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Virology Research Journal

Volume 1 Issue 4

Vaccines World 2017

Notes:

Page 45

November 09-10, 2017 Vienna, Austria

21

st

World Congress and Exhibition on

VACCINES, VACCINATION & IMMUNIZATION

Tumor liberated protein (TLP) as potential

vaccine for lung cancer patients

Giulio Tarro

Foundation T. & L. de Beaumont Bonelli for cancer research, Italy

T

umor liberated protein (TLP) has been previously

describedas aTAA(complex) present in the sera fromlung

cancer patients with early stage disease. Since early detection

improves overall survival in lung cancer, identification of

screening biomarkers for patients at risk for the development

of this disease represents an important target. Starting from

the peptide epitope RTNKEASI previously isolated from TLP

complexes, we generated a rabbit anti-RTNKEASI serum.

This antiserum detected and immunoprecipitated a 55 kDa

protein band in the lysate of the lung cancer cell line A549.

This protein band was identified as aldehyde dehydrogenase

isoform 1A1 through mass spectrometry, revealing the

molecular nature of at least one component of the previously

described TLP complex. Next, we screened a cohort of 29

lung cancer patients (all histologies), 17 patients with non-

neoplastic lung pathologies and nine healthy donors for the

presence of serum ALDH1A1 and global serum ALDH by

enzyme-linked immunosorbent assay. This analysis indicated

that the presence of ALDH was highly restricted to patients

with lung cancer. Interestingly, the global ALDH test detected

more lung cancer patients compared to the ALDH1A1-

specific test, suggesting that other ALDH isoforms might add

to the sensitivity of the assay. Our data suggest that ALDH

levels may therefore be evaluated as part of a marker panel

for lung cancer screening. Finally, the ability of the immune

system to recognize a TAA, enables the development of a

vaccine approach for preventive and therapeutic application

and represents a main target of this field of research.

giuliotarro@gmail.com

Virol Res J 2017, 1:4