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是否有临床需要一种诊断检测方法来检测特定于链类型的抗 A 和抗 B?

Is there a clinical need for a diagnostic test allowing detection of chain type-specific anti-A and anti-B?

机构信息

AbSorber AB and the Division of Clinical Immunology and Transfusion Medicine, Karolinska Institute, Stockholm, Sweden.

出版信息

Transfusion. 2011 Mar;51(3):494-503. doi: 10.1111/j.1537-2995.2010.02870.x. Epub 2010 Sep 16.

Abstract

BACKGROUND

Hemagglutination for detection and semiquantification of ABO antibodies is associated with large center-to-center variations and poor reproducibility. Because acceptance for transplantation and diagnosis of rejection in ABO-incompatible transplantation rely on the levels and specificity of ABO antibodies, reproducible tests that allow their detection and specificity determination are required.

STUDY DESIGN AND METHODS

The level of chain type-specific anti-A and anti-B were analyzed in the sera of 44 healthy individuals of known ABO blood group using an enzyme-linked immunosorbent assay (ELISA) with polyacrylamide (PAA) conjugates of blood group A and B trisaccharides or Type 2 chain A and B tetrasaccharides. Selected sera were further analyzed by hemagglutination and in an ELISA with Types 1 to 4 chain A or B neoglycolipids (NGL) as antigens.

RESULTS

Immunoglobulin (Ig)G anti-A and anti-B levels were higher (p ≤ 0.05) in blood group O than in B and A individuals. More IgM anti-A and anti-B cross-reactivity was detected in AB serum on PAA-conjugated A and B trisaccharides than on the tetrasaccharides. One of 11 blood group B and two of 12 A individuals had IgG antibodies binding the tetrasaccharide despite lack of, or very low reactivity with, the trisaccharides. IgG antibodies preferring the A and B Type 2 tetrasaccharides were of the IgG2 subclass. The NGL ELISA further supported the presence of chain type-specific anti-A and -B antibodies among nonsensitized, healthy individuals.

CONCLUSION

An ELISA with structurally defined ABH antigens will allow the antibody class and fine specificity of ABO antibodies to be determined, which may improve risk assessment in ABO-incompatible transplantation.

摘要

背景

用于检测和半定量 ABO 抗体的血凝法存在较大的中心-中心差异和较差的重现性。由于 ABO 不相容移植中移植的接受和排斥的诊断依赖于 ABO 抗体的水平和特异性,因此需要可重复的检测方法来检测和确定其特异性。

研究设计与方法

使用具有 A 型和 B 型三糖的聚丙烯酰胺(PAA)缀合物或 2 型 A 和 B 四糖的酶联免疫吸附试验(ELISA)分析 44 名已知 ABO 血型个体血清中的链型特异性抗-A 和抗-B 水平。选择的血清进一步通过血凝法和 ELISA 进行分析,抗原为 A 或 B 型 1 至 4 型链的新糖脂(NGL)。

结果

与 B 型和 A 型个体相比,O 型个体的 IgG 抗-A 和抗-B 水平更高(p ≤ 0.05)。在 PAA 缀合的 A 和 B 三糖上检测到更多的 AB 血清 IgM 抗-A 和抗-B 交叉反应性,而在四糖上则较少。尽管缺乏或仅有很低的三糖反应性,但 11 名 B 型个体中的 1 名和 12 名 A 型个体中的 2 名具有结合四糖的 IgG 抗体。优先结合 A 和 B 型 2 型四糖的 IgG 抗体属于 IgG2 亚类。NGL ELISA 进一步支持在未致敏的健康个体中存在链型特异性抗-A 和抗-B 抗体。

结论

具有结构定义的 ABO 抗原的 ELISA 将允许确定 ABO 抗体的抗体类别和精细特异性,这可能会改善 ABO 不相容移植中的风险评估。

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