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IgG抗Jka/Jkb抗体不太可能补体结合。

IgG anti-Jka/Jkb antibodies are unlikely to fix complement.

作者信息

Yates J, Howell P, Overfield J, Voak D, Downie D M, Austin E B

机构信息

Manchester Blood Centre, UK.

出版信息

Transfus Med. 1998 Jun;8(2):133-40. doi: 10.1046/j.1365-3148.1998.00139.x.

Abstract

Antibodies in the Kidd blood group system show a great deal of serological variability, are notoriously elusive and hence evoke difficulties in detection. However, they have been regularly reported as causing severe immediate or delayed haemolytic transfusion reactions and this clinical potential has been largely attributed to their complement binding ability. In initial investigations on 43 anti-Jka/Jkb sera with a range of titres of IgG antibody only a few seemed to fix complement, though following repeated tests on 20 of these sera a further five were shown to bind complement, making a total of 12 (27.9%) showing evidence of complement binding. Twenty-three sera were unavailable for re-testing. Subsequent tests revealed that only those sera which showed direct agglutination or were positive with an anti-IgM reagent in an indirect antiglobulin test (IAT) fixed complement. Evaluations on the IgG fractions of six selected potent anti-Jka sera failed to reveal any complement-fixing ability although all the original sera bound complement avidly and contained variable amounts of IgM antibody, some at very low subagglutinating levels. These findings challenge past perceptions and give cause for reflection on the changing methodologies and strategies which could unduly compromise the detection of these potentially clinically damaging antibodies.

摘要

基德血型系统中的抗体表现出大量的血清学变异性,极其难以捉摸,因此在检测方面存在困难。然而,它们经常被报道会引起严重的即刻或延迟溶血性输血反应,这种临床潜在影响很大程度上归因于它们结合补体的能力。在对43份具有一系列IgG抗体效价的抗Jka/Jkb血清进行的初步研究中,只有少数血清似乎能结合补体,不过在对其中20份血清进行重复检测后,又有5份被证明能结合补体,总共12份(27.9%)显示出补体结合的证据。有23份血清无法进行重新检测。后续检测表明,只有那些在直接抗球蛋白试验(IAT)中显示直接凝集或用抗IgM试剂呈阳性的血清才能结合补体。对6份选定的强效抗Jka血清IgG组分的评估未能发现任何补体结合能力,尽管所有原始血清都能强烈结合补体且含有不同量的IgM抗体,有些IgM抗体处于非常低的亚凝集水平。这些发现挑战了以往的认知,并促使人们反思不断变化的方法和策略,这些方法和策略可能会不适当地影响对这些具有潜在临床损害性抗体的检测。

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