OSE Immunotherapeutics Announces Peer-Reviewed Publication on Novel Myeloid Immune Checkpoint CLEC-1 in Journal of Immunology
02 Abril 2024 - 11:30PM
OSE Immunotherapeutics Announces Peer-Reviewed Publication on Novel
Myeloid Immune Checkpoint CLEC-1 in Journal of Immunology
OSE Immunotherapeutics Announces
Peer-Reviewed Publication on Novel Myeloid Immune
Checkpoint CLEC-1in Journal of
Immunology
Nantes, France – April 2, 2024 – 7:30 am
CET – OSE Immunotherapeutics SA
(ISIN: FR0012127173; Mnemo: OSE) today announced the
publication of novel data in the peer-reviewed Journal of
Immunology (1) on a first-in-class research program with CLEC-1,
its novel myeloid immune checkpoint target for cancer
immunotherapy.
The academic collaboration conducted with Dr
Elise Chiffoleau’s team at the Center for Translational Research in
Transplantation and Immunology (2) has led to the identification of
CLEC-1 as a checkpoint, a receptor expressed by myeloid cells
inhibiting key myeloid cell functions, and T-cell cross-priming and
hence limiting anti-tumor immune responses. In the new publication,
the collaborative research work confirmed and reinforced the
potential of CLEC-1 as a novel myeloid immune checkpoint regulating
acute immune responses.
The article, titled “CLEC-1 restrains
acute inflammatory response and recruitment of neutrophils
following tissue injury” concludes that CLEC-1 acts as an
immune checkpoint for the control of acute immune response and
restrains myeloid cell infiltration and associated
inflammation.
Dr Elise Chiffoleau, INSERM scientist, said: “We
are very pleased to have these novel research data published in
“Journal of Immunology”, an internationally recognized scientific
journal. Our collaborative work shows, for the first time, that
CLEC-1 acts as an immune checkpoint for the control of acute immune
responses in the context of sterile inflammation. Additionally, its
pharmacological blockade with monoclonal antibodies can release
breaks on innate immune responses involved in various type of
diseases, in particular in immune responses against cancers.”
(1) CLEC-1 restrains acute inflammatory response and
recruitment of neutrophils following tissue injury
Camille Ligeron*†1, Javier Saenz†1 1, Berangere
Evrard†, Marion Drouin*†, Emmanuel Merieau†, Caroline Mary*, Kevin
Biteau*, Emmanuelle Wilhelm*, Cécile Batty*, Vanessa Gauttier*,
Irene Baccelli*, Nicolas Poirier*, Elise Chiffoleau†.* OSE
Immunotherapeutics, 22 Boulevard Benoni Goullin, Nantes, France.†
Nantes Université, Inserm, Centre de Recherche en Transplantation
et ImmunologieTranslationnelle, UMR 1064, ITUN, F-44000 Nantes,
France
(2) Collaborative academic program
between OSE Immunotherapeutics and Dr Elise Chiffoleau’s research
teams (Center for Research in Transplantation and Translational
Immunology (CR2TI), UMR1064, INSERM, Nantes University at
Nantes University Hospital,
https://cr2ti.univ-nantes.fr/research/team-1).
ABOUT OSE IMMUNOTHERAPEUTICS
OSE Immunotherapeutics is a biotech company
dedicated to developing first-in-class assets in immuno-oncology
(IO) and immuno-inflammation (I&I). The Company’s current
well-balanced first-in-class clinical pipeline includes:
-
Tedopi® (immunotherapy activating
tumor specific T-cells, off-the-shelf, neoepitope-based): this
cancer vaccine is the Company’s most advanced product; positive
results from the Phase 3 trial (Atalante 1) in Non-Small Cell Lung
Cancer patients in secondary resistance after checkpoint inhibitor
failure. Other Phase 2 trials, sponsored by clinical oncology
groups, of Tedopi® in combination are ongoing in solid tumors.
- OSE-279
(anti-PD1): first positive results in the ongoing Phase 1/2 in
solid tumors.
- OSE-127 -
lusvertikimab (humanized monoclonal antibody antagonist of IL-7
receptor); ongoing Phase 2 in Ulcerative Colitis (sponsor OSE
Immunotherapeutics); ongoing preclinical research in leukemia (OSE
Immunotherapeutics).
- FR-104/VEL-101
(anti-CD28 monoclonal antibody): developed in partnership with
Veloxis Pharmaceuticals, Inc. in transplantation; ongoing Phase 1/2
in renal transplant (sponsor Nantes University Hospital);
successful Phase 1 in the US (sponsor Veloxis Pharmaceuticals,
Inc.).
- BI 765063 and
BI 770371 (anti-SIRPα monoclonal antibody on
CD47/SIRPα pathway) developed in partnership with Boehringer
Ingelheim in advanced solid tumors; positive Phase 1 dose
escalation results in monotherapy and in combination, in particular
with anti-PD-1 antibody ezabenlimab; international Phase 1b ongoing
clinical trial in combination with ezabenlimab alone or with other
drugs in patients with recurrent/metastatic head and neck squamous
cell carcinoma (HNSCC) and hepatocellular carcinoma (HCC).
- OSE-230 (ChemR23
agonist mAb) developed in partnership with AbbVie in chronic
inflammation.
OSE Immunotherapeutics expects to generate
further significant value from its three proprietary drug discovery
platforms, which are central to its ambitious goal to deliver
next-generation first-in-class immunotherapies:
- Pro-resolutive mAb
platform focused on targeting and advancing inflammation
resolution and optimizing the therapeutic potential of targeting
Neutrophils and Macrophages in I&I. OSE-230
(licensed to AbbVie) is the first candidate generated by the
platform, additional discovery programs ongoing on new
pro-resolutive GPCRs.
- Myeloid Checkpoint
platform focused on optimizing the therapeutic potential
of myeloid cells in IO by targeting immune regulatory receptors
expressed by Macrophages and Dendritic cells. BI
765063 and BI 770371 (licensed to
Boehringer Ingelheim) are the most advanced candidates generated by
the platform. Ongoing additional discovery programs, in particular
with positive preclinical results obtained in monotherapy with new
anti-CLEC-1 mAbs.
- Cytokine platform
focused on leveraging the Cis-Delivery of cytokine in IO and
I&I. BiCKI® is a bispecific fusion protein platform built on
the key backbone component of anti-PD1 combined with a new
immunotherapy target to increase anti-tumor efficacy.
BiCKI®-IL-7v is the most advanced
BiCKI® candidate targeting anti-PD1xIL-7. Ongoing additional
discovery programs on Cis-Demasking technologies.
Additional information about OSE
Immunotherapeutics assets is available on the Company’s website:
www.ose-immuno.com. Click and follow us on X and LinkedIn
:https://twitter.com/i/flow/login?redirect_after_login=%2Fi%2Fflow%2Floginhttps://www.linkedin.com/company/ose-immunotherapeutics/
Contacts
OSE
ImmunotherapeuticsSylvie
Détrysylvie.detry@ose-immuno.comNicolas PoirierChief Executive
Officer nicolas.poirier@ose-immuno.com |
French
Media: FP2COMFlorence
Portejoiefportejoie@fp2com.fr+33 6
07 768 283U.S. Media
ContactRooneyPartners LLCKate
Barrettekbarrette@rooneypartners.com+1 212 223 0561 |
|
Forward-looking statementsThis
press release contains express or implied information and
statements that might be deemed forward-looking information and
statements in respect of OSE Immunotherapeutics. They do not
constitute historical facts. These information and statements
include financial projections that are based upon certain
assumptions and assessments made by OSE Immunotherapeutics’
management in light of its experience and its perception of
historical trends, current economic and industry conditions,
expected future developments and other factors they believe to be
appropriate.These forward-looking statements include statements
typically using conditional and containing verbs such as “expect”,
“anticipate”, “believe”, “target”, “plan”, or “estimate”, their
declensions and conjugations and words of similar import. Although
the OSE Immunotherapeutics management believes that the
forward-looking statements and information are reasonable, the OSE
Immunotherapeutics’ shareholders and other investors are cautioned
that the completion of such expectations is by nature subject to
various risks, known or not, and uncertainties which are difficult
to predict and generally beyond the control of OSE
Immunotherapeutics. These risks could cause actual results and
developments to differ materially from those expressed in or
implied or projected by the forward-looking statements. These risks
include those discussed or identified in the public filings made by
OSE Immunotherapeutics with the AMF. Such forward-looking
statements are not guarantees of future performance. This press
release includes only summary information and should be read with
the OSE Immunotherapeutics Universal Registration Document filed
with the AMF on May 2, 2023, including the annual financial report
for the fiscal year 2022, available on the OSE Immunotherapeutics’
website. Other than as required by applicable law, OSE
Immunotherapeutics issues this press release at the date hereof and
does not undertake any obligation to update or revise the
forward-looking information or statements.
- EN_240402_CLEC-1_Journal of Immunol
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