Skip to content
2000
Volume 1, Issue 3
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

Peptide based vaccine design for cancer immunotherapy is currently being used in clinical trials for malignant melanoma with much success. Administration of synthetic peptides derived from proteins overexpressed in tumour cells (tumour-associated antigens) can elicit tumour-specific CD8+ T cell responses in vitro and in vivo. Currently, a number of tumour antigens from overexpressed cancer proteins such as mucin 1 (MUC1), survivin, carcinoembryonic antigen (CEA), telomerase reverse transcriptase (TERT) and HER- 2 / neu are examples of cancers whereby peptide based vaccinations are being tested for potential immunotherapy. In this review, we discuss some examples of the work being investigated with these cancer proteins, limitations to this therapy and suggestions of future directions to improve the efficacy of this treatment.

Loading

Article metrics loading...

/content/journals/lddd/10.2174/1570180043398894
2004-07-01
2025-09-29
Loading full text...

Full text loading...

/content/journals/lddd/10.2174/1570180043398894
Loading

  • Article Type:
    Review Article
Keyword(s): cancer immunotherapy; cytotoxic t cells; muc1; peptide; tumour associated antigens
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test