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Immunoisolation

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Sequestration of cells within a semi-permeable membrane ... Allogeneic or xenogeneic? Primary post-mitotic cells? Mitotically active cells? ... – PowerPoint PPT presentation

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Title: Immunoisolation


1
Immunoisolation
  • Beth Zielinski-Habershaw, Ph.D.

2
Why organ replacement?
  • Irreversible organ/tissue damage
  • Metabolic insufficiencies
  • Molecular dysfunction
  • Solution
  • Donor transplantation
  • Artificial repair and replacement

3
Need?
4
Donor transplantation
  • Pros
  • Replicates tissues natural function
  • Cons
  • Supply constraints
  • Immune rejection

5
Artificial repair and replacement
  • Pros
  • No immune suppression required
  • No supply constraints
  • Cons
  • Full replacement of function?
  • Biocompatibility

6
The alternative
  • Immunoisolation

7
Immunoisolation
  • Sequestration of cells within a semi-permeable
    membrane
  • Delivery of therapeutic agents to host by
    encapsulated cells
  • Separation between host immune components and
    encapsulated cells

8
Bioartificial organs
  • History
  • 1970
  • Chick et al
  • Bioartificial pancreas
  • 1980
  • Lim and Sun
  • Alginate-encapsulated allogeneic islets
  • 1980-present
  • Immunoisolatory therapy for treatments of
    diabetes, chronic pain, neurodegenerative
    diseases, cancer

9
Theory
Macroencapsulation
Microencapsulation
10
Issues
  • Membrane characteristics
  • Pore size
  • Thickness
  • Tortuosity
  • Polymer/device characteristics
  • Thermomechanical stability
  • Geometry
  • Biodegradability
  • Retrievability
  • Scale-up

11
Issues
  • Cells/Cell sourcing
  • Allogeneic or xenogeneic?
  • Primary post-mitotic cells?
  • Mitotically active cells?
  • Genetically engineered cell lines?

12
Capsule format
  • Microcapsules
  • Interfacial coacervation
  • Cells entrapped during manufacturing of
    microcapsule device
  • Macrocapsules
  • Co-extruded phase inversion
  • Simultaneous fiber formation and loading
  • Phase inversion and filling
  • Cells encapsulated following formation of stock
    fiber

13
Matrices
  • Adherent and non-adherent cell types?
  • Growth or protein production enhancement?
  • Viability?
  • Preloading of desired matrix?
  • Simultaneous loading of matrix and cells?
  • Simultaneous formation of capsules with matrix
    and cells included?

14
Microencapsulation techniques
15
Macroencapsulation techniques
  • Co-extrusion
  • Cells extruded into fiber along with polymer
  • Exposure to organic solvents
  • Post-extruded filling
  • Loading of preformed capsules
  • Sealing of capsule ends

16
Host immune responses
  • Cellular
  • Macrophage
  • Giant cells/FBR
  • Neutrophils
  • Antibody
  • IgM
  • IgG
  • IgA?
  • Complement
  • Alone or in conjunction with cellular or antibody
    responses

17
Host immune responses
Antibody response
Macrophage/neutrophil activation Complement
activation
18
Current Applications
  • Chronic Pain
  • Diabetes
  • Cancer
  • ALS
  • Neurotrophic release

19
Current applications
  • Neurotech USA
  • RenaMed Therapeutics

20
Future directions
  • Microvascularization
  • Biodegradable microspheres
  • Photopolymerized conformal coatings
  • Programmable death
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