Residual MHC class II expression on mature dendritic cells and activated B cells in RFX5-deficient mice

被引:59
|
作者
Clausen, BE
Waldburger, JM
Schwenk, F
Barras, E
Mach, B
Rajewsky, K
Förster, I
Reith, W
机构
[1] Univ Cologne, Inst Genet, D-50931 Cologne, Germany
[2] Univ Geneva, Sch Med, Louis Jeantet Lab Mol Genet, Dept Genet & Microbiol, CH-1211 Geneva 4, Switzerland
关键词
D O I
10.1016/S1074-7613(00)80467-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients with major histocompatibility complex class II (MHC-II) deficiency are known to carry mutations in either the RFX complex or the trans-activator CIITA. While the pivotal role of CIITA for MHC-II gene transcription is supported by the essential absence of MHC-II molecules in CIITA-deficient mice, we demonstrate here that RFX5(-/-) mice retain expression of MHC-II in thymic medulla, mature dendritic cells, and activated B cells. Nevertheless, RFX5(-/-) mice develop a severe immunodeficiency due to the lack of MHC-II in thymic cortex, failure of positive selection of CD4(+) T cells, and absence of MHC-II on resting B cells and resident or IFN gamma-activated macrophages. This differential requirement for CIITA and RFX5 in subsets of antigen-presenting cells may be specific for the mouse; it may, however, also exist in humans without having been noticed so far.
引用
收藏
页码:143 / 155
页数:13
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