Heat shock proteins in cancer immunotherapy

Gann Monographs on Cancer Research

Volumn 48, Issue , 1999, Pages 201-209

  Udono, H ^a   Suto, R ^a   Tamura, Y ^a   Matsutake, T ^a   Srivastava, P K ^a  

^a NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CANCER VACCINE; HEAT SHOCK PROTEIN; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; TUMOR ANTIGEN;

ANIMAL CELL; ANIMAL MODEL; ANTIGEN PRESENTATION; CANCER IMMUNOTHERAPY; CYTOTOXIC T LYMPHOCYTE; IMMUNIZATION; MAJOR HISTOCOMPATIBILITY COMPLEX; MOUSE; NONHUMAN; PRIORITY JOURNAL; REVIEW; T LYMPHOCYTE; TUMOR GROWTH;

EID: 0033302920     PISSN: 00720151     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Review

References (25)

1. Cross-priming of minor histocompatibility antigen specific cytotoxic T cells upon immunization with the heatshock protein gp96
2. Influences of transporter associated with antigen processing (TAP) on the repertoire of peptides associated with the endoplasmic reticulum-resident stress protein gp96
3. Heat shock protein-peptide complexes, reconstituted in vitro, elicit peptide-specific cytotoxic T lymphocyte response and tumor immunity
4. Immunization with a lymphocytic choriomeningitis virus peptide mixed with heat shock protein 70 results in protective antiviral immunity and specific cytotoxic T lymphocytes
5. Generation of heat shock protein-based vaccines by intracellular loading of gp96 with antigenic peptides
6. Isolation of MHC class I-restricted tumor antigen peptide and its precursors associated with heat shock proteins hsp 70, hsp 90 and gp96
7. γδ T cell recognition of tumor Ig peptide
8. Expression levels of stress protein gp96 are not limiting for major histocompatibility complex class I-restricted antigen presentation
9. Protein disulfide isomerase is the dominant acceptor for peptides translocated into the endoplasmic reticulum
10. Novel peptide-binding proteins and peptide transport in normal and TAP-deficient microsomes
11. Heat shock protein 72 on tumor cells: A recognition structure for natural killer cells
12. Isolation of an immunodominant viral peptide that is endogenously bound to the stress protein GP96/GRP94
13. TAP-translocated peptides specifically bind proteins in the endoplasmic reticulum, including gp96, protein disulfide isomerase and calreticulin
14. Heat shock proteins in immune response to cancer: The Fourth Paradigm
15. Tumor rejection antigens of chemically induced tumors of inbred mice
16. Heat shock proteins transfer peptides during antigen processing and CTL priming
17. A mechanism for the specific immunogenicity of heat shock protein-chaperoned peptides
18. Heat shock fusion proteins as vehicles for antigen delivery into the major histocompatibility complex class I presentation pathway
19. Immunotherapy of tumors with autologous tumor-derived heat shock protein preparation
20. 70kDa heat shock cognate protein is a transformation associated antigen and a possible target for host's anti-tumor immunity
21. Cellular requirements for tumor-specific immunity elicited by heat shock proteins: Tumor rejection antigen gp96 primes CD8+ T cells in vivo
22. Comparison of tumor specific immunogenicities of stress induced proteins gp96, hsp90 and hsp70
23. Heat shock protein 70 associated peptides elicit specific cancer immunity
24. Identification of a unique antigen peptide pRL1 on BALB/c RL♂1 leukemia recognized by cytotoxic T lymphocytes and its relation to the Akt oncogene
25. A mouse tumor specific transplantation antigen is a heat shock related protein