MICE LACKING MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I AND CLASS-II MOLECULES

被引:232
作者
GRUSBY, MJ
AUCHINCLOSS, H
LEE, R
JOHNSON, RS
SPENCER, JP
ZIJLSTRA, M
JAENISCH, R
PAPAIOANNOU, VE
GLIMCHER, LH
机构
[1] HARVARD UNIV,SCH PUBL HLTH,DEPT CANC BIOL,BOSTON,MA 02115
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02115
[3] MASSACHUSETTS GEN HOSP,SURG SERV,TRANSPLANTAT UNIT,BOSTON,MA 02114
[4] MASSACHUSETTS GEN HOSP,DEPT SURG & PATHOL,BOSTON,MA 02114
[5] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,BOSTON,MA 02115
[6] HARVARD UNIV,SCH MED,DEPT BIOL CHEM & MOLEC PHARMACOL,BOSTON,MA 02115
[7] TUFTS UNIV,SCH MED & VET MED,DEPT PATHOL,BOSTON,MA 02111
[8] MIT,DEPT BIOL,CAMBRIDGE,MA 02142
[9] MIT,WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142
关键词
D O I
10.1073/pnas.90.9.3913
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
Mice lacking major histocompatibility complex (MHC) antigens were generated by mating beta2-microglobulin-deficient, and therefore class I-deficient, animals with MHC class II-deficient animals. When housed under sterile conditions, the resulting MHC-deficient mice appear healthy, survive for many months, and breed successfully. Phenotypically, MHC-deficient mice are depleted of CD4+ and CD8+ T cells in peripheral lymphoid organs due to a lack of appropriate restricting elements. In contrast, the B-cell compartment of these animals appears intact, and MHC-deficient mice can mount specific antibody responses when challenged with a T-independent antigen. Spleen cells from MHC-deficient animals are poor stimulators and responders in a mixed lymphocyte reaction. Despite their relatively weak cellular immune responses in vitro, MHC-deficient mice reject allogeneic skin grafts with little delay, and grafts from MHC-deficient animals are rapidly rejected by normal allogeneic recipients. Taken together, these results emphasize the plasticity of the immune system and suggest that MHC-deficient mice may be useful for examining compensatory mechanisms in severely immunocompromised animals.
引用
收藏
页码:3913 / 3917
页数:5
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