Press J L, Giorgetti C A, Busby W F
Department of Biology and Rosenstiel Research Center, Brandeis University, Waltham, MA 02254-9110.
Mol Immunol. 1991 Nov;28(11):1217-24. doi: 10.1016/0161-5890(91)90008-8.
Our previous studies of the neonatal primary response to (T,G)-A--L showed that the majority of anti-(T,G)-A--L antibodies bind the copolymer L-Glu:L-Tyr (GT), share idiotypy (Id), and use the H10 germline VH gene from the VHJ558 family and a V kappa 1 gene. We also identified two hybridomas from different neonatal donors that produced GT+, Id+ antibodies using a V kappa 1 gene with a VH gene from the VH36-60 family. In the study reported here, we show that both neonatal hybridomas use the same germline VH gene from the VH36-60 gene family. However, the VH gene sequence is different from previously identified germline genes of the VH36-60 gene family. To determine whether the expressed heavy chain gene had undergone somatic mutation, we isolated the corresponding germline gene from kidney DNA. Sequence analysis of this gene shows that it is a new member of the VH36-60 family which is not mutated in the neonatal antibodies. Furthermore, the deduced amino acid sequences of the two neonatal antibodies are identical not only in the VH region but also in the VH-D-JH joins, suggesting that there is a strong selection for CDRIII among neonatal anti-(T,G)-A--L antibodies using this germline gene (designated here as VH3A1) with a V kappa 1 gene. Also, the VH gene from the VH36-60 family that we showed previously was used by an adult memory B cell clone specific for (T,G)-A--L, can now be identified as a rearrangement of the VH3A1 germline gene. Elucidation of the germline variable region genes that are used in the antigen-specific neonatal response will help us understand the mechanisms that shape the preimmune B cell repertoire during B cell development.
我们之前对新生儿对(T,G)-A--L的初次反应的研究表明,大多数抗(T,G)-A--L抗体结合共聚物L-Glu:L-Tyr(GT),具有独特型(Id),并使用来自VHJ558家族的H10胚系VH基因和一个Vκ1基因。我们还从不同的新生儿供体中鉴定出两个杂交瘤,它们使用来自VH36-60家族的VH基因和Vκ1基因产生GT +、Id +抗体。在本文报道的研究中,我们表明这两个新生儿杂交瘤都使用来自VH36-60基因家族的相同胚系VH基因。然而,VH基因序列与先前鉴定的VH36-60基因家族的胚系基因不同。为了确定表达的重链基因是否经历了体细胞突变,我们从肾脏DNA中分离出相应的胚系基因。该基因的序列分析表明它是VH36-60家族的一个新成员,在新生儿抗体中未发生突变。此外,两种新生儿抗体的推导氨基酸序列不仅在VH区域相同,而且在VH-D-JH连接处也相同,这表明在使用该胚系基因(此处指定为VH3A1)和Vκ1基因的新生儿抗(T,G)-A--L抗体中,CDRIII存在强烈的选择。此外,我们之前展示的来自VH36-60家族的VH基因被一个针对(T,G)-A--L的成人记忆B细胞克隆所使用,现在可以被鉴定为VH3A1胚系基因的重排。阐明在抗原特异性新生儿反应中使用的胚系可变区基因将有助于我们理解在B细胞发育过程中塑造免疫前B细胞库的机制。