Enhancing therapeutic HPV DNA vaccine potency through depletion of CD4+CD25+ T regulatory cells

被引:41
作者
Chuang, Chi-Mu [4 ,5 ]
Hoory, Talia
Monie, Archana
Wu, Annie
Wang, Mei-Cheng [3 ]
Hung, Chien-Fu [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Johns Hopkins Med Inst, Baltimore, MD 21231 USA
[2] Johns Hopkins Med Inst, Dept Oncol, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Dept Biostat, Baltimore, MD 21205 USA
[4] Taipei Vet Gen Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[5] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
关键词
PC61; Regulatory T cells (Tregs); DNA vaccine; Heat shock protein 70 (Hsp70); IMMUNE-RESPONSE; CANCER; SUPPRESSION; PEPTIDES; PROTEINS; TREGS; FOXP3; GENE;
D O I
10.1016/j.vaccine.2008.11.042
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Therapeutic human papillomavirus (HPV) vaccines targeting E6 and/or E7 antigens represent an opportunity to control HPV-associated lesions. We have previously generated several therapeutic DNA vaccines targeting HPV-16 E7 antigen and generated significant antitumor effects. Since regulatory T cells (Tregs) play an important role in suppressing immune responses against tumors by immunotherapy, such as DNA vaccines, we tested if the therapeutic effects of a DNA vaccine encoding E7 linked to heat shock protein 70 (Hsp70) can be improved by a strategy to deplete Tregs using a anti-CD25 monoclonal antibody (PC61) in vaccinated mice. We found that administration of PC61 prior to vaccination with E7/Hsp70 DNA was capable of generating higher levels of E7-specific CD8(+) T cells compared to the control antibody, leading to significantly improved therapeutic and long-term protective antitumor effects against an E7-expressing tumor, TC-1. Thus, a strategy to deplete CD4(+)CD25(+) Tregs in conjunction with therapeutic tumor antigen-specific DNA vaccine may represent a potentially promising approach to control tumor. The clinical implications of our study are discussed. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:684 / 689
页数:6
相关论文
共 37 条
[1]   Regulatory T cells under scrutiny [J].
Bach, JF .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (03) :189-198
[2]  
Chen CH, 2000, CANCER RES, V60, P1035
[3]   DNA-based immunization by in vivo transfection of dendritic cells [J].
Condon, C ;
Watkins, SC ;
Celluzzi, CM ;
Thompson, K ;
Falo, LD .
NATURE MEDICINE, 1996, 2 (10) :1122-1128
[4]   Specific recruitment of regulatory T cells in ovarian carcinoma fosters immune privilege and predicts reduced survival [J].
Curiel, TJ ;
Coukos, G ;
Zou, LH ;
Alvarez, X ;
Cheng, P ;
Mottram, P ;
Evdemon-Hogan, M ;
Conejo-Garcia, JR ;
Zhang, L ;
Burow, M ;
Zhu, Y ;
Wei, S ;
Kryczek, I ;
Daniel, B ;
Gordon, A ;
Myers, L ;
Lackner, A ;
Disis, ML ;
Knutson, KL ;
Chen, LP ;
Zou, WP .
NATURE MEDICINE, 2004, 10 (09) :942-949
[5]   Regulatory T-cell development: is Foxp3 the decider? [J].
Curiel, Tyler J. .
NATURE MEDICINE, 2007, 13 (03) :250-253
[6]   Tregs and rethinking cancer immunotherapy [J].
Curiel, Tyler J. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (05) :1167-1174
[7]  
Donnelly JJ, 1997, ANNU REV IMMUNOL, V15, P617, DOI [10.1146/annurev.immunol.15.1.617, 10.1016/S0024-3205(96)00502-4]
[8]   Mechanisms of immune evasion by tumors [J].
Drake, CG ;
Jaffee, E ;
Pardoll, DM .
ADVANCES IN IMMUNOLOGY, VOL 90: CANCER IMMUNOTHERAPY, 2006, 90 :51-81
[9]   The immunobiology of cancer immunosurveillance and immunoediting [J].
Dunn, GP ;
Old, LJ ;
Schreiber, RD .
IMMUNITY, 2004, 21 (02) :137-148
[10]   Sunitinib Reverses Type-1 Immune Suppression and Decreases T-Regulatory Cells in Renal Cell Carcinoma Patients [J].
Finke, James H. ;
Rini, Brian ;
Ireland, Joanna ;
Rayman, Patricia ;
Richmond, Amy ;
Golshayan, Ali ;
Wood, Laura ;
Elson, Paul ;
Garcia, Jorge ;
Dreicer, Robert ;
Bukowski, Ronald .
CLINICAL CANCER RESEARCH, 2008, 14 (20) :6674-6682