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Treatment of squamous carcinoma in mice with a vaccine enriched for cells that induce immunity to squamous carcinoma—A new vaccination strategy
Author(s) -
Chopra Amla,
Kim Tae Sung,
OSullivan InSug,
Martinez Don,
Cohen Edward P.
Publication year - 2006
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.21844
Subject(s) - transfection , biology , dna vaccination , population , antigen , vaccination , cell culture , immunology , mhc class i , antibody , cancer research , microbiology and biotechnology , virology , major histocompatibility complex , immunization , medicine , genetics , environmental health
Abstract We report a new vaccination strategy for squamous cell carcinoma (SCC). The vaccine was prepared by transfer of unfractionated DNA‐fragments (25 kb) from squamous carcinoma cells (KLN205, DBA/2 origin (H‐2 d )) into LM mouse fibroblasts (C3H/He origin; H‐2 k ), a highly immunogenic cell line. To enhance their nonspecific immunogenic properties, the fibroblasts were modified before DNA transfer to secrete IL‐2 and to express additional allogeneic MHC class I determinants. As the transferred DNA integrates into the genome of the recipient cells, and is replicated as the cells divide, sufficient DNA to prepare the vaccine could be obtained from as few as 10 7 squamous carcinoma cells (4 mm tumor). Since only a small proportion of the transfected cell‐population was expected to have incorporated genes specifying antigens associated with the squamous carcinoma cells (TAA), we devised a novel approach to enrich the vaccine for cells that induce immunity to the SCC. Aliquots of the transfected population were divided into 10 small pools (initial inoculums = 1 × 10 3 ). We reasoned that if the starting inoculums were sufficiently small, then the distribution of highly immunogenic and weakly immunogenic cells in each pool would not be the same. Cells from individual pools were allowed to increase in number. A portion of the expanded cell populations were maintained frozen/viable for later recovery. The remaining portions were used to immunize naïve DBA/2 mice. Pools containing greater numbers of immunogenic cells were identified by 2 independent assays. Frozen aliquots of cells from the pool that stimulated immunity to the squamous carcinoma to the greatest extent were recovered and subdivided for additional rounds of immune selection. Enhanced immunity to squamous carcinoma mediated by CD8+ T cells was induced in tumor‐bearing mice treated solely by immunization with the enriched cell‐population. © 2006 Wiley‐Liss, Inc.