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HIV感染儿童坏死性小肠结肠炎中TNF系统激活及TNFα信使转录物高表达的证据

Evidence of TNF system activation and high expression of TNF alpha messenger transcripts in necrotizing enterocolitis of HIV-infected children.

作者信息

Ispas D

机构信息

Dr. Victor Babeş Clinic Hospital for Infectious and Tropical Diseases, Bucharest.

出版信息

Rom J Virol. 1999 Jan-Dec;50(1-4):53-70.

Abstract

TNF alpha contributes to the necrotizing enterocolitis (NEC) pathogenesis. To date, this clinical entity of neonates was never described in HIV-infected children. In 15 HIV-positive children with histological evidence of various intestinal lesions resembling NEC, we have studied serum TNF alpha and soluble TNF receptor concentrations by ELISAs, and archived paraffin embedded intestinal tissues by in situ hybridization with DIG-labeled RNA probes for TNF alpha messenger transcripts. We found increased levels of TNF alpha and soluble receptors, proving TNF alpha system activation. We detected TNF alpha messenger transcripts in all cases, regardless of the presence of microbial pathogens at intestinal level. Since HIV can infect many cells of the gastrointestinal tract, also triggering the secretion of TNF alpha, we concluded that factors contributing to NEC pathogenesis in HIV-infected children are complex. At least the nutritional and immunological status are involved, other viral co-infections, opportunistic microbes (such as mycobacteria), and pathogenic activities of HIV. All together enhance both circulating TNF alpha system and its cytotoxic effects at intestinal level.

摘要

肿瘤坏死因子α(TNFα)促成坏死性小肠结肠炎(NEC)的发病机制。迄今为止,从未在感染人类免疫缺陷病毒(HIV)的儿童中描述过这种新生儿临床病症。在15名有各种类似NEC肠道病变组织学证据的HIV阳性儿童中,我们通过酶联免疫吸附测定(ELISA)研究了血清TNFα和可溶性TNF受体浓度,并通过用地高辛(DIG)标记的RNA探针原位杂交检测存档的石蜡包埋肠道组织中的TNFα信使转录本。我们发现TNFα和可溶性受体水平升高,证明TNFα系统被激活。我们在所有病例中均检测到TNFα信使转录本,无论肠道水平是否存在微生物病原体。由于HIV可感染胃肠道的许多细胞,也会触发TNFα的分泌,我们得出结论,导致HIV感染儿童发生NEC发病机制的因素很复杂。至少涉及营养和免疫状况、其他病毒合并感染、机会性微生物(如分枝杆菌)以及HIV的致病活性。所有这些共同增强了循环TNFα系统及其在肠道水平的细胞毒性作用。

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