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A. S. Evans
Researcher at University of Wales
Publications - 12
Citations - 1430
A. S. Evans is an academic researcher from University of Wales. The author has contributed to research in topics: Immunotherapy & Cytotoxic T cell. The author has an hindex of 10, co-authored 12 publications receiving 1397 citations. Previous affiliations of A. S. Evans include University Hospital of Wales.
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Journal ArticleDOI
A recombinant vaccinia virus encoding human papillomavirus types 16 and 18, E6 and E7 proteins as immunotherapy for cervical cancer
L. K. Borysiewicz,Alison Nina Fiander,M. Nimako,Stephen Man,Gavin William Grahame Wilkinson,D. Westmoreland,A. S. Evans,Malcolm Adams,Simon N. Stacey,Mike Boursnell,E. Rutherford,Julian Hickling,Stephen Charles Inglis +12 more
TL;DR: Examination of the clinical and environmental safety and immunogenicity in the first clinical trial of a live recombinant vaccinia virus expressing the E6 and E7 proteins of HPV 16 and 18 found vaccination resulted in no significant clinical side-effects and there was no environmental contamination by live TA-HPV.
Journal Article
Infiltration of Cervical Cancer Tissue with Human Papillomavirus-specific Cytotoxic T-Lymphocytes
TL;DR: In this paper, the authors identified HLA-A*0201-restricted peptide-specific CTLs in the peripheral blood (four of five patients), draining lymph nodes (three of four patients) and tumors (one of three patients) of cervical cancer patients.
Journal ArticleDOI
Infiltration of cervical cancer tissue with human papilloma virus-specific cytotoxic T-lymphocytes
TL;DR: This is the first demonstration that virus-specific CTLs infiltrate the virus-associated tumor, where they may play an important role in restricting disease progression.
Journal ArticleDOI
Clinical studies of human papilloma vaccines in pre-invasive and invasive cancer.
Malcolm Adams,Leszek K. Borysiewicz,Alison Nina Fiander,Stephen Man,Bharat Jasani,Hossein Navabi,C. Lipetz,A. S. Evans,Malcolm David Mason +8 more
TL;DR: It appears therefore feasible to induce HPV specific CTL responses in patients with cervical cancer using several vaccine strategies, however, further clinical trials are needed to determine the full anti-tumour potential of this vaccine based immunotherapy.
Journal ArticleDOI
Antigen Processing Defects in Cervical Carcinomas Limit the Presentation of a CTL Epitope from Human Papillomavirus 16 E6
Mererid Evans,Leszek K. Borysiewicz,A. S. Evans,Martin Rowe,Matthew Jones,Uzi Gileadi,Vincenzo Cerundolo,Stephen Man +7 more
TL;DR: Presentation of the HPV16 E629–38 epitope in cervical carcinoma cell lines is limited both by the level of TAP expression and by the low level or availability of the source HPV E6 oncoprotein, which place constraints on the use of this, and potentially other, HPV-derived CTL epitopes for the immunotherapy of cervical cancer.