Serum and ascites neutralizing antibodies in ovarian cancer patients treated with intraperitoneal adenoviral gene therapy

被引:41
作者
Hemminki, A
Wang, MH
Desmond, RA
Strong, TV
Alvarez, RD
Curiel, DT
机构
[1] Univ Alabama, Div Human Gene Therapy, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama, Div Human Gene Therapy, Dept Pathol, Birmingham, AL 35294 USA
[3] Univ Alabama, Div Human Gene Therapy, Dept Surg, Birmingham, AL 35294 USA
[4] Univ Alabama, Gene Therapy Ctr, Birmingham, AL 35294 USA
[5] Univ Alabama, Dept Biomed Engn, Birmingham, AL 35294 USA
[6] Univ Alabama, Ctr Comprehens Canc, Biostat Unit, Birmingham, AL 35294 USA
[7] Univ Alabama, Dept Med, Div Hematol Oncol, Birmingham, AL 35294 USA
[8] Univ Alabama, Dept Obstet & Gynecol, Birmingham, AL 35294 USA
关键词
D O I
10.1089/10430340260185139
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Neutralizing antibodies (NAbs) can inhibit gene transfer by adenovirus in preclinical models, but this has not been confirmed in human trials, which have mostly utilized local delivery. Heretofore, it has not been studied whether intraperitoneal administration of adenovirus to ovarian cancer patients results in induction of NAbs in ascites or serum. Also, it is not known how ascites and serum NAbs correlate, or if preexisting ascites NAbs block gene transfer in humans. Before treatment, 33% of patients had an NAb titer of >1000. Good correlation existed between serum and ascites NAb titers before (p = 0.0003) and after (p = 0.0008) treatment, and serum and ascites NAb titers were rapidly induced after treatment. Transgene expression was affected but not prevented by preexisting NAbs. Total anti-adenoviral antibodies did not correlate well with NAbs and the administered dose did not affect the level of NAb induction. Although serum and ascites NAbs correlated well, serum total protein concentration was over 4-fold higher, suggesting selective accumulation of proteins in ascites. These results imply that serum NAbs can be used as a surrogate for ovarian cancer-associated ascites NAbs. Also, although NAbs did not prevent gene transfer, it could be useful to attempt removal of ascites before intraperitoneal adenoviral therapy.
引用
收藏
页码:1505 / 1514
页数:10
相关论文
共 30 条
[1]  
Alvarez RD, 2000, CLIN CANCER RES, V6, P3081
[2]   Adenoviral-mediated suicide gene therapy for ovarian cancer [J].
Alvarez, RD ;
Gomez-Navarro, J ;
Wang, MH ;
Barnes, MN ;
Strong, TV ;
Arani, RB ;
Arafat, W ;
Hughes, JV ;
Siegal, GP ;
Curiel, DT .
MOLECULAR THERAPY, 2000, 2 (05) :524-530
[3]   Using a tropism-modified adenoviral vector to circumvent inhibitory factors in ascites fluid [J].
Blackwell, JL ;
Li, H ;
Gomez-Navarro, J ;
Dmitriev, I ;
Krasnykh, V ;
Richter, CA ;
Shaw, DR ;
Alvarez, RD ;
Curiel, DT ;
Strong, TV .
HUMAN GENE THERAPY, 2000, 11 (12) :1657-1669
[4]  
BULLER RE, 2001, P AN M AM SOC CLIN, V20, pA262
[5]   Pre-existent adenovirus antibody inhibits systemic toxicity and antitumor activity of CN706 in the nude mouse LNCaP xenograft model: Implications and proposals for human therapy [J].
Chen, Y ;
Yu, DC ;
Charlton, D ;
Henderson, DR .
HUMAN GENE THERAPY, 2000, 11 (11) :1553-1567
[6]   Stealth adenoviruses blunt cell-mediated and humoral immune responses against the virus and allow for significant gene expression upon readministration in the lung [J].
Croyle, MA ;
Chirmule, N ;
Zhang, Y ;
Wilson, JM .
JOURNAL OF VIROLOGY, 2001, 75 (10) :4792-4801
[7]  
DeWeese TL, 2001, CANCER RES, V61, P7464
[8]  
Gahéry-Ségard H, 1998, J VIROL, V72, P2388
[9]   Phase I trial of recombinant adenovirus gene transfer in lung cancer - Longitudinal study of the immune responses to transgene and viral products [J].
GaherySegard, H ;
MolinierFrenkel, V ;
LeBoulaire, C ;
Saulnier, P ;
Opolon, P ;
Lengagne, R ;
Gautier, E ;
LeCesne, A ;
Zitvogel, L ;
Venet, A ;
Schatz, C ;
Courtney, M ;
LeChevalier, T ;
Tursz, T ;
Guillet, JG ;
Farace, F .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (09) :2218-2226
[10]  
Ganly I, 2000, CLIN CANCER RES, V6, P798