Posted by on February 13, 2018 5:40 am
Categories: Crispr Articles

Source: Two Issued US Patents Granted to Cellectis for CRISPR Use in T-Cells

NEW YORK–()–Regulatory News:

(Paris:ALCLS) (NASDAQ:CLLS), a clinical-stage biopharmaceutical company
focused on developing immunotherapies based on gene-edited allogeneic
CAR T-cells (UCART), announced today the issuance of two U.S. patents –
US 9,855,297 and US 9,890,393 – for the invention of certain uses of
RNA-guided endonucleases, such as Cas9 or Cpf1, for the genetic
engineering of T-cells. The patents came into force on January 2nd,
2018and February 13th, 2018, respectively.

Both patents claim methods by which T-cells are gene edited using
transient expression of CRISPR/Cas9 components. These inventions are
based on the early work initiated by inventors at Cellectis when the
CRISPR technology first came to light.

These therapeutic-focused patents follow the grant by the European
Patent Office of patent No. EP3004337 for similar inventions and
previous intellectual property that Cellectis has obtained over the last
two decades for major gene editing technologies including meganucleases,

“Cellectis is a pioneering gene editing company that has always been
keen to be at the forefront of all gene editing technologies,” said Dr.
André Choulika, Cellectis Chairman & CEO. “We have been the first to
explore the potential of CRISPR in its early days in various
applications, including therapeutics and plants. These early findings
ultimately led to the grant of this set of new patents. As such, these
patents only reinforce Cellectis’ leadership position in the gene
editing industry.”

Convinced of their strong value for the future development of engineered
CAR T-cells, Cellectis will make these patents available for licensing
to companies that are willing to use CRISPR technologies in T-cells. The
technical knowledge in these patents could, for example, help users
engineer allogeneic CAR T-cells while suppressing genes involved in
checkpoint inhibitions, such as PD-1, engineer drug resistance, or
remove MHC (Major Histocompatibility Complex) related genes. The
technology could also be used to insert a DNA CAR construct by gene
targeting a specific locus in the genome of T-cells.

The inventors of these patents are Dr. André Choulika, Chairman & CEO of
Cellectis and one of the pioneers in the development of nuclease-based
genome editing technologies; Dr. Philippe Duchateau, Cellectis Chief
Scientific Officer and seasoned gene editing expert; and Dr. Laurent
Poirot, Cellectis Head of Early Discovery and expert of gene functions
in immune cells.

Claims 1 and 2 of US 9,855,297:

1. A method of preparing genetically modified primary T-cells for
immunotherapy comprising the steps of: (a) transfecting mRNA encoding an
RNA-guided endonuclease into the primary T-cells, wherein the RNA-guided
endonuclease is expressed from the transfected m RNA; (b) introducing a
DNA vector that encodes a specific guide RNA, wherein the specific guide
RNA directs the RNA-guided endonuclease to at least one targeted locus
in the T-cell genome into the primary T-cells; (c) cleaving at least one
targeted locus in the T-cell genome with the RNA-guided endonuclease;
(d) generating a genetic modification at the site of the cleavage; and
(e) expanding the resulting genetically modified T-cells.

2. The method of claim 1, wherein the RNA-guided endonuclease is Cas9.

Claim 1 of US 9,890,393:

1. A method of preparing T-cells for immunotherapy comprising the step

(a) genetically modifying primary T-cells by introduction and/or
expression into the cells of at least:

– a RNA-guided endonuclease; and

– a specific guide RNA that directs said endonuclease to at least one
targeted locus in the T-cell genome,

wherein said RNA-guided endonuclease is expressed from transfected mRNA;

wherein said RNA-guided endonuclease comprises the amino acid sequence
set forth in SEQ ID NO:1 or SEQ ID NO:2; and

(b) expanding the resulting cells.

About Cellectis

Cellectis is a clinical-stage biopharmaceutical company focused on
developing a new generation of cancer immunotherapies based on
gene-edited T-cells (UCART). By capitalizing on its 18 years of
expertise in gene editing – built on its flagship TALEN® technology and
pioneering electroporation system PulseAgile – Cellectis uses the power
of the immune system to target and eradicate cancer cells.

Using its life-science-focused, pioneering genome engineering
technologies, Cellectis’ goal is to create innovative products in
multiple fields and with various target markets.

Cellectis is listed on the Nasdaq market (ticker: CLLS) and on Euronext
Growth (ticker: ALCLS). To find out more about us, visit our website:

Talking about gene editing? We do it. TALEN® is a registered trademark
owned by the Cellectis Group.


This press release contains “forward-looking” statements that are based
on our management’s current expectations and assumptions and on
information currently available to management. Forward-looking
statements involve known and unknown risks, uncertainties and other
factors that may cause our actual results, performance or achievements
to be materially different from any future results, performance or
achievements expressed or implied by the forward-looking statements.
Further information on the risks factors that may affect company
business and financial performance, is included in filings Cellectis
makes with the Security Exchange Commission from time to time and its
financial reports. Except as required by law, we assume no obligation to
update these forward-looking statements publicly, or to update the
reasons actual results could differ materially from those anticipated in
the forward-looking statements, even if new information becomes
available in the future.

Published at Tue, 13 Feb 2018 05:01:00 +0000

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