Selective destruction by formaldehyde fixation of an H-2Kb serological determinant involving lysine 89 without loss of T-cell reactivity
Selective destruction by formaldehyde fixation of an H-2Kb serological determinant involving lysine 89 without loss of T-cell reactivity
复制标题
通过甲醛固定选择性破坏涉及赖氨酸 89 的 H-2Kb 血清学决定簇,且不损失 T 细胞反应性
DOI:
10.1007/bf00375375
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发表时间:
2004
期刊:
影响因子:
3.2
通讯作者:
A. Schmitt
中科院分区:
文献类型:
--
作者:
C. Hua;C. Langlet;M. Buferne;A. Schmitt
In preparation for functional analyses, a study of the binding of H-2Kb-specific monoclonal antibodies (mAb) to formaldehyde (FOR)-fixed H-2b spleen or tumor cells revealed that three of nine mAb tested had lost reactivity with the FOR-fixed cells, whereas the reactivity of the other mAb generally did not diminish. Comparison of the reactivity of these mAb on untreated H-2Kbm mutant cells and on FOR-treated H-2Kb cells suggests that for three mAb the total loss of reactivity on the latter could be a consequence of the alteration by FOR of lysine 89, which is substituted by alanine in mutant bm3. H-2KPb-specific alloreactive polyclonal or monoclonal CTL, all of which had retained reactivity with bm3 target cells, had also retained reactivity with FOR-fixed H-2b cells as indicated by cold target inhibition studies. The H-2Kb-specific CTL were probably reactive with “conformational” determinants of H-2Kb, which are dependent on the integrity of both the α1 and the α2 domains of the H-2Kb molecule. Results are compatible with FOR treatment selectively affecting a serological determinant in the α1 domain without affecting conformational-type CTL determinants.