IMMUNIZATION OF HU-PBL-SCID MICE AND THE RESCUE OF HUMAN MONOCLONAL FAB FRAGMENTS THROUGH COMBINATORIAL LIBRARIES

被引:138
作者
DUCHOSAL, MA
EMING, SA
FISCHER, P
LETURCQ, D
BARBAS, CF
MCCONAHEY, PJ
CAOTHIEN, RH
THORNTON, GB
DIXON, FJ
BURTON, DR
机构
[1] SCRIPPS RES INST, DEPT MOLEC BIOL, LA JOLLA, CA 92037 USA
[2] RW JOHNSON PHARMACEUT RES INST, SAN DIEGO, CA 92121 USA
[3] UNIV SHEFFIELD, KREBS INST, DEPT MOLEC BIOL & BIOTECHNOL, SHEFFIELD S10 2TN, S YORKSHIRE, ENGLAND
关键词
D O I
10.1038/355258a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ANTIBODIES are usually prepared from recently boosted animals and reflect ongoing immune responses 1-6. In humans, this is restrictive as ethical constraints generally prevent antigen-boosting. Therefore the rich memory compartment of human antibody responses remains largely untapped 7. Severe combined immune deficiency (SCID) mice 8 populated with human cells 9-11 allow the stimulation of human antibody memory without the usual constraints. Here we show how peripheral blood lymphocytes can be stimulated by antigen to produce large secondary responses after transfer to SCID mice. Specific monoclonal human Fab fragments can then be isolated from the mice by repertoire cloning even when the human donor's last contact with antigen was more than 17 years ago.
引用
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页码:258 / 262
页数:5
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