Evolution pattern of auto-antibodies against oxidized low-density lipoproteins in renal transplant recipients

被引:5
|
作者
Kandoussi, AM
Glowacki, F
Duriez, P
Tacquet, A
Fruchart, JC
Noël, C
机构
[1] Inst Pasteur, Inserm U 325, F-59019 Lille, France
[2] Hop Calmette, Clin Nephrol A, Lille, France
来源
NEPHRON | 2001年 / 89卷 / 03期
关键词
malondialdehyde-modified low-density lipoprotein; Cu2+-oxidized low-density lipoprotein; auto-antibody; ciclosporin A; lag phase; renal transplantation;
D O I
10.1159/000046090
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
An increased degree of oxidative stress in renal transplant recipients and a possible role of ciclosporin A (Cs-A) immunosuppressive therapy in this process have already been described. However, prospective data using in vivo markers and the influence of Cs-A in the oxidizability of low-density lipoprotein (LDL) are scarce. We aimed at investigating in this prospective study the evolution pattern of auto-antibodies directed against malondialdehyde-modified LDL (MDA-LDL) and Cu2+-oxidized LDL in 28 stable renal transplant recipients on Cs-A immunosuppressive therapy before and after 3 successive years of renal transplantation. Also, the effect of enrichment of LDL with Cs-A on the susceptibility of LDL to in vitro oxidation was tested. The results showed a significant increase of both auto-antibody titres (MDA-LDL and Cu2+-oxidized LDL) after 1 year, and the values remained high during the 2nd and the 3rd year following transplantation. The yearly mean relative variations of auto-antibodies against MDA-LDL and Cu2+-oxidized LDL during the follow-up period were 133, 149, and 137%, and 111, 115, and 117%, respectively. A significant correlation was observed during the 1st year between Cs-A trough blood level and Cu2+-oxidized LDL auto-antibody: r = 0.04 (p = 0.046). Incorporation of Cs-A into LDL from healthy volunteers showed no changes during the lag phase in comparison with Cs-A-free LDL, indicating that Cs-A had no effect on in vitro LDL oxidizability. Our results suggest that Cs-A may be involved earlier in the LDL oxidation, but the mechanism by which it acts is still unclear. Copyright (C) 2001 S. Karger AG, Basel.
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页码:303 / 308
页数:6
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