AUTOLOGOUS, ORTHOTOPIC THYROID FOLLICULAR CELL TRANSPLANTATION - A SURGICAL COMPONENT OF EXVIVO SOMATIC GENE-THERAPY

被引:13
作者
OMALLEY, BW
FINEGOLD, MJ
LEDLEY, FD
机构
[1] BAYLOR COLL MED,HOWARD HUGHES MED INST,DEPT CELL BIOL,1 BAYLOR PLAZA,HOUSTON,TX 77030
[2] BAYLOR COLL MED,HOWARD HUGHES MED INST,DEPT PATHOL,HOUSTON,TX 77030
[3] BAYLOR COLL MED,HOWARD HUGHES MED INST,DEPT OTORHINOLARYNGOL & COMMUNICAT SCI,HOUSTON,TX 77030
[4] BAYLOR COLL MED,HOWARD HUGHES MED INST,DEPT PEDIAT,HOUSTON,TX 77030
关键词
D O I
10.1177/019459989310800107
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Ex vivo strategies for somatic gene therapy involve the harvest of primary cells from patients, the transfer of novel genetic material into these cells in cell culture, and reimplantation of the genetically engineered cells back into patients. In consideration of methods for targeting somatic gene therapy to the thyroid, we have studied the autologous, orthotopic transplantation of thyroid follicular cells in a canine model. Using the fluorescent dye Dil, we were able to stain follicular cells in vitro before transplantation and then follow the pattern of engraftment through histologic sectioning and microscopy up to 14 days after transplantation. The transplantations involved the direct injection of intact and disrupted follicles into a remaining thyroid lobe after cell harvest from the contralateral lobe. We also demonstrated engraftment of individual follicular cells recovered from primary monolayer cultures. Histologic studies revealed the presence of transplanted cells and follicles as well as focal regions of granulomatous reaction in close relation to the engrafted material. These studies demonstrate the feasibility of autologous, orthotopic transplantation of thyroid follicular cells. This method is an essential component of ex vivo strategies for targeting somatic gene therapy to the thyroid gland.
引用
收藏
页码:51 / 62
页数:12
相关论文
共 29 条
[1]   PROSPECTS FOR HUMAN-GENE THERAPY [J].
ANDERSON, WF .
SCIENCE, 1984, 226 (4673) :401-409
[2]  
ASHER AL, 1991, J IMMUNOL, V146, P3227
[3]   SYSTEMIC DELIVERY OF RECOMBINANT PROTEINS BY GENETICALLY MODIFIED MYOBLASTS [J].
BARR, E ;
LEIDEN, JM .
SCIENCE, 1991, 254 (5037) :1507-1509
[4]  
BARTHELD CS, 1990, J HISTOCHEM CYTOCHEM, V38, P725
[5]   RECONSTRUCTION OF A THYROID-GLAND EQUIVALENT FROM CELLS AND MATRIX MATERIALS [J].
BELL, E ;
MOORE, H ;
MITCHIE, C ;
SHER, S ;
COON, H .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1984, 232 (02) :277-285
[6]   LYMPHOCYTE GENE-THERAPY [J].
CULVER, KW ;
ANDERSON, WF ;
BLAESE, RM .
HUMAN GENE THERAPY, 1991, 2 (02) :107-109
[7]   PROGRESS TOWARD HUMAN-GENE THERAPY [J].
FRIEDMANN, T .
SCIENCE, 1989, 244 (4910) :1275-1281
[8]  
FRIEDMANN T, 1983, GENE THERAPY FACT FI
[9]   DIL AND DIO - VERSATILE FLUORESCENT DYES FOR NEURONAL LABELING AND PATHWAY TRACING [J].
HONIG, MG ;
HUME, RI .
TRENDS IN NEUROSCIENCES, 1989, 12 (09) :333-&
[10]  
HONIG MG, 1989, TRENDS NEUROSCI, V12, P336