Tumor cell lysates as immunogenic sources for cancer vaccine design
Author
dc.contributor.author
González, Fermín E.
Author
dc.contributor.author
Gleisner, Alejandra
Author
dc.contributor.author
Falcón Beas, Felipe
Author
dc.contributor.author
Osorio, Fabiola
Author
dc.contributor.author
López, Mercedes N.
Author
dc.contributor.author
Salazar Onfray, Flavio
Admission date
dc.date.accessioned
2019-03-18T11:52:07Z
Available date
dc.date.available
2019-03-18T11:52:07Z
Publication date
dc.date.issued
2014
Cita de ítem
dc.identifier.citation
Human Vaccines & Immunotherapeutics 10:11, 3261--3269; November 2014
Identifier
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2164554X
Identifier
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21645515
Identifier
dc.identifier.other
10.4161/21645515.2014.982996
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/166455
Abstract
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Autologous dendritic cells (DCs) loaded with tumor-associated antigens (TAAs) are a promising immunologicaltool for cancer therapy. These stimulate the antitumorresponse and immunological memory generation.Nevertheless, many patients remain refractory to DCapproaches. Antigen (Ag) delivery to DCs is relevant tovaccine success, and antigen peptides, tumor-associatedproteins, tumor cells, autologous tumor lysates, and tumor-derived mRNA have been tested as Ag sources. Recently, DCsloaded with allogeneic tumor cell lysates were used to inducea potent immunological response. This strategy provides areproducible pool of almost all potential Ags suitable forpatient use, independent of MHC haplotypes or autologoustumor tissue availability. However, optimizing autologoustumor cell lysate preparation is crucial to enhancing efficacy.This review considers the role of cancer cell-derived lysates asa relevant source of antigens and as an activating factor forexvivotherapeutic DCs capable of responding to neoplasticcells. These promising therapies are associated with theprolonged survival of advanced cancer patients.