Hunt J S, Jadhav L, Chu W, Geraghty D E, Ober C
Departments of Anatomy and Cell Biology and Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS 66160-7400, USA.
Am J Obstet Gynecol. 2000 Sep;183(3):682-8. doi: 10.1067/mob.2000.106762.
Soluble isoforms of the HLA class Ib gene HLA-G have been identified at the maternal-fetal interface. Because soluble forms of other HLA class I antigens modulate T-cell reactivity and induce cellactivated apoptosis, our goal was to determine whether soluble HLA-G circulates in maternal or fetal blood and to identify the specific isoform.
Capture enzyme-linked immunosorbent assays with mouse monoclonal antibodies directed toward an epitope present on all isoforms of soluble HLA-G were constructed to identify soluble HLA-G in 44 serum samples from nonpregnant control subjects, 129 serum samples from pregnant women, and 10 samples of term cord blood. Distinguishing between soluble HLA-G1, which is composed of heavy chains complexed with light chains (beta(2)-microglobulin), and soluble HLA-G2, which consists only of heavy chains, was achieved by substituting a monoclonal antibody that requires beta(2)-microglobulin for binding (W6/32) in the capture phase of the enzyme-linked immunosorbent assay.
Capture enzyme-linked immunosorbent assays with mouse anti-soluble HLA-G showed that soluble HLA-G was present at all stages of gestation and that levels of soluble HLA-G were statistically significantly higher in serum samples from pregnant women than in serum samples from nonpregnant women. In contrast, W6/32 failed to detect soluble HLA-G in serum samples from pregnant women. Cord serum samples did not contain detectable soluble HLA-G.
Collectively, the data indicate that pregnancy is characterized by the presence of soluble HLA-G circulating in maternal blood and strongly suggest that the major isoform is soluble HLA-G2.
已在母胎界面鉴定出HLA - Ib类基因HLA - G的可溶性异构体。由于其他HLA - I类抗原的可溶性形式可调节T细胞反应性并诱导细胞活化凋亡,我们的目标是确定可溶性HLA - G是否在母体或胎儿血液中循环,并鉴定其具体异构体。
构建了捕获酶联免疫吸附测定法,使用针对可溶性HLA - G所有异构体上存在的一个表位的小鼠单克隆抗体,以鉴定来自非妊娠对照受试者的44份血清样本、来自孕妇的129份血清样本和10份足月脐带血样本中的可溶性HLA - G。通过在酶联免疫吸附测定法的捕获阶段替换一种需要β2 -微球蛋白结合的单克隆抗体(W6/32),区分由与轻链(β2 -微球蛋白)复合的重链组成的可溶性HLA - G1和仅由重链组成的可溶性HLA - G2。
用小鼠抗可溶性HLA - G的捕获酶联免疫吸附测定法显示,可溶性HLA - G在妊娠的所有阶段均存在,且孕妇血清样本中可溶性HLA - G的水平在统计学上显著高于非孕妇血清样本。相比之下,W6/32未能在孕妇血清样本中检测到可溶性HLA - G。脐带血清样本中未检测到可溶性HLA - G。
总体而言,数据表明妊娠的特征是母体血液中存在循环的可溶性HLA - G,并强烈提示主要异构体是可溶性HLA - G2。