dye associated with each labeled reporter. The lasers and labels of this example are adjusted to match those of available variants of the Applicant's CytoFLEX cytometer. The second row indicates the label associated with each labeled reporter; the third row indicates specificity: the cellular components against which the labeled reporter is directed.

[0044] FIG. 3 shows variations between cells from different donors with and without treatment by Obinituzumab. The cells were analyzed using the extracellular panel described above and measured in a CytoFLEX cytometer gating to isolate NK cells. The bars show the expression of CD16 on NK cells from various donors. Note the very heterogeneous ability of NK Cells to internalize CD16 upon binding with Obinituzumab.

[0045] FIG. 4 shows variations between cells from the same set of donors using the same extracellular panel described above. When compared to resting NK cells, fully activated NK cells present a higher percentage of KIR positive cells. This illustrates in part the utility of different assay outputs even with the same panel.

[0046] The results of tests for extracellular markers showed the following. A large heterogeneity of response between the different donors tested was seen. There was no apparent correlation between studied parameters and magnitude of B cell depletion. The percentage of triply positive NK cells (CD69.sup.+CD107a.sup.+CD54) was most correlated with activation. Fully activated NK cells were significantly more KIR positive than the resting ones.

TABLE-US-00002 TABLE 2 Intracellular panel Violet Laser (405 nm) Blue Laser (488 nm) Red laser (638 nm) PB KrO A488 PE ECD PECy5 PECy7 APC APC- APC- A700 A750 IFN CD45 IL8 IL6 CD16 CD19 CD3 + CD14 IL10 TNF CD56

[0047] An intracellular panel of the invention is presented in Table 2 above; the description of each line of the table is the same as that for the extracellular panel. As in the case of the extracellular panel, the intracellular panel has been developed to enable the concomitant monitoring of B cell depletion as well as NK cell activation upon a stimulation with an anti-CD20 therapeutic antibody. It is not presently known which cytokines and/or which cell types are the most responsible for IRRs. It is interesting to mention that therapeutic mAbs/fusion protein the cytokines followed here do already exist. If it is found that one of the cytokines is more particularly responsible for potential IRRs in a given patient, the appropriate drug to counter that cytokine effect could be added to the therapeutic cocktails of the considered patient to minimize the probability of the occurrence of IRRs. Likewise, the present invention can be used to determine whether one of the cytokines is more particularly responsible for the cytokine release syndrome (CRS) in a given patient, and the appropriate drug to counter that cytokine effect could be administered to the patient.

[0048] As in in the case of the extracellular panel, a large heterogeneity of response between the different donors tested was observed. Three main profiles have been identified when focusing on monocytes (n=13): donors mainly expressing IL8 (n=10), donors mainly expressing IL8 and IL6 (n=2) and donors mainly expressing IL8 and TNF (n=1). No IL10 expression was observed on monocytes under the tested conditions. Production of IFN and TNF observed on NK cells but required brefeldine conditions different from monocytes.

[0049] Considering that anaphylactic shocks are also listed as potential IRR a panel in Table 3 below (including CD203c, CD63, CD3, CRTH2, and CD45) to determine basophil activation is also useful to characterize the basophil activation status upon therapeutic mAb stimulation, especially when considering mAbs with murine amino acid sequences and/or glycosylation moieties.

TABLE-US-00003 TABLE 3 Violet Laser (405 nm) Blue Laser (488 nm) Red laser (638 nm) PB KrO FITC/A488 PE ECD PECy5 PECy7 APC/A647 APC- APC- A700 A750 CD63 CD45 CD3 CD203c CDTH2

[0050] To help the model to be finalized, additional information such as CD16 variant might be needed for each patient and future experiments will help us characterize the importance of each of the above panels.

[0051] Another set or extracellular and intracellular panels useful in the invention are presented in Tables 4 and 5, below.

TABLE-US-00004 TABLE 4 Extracellular panel VIOLET LASER RED LASER (405 NM) BLUE LASER (488 NM) (638 NM) PB KrO FITC PE ECO PEcy5.5 PECy7 APC APC-A700 APC-A750 CD107a CD45 CD54 CD14 CD137 CD19 CD56 CD69 CD3 CD16

TABLE-US-00005 TABLE 5 Intracellular Panel VIOLET LASER RED LASER (405 NM) BLUE LASER (488 NM) (638 NM) PB KrO FITC PE ECD PEcy5.5 PECy7 APC APC-A700 APC-A750 INFy CD45 IL8 IL6 CD14 CD19 CD56 CD16 TNF CD3

[0052] The ability to assess the function anti-CD20 mAb using the above panels is shown in FIGS. 5A-5F.

Anti-TNF Antibodies

[0053] The approach demonstrated above can also be applied to soluble molecules, such as TNF. The mechanisms of actions mediated by soluble (sTNF) and membrane-bound (tmTNF) are illustrated in FIG. 7. The methods of the invention can be used, for example, to stratify patients and personalize patients over time. Panels useful for Anti-TNF, mAbs are presented in Tables 6 and 7.

TABLE-US-00006 TABLE 6 Extacellular panel VIOLET LASER RED LASER (405 NM) BLUE LASER (488 NM) (638 NM) PB KrO FITC PE ECD PEcy5.5 PECy7 APC APCA700 APC-A750 CD3 CD45 CD54 TNFR2 CD14 CD19 CD56 CD69 TNF CD16

TABLE-US-00007 TABLE 7 Intracellular Panel VIOLET LASER RED LASER (405 NM) BLUE LASER (488 NM) (638 NM) PB KrO FITC PE ECD PEcy5.5 PECy7 APC APC- APC- A700 A750 IL10 CD45 IL8 IL6 CD14 CD3 CD56 CD69 TNF CD16

[0054] The results of assays using these panels to monitor various mechanisms of action are shown in FIGS. 8-10.

[0055] It is understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and scope of the appended claims. All publications, patents, and patent applications cited herein are hereby incorporated by reference in their entirety for all purposes.