PT  - JOURNAL ARTICLE
AU  - Lendvai, Nikoletta
AU  - Gnjatic, Sacha
AU  - Ritter, Erika
AU  - Mangone, Michael
AU  - Austin, Wayne
AU  - Reyner, Karina
AU  - Jayabalan, David
AU  - Niesvizky, Ruben
AU  - Jagannath, Sundar
AU  - Bhardwaj, Nina
AU  - Chen-Kiang, Selina
AU  - Old, Lloyd J.
AU  - Cho, Hearn Jay
TI  - Cellular immune responses against CT7 (MAGE-C1) and humoral responses against other cancer-testis antigens in multiple myeloma patients
DP  - 2010 Jan 01
TA  - Cancer Immunity Archive
PG  - 4
VI  - 10
IP  - 1
4099  - http://cancerimmunolres.aacrjournals.org/content/10/1/4.short
4100  - http://cancerimmunolres.aacrjournals.org/content/10/1/4.full
SO  - Cancer Immun2010 Jan 01; 10
AB  - The type I melanoma antigen gene (MAGE) proteins CT7 (MAGE-C1) and MAGE-A3 are commonly expressed in multiple myeloma (MM), and their expression correlates with increased plasma cell proliferation and poor clinical outcome. They belong to the cancer-testis antigen (CTAg) group of tumor-associated proteins, some of which elicit spontaneous immune responses in cancer patients. CT7 and MAGE-A3 are promising antigenic targets for therapeutic tumor vaccines in myeloma; therefore, it is critical to determine if they are immunogenic in MM patients. We analyzed cellular and humoral immune responses against CTAgs in patients with plasma cell dyscrasias: MM, monoclonal gammopathy of undetermined significance (MGUS), and Waldenström's macroglobulinemia (WM). Bone marrow lymphocytes from two of four untreated MM patients exhibited CT7-specific cellular immune responses as measured by an autologous cellular immunity assay, the first such immune response to CT7 to be reported in cancer patients. Sera from 24 patients were screened by ELISA for humoral immune responses to CTAgs. Two patients with MM demonstrated positive titers, one for MAGE-A1 and the other for SSX1. These data demonstrate that CTAgs, particularly CT7, are immunogenic in MM patients and merit further exploration as targets of immunological therapy in MM.This article was published in Cancer Immunity, a Cancer Research Institute journal that ceased publication in 2013 and is now provided online in association with Cancer Immunology Research.