Cumano A, Rajewsky K
EMBO J. 1986 Oct;5(10):2459-68. doi: 10.1002/j.1460-2075.1986.tb04522.x.
The nucleotide sequences of the variable regions of lambda 1 chain bearing anti-NP antibodies from the secondary response of C57BL/6 mice were determined. The data indicate that the V186.2 VH gene which dominates the primary anti-NP response is expressed in nine out of 10 secondary response antibodies and is extensively mutated. In the V lambda 1 regions somatic mutations are less frequent. While point mutations predominate, there is suggestive evidence for two conversion events, one involving a one-codon deletion. Most, but not all, secondary response antibodies have a higher affinity (up to 10-fold) for the hapten than is seen in the primary response. The increase in affinity correlates with 'parallel' mutations in CDRs of H and L chains, likely to play a role in hapten binding. The analysis of VDJH rearrangements demonstrates that the secondary response lambda 1 chain-bearing antibodies are produced by a diverse set of B cell clones, which are only rarely expressed in primary responses. These clones are characterized by N-sequence-mediated heterogeneity in the 3' half of CDR3, where the germ line sequence of the D element DFl16.1 predominates in primary response antibodies. The antibodies analyzed in this and in previous work were isolated from idiotypically suppressed mice in order to evaluate whether, intraclonally, idiotype suppression selects antibody mutants into the memory pool, through suppression of the wild-type. A selection of this type was not detectable. However, idiotype suppression may control the pattern of clonotypes expressed in the primary versus the secondary response.
测定了C57BL/6小鼠二次免疫应答中携带抗NP抗体的λ1链可变区的核苷酸序列。数据表明,在初次抗NP应答中占主导地位的V186.2 VH基因在10种二次免疫应答抗体中的9种中表达,并且发生了广泛的突变。在Vλ1区域,体细胞突变较少见。虽然点突变占主导,但有证据暗示存在两次转换事件,其中一次涉及一个密码子的缺失。大多数(但不是全部)二次免疫应答抗体对半抗原的亲和力比初次免疫应答中的抗体高(高达10倍)。亲和力的增加与重链和轻链互补决定区(CDR)中的“平行”突变相关,这些突变可能在半抗原结合中起作用。对VDJH重排的分析表明,二次免疫应答中携带λ1链的抗体由多种B细胞克隆产生,这些克隆在初次免疫应答中很少表达。这些克隆的特征是CDR3 3'端由N序列介导的异质性,其中D元件DFl16.1的种系序列在初次免疫应答抗体中占主导。在本研究及之前的研究中分析的抗体是从独特型抑制的小鼠中分离出来的,以评估在克隆内独特型抑制是否通过抑制野生型将抗体突变体选择进入记忆库。未检测到这种类型的选择。然而,独特型抑制可能控制初次免疫应答与二次免疫应答中表达克隆型的模式。