U. Sahin et al., HUMAN NEOPLASMS ELICIT MULTIPLE SPECIFIC IMMUNE-RESPONSES IN THE AUTOLOGOUS HOST, Proceedings of the National Academy of Sciences of the United Statesof America, 92(25), 1995, pp. 11810-11813
Expression of cDNA libraries from human melanoma, renal cancer, astroc
ytoma, and Hodgkin disease in Escherichia coli and screening for clone
s reactive with high-titer IgG antibodies in autologous patient serum
lead to the discovery of at least four antigens with a restricted expr
ession pattern in each tumor, Besides antigens known to elicit T-cell
responses, such as MAGE-1 and tyrosinase, numerous additional antigens
that were overexpressed or specifically expressed in tumors of the sa
me type were identified, Sequence analyses suggest that many of these
molecules, besides being the target of a specific immune response, mig
ht be of relevance for tumor growth, Antibodies to a given antigen wer
e usually confined to patients with the same tumor type. The unexpecte
d frequency of human tumor antigens, which can be readily defined at t
he molecular level by the serological analysis of autologous tumor cDN
A expression cloning, indicates that human neoplasms elicit multiple s
pecific immune responses in the autologous host and provides diagnosti
c and therapeutic approaches to human cancer.