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PMID: 8376942 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Heat shock protein 70-associated peptides elicit specific cancer immunity.

The Journal of experimental medicine ·Vol. 178 ·No. 4 ·1993-10-01 ·Pages 1391-6

Udono H, Srivastava PK

Abstract

Vaccination of mice with heat shock protein 70 (hsp70) preparations derived from the Meth A sarcoma, but not from normal tissues, renders the mice immune to a substantial challenge with Meth A sarcoma. The immunogenicity is dose dependent and tumor specific. Treatment of an antigenically active hsp70 preparation with ATP followed by removal of low-molecular weight material leaves hsp70 intact, as judged by SDS-PAGE but results in loss of antigenicity, as judged by tumor rejection assays. Separation of this low-molecular weight material on a C18 reverse-phase column shows a diverse array of peptides with molecular mass between 1,000 and 5,000 daltons. Our data indicate that antigenicity of hsp70 preparations derives, not from hsp70 per se, but from associated peptides. These observations may suggest a novel method of using the peptide-binding property of hsp70 for specific vaccination against cancer and infectious diseases.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Female Heat-Shock Proteins/immunology Methylcholanthrene Mice Mice, Inbred BALB C Neoplasm Transplantation Peptides/immunology Sarcoma, Experimental/chemically induced,immunology
Chemicals
Heat-Shock Proteins Peptides Methylcholanthrene Adenosine Triphosphate
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Udono H
Department of Pharmacology, Mount Sinai School of Medicine, New York, New York 10029.
Srivastava P K
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1993-10-01
Pages
1391-6
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2191193
Subset
IM
Grants
NCI NIH HHS · CA-44786 · United States
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