不同慢性阻塞性肺病表现的 PiMM 和 PiZZ 患者血浆中的α2-巨球蛋白和α1-抗胰蛋白酶水平之间存在关联。

IF 2.5 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinical biochemistry Pub Date : 2024-02-29 DOI:10.1016/j.clinbiochem.2024.110736
Urszula Lechowicz , Beatriz Martinez-Delgado , Bin Liu , Sabine Wrenger , Adriana Rozy , Aneta Zdral , David S. DeLuca , Tobias Welte , Sabina Janciauskiene , Joanna Chorostowska-Wynimko
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We aimed to investigate putative differences in plasma levels of acute phase proteins (APP) between PiMM and PiZZ subjects and to determine plasma Z-AAT polymer levels in PiZZ subjects.</p></div><div><h3>Materials and methods</h3><p>Nephelometric analysis of seven plasma APPs was performed in 67 PiMM and 44 PiZZ subjects, of whom 43 and 42, respectively, had stable COPD. Of the PiZZ-COPD patients, 21 received and 23 did not receive intravenous therapy with human AAT preparations (IV-AAT). Plasma levels of Z-AAT polymers were determined by Western blotting using specific mouse monoclonal antibodies (2C1 and LG96).</p></div><div><h3>Results</h3><p>In addition to lower plasma AAT, PiZZ patients had higher α2-macroglobulin (A2MG) levels than PiMM patients. In contrast, PiZZ who received IV-AAT had higher AAT values but lower A2MG values than PiZZ without IV-AAT. 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引用次数: 0

摘要

导言:与正常的 PiMM 相比,严重的 α1-抗胰蛋白酶(AAT)PiZZ(Glu342Lys)基因型缺乏症患者罹患与 Z-AAT 聚合物和中性粒细胞炎症相关的早发慢性阻塞性肺病(COPD)/肺气肿的风险更高。我们旨在研究 PiMM 和 PiZZ 受试者血浆中急性期蛋白(APP)水平的假定差异,并确定 PiZZ 受试者血浆中 Z-AAT 聚合物的水平:对 67 名 PiMM 和 44 名 PiZZ 受试者的七种血浆 APP 进行了尼泊金测定分析,其中分别有 43 名和 42 名受试者患有稳定的慢性阻塞性肺病。在 PiZZ-COPD 患者中,21 人接受了人 AAT 制剂(IV-AAT)静脉注射治疗,23 人未接受治疗。使用特异性小鼠单克隆抗体(2C1 和 LG96)通过 Western 印迹法测定血浆中 Z-AAT 聚合物的水平:结果:与 PiMM 患者相比,PiZZ 患者除了血浆 AAT 水平较低外,α2-巨球蛋白(A2MG)水平也较高。相比之下,接受 IV-AAT 的 PiZZ 比未接受 IV-AAT 的 PiZZ 的 AAT 值更高,但 A2MG 值更低。无论 AAT 基因型如何,AAT 水平都与 A2MG 成反比,AAT/A2MG 比值与肺弥散能力(DCLO%)相关。所有 PiZZ 患者的循环 Z-AAT 聚合物水平都与 A2MG 直接相关。在未接受 IV-AAT 治疗的 PiZZ 患者中,聚合物水平与 1 秒用力呼气量与用力肺活量(FEV1/FVC)之比成反比:联合测量血浆 AAT 和 A2MG 水平可能对评估慢性阻塞性肺病的进展具有临床价值,需要进一步关注。
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An association between plasma levels of α2-macroglobulin and α1-antitrypsin in PiMM and PiZZ individuals differing in COPD presentation

Introduction

Compared to normal PiMM, individuals with severe α1-antitrypsin (AAT) PiZZ (Glu342Lys) genotype deficiency are at higher risk of developing early-onset chronic obstructive pulmonary disease (COPD)/emphysema associated with Z-AAT polymers and neutrophilic inflammation. We aimed to investigate putative differences in plasma levels of acute phase proteins (APP) between PiMM and PiZZ subjects and to determine plasma Z-AAT polymer levels in PiZZ subjects.

Materials and methods

Nephelometric analysis of seven plasma APPs was performed in 67 PiMM and 44 PiZZ subjects, of whom 43 and 42, respectively, had stable COPD. Of the PiZZ-COPD patients, 21 received and 23 did not receive intravenous therapy with human AAT preparations (IV-AAT). Plasma levels of Z-AAT polymers were determined by Western blotting using specific mouse monoclonal antibodies (2C1 and LG96).

Results

In addition to lower plasma AAT, PiZZ patients had higher α2-macroglobulin (A2MG) levels than PiMM patients. In contrast, PiZZ who received IV-AAT had higher AAT values but lower A2MG values than PiZZ without IV-AAT. Regardless of the AAT genotype, AAT levels were inversely correlated with A2MG, and the AAT/A2MG ratio was correlated with lung diffusion capacity (DCLO%). All PiZZ patients had circulating Z-AAT polymer levels that correlated directly with A2MG. In PiZZ without IV-AAT therapy polymer levels correlated inversely with the ratio of forced expiratory volume in 1 s to forced vital capacity (FEV1/FVC).

Conclusion

Combined measurement of plasma AAT and A2MG levels may be of clinical value in assessing the progression of COPD and requires further attention.

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来源期刊
Clinical biochemistry
Clinical biochemistry 医学-医学实验技术
CiteScore
5.10
自引率
0.00%
发文量
151
审稿时长
25 days
期刊介绍: Clinical Biochemistry publishes articles relating to clinical chemistry, molecular biology and genetics, therapeutic drug monitoring and toxicology, laboratory immunology and laboratory medicine in general, with the focus on analytical and clinical investigation of laboratory tests in humans used for diagnosis, prognosis, treatment and therapy, and monitoring of disease.
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