Sieckmann D G, Stall A M, Subbarao B
Naval Medical Research Institute, Bethesda, MD 20814-5055.
Hybridoma. 1991 Feb;10(1):121-35. doi: 10.1089/hyb.1991.10.121.
An IgG1 mouse monoclonal antibody (MAb) specific for a mouse IgM allotypic determinant in the a, c, f, g, h, and j haplotypes was derived from a fusion of SP2/O-Ag14 mouse myeloma cells with C57BL/6 mouse spleen cells (Igh-Cb) immune to TC31, a MAb of the IgMa allotype. MAb from one hybridoma derived from this fusion (designated DS1) was demonstrated to bind in an ELISA to immunoglobulin bearing the IgMa allotype (TC31, MOPC104E), but not to immunoglobulin bearing the IgMb allotype (C.BPC112). Fluorescein-conjugated DS1 was shown to bind to the surface of BALB/cByJ splenic B cells, but was shown to have negligible binding on C57BL/6J cells. Similarly, DS1-conjugated Sepharose beads were able to stimulate in vitro proliferation of BALB/c, but not C57BL/6 splenic B cells. DS1 was unable to bind to spleen cells from BALB/c allotype congenic strains, BAB/14 (Igh-Cb) and C.AL-20 (Igh-Co), demonstrating that DS1 recognizes a determinant under the control of a gene linked to the Igh-C gene complex. Using sera from recombinant inbred lines, the determinant defined by DS1 was shown to be linked to the Igh-1 locus. Furthermore, the determinant was localized to the CH1 domain of the mu heavy chain. Sera from BALB/cByJ, NMRI, CBA/J, SEA/GnJ, RIIIs/J, and CE/J mouse strains were shown to bind to DS1 in an ELISA, while sera from A/J, SJL/J, NZB/B1NJ, AKR/J, C57BL/6J, and C57BL/10SnJ mouse strains did not bind to DS1. From these data we propose that DS1 is reactive with specificity Igh-6.1, which was originally defined by an allotypic antiserum developed by Black et al. (Immunogenetics 7:213, 1978).
一种针对a、c、f、g、h和j单倍型中小鼠IgM同种异型决定簇的IgG1小鼠单克隆抗体(MAb),是通过将SP2/O-Ag14小鼠骨髓瘤细胞与对IgMa同种异型的单克隆抗体TC31免疫的C57BL/6小鼠脾细胞(Igh-Cb)融合而获得的。来自该融合产生的一个杂交瘤的单克隆抗体(命名为DS1)在酶联免疫吸附测定(ELISA)中被证明能与带有IgMa同种异型的免疫球蛋白(TC31、MOPC104E)结合,但不能与带有IgMb同种异型的免疫球蛋白(C.BPC112)结合。荧光素偶联的DS1被证明能与BALB/cByJ脾B细胞表面结合,但在C57BL/6J细胞上的结合可忽略不计。同样,DS1偶联的琼脂糖珠能够刺激BALB/c脾B细胞的体外增殖,但不能刺激C57BL/6脾B细胞。DS1不能与BALB/c同种异型近交系BAB/14(Igh-Cb)和C.AL-20(Igh-Co)的脾细胞结合,这表明DS1识别与Igh-C基因复合体连锁的基因控制下的一个决定簇。使用重组近交系的血清,DS1定义的决定簇被证明与Igh-1位点连锁。此外,该决定簇定位于μ重链的CH1结构域。在ELISA中,来自BALB/cByJ、NMRI、CBA/J、SEA/GnJ、RIIIs/J和CE/J小鼠品系的血清被证明能与DS1结合,而来自A/J、SJL/J、NZB/B1NJ、AKR/J、C57BL/6J和C57BL/10SnJ小鼠品系的血清不与DS1结合。根据这些数据,我们提出DS1与特异性Igh-6.1反应,该特异性最初由Black等人(《免疫遗传学》7:213,1978)开发的一种同种异型抗血清定义。