JP2017538669A5 - - Google Patents

Download PDF

Info

Publication number
JP2017538669A5
JP2017538669A5 JP2017520986A JP2017520986A JP2017538669A5 JP 2017538669 A5 JP2017538669 A5 JP 2017538669A5 JP 2017520986 A JP2017520986 A JP 2017520986A JP 2017520986 A JP2017520986 A JP 2017520986A JP 2017538669 A5 JP2017538669 A5 JP 2017538669A5
Authority
JP
Japan
Prior art keywords
pharmaceutical composition
composition according
group
mdsc
human genetic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2017520986A
Other languages
English (en)
Japanese (ja)
Other versions
JP2017538669A (ja
JP6918279B2 (ja
Filing date
Publication date
Priority claimed from EP14190370.8A external-priority patent/EP3012271A1/en
Application filed filed Critical
Publication of JP2017538669A publication Critical patent/JP2017538669A/ja
Publication of JP2017538669A5 publication Critical patent/JP2017538669A5/ja
Priority to JP2021102148A priority Critical patent/JP7253008B2/ja
Application granted granted Critical
Publication of JP6918279B2 publication Critical patent/JP6918279B2/ja
Priority to JP2023047480A priority patent/JP2023078398A/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017520986A 2014-10-24 2015-10-21 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物 Active JP6918279B2 (ja)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2021102148A JP7253008B2 (ja) 2014-10-24 2021-06-21 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物
JP2023047480A JP2023078398A (ja) 2014-10-24 2023-03-24 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP14190370.8A EP3012271A1 (en) 2014-10-24 2014-10-24 Method and compositions for inducing differentiation of myeloid derived suppressor cell to treat cancer and infectious diseases
EP14190370.8 2014-10-24
PCT/IB2015/058124 WO2016063233A1 (en) 2014-10-24 2015-10-21 Method and compositions for inducing differentiation of myeloid derived suppressor cell to treat cancer and infectious diseases

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2021102148A Division JP7253008B2 (ja) 2014-10-24 2021-06-21 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物

Publications (3)

Publication Number Publication Date
JP2017538669A JP2017538669A (ja) 2017-12-28
JP2017538669A5 true JP2017538669A5 (https=) 2018-11-29
JP6918279B2 JP6918279B2 (ja) 2021-08-11

Family

ID=51868772

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2017520986A Active JP6918279B2 (ja) 2014-10-24 2015-10-21 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物
JP2021102148A Active JP7253008B2 (ja) 2014-10-24 2021-06-21 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物
JP2023047480A Pending JP2023078398A (ja) 2014-10-24 2023-03-24 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2021102148A Active JP7253008B2 (ja) 2014-10-24 2021-06-21 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物
JP2023047480A Pending JP2023078398A (ja) 2014-10-24 2023-03-24 癌および感染症の治療のために骨髄由来抑制細胞分化を誘導する方法および組成物

Country Status (9)

Country Link
US (3) US20170247464A1 (https=)
EP (4) EP3012271A1 (https=)
JP (3) JP6918279B2 (https=)
CA (1) CA2964203C (https=)
DK (2) DK3209691T3 (https=)
ES (2) ES3060595T3 (https=)
HU (1) HUE050318T2 (https=)
PL (2) PL3783027T3 (https=)
WO (1) WO2016063233A1 (https=)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015109391A1 (en) 2014-01-24 2015-07-30 Children's Hospital Of Eastern Ontario Research Institute Inc. Smc combination therapy for the treatment of cancer
WO2017027422A1 (en) 2015-08-07 2017-02-16 Alexo Therapeutics Inc. Constructs having a sirp-alpha domain or variant thereof
EP3341015B2 (en) 2015-08-26 2023-12-27 The Board of Trustees of the Leland Stanford Junior University Enhanced depletion of targeted cells with cd47 blockade and an immune costimulatory agonist
JP7078533B2 (ja) * 2015-10-21 2022-05-31 オーエスイー イムノセラピューティクス 炎症促進性細胞へのマクロファージ分極を改変して癌を治療するための抗SIRPa化合物
RS66062B1 (sr) 2016-04-14 2024-11-29 Ose Immunotherapeutics Nova anti-sirpa antitela i njihove terapijske primene
KR102379464B1 (ko) 2016-06-20 2022-03-29 키맵 리미티드 항-pd-l1 항체
US20190153095A1 (en) * 2016-07-05 2019-05-23 National University Corporation Kobe University Antitumor Agent
JOP20190009A1 (ar) * 2016-09-21 2019-01-27 Alx Oncology Inc أجسام مضادة ضد بروتين ألفا منظم للإشارات وطرق استخدامها
CN118027200A (zh) 2016-12-09 2024-05-14 艾利妥 抗SIRPα抗体及其使用方法
US11566060B2 (en) 2017-01-05 2023-01-31 Kahr Medical Ltd. PD1-CD70 fusion protein and methods of use thereof
LT3565579T (lt) 2017-01-05 2023-09-11 Kahr Medical Ltd. Pd1-41bbl sulietas baltymas ir jo panaudojimo būdai
PT3565828T (pt) 2017-01-05 2022-02-08 Kahr Medical Ltd Proteína de fusão sirp1 alfa-41bbl e seus métodos de utilização
WO2018127918A1 (en) 2017-01-05 2018-07-12 Kahr Medical Ltd. A sirp alpha-cd70 fusion protein and methods of use thereof
WO2018136659A1 (en) * 2017-01-18 2018-07-26 Nant Holdings Ip, Llc Modulation of tumor cell susceptibility
US20200306300A1 (en) * 2017-02-15 2020-10-01 The Regents Of The University Of California Compositions and methods for activating nk cells
JP7262440B2 (ja) 2017-08-02 2023-04-21 フェインズ セラピューティクス,インコーポレーテッド 抗cd47抗体及びその使用
JP7395471B2 (ja) 2017-10-13 2023-12-11 オーセ イミュノセラピューティクス 改変抗SIRPa抗体及びその使用
AU2019233577A1 (en) 2018-03-13 2020-09-03 Ose Immunotherapeutics Use of anti-human SIRPa v1 antibodies and method for producing anti-SIRPa v1 antibodies
MX2020009774A (es) 2018-03-21 2020-10-08 Alx Oncology Inc Anticuerpos contra proteína alfa reguladora de señal y métodos de uso.
EP3802602A1 (en) 2018-05-25 2021-04-14 Alector LLC Anti-sirpa antibodies and methods of use thereof
US11759485B2 (en) 2018-06-14 2023-09-19 Meiji Co., Ltd. Composition for enhancing immune checkpoint blockade therapy
US12134638B2 (en) 2018-07-11 2024-11-05 Kahr Medical Ltd. SIRPalpha-4-1BBL variant fusion protein and methods of use thereof
KR20210044221A (ko) 2018-07-11 2021-04-22 카 메디컬 리미티드 Pd1-4-1bbl 변이체 융합 단백질 및 이의 사용 방법
US11591390B2 (en) 2018-09-27 2023-02-28 Celgene Corporation SIRP-α binding proteins and methods of use thereof
SG11202102851XA (en) 2018-09-27 2021-04-29 Celgene Corp SIRPa BINDING PROTEINS AND METHODS OF USE THEREOF
US12331320B2 (en) 2018-10-10 2025-06-17 The Research Foundation For The State University Of New York Genome edited cancer cell vaccines
BR112021007286A2 (pt) * 2018-10-19 2021-07-27 Ohio State Innovation Foundation células furtivas terapêuticas nanoprojetadas
BR112021024003A2 (pt) 2019-05-31 2022-04-19 Alx Oncology Inc Métodos de tratamento de câncer com fusão sirp alfa-fc em combinação com um inibidor de checkpoint imunológico
CN114206912B (zh) 2019-06-07 2025-02-11 Alx肿瘤生物技术公司 用于在血清学测定中减少结合cd47的药物的干扰的方法和试剂
AU2020394204A1 (en) 2019-11-27 2022-06-02 ALX Oncology Inc. Combination therapies for treating cancer
US12343377B2 (en) 2020-06-01 2025-07-01 ALX Oncology Inc. Combination therapies comprising a hypomethylation agent for treating cancer
CN111808800B (zh) * 2020-07-20 2022-08-26 中南大学湘雅二医院 一种体外诱导免疫抑制性髓系抑制细胞及其制备和应用
WO2022120286A1 (en) 2020-12-06 2022-06-09 ALX Oncology Inc. Multimers for reducing the interference of drugs that bind cd47 in serological assays
JP2024520902A (ja) 2021-05-13 2024-05-27 エーエルエックス オンコロジー インコーポレイテッド がんを治療するための併用療法
WO2023020459A1 (zh) 2021-08-17 2023-02-23 杭州九源基因工程有限公司 靶向SIRPα的单克隆抗体及其用途
JP2025523369A (ja) 2022-06-01 2025-07-23 エーエルエックス オンコロジー インコーポレイテッド 尿路上皮癌腫を治療するための併用療法
EP4619435A1 (en) 2022-11-16 2025-09-24 Boehringer Ingelheim International GmbH Predictive efficacy biomarkers for anti-sirpa antibodies
CN115896015B (zh) * 2023-02-08 2023-09-29 上海诚益生物科技有限公司 一种髓系来源抑制性细胞的体外培养方法
CN117054649A (zh) * 2023-08-04 2023-11-14 广州中医药大学第一附属医院 一种慢性萎缩性胃炎向胃癌转化标志物及其应用

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1048299A1 (en) 1999-04-28 2000-11-02 Faculteit der Geneeskunde van de Vrije Universiteit Method for inhibiting cell functioning for use in anti-inflammatory and anti-tumour therapies
JP3936673B2 (ja) 2003-06-02 2007-06-27 国立大学法人群馬大学 Cd47部分ペプチドと抗shps−1モノクロナール抗体
EP2630966B1 (en) * 2007-10-12 2017-04-19 Massachusetts Institute of Technology Vaccine nanotechnology
AU2009205665B2 (en) * 2008-01-15 2013-12-05 The Board Of Trustees Of The Leland Stanford Junior University Methods for manipulating phagocytosis mediated by CD47
EP2111869A1 (en) 2008-04-23 2009-10-28 Stichting Sanquin Bloedvoorziening Compositions and methods to enhance the immune system
PL2995315T3 (pl) 2009-05-15 2024-04-22 University Health Network Kompozycje i sposoby leczenia nowotworów hematologicznych celujące w oddziaływanie sirp alfa-cd47
GB201015765D0 (en) * 2010-09-21 2010-10-27 Immatics Biotechnologies Gmbh Use of myeloid cell biomarkers for the diagnosis of cancer
EP3682896A1 (en) * 2011-04-28 2020-07-22 University of Southern California Human myeloid derived suppressor cell cancer markers
WO2013056352A1 (en) * 2011-10-19 2013-04-25 University Health Network Antibodies and antibody fragments targeting sirp-alpha and their use in treating hematologic cancers
SI2804617T1 (sl) 2012-01-17 2020-10-30 The Board Of Trustees Of The Leland Stanford Junior University Visokoafinitetni SIRP-alfa reagenti
CN105101997B (zh) * 2013-02-06 2018-11-09 印希彼有限合伙公司 不减少血小板和不减少血红细胞的cd47抗体及其使用方法
AU2015229448B2 (en) 2014-03-11 2020-09-03 The Board Of Trustees Of The Leland Stanford Junior University Anti SIRP-alpha antibodies and Bi-specific Macrophage Enhancing antibodies

Similar Documents

Publication Publication Date Title
JP2017538669A5 (https=)
Chen et al. Induced expression of B7-H3 on the lung cancer cells and macrophages suppresses T-cell mediating anti-tumor immune response
Gottstein et al. Susceptibility versus resistance in alveolar echinococcosis (larval infection with Echinococcus multilocularis)
Khammari et al. Treatment of metastatic melanoma with autologous Melan-A/MART-1-specific cytotoxic T lymphocyte clones
MX2019005125A (es) Variantes de superficie celular discernibles inmunologicamente para uso en terapia celular.
EA201792497A1 (ru) Антитела к gitr для диагностики злокачественной опухоли
JP2009525478A5 (https=)
Conti et al. Microenvironment, Oncoantigens, and Antitumor Vaccination: Lessons Learned from BALB‐neuT Mice
EP4335931A3 (en) Therapeutic and diagnostic methods for cancer
MX2023001945A (es) Composiciones y metodos para el cribado de tumores solidos.
EA201591219A1 (ru) Антитела против lamp1 и конъюгаты антитела и лекарственного средства, а также их применение
EP1966370A1 (en) Method for treating disseminated cancer
WO2019079624A3 (en) Msi from liquid biopsies
Costa et al. Diagnosis of human strongyloidiasis: Application in clinical practice
WO2021150936A1 (en) Oncolytic virus compositions including il-15 complex and methods for the treatment of cancer
WO2020081579A8 (en) Monoclonal antibodies against human dickkopf3 and uses thereof
Woller et al. Virus infection, inflammation and prevention of cancer
Goto et al. DSP-7888, a novel cocktail design of WT1 peptide vaccine, and its combinational immunotherapy with immune checkpoint-blocking antibody against PD-1
Cachot et al. 545 Tumor-specific cytolytic CD4 T cells mediate protective immunity against human cancer
CN116940378A (zh) 神经内分泌癌的治疗
Jacobsen et al. 544 Multiomic characterization of T-cell populations at the single-cell level utilizing sensitive dextramers and BD® AbSeq on the BD RhapsodyTM Single-Cell Analysis system
Jackson et al. Immu-18. Immunogenomic responder phenotype from a phase I trial of anti-LAG3 or anti-CD137 alone and in combination with anti-PD-1 in patients with recurrent GBM
Jin et al. IMMU-15. A UNIQUE SELF-STIMULATIVE PROPERTY OF CD70 CAR ADVANCES T CELL FUNCTION AND ANTI-TUMOR RESPONSE IN GLIOBLASTOMA
Vaishnav et al. Nanobytes-molecular and immuno-oncology
Laspidea et al. IMMU-14. ONCOLYTIC VIRUS EXPRESSING A POSITIVE IMMUNE CHECKPOINT MODULATOR AS A THERAPEUTIC APPROACH FOR DIPG