抗中性粒细胞胞浆抗体(ANCA)在疟疾中的作用。

Indian journal of malariology Pub Date : 2002-09-01
Vandana Pradhan, S S Badakere, U Shankarkumar, Y S Iyer, K Ghosh, D Karnad
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引用次数: 0

摘要

对173例急性住院疟疾患者进行了抗核抗体(ANA)、抗双链DNA(抗dsdna)、抗组蛋白抗体(AHA)、抗中性粒细胞胞浆抗体(ANCA)、抗髓过氧化物酶(抗mpo)、抗蛋白酶3(抗pr3)和抗乳铁蛋白(抗lf)抗体等自身抗体的研究,其中160例为恶性疟原虫,13例为间日疟原虫。采用间接免疫荧光(IIF)显微镜、共聚焦显微镜和ELISA等标准方法对自身抗体进行鉴定和定量,并研究PMN和HL-60细胞上的IIF模式进行ANCA分类。用HEp-2细胞检测ANA,用ELISA检测抗dsdna、AHA、抗mpo、抗pr3和抗lf。疟疾患者血清显示明显的免疫荧光染色模式,其中恶性疟原虫组23.8%的病例存在ANA,而间日疟原虫组为15.4%,恶性疟原虫组和间日疟原虫组分别有20%和15.4%的病例存在ANCA。一个有趣的观察结果是,在所有ANCA阳性患者中,59%为p-ANCA, 5.9%为c-ANCA, 44.1%为“非典型”或X-ANCA模式。p-ANCA阳性与c-ANCA阳性比较,OR = 16, chi 2 = 16.43, EF = 0.46, p值= 5.037 e0.5,具有良好的统计学相关性。ELISA检测结果显示,恶性疟原虫抗mpo阳性率为31.2%,抗pr3阳性率为6.2%,2例间日疟原虫抗mpo阳性率为6.2%。40.6%的病例存在抗lf。恶性疟原虫和间日疟原虫都不含有与狼疮自身抗体特异性相似的自身抗体,如双链DNA (dsDNA)。在某些类型的疟疾感染中也会出现ANCA阳性,同时存在各种自身抗体,这从临床角度来看很重要,在疟疾流行的地理区域应仔细评估。它还提醒我们注意这样一个事实,即在易感个体中反复感染疟疾的情况下,通过ANCA途径发展的血管疾病可能导致肾脏和其他并发症。
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Anti-neutrophil cytoplasmic antibodies (ANCA) in malaria.

Various autoantibodies like anti-nuclear antibodies (ANA), anti-double stranded DNA (anti-dsDNA), anti-histone antibodies (AHA), anti-neutrophil cytoplasmic antibodies (ANCA), anti-myeloperoxidase (anti-MPO), anti-proteinase3 (anti-PR3) and anti-lactoferrin (anti-LF) antibodies were studied in 173 acute hospitalised patients suffering from malaria of which 160 patients had P. falciparum and remaining 13 had P. vivax infection. Standard methods like indirect immunofluorescence (IIF) microscopy along with Confocal microscopy and ELISA were used for identifying and quantifying the autoantibodies and IIF patterns on PMN and HL-60 cells were studied for ANCA classification. Also HEp-2 cells were used for ANA detection, while estimation of anti-dsDNA, AHA, anti-MPO, anti-PR3 and anti-LF were tested using ELISA. Sera from malaria patients showed prominent immunofluorescence staining patterns where 23.8% cases had ANA in P. falciparum group as compared to 15.4% in P. vivax group and ANCA was found to be present in 20% in P. falciparum and 15.4% in P. vivax group. An interesting observation was that, of the total ANCA positives, 59% had p-ANCA, 5.9% had c-ANCA and 44.1% of the cases showed the 'atypical' or X-ANCA pattern. When p-ANCA positivity was compared with c-ANCA positivity among these patients, a good statistical correlation was noted with OR = 16, chi 2 = 16.43, EF = 0.46 and p-value = 5.037E 0.5. ELISA showed 31.2% anti-MPO and 6.2% anti-PR3 in P. falciparum cases while the two ANCA positive cases in P. vivax had anti-MPO. Anti-LF was found to be present in 40.6% cases. Neither the P. falciparum nor P. vivax contained autoantibodies with specificities similar to the characteristic lupus autoantibodies such as double stranded DNA (dsDNA). ANCA positivity develops in some types of malarial infection also with the presence of various autoantibodies which is important from a clinical point of view and should be carefully evaluated in those geographic areas where malaria is endemic. It also alerts us to the fact, whether in cases of repeated malarial infections in susceptible individuals, vasculitic disorders, which through ANCA pathways develop, could lead to renal and other complications.

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