Tyrey L
Department of Obstetrics and Gynecology, Duke University Medical Center, Durham, NC 27710, USA.
Semin Oncol. 1995 Apr;22(2):121-9.
Modern HCG assay methodology provides a level of sensitivity such that "HCG" immunoactivity in normal individuals or other unexplained low-level "HCG" measurements may be problematic. Two-site assays improve specificity for authentic HCG by selectively measuring intact hormone, and such measures correlate well with biological activity. In some cases, 125I has been replaced with nonradioisotopic labels without sacrificing sensitivity. On the negative side, such two-site assays will not reveal the presence of free subunit that may originate from trophoblastic tissue. Because free beta subunit appears in the sera of patients with GTD, monitoring intact HCG alone may pose a risk. Thus, some form of subunit monitoring by total-beta or free-beta assay is desirable. If the beta subunit/HCG ratio reflects the degree of trophoblastic cell differentiation and aggressiveness, a combination of specific whole molecule and free subunit measurements may provide the ideal monitoring for GTD.
现代的人绒毛膜促性腺激素(HCG)检测方法具有一定的灵敏度,以至于正常个体中的“HCG”免疫活性或其他不明原因的低水平“HCG”测量结果可能存在问题。双位点检测通过选择性地测量完整激素来提高对真实HCG的特异性,并且这些测量结果与生物活性密切相关。在某些情况下,125I已被非放射性同位素标记所取代,而不影响灵敏度。不利的一面是,这种双位点检测无法检测到可能源自滋养层组织的游离亚基的存在。由于游离β亚基会出现在妊娠滋养细胞疾病(GTD)患者的血清中,仅监测完整的HCG可能会带来风险。因此,采用某种形式的通过总β或游离β检测进行亚基监测是可取的。如果β亚基/HCG比值反映了滋养层细胞的分化程度和侵袭性,那么特定的完整分子和游离亚基测量相结合可能为GTD提供理想的监测方法。