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. Author manuscript; available in PMC: 2013 Jul 24.
Published in final edited form as: J Allergy Clin Immunol. 2010 Jan 12;125(2 0 2):S272–S283. doi: 10.1016/j.jaci.2009.09.045

TABLE I.

Human TAs that are candidates for immune therapies*

TA category Examples
Oncofetal Oncofetal antigen/immature laminin receptor (OFA/iLRP)
Glypican 3 (heparan sulfate protoglycan)
α-Fetoprotein (AFP)
Carcinoembryonic antigen (CEA)
Oncogenes The RAS family: p53, Her2 neu
Cancer testis (CT) antigens: MAGE-1
 BAGE
 GAGE
 NY-ESO-1/LAGE
 SAGE
 Other 35–40 CT antigens mapping to chromosome X (CT-X) or distributed throughout the genome (non-X CT)
Human melanoma antigens MART-1/MELAN-A
 Gp100/pmel 17
 Tyrosinase
 Tyrosinase related proteins (TRP) 1 and 2
 Chondroitin sulfate proteoglycan (CSPG4)
Human glioma antigens IL-13 receptor α2
 Eph A2
 Survivin
 EGFR variant III (EGFRvIII)
Head and neck cancer antigens EGFR
 Human papilloma virus (HPV 16 or 18)
 Aldehyde dehydrogenase A1 (ALDHA1)
 CSPG4
Normal overexpressed or modified antigens MUC-1
 Cyclin-B1
 Prostate-specific antigen (pSA)
 Prostate membrane-specific Ag (PMSA)
*

The actual list of TAs available for immune therapies is much longer. The reader is referred to a more comprehensive recent listing of these antigens.36,37