S. Janetzki et al., Immunization of cancer patients with autologous cancer-derived heat shock protein gp96 preparations: A pilot study, INT J CANC, 88(2), 2000, pp. 232-238
Heat shock protein (HSP)-peptide complexes isolated from murine cancers eli
cit protective immunity and T lymphocytes specific for the cancer from whic
h the HSPs are isolated. A pilot study was designed to test the feasibility
, immunogenicity and toxicity of such treatment in cancer patients. Sixteen
patients with assorted advanced malignancies, which had become refractory
to established therapies, were recruited. The gp96 vaccine was prepared for
each patient from tumor obtained from that patient, Anti-tumor immune resp
onses were evaluated using Elispot assays of T cells in peripheral blood af
ter minimal in vitro stimulation, No unacceptable vaccine-related toxicitie
s or auto-immune reactions were observed, Immunization with autologous gp96
elicited MHC I-restricted, tumor-specific CD8(+) T lymphocytes in 6/12 pat
ients immunized, In addition, expansion of the NK cell population was seen
in 8/13 of patients immunized. These observations are entirely consistent w
ith the murine experience and form a firm basis for future trials with clin
ical end points, using autologous, patient-specific HSP-peptide vaccines. I
nt, J. Cancer 88:232-238, 2000, (C) 2000 Wiley-Liss, Inc.