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S e p t e m b e r 1 0 - 1 1 , 2 0 1 8 | D u b l i n , I r e l a n d

Cell and Gene Therapy 2018 & Clinical Microbiology Congress 2018

Note:

Page 8

allied

academies

CLINICAL AND MEDICAL MICROBIOLOGY

CELL AND GENE THERAPY

&

World Congress on

International Conference on

Joint Event on

Biomedical Research

|

ISSN: 0976-1683

|

Volume 29

Shirley O’Dea, Biomed Res 2018, Volume 29 | DOI: 10.4066/biomedicalresearch-C3-006

IN VIVO

ENGRAFTMENT OF T CELLS

TRANSFECTED USING SOLUPORE

®

IS SUPERIOR COMPARED WITH

ELECTROPORATION-BASED SYSTEMS

S

olupore is a vector-free intracellular delivery platform that enables

development and manufacture of cell therapies. Membrane disruption-

based methods, such as Solupore

®

, that enable intracellular delivery of various

cargotypesforclinicalapplicationshavebeenproposedasattractivecandidates

as next-generation delivery modalities because of potential benefits for safety,

regulation and production. Electroporation is the most widely used method

currently, this includes electroporation-based methods such as nucleofection,

however disadvantages include toxicity and proliferation stalling. Solupore

®

uses reversible permeabilization to achieve rapid intracellular delivery of

cargos with varying compositions, properties and sizes. A permeabilizing

delivery solution containing a low level of ethanol is used as the permeabilizing

agent. The technology achieves intracellular delivery and subsequent reversal

of cell permeabilization by precisely controlling the contact of the target cells

with this solution. The process is rapid and cargo transfers directly into the

cytoplasm by diffusion in an endocytic-independent manner. We have termed

the method soluporation. Comparisons of the phenotype and functionality

of primary human T cells following soluporation (Solupore

®

), nucleofection

(4D-Nucleofector

TM

) and electroporation (Neon

®

) are outlined in this work. The

extent to which the transfection systems perturb T cells was investigated as

well as the effects on cell functionality. The results presented demonstrate that

the Solupore

®

 technology does not perturb gene expression or cell surface

markers in T cells. Furthermore, cell proliferation and

in vivo

engraftment is

superior in soluporated cells compared with nucleofected cells. Thus, the

Solupore technology is gentle yet highly reproducible, automated, and scalable

and has the potential to enable a broad range of T cell engineering applications.

Biography

Shirley O’Dea has co-founded Avectas Ltd., in 2012

and is the company’s CSO. She is charged with

overseeing scientific programs. Her basic research

provides a strong pipeline of applications for Av-

ectas technology. She has previously served as a

Principal Investigator with Johnson and Johnson

and has led a large academic group specializing

in Lung Biology at National University of Ireland,

Maynooth.

sodea@avectas.com

Shirley O’Dea

Avectas Ltd., Ireland