The identification of tumor-associated antigens recognized by cellular or h
umoral effecters of the immune system has opened new perspectives for cance
r immunotherapy. Different categories of cancer-associated antigens have be
en described as targets for CD8+ T cells in vitro and in vivo: (1) 'cancer-
testis' (CT) antigens expressed in different tumors and normal testis; (2)
melanocyte differentiation antigens; (3) point mutations of normal genes; (
4) antigens that are overexpressed in malignant tissues, and (5) viral anti
gens. Clinical trials with antigenic peptides have been initiated to induce
specific immunological responses in vivo. Immunological and clinical param
eters for the assessment of peptide-specific reactions have been defined: D
TH, CD8+ T cell, autoimmune and tumor regression responses. Preliminary res
ults show that tumor-associated peptides alone elicit specific DTH and CD8 T cell responses associated with tumor regression after intradermal vaccin
ation. Granulocyte macrophage colony-stimulating factor has been shown to e
nhance peptide-specific immune reactions by amplification of dermal antigen
-presenting dendritic cells. Complete tumor regressions have been observed
after the induction of CD8+ T cell responses by peptide immunization. Based
on these results, active immunotherapy with tumor-associated antigens may
be a promising approach for patients in adjuvant treatment situations, who
are at high risk for tumor recurrence. Recently, a strategy utilizing spont
aneous antibody responses to tumor-associated antigens (SEREX) has led to t
he identification of a new CT antigen, NV-ESO-1. NY-ESO-1-specific spontane
ous humoral and cellular immune responses were found in approximately 50% o
f patients with NY-ESO-1-positive tumors. Clinical studies have been initia
ted to evaluate the immunological effects of immunization with NY-ESO-1 pep
tides in cancer patients with detectable or absent immunity against NY-ESO-
1. Copyright (C) 2001 S. Karger AG, Basel.