Tumor-specific, cytotoxic T-lymphocyte response after idiotype vaccination for B-cell, non-Hodgkin's lymphoma

被引:105
作者
Nelson, EL
Li, XB
Hsu, FJ
Kwak, LW
Levy, R
Clayberger, C
Krensky, AM
机构
[1] NCI, CLIN RES BRANCH, FREDERICK, MD 21701 USA
[2] STANFORD UNIV, SCH MED, DEPT MED, DIV ONCOL, STANFORD, CA 94305 USA
[3] STANFORD UNIV, SCH MED, DEPT CARDIOTHORAC SURG, STANFORD, CA 94305 USA
[4] STANFORD UNIV, SCH MED, DEPT PEDIAT, DIV IMMUNOL & TRANSPLANTAT BIOL, STANFORD, CA 94305 USA
[5] NCI, CLIN RES BRANCH, FREDERICK, MD 21701 USA
关键词
D O I
10.1182/blood.V88.2.580.bloodjournal882580
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with non-Hodgkin's B-cell lymphoma who received an antitumor vaccine lg idiotypic lg protein showed humoral and proliferative immune responses. Because immunity to some antigens, including tumor antigens and human pathogenic viruses, may be better correlated with the cytolytic cellular immune response, we evaluated 16 non-Hodgkin's lymphoma patients immunized with autologous idiotypic lg molecules for changes in tumor-specific cytotoxic T-lymphocyte precursor (CTLp) frequency using limiting dilution analysis. Eleven patients had a significant increase in tumor-specific CTLp, Eight of these 11 patients remain without evidence of disease or with stable minimal disease, In contrast, all five patients who did not have a significant change in tumor-specific CTLp have developed progressive disease, Patient vaccination with tumor-associated protein antigens can increase tumor-specific CTLp frequencies. The correlation of increased tumor-specific CTLp with freedom from progression is significant at P = .002, This study indicates that measurement of CTLp frequencies are relevant to the clinical evaluation of human tumor vaccines and suggests that cell-mediated cytolytic immune responses may be an important determinant of vaccine efficacy. (C) 1996 by The American Society of Hematology.
引用
收藏
页码:580 / 589
页数:10
相关论文
共 87 条
[1]   CELL-MEDIATED-IMMUNITY TO VARICELLA-ZOSTER VIRUS [J].
ARVIN, AM .
JOURNAL OF INFECTIOUS DISEASES, 1992, 166 :S35-S41
[2]  
BARTH A, 1994, CANCER RES, V54, P3342
[3]  
Bender B S, 1992, Semin Respir Infect, V7, P38
[4]  
BUKOWSKI JF, 1994, J IMMUNOL, V153, P5133
[5]  
BYSTRYN JC, 1993, ANN NY ACAD SCI, V690, P190
[6]  
Campbell M J, 1989, Int Rev Immunol, V4, P251, DOI 10.3109/08830188909044782
[7]   RECOGNITION OF AN IMMUNOGLOBULIN V(H) EPITOPE BY INFLUENZA VIRUS-SPECIFIC CLASS-I MAJOR HISTOCOMPATIBILITY COMPLEX-RESTRICTED CYTOLYTIC T-LYMPHOCYTES [J].
CAO, WX ;
MYERSPOWELL, BA ;
BRACIALE, TJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (01) :195-202
[8]  
CARBONE PP, 1971, CANCER RES, V31, P1860
[9]   MOUSE X HUMAN HETEROHYBRIDOMAS AS FUSION PARTNERS WITH HUMAN B-CELL TUMORS [J].
CARROLL, WL ;
THIELEMANS, K ;
DILLEY, J ;
LEVY, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 89 (01) :61-72
[10]   IDENTIFICATION OF POTENTIAL CTL EPITOPES OF TUMOR-ASSOCIATED ANTIGEN MAGE-1 FOR 5 COMMON HLA-A ALLELES [J].
CELIS, E ;
FIKES, J ;
WENTWORTH, P ;
SIDNEY, J ;
SOUTHWOOD, S ;
MAEWAL, A ;
DELGUERCIO, MF ;
SETTE, A ;
LIVINGSTON, B .
MOLECULAR IMMUNOLOGY, 1994, 31 (18) :1423-1430