Matossian-Rogers A, DeGiorgi L, Povey S
Immunogenetics. 1983;18(6):639-48. doi: 10.1007/BF00345971.
In this report we describe a new diallelic gene system, Arpa and Arpb, which codes for surface antigens on murine lymphocytes. Arpb is present only in a mutant strain of BALB/c which is designated BALB/c-Arpb. Normal BALB/c and all other strains of mice tested express Arpa. The Arpb mutation is associated with a newly discovered polymorphism of the Peptidase-7 enzyme, Pep-7b, which codes for a variant form of the enzyme with a faster anodal mobility on electrophoresis than the commonly known form. The Arp locus controls a range of alloimmune interactions between Arp incompatible lymphocytes. These include mixed lymphocyte reactivity, host-versus-graft and graft-versus-host reactions and the development of weak cytotoxic but strong cytostatic effector lymphocytes which are allo- as well as autoreactive. The association between Arp and Pep-7 and the biological significance of the Arp locus are discussed.
在本报告中,我们描述了一种新的双等位基因系统Arpa和Arpb,它们编码小鼠淋巴细胞表面抗原。Arpb仅存在于BALB/c的一个突变株中,该突变株被命名为BALB/c-Arpb。正常的BALB/c以及所有其他测试的小鼠品系都表达Arpa。Arpb突变与新发现的肽酶-7(Pep-7)酶的多态性有关,Pep-7b编码该酶的一种变体形式,在电泳中其阳极迁移速度比常见形式更快。Arp基因座控制Arp不相容淋巴细胞之间的一系列同种免疫相互作用。这些相互作用包括混合淋巴细胞反应、宿主抗移植物和移植物抗宿主反应,以及弱细胞毒性但强细胞抑制性效应淋巴细胞的发育,这些淋巴细胞具有同种反应性和自身反应性。本文讨论了Arp与Pep-7之间的关联以及Arp基因座的生物学意义。