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Ann Clin Trials Vaccines Res. 2017 | Volume 1 Issue 2

Global Vaccines & Vaccination Summit & B2B

November 01-02, 2017 | Toronto, Canada

A rapid platform immunogenicity testing of cancer (neo) epitopes amenable to predict responders

from non-responders

Pirouz Daftarian

and

Marc Delcommenne

MBL International Corporation, USA

O

nly a fraction of cancer patients benefits from immune

checkpoint blockades (ICB). Those who respond to ICB

have some intrinsic anti-tumor immune responses. The

effectiveness of such therapies depends on the intrinsic

antitumor immunity namely preexisting tumor-specific

cytotoxic T cells. A notion that has intensified research

studies on cancer vaccines to assist ICB, with an aim to

treat those cancer patients that currently do not respond

to ICB therapies. In the recent years, the research tools and

technologies for the identification of cancer mutations and

of potential neoepitopes have improved dramatically, to the

point that they have never been this promising. However,

such candidate neoepitopes must be validated functionally

for their immunogenicity, only those that are expressed

and can be processed and presented are real neoepitopes.

A solid characterization or indication of true neoepitopes

is that they can bind to the MHC groove. Indeed, it is

difficult to make a verdict on the immunogenicity of (neo)

epitopes without a rapid method to measure the binding

of these peptides to MHC of the hosts. We have devised a

rapid, user-friendly peptide exchange tetramer assay (that

can help determine the binding of novel peptides to MHC

class I molecules and to generate new specificity MHC class

I tetramers for peptide specific T cell detection. Here, we

show data on the validation of the platform and present

data on how this platform may be used to discriminate

responders from non-responders. For the validation of

the platform, peptides were assessed for their HLA-A2402

binding and data from three different laboratories. Studies

are ongoing to determine how this assay may discriminate

between responders and non-responders to peptide based

vaccine therapy, which will be discussed.

Speaker Biography

Pirouz Daftarian is the Applications Manager, at MBL International focusing on

applications in immuno-oncology. He is also a Volunteer Assistant Professor University

of Miami, USA. He is a Vaccinologist/Immuno-Oncologist with 20 years of experience

in T-cell biology, vaccine development. IVD assay development for I-O biomarker and

surrogates of tumor rejection. He has nine patents and more than 50 publications in

peer reviewed journals.

e:

pdaftarian@jsrmicro.com