FIELD: medicine.
SUBSTANCE: group of inventions refers to medicine, namely to immunology, and can be used to produce immunostimulating polypeptide derivative of transcription transactivation (Tat). Immunostimulating polypeptide derivative of the transactional transactivation agent has an amino acid sequence comprising the following sequence: (i) a transcription factor domain sequence of human immunodeficiency virus (HIV) (TAT) protein or monkey immunodeficiency virus, having the amino acid sequence SEQ ID NO: 96, 97 or 98, (ii) a sequence of a cysteine-rich domain from monkey immunodeficiency virus, HIV or defensin, having more than 85 % sequence identity to the amino acid sequence of one of SEQ ID NO: 124–132, and (iii) a sequence of the C-terminal domain of the HIV protein Tat or the immunodeficiency virus of monkeys, having more than 85 % sequence identity to the amino acid sequence of one of SEQ ID NO: 133–150, wherein the polypeptide derivative Tat is not one of SEQ ID NO: 2, 3 or 4. Group of inventions also involves the use of Tat for inhibiting suppression of an antitumour immune response in a patient with cancer, for treating an expressing PD-L1 tumour.
EFFECT: using the given group of inventions enables to overcome the PD-1/PD-L1 signal transmission pathway in PD-L1-expressing mammary gland cancer by administering the polypeptide derivative of Tat, and also reverses the immunosuppression periodically occurring during the progression of cancer, and restores immunoreactivity.
19 cl, 5 ex, 4 tbl, 14 dwg
| Title |
Year |
Author |
Number |
| PHARMACEUTICAL COMPOSITION POSSESSING ANTITUMOUR EFFECT, AND METHOD FOR REDUCING PD-L1 INHIBITING EFFECT ON HUMAN T-CELLS |
2016 |
|
RU2688692C2 |
| REDUCTION OF TUMOR MASS BY INJECTING CCR1 ANTAGONISTS IN COMBINATION WITH PD-1 INHIBITORS OR PD-L1 INHIBITORS |
2017 |
- Sharo Izrael
- Chon Khejyun
- Shall Tomas Dzh.
- Chzhan Penli
|
RU2745195C2 |
| COMBINED METHODS OF THERAPY FOR TREATMENT OF CANCEROUS TUMORS |
2017 |
- Sherts, Avigdor
- Salomon, Joram
- Agemi, Lilakh
- Khamri, Rakhel
- Prajs, Dina
- Kim, Kvankhi
- Koulmen, Dzhonatan
|
RU2747258C2 |
| METHODS OF TREATING CANCER USING PD-1 AND PD-L1 ANTAGONISTS IN COMBINATION WITH RADIATION THERAPY |
2015 |
- Stewart, Ross
- Morrow, Michelle
- Wilkinson, Robert
- Poon, Edmund
- Dovedi, Simon
- Illidge, Tim
|
RU2711408C2 |
| TREATMENT OF INFLAMMATION, AUTOIMMUNE, AND NEURODEGENERATIVE DISORDERS WITH IMMUNOSUPPRESSIVE TAT DERIVATIVE POLYPEPTIDES |
2013 |
- Goldberg Dzhoshua
- Bir Kolin
- Khotts-Bikhofsits Kristof
- Khenskom Sofi
|
RU2653754C2 |
| COMBINATION THERAPY USING CC CHEMOKINE RECEPTOR 4 (CCR4) ANTAGONISTS AND ONE OR MORE CHECKPOINT INHIBITORS |
2019 |
- Li, Shijie
- Mali, Venkat Reddy
- Singh, Rajinder
- Yang, Ju
- Zhang, Penglie
|
RU2810717C2 |
| COMPOSITIONS AND METHODS OF IMMUNOTHERAPY |
2014 |
- Brentdzhens Rener Dzh.
- Dzhekson Kholli Dzh.
|
RU2680010C2 |
| STABLE COMPOSITIONS OF ANTIBODIES AGAINST PROGRAMMABLE DEATH RECEPTOR OF PD-1 PERSON AND RELATED TREATMENT |
2012 |
- Sharma Manodzh K.
- Narasimkhan Chakravarti Nachu
- Gergich Kevin Dzhejms
- Kang Soonmo Piter
|
RU2633509C2 |
| ANTICANCER AGENT |
2016 |
- Odagami, Takenao
- Kouji, Hiroyuki
- Ozawa, Yoichi
- Hori, Yusaku
|
RU2729936C2 |
| CONTROL POINT INHIBITOR AND WHOLE MYCOBACTERIAL CELLS FOR USE IN CANCER THERAPY |
2016 |
- Akle Charles
- Brunet Laura Rosa
|
RU2733033C2 |