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Late Infantile Batten Disease
Martin L. Katz, Principal Investigator, University of Missouri School of Medicine, Mason Eye Institute, Columbia, MO 65212 E-mail: katzm@health.missouri.edu
1
APPROACHES FOR TREATING CLN2
CLN2 Therapy Studies from the Neurodegenerative Diseases Research Laboratory
The cause of CLN2 is the lack of a protein
(enzyme) called tripeptidyl peptidase-1 (TPP1).
TPP1 is required for the breakdown of old damaged
proteins that cells need to get rid of.
If TPP1 is missing or defective the proteins and
fragments cannot be chopped up properly so they
aggregate and build up inside cells
2
The aggregates that accumulate in nerve cells in
CLN2 give off a golden yellow glow when slices of
tissue are viewed with fluorescence microscopy.
Brain Brain Spinal Cord
5It should be possible to cure CLN2 by
providing nerve and other cells with the
normal form of the TTP1 Protein.
Cells will take up TPP1 supplied to them.
The TPP1 protein will attach
to the surfaces of most cells.
After it attaches, the protein
is taken up into cells in small
vesicles. These vesicles
deliver the protein to a
specialized structure in the
cell called the lysosome. In
the lysosome the TPP1
enzyme carries out its
normal function of breaking
down old and damaged
proteins.
3
4 TPP1 can be delivered widely throughout
the brain and spinal cord via the cerebral
spinal fluid.
Three Approaches for Delivering TPP1 to
the Cerebrospinal Fluid
6
Enzyme Infusion
Gene Therapy
Stem Cell Delivery
These approaches for therapy are being
tested in a Dachshund model for CLN2.
TPP1 is made by cells in culture, purified, and
then infused into the CSF. A clinical trial using
this approach is planned by BioMarin for 2013.
Copies of the TPP1 gene are made by cells in
culture, purified, and then infused into the
CSF. The genes are taken up by cells in the
brain and direct the cells to make and release
the TPP1 protein which then flows through the
CSF.
Cultured stem cells are programmed to make
large amounts of the TPP1 protein. These cells
are implanted into the CSF where they take up
residence and release the protein.
INTRODUCTION
A primary goal of the Neurodegenerative
Diseases Research Laboratory (NDRL) is to
develop a cure for the CLN2 form of Batten
disease.
Using a dog model we are evaluating 3
approaches to treatment: enzyme replacement
therapy; gene therapy; and stem cell therapy.
The cerebrospinal fluid
(CSF) is made in the brain
and circulates around the
entire brain and the spinal
cord.
The CSF flows through the
subarachnoid spaces where it
is in very close contact with
most structures and cells of the
brain.

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Lincl katz

  • 1. Late Infantile Batten Disease Martin L. Katz, Principal Investigator, University of Missouri School of Medicine, Mason Eye Institute, Columbia, MO 65212 E-mail: katzm@health.missouri.edu 1 APPROACHES FOR TREATING CLN2 CLN2 Therapy Studies from the Neurodegenerative Diseases Research Laboratory The cause of CLN2 is the lack of a protein (enzyme) called tripeptidyl peptidase-1 (TPP1). TPP1 is required for the breakdown of old damaged proteins that cells need to get rid of. If TPP1 is missing or defective the proteins and fragments cannot be chopped up properly so they aggregate and build up inside cells 2 The aggregates that accumulate in nerve cells in CLN2 give off a golden yellow glow when slices of tissue are viewed with fluorescence microscopy. Brain Brain Spinal Cord 5It should be possible to cure CLN2 by providing nerve and other cells with the normal form of the TTP1 Protein. Cells will take up TPP1 supplied to them. The TPP1 protein will attach to the surfaces of most cells. After it attaches, the protein is taken up into cells in small vesicles. These vesicles deliver the protein to a specialized structure in the cell called the lysosome. In the lysosome the TPP1 enzyme carries out its normal function of breaking down old and damaged proteins. 3 4 TPP1 can be delivered widely throughout the brain and spinal cord via the cerebral spinal fluid. Three Approaches for Delivering TPP1 to the Cerebrospinal Fluid 6 Enzyme Infusion Gene Therapy Stem Cell Delivery These approaches for therapy are being tested in a Dachshund model for CLN2. TPP1 is made by cells in culture, purified, and then infused into the CSF. A clinical trial using this approach is planned by BioMarin for 2013. Copies of the TPP1 gene are made by cells in culture, purified, and then infused into the CSF. The genes are taken up by cells in the brain and direct the cells to make and release the TPP1 protein which then flows through the CSF. Cultured stem cells are programmed to make large amounts of the TPP1 protein. These cells are implanted into the CSF where they take up residence and release the protein. INTRODUCTION A primary goal of the Neurodegenerative Diseases Research Laboratory (NDRL) is to develop a cure for the CLN2 form of Batten disease. Using a dog model we are evaluating 3 approaches to treatment: enzyme replacement therapy; gene therapy; and stem cell therapy. The cerebrospinal fluid (CSF) is made in the brain and circulates around the entire brain and the spinal cord. The CSF flows through the subarachnoid spaces where it is in very close contact with most structures and cells of the brain.