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吸附后ELISA中抗AT1R反应性丧失——假反应性还是检测干扰?

Loss of anti-AT1R reactivity in ELISA post-adsorption - False reactivity or interference in the assay?

作者信息

Xu Qingyong, Johnson Kurt P, Hardiman Maura, Helmick Dennis, Zeevi Adriana

机构信息

Department of Pathology, University of Pittsburgh Medical Center, United States.

Department of Pathology, University of Pittsburgh Medical Center, United States.

出版信息

Hum Immunol. 2023 Apr;84(4):286-289. doi: 10.1016/j.humimm.2023.02.001. Epub 2023 Feb 8.

Abstract

Autoantibodies to Angiotensin II type 1 receptor (AT1R) are associated with detrimental outcomes in organ transplants. However, reports showed that adsorption with latex beads reduced positive anti-AT1R antibodies, suggesting possible false reactivity. To investigate this conundrum, we studied 11 samples positive for AT1R antibodies with an ELISA kit before and after adsorption. Adsorption significantly reduced the measurable level of AT1R antibodies (28.3 ± 9.8 vs. 6.3 ± 3.0 U/ml, p < 0.001). AT1R antibodies were lower when post-adsorption serum was added back at 1:1 ratio to the neat serum compared to the diluent control (8.6 ± 4.2 vs. 18.1 ± 10.3 U/ml, p = 0.02). Sham adsorption with the buffer from Adsorb Out™ kit without beads also suppressed the detection of anti-AT1R antibodies (32.7 ± 9.1 vs. 8.1 ± 3.9 U/ml, p < 0.001). Thus, rather than actively removing nonspecific antibodies by the beads, the adsorption process introduces soluble factors that interfere with the detection of anti-AT1R antibodies with the ELISA kit.

摘要

抗血管紧张素II 1型受体(AT1R)自身抗体与器官移植的不良后果相关。然而,报告显示用乳胶珠吸附可降低抗AT1R抗体阳性率,提示可能存在假反应性。为研究这一难题,我们用ELISA试剂盒对11份AT1R抗体阳性样本在吸附前后进行了检测。吸附显著降低了可检测到的AT1R抗体水平(28.3±9.8 vs. 6.3±3.0 U/ml,p<0.001)。与稀释剂对照相比,将吸附后血清以1:1比例回加至纯血清时,AT1R抗体水平更低(8.6±4.2 vs. 18.1±10.3 U/ml,p=0.02)。用不含珠子的Adsorb Out™试剂盒缓冲液进行假吸附也抑制了抗AT1R抗体的检测(32.7±9.1 vs. 8.1±3.9 U/ml,p<0.001)。因此,吸附过程并非通过珠子有效去除非特异性抗体,而是引入了干扰ELISA试剂盒检测抗AT1R抗体的可溶性因子。

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