Affinity maturation without germinal centres in lymphotoxin-alpha-deficient mice

被引:286
作者
Matsumoto, M
Lo, SF
Carruthers, CJL
Min, JJ
Mariathasan, S
Huang, GM
Plas, DR
Martin, SM
Geha, RS
Nahm, MH
Chaplin, DD
机构
[1] WASHINGTON UNIV,SCH MED,CTR IMMUNOL,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT INTERNAL MED,ST LOUIS,MO 63110
[3] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63110
[4] WASHINGTON UNIV,SCH MED,HOWARD HUGHES MED INST,ST LOUIS,MO 63110
[5] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02138
关键词
D O I
10.1038/382462a0
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
AFFINITY maturation by somatic hypermutation is thought to occur within germinal centres(1-4). Mice deficient in lymphotoxin-alpha (LT alpha(-/-) mice) have no lymph nodes or Peyer's patches(5,6), and fail to form germinal centres in the spleen(7). We tested whether germinal centres are essential for maturation of antibody responses to T-cell-dependent antigens. LT alpha(-/-) mice immunized with low doses of (4-hydroxy-3-nitrophenyl)acetyl-ovalbumin (NP-OVA) showed dramatically impaired production of high-affinity anti-NP IgG1. However, LT alpha(-/-) mice immunized with high doses of NP-OVA, even though they failed to produce germinal centres, manifested a high-affinity anti-NP IgG1 response similar to wild-type mice. Furthermore, when LT alpha(-/-) mice were multiply immunized with high doses of NP-OVA, the predominantly expressed anti-NP Vu gene segment VH186.2 showed somatic mutations typical of affinity maturation(8). Thus, B-cell memory and affinity maturation are not absolutely dependent on the presence of germinal centres.
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页码:462 / 466
页数:5
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