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人类中性粒细胞抗原 3 基因型对 TRALI 两事件模型中中性粒细胞介导的内皮细胞细胞毒性的影响。

Human neutrophil antigen 3 genotype impacts neutrophil-mediated endothelial cell cytotoxicity in a two-event model of TRALI.

机构信息

Clinical Services and Research, Australian Red Cross Lifeblood, Brisbane, Queensland, Australia.

Transplantation and Immunogenetics Services, Australian Red Cross Lifeblood, Brisbane, Queensland, Australia.

出版信息

Blood Transfus. 2022 Nov;20(6):465-474. doi: 10.2450/2022.0013-22. Epub 2022 May 19.

Abstract

BACKGROUND

Antibodies against human neutrophil antigen (HNA)-3a are associated with severe cases of transfusion-related acute lung injury (TRALI). The HNA-3 system is located on choline transporter-like 2 (CTL-2) protein. CTL-2 is encoded by the gene SLC44A2 and a single-nucleotide polymorphism c.461G>A results in two antigens: HNA-3a and HNA-3b. Three HNA-3 genotypes/ phenotypes exist: HNA-3aa, HNA-3bb, and HNA-3ab. Two different pathways of anti-HNA-3a TRALI have been described: a two-hit neutrophil-dependent pathway and a one-hit neutrophil-independent pathway. However, it is not clear whether HNA-3ab heterozygous patients have a lower risk of anti-HNA-3a-mediated TRALI compared to HNA-3aa homozygous patients.

MATERIALS AND METHODS

Healthy volunteers were genotyped for HNA-3 by real-time polymerase chain reaction, and phenotyped for HNA-3a by granulocyte immunofluorescence test (GIFT) and granulocyte agglutination test (GAT) against two donor sera containing anti-HNA-3a antibodies. The two sera were also used in in vitro models of human pulmonary microvascular endothelial cell (HLMVEC) cytotoxicity to investigate pathways of TRALI development.

RESULTS

For both anti-HNA-3a sera, GIFT results matched the genotype, with a lower GIFT ratio for HNA-3ab neutrophils compared to HNA-3aa neutrophils, whereas GAT results showed no difference in agglutination. HLMVEC cytotoxicity was not observed in a one-hit neutrophil-independent model but was observed in a two-hit neutrophil-dependent model. Differences in cytotoxicity were observed between the two anti-HNA-3a sera used. Consistent with reduced HNA-3a antigen density as measured by GIFT, HNA-3ab neutrophils mediated less HLMVEC cytotoxicity than HNA-3aa neutrophils.

CONCLUSION

HNA-3 genotype and HNA-3a antigen expression impacted the severity of anti-HNA-3a-mediated HLMVEC cytotoxicity in a two-hit neutrophil-dependent model of TRALI. Different HNA-3a antibodies might also impact the magnitude of HLMVEC cytotoxicity.

摘要

背景

针对人类中性粒细胞抗原(HNA)-3a 的抗体与输血相关急性肺损伤(TRALI)的严重病例有关。HNA-3 系统位于胆碱转运蛋白样 2(CTL-2)蛋白上。CTL-2 由基因 SLC44A2 编码,单核苷酸多态性 c.461G>A 导致两种抗原:HNA-3a 和 HNA-3b。存在三种 HNA-3 基因型/表型:HNA-3aa、HNA-3bb 和 HNA-3ab。已经描述了两种抗 HNA-3a TRALI 的不同途径:依赖中性粒细胞的双打击途径和不依赖中性粒细胞的单打击途径。然而,目前尚不清楚 HNA-3ab 杂合患者与 HNA-3aa 纯合患者相比,是否具有较低的抗 HNA-3a 介导的 TRALI 风险。

材料和方法

通过实时聚合酶链反应对健康志愿者进行 HNA-3 基因分型,通过粒细胞免疫荧光试验(GIFT)和粒细胞凝集试验(GAT)对两种含有抗 HNA-3a 抗体的供体血清进行 HNA-3a 表型检测。还使用这两种血清在体外人肺微血管内皮细胞(HLMVEC)细胞毒性模型中研究 TRALI 发展的途径。

结果

对于两种抗 HNA-3a 血清,GIFT 结果与基因型匹配,HNA-3ab 中性粒细胞的 GIFT 比值低于 HNA-3aa 中性粒细胞,而 GAT 结果显示凝集无差异。在不依赖中性粒细胞的单次打击模型中未观察到 HLMVEC 细胞毒性,但在依赖中性粒细胞的两次打击模型中观察到了细胞毒性。两种抗 HNA-3a 血清之间观察到细胞毒性的差异。与 GIFT 测量的 HNA-3a 抗原密度降低一致,HNA-3ab 中性粒细胞介导的 HLMVEC 细胞毒性低于 HNA-3aa 中性粒细胞。

结论

在 TRALI 的依赖中性粒细胞的两次打击模型中,HNA-3 基因型和 HNA-3a 抗原表达影响抗 HNA-3a 介导的 HLMVEC 细胞毒性的严重程度。不同的 HNA-3a 抗体也可能影响 HLMVEC 细胞毒性的程度。

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Molecular Genetics of the Human Neutrophil Antigens.人类中性粒细胞抗原的分子遗传学
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