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对感染艾滋病毒患者非刺激性唾液中溶菌酶浓度和过氧化物酶活性的评估。

The evaluation of lysozyme concentration and peroxidase activity in non-stimulated saliva of patients infected with HIV.

作者信息

Klimiuk A, Waszkiel D, Jankowska A, Zelazowska-Rutkowska B, Choromańska M

机构信息

Department of Conservative Dentistry, Medical University of Białystok, Poland.

出版信息

Adv Med Sci. 2006;51 Suppl 1:49-51.

Abstract

PURPOSE

The aim of the study was the comparison of lysozyme concentration and peroxidase activity in mixed, non-stimulated saliva of HIV-positive patients and healthy subjects.

MATERIAL AND METHODS

The study was carried out in the group of 37 patients infected with HIV. The control group comprised of non-infected individuals, counterpart of the examined group. Mixed non-stimulated saliva, collected using expectoration method in the amount of 3-5 ml 2 hours after meal, was used for the study. Saliva samples were centrifuged, divided into portions 200 microl each, and stored at -80 degrees C. Peroxidase activity was determined using the method by Mansson-Rahemtull et al. Lysozyme concentrations were determined with the use of radial immunodiffusion method, ready-made kits (Human NL Nanorid plate--The Binding Site Ltd., UK).

RESULTS

Higher concentrations of lysozyme as well as peroxidase activity were observed in the group of patients with HIV as compared to the control group, and they were 35.08 microg/ml, 46.74 IU/1, 21.3 microg/ml, 37.73 IU/l, respectively. The difference was statistically significant only in case of peroxidase activity.

CONCLUSIONS

  1. HIV infection triggers immune mechanisms, that are manifested by the increase in salivary enzymes responsible for local non-specific resistance. 2. The immunological resistance decrease, manifested by the drop of the absolute number of CD4 lymphocytes T, is compensated by the increase in lysozyme concentration and peroxidase activity in non-stimulated saliva of HIV-positive patients.
摘要

目的

本研究旨在比较HIV阳性患者和健康受试者混合非刺激性唾液中的溶菌酶浓度和过氧化物酶活性。

材料与方法

对37例HIV感染患者进行了研究。对照组由未感染个体组成,与研究组相对应。采用咳痰法在饭后2小时收集3 - 5毫升混合非刺激性唾液用于研究。唾液样本离心后,分成每份200微升的部分,并储存在-80℃。过氧化物酶活性采用Mansson-Rahemtull等人的方法测定。溶菌酶浓度采用放射免疫扩散法,使用现成的试剂盒(Human NL Nanorid plate - The Binding Site Ltd., UK)测定。

结果

与对照组相比,HIV患者组中观察到更高的溶菌酶浓度以及过氧化物酶活性,分别为35.08微克/毫升、46.74国际单位/升、21.3微克/毫升、37.73国际单位/升。仅过氧化物酶活性的差异具有统计学意义。

结论

  1. HIV感染触发免疫机制,表现为负责局部非特异性抵抗的唾液酶增加。2. HIV阳性患者非刺激性唾液中溶菌酶浓度和过氧化物酶活性的增加补偿了CD4淋巴细胞T绝对数量下降所表现出的免疫抵抗降低。

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