You’re using a public version of DrugPatentWatch with 5 free searches available | Register to unlock more free searches. CREATE FREE ACCOUNT

Last Updated: March 28, 2024

Claims for Patent: 5,837,467


✉ Email this page to a colleague

« Back to Dashboard


Summary for Patent: 5,837,467
Title: Method for predicting the response to treatment with BCG of superficial bladder carcinoma
Abstract:The invention relates to a method and kit for the prediction of the response of a patient suffering from superficial bladder carcinoma to treatment with bacillus Calmette-Guerin (BCG), by calculating the inducibility of the Interleukin-2 (IL-2) gene of the patient in a sample of peripheral blood mononuclear (PBM) cells from the patient receiving BCG. The method includes the steps of culturing at least two aliquots of PBM from the patient where the cells in a first aliquot are cultured in the presence of an inducing agent for inducing expression of the IL-2 gene and the cells in the second aliquot are cultured in the absence of the inducing agent. The extent of expression of the IL-2 gene is quantitatively determined for each aliquot. The ratio of the extent of the expression of the IL-2 gene in the first aliquot to the extent of the expression of the IL-2 gene in the second aliquot is calculated, the ratio providing a measure of the inducibility of the IL-2 gene. The inducibility is in a direct relationship with the probability of entering remission, relapse or persistence of bladder carcinoma in the patient. Patients with a ratio below about 1.5 can be treated either with a cytokine preparation, a second course of treatment with the BCG or a second course of treatment with the BCG in combination with a cytokine preparation to improve response.
Inventor(s): Kaempfer; Raymond (Jerusalem, IL), Shapiro; Amos (Mevaseret Ziyon, IL)
Assignee: Yissum Research Development Company of the Hebrew University of Jerusalem (Jerusalem, IL) Hadasit Medical Research Services and Development Company Ltd. (Jerusalem, IL)
Application Number:08/786,503
Patent Claims:1. A method for the prediction of the response of a patient suffering from superficial bladder carcinoma to treatment with bacillus Calmette-Guerin (BCG), by calculating the inducibility of the Interleukin-2 (IL-2) gene of the patient in a sample of peripheral blood mononuclear cells from the patient, comprising the steps of:

a) dividing at least one peripheral blood sample collected from a patient in the course of treatment of the patient with BCG, at least one week after said treatment, into at least two aliquots;

b) culturing the cells in each aliquot obtained in step (a) wherein:

(i) the cells in a first aliquot are cultured in the presence of an inducing agent for inducing expression of the IL-2 gene, and

(ii) the cells in a second aliquot are cultured in the absence of the inducing agent;

c) determining quantitatively the extent of expression of the IL-2 gene in each aliquot;

d) calculating the ratio of the extent of the expression of the IL-2 gene in the first aliquot to the extent of the expression of the IL-2 gene in the second aliquot wherein the ratio is providing a measure of the inducibility of the IL-2 gene wherein

the inducibility being in direct relationship with the probability of entering remission, relapse or persistence of bladder carcinoma in the patient.

2. The method according to claim 1 wherein said step determining quantitatively the extent of expression of the IL-2 gene in each aliquot is further defining as

a) isolating RNA from each of the aliquots;

b) blotting RNA isolated from each aliquot onto a support matrix; and

c) hybridizing each of the blotted RNA obtained in step (b) with a labeled riboprobe specific to the IL-2 gene.

3. The method according to claim 2 wherein said step isolating RNA is further defining as

a) lysing each of the cell cultures obtained by the addition a suitable lysing agent;

b) homogenizing each of the lysates obtained and subsequently selectively precipitating the RNA in each of the lysates by a suitable precipitating agent.

4. The method according to claim 3 wherein the lysing agent is selected from the group consisting of guanidinium-hydrochloride and guanidinium thiocyanate.

5. The method according to claim 3 wherein the precipitating agent is selected from the group consisting of sodium or potassium acetate or absolute ethanol.

6. The method according to claim 1 wherein the inducing agent is selected from the group consisting of phytohemagglutinin (PHA) or concanavalin A.

7. The method according to claim 1 wherein the BCG is administered to the patient repeatedly and the peripheral blood sample(s) are collected at a suitable time in the course of the repeated administrations of BCG.

8. The method according to claim 7 wherein the BCG is administered to the patient on a weekly basis and the peripheral blood sample/s are collected before the third and/or fourth weeks of administration of BCG.

9. A method of improving the response of a patient suffering from superficial bladder carcinoma to treatment with BCG by calculating the inducibility of the IL-2 gene of the patient in a sample of peripheral blood mononuclear cells from the patient by the method according to claim 1 and, in case the ratio is below about 1.5, the patient is subjected to treatment selected from the group consisting of administering to the patient a suitable cytokine preparation, administering to the patient a second course of treatment with BCG, and administering to the patient a second course of treatment with the BCG in combination with a cytokine preparation.

10. A method according to claim 9 wherein the cytokine preparation is recombinant.

11. A method according to claim 9 wherein the cytokine preparation is a natural cell product.

12. A method according to claim 10 wherein the cytokine preparation is recombinant IL-2.

13. A diagnostic kit for the determination of the inducibility of the IL-2 gene in a sample of peripheral blood mononuclear cells from a patient suffering from superficial bladder carcinoma, for use in the prediction of the response of the patient subjected to treatment with bacillus Calmette-Guerin (BCG) comprising:

an inducing agent; a lysing agent; a precipitating agent; a prehybridization buffer; and a riboprobe, specific to the IL-2 gene; positive control samples comprising a cell sample of peripheral blood mononuclear cells from a patient responsive to treatment with BCG or negative control samples comprising a cell sample of peripheral blood mononuclear cells from a patient nonresponsive to treatment with BCG.

14. A kit according to claim 13 wherein said inducing agent is selected from the group consisting of phytohemagglutinin (PHA) and concanavalin A.

15. A kit according to claim 13 wherein said lysing agent is selected from the group consisting of guanidinium-hydrochloride and guanidinium thiocyanate.

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.