FIELD: medicine.
SUBSTANCE: group of inventions relates to medicine, namely, the prediction or monitoring of the future or current response of a patient suffering from cancer to a TLR-9 agonist treatment. For this purpose, the frequency of activated natural killer T (NKT) cells is determined, where the patient responding to the TLR-9 agonist treatment has a frequency of at least 3 % activated NKT cells of the whole NKT cell population. At the same time, the patient responding to treatment has a prolonged survival time without progression. Further, the TLR-9 agonist is a DNA construct from a covalently continuous, partially self-complementary DNA strand having a double-stranded stem with single-stranded end loops bearing unmethylated CG motif, wherein the DNA construct comprises at least one sequence motif N1N2CGN3N4, where N1N2 and N3N4 represent any combination of A, C, T and G, and C is deoxycytidine, G is deoxyguanosine, A is deoxyadenosine, and T is deoxythymidine. Also, the group of inventions relates to the use of a TLR-9 agonist representing a DNA construct for the treatment of cancer.
EFFECT: use of this group of inventions allows the use of activated NKT cells as a biomarker for patients undergoing TLR-9 agonist treatment.
14 cl, 2 tbl, 4 dwg
Title | Year | Author | Number |
---|---|---|---|
NON-CODING IMMUNOMODULATORY DNA CONSTRUCT | 2011 |
|
RU2583291C2 |
COMBINATION INCLUDING IMMUNE-STIMULATING OLIGONUCLEOTIDES | 2016 |
|
RU2766693C2 |
COVALENTLY CLOSED NON-CODING IMMUNOMODULATORY DNA CONSTRUCT | 2015 |
|
RU2668387C2 |
ALLOGENEIC ANTITUMOR THERAPEUTIC MEDICATION | 2004 |
|
RU2354694C2 |
CONCATEMERS FOR IMMUNE MODULATION | 2010 |
|
RU2556119C2 |
USE OF STRUCTURE FOR DNA EXPRESSION | 2011 |
|
RU2598713C2 |
DNA CONSTRUCT FOR EXPRESSION | 2011 |
|
RU2604186C2 |
PROSTATE-ASSOCIATED ANTIGENS AND IMMUNOTHERAPEUTIC REGIMENS BASED ON VACCINES | 2013 |
|
RU2737765C2 |
PROSTATE-ASSOCIATED ANTIGENS AND IMMUNOTHERAPY SCHEMES BASED ON VACCINES | 2013 |
|
RU2609651C2 |
METHOD FOR TREATING THRICE-NEGATIVE BREAST CANCER | 2017 |
|
RU2757905C2 |
Authors
Dates
2018-11-14—Published
2014-05-15—Filed