Cellular immune responses against CT7 (MAGE-C1) and humoral responses against other cancer-testis antigens in multiple myeloma patients.

TitleCellular immune responses against CT7 (MAGE-C1) and humoral responses against other cancer-testis antigens in multiple myeloma patients.
Publication TypeJournal Article
Year of Publication2010
AuthorsLendvai N, Gnjatic S, Ritter E, Mangone M, Austin W, Reyner K, Jayabalan D, Niesvizky R, Jagannath S, Bhardwaj N, Chen-Kiang S, Old LJ, Cho HJay
JournalCancer Immun
Volume10
Pagination4
Date Published2010 Jan 29
ISSN1424-9634
KeywordsAged, Antigens, Neoplasm, Cell Separation, Enzyme-Linked Immunosorbent Assay, Female, Flow Cytometry, Fluorescent Antibody Technique, Humans, Immunity, Cellular, Immunity, Humoral, Male, Middle Aged, Multiple Myeloma, Neoplasm Proteins, Reverse Transcriptase Polymerase Chain Reaction
Abstract

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.

Alternate JournalCancer Immun
PubMed ID20108890
PubMed Central IDPMC2926649
Grant ListK01 CA115917 / CA / NCI NIH HHS / United States
K01 CA115917-04 / CA / NCI NIH HHS / United States
NCI K01-CA115917 / CA / NCI NIH HHS / United States
Related Faculty: 
Selina Chen-Kiang, Ph.D.

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