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感染猴免疫缺陷病毒(SIV)的恒河猴肠道中缺乏SIV特异性IgA反应。

Lack of simian immunodeficiency virus (SIV) specific IgA response in the intestine of SIV infected rhesus macaques.

作者信息

Schäfer F, Kewenig S, Stolte N, Stahl-Hennig C, Stallmach A, Kaup F-J, Zeitz M, Schneider T

机构信息

Department of Internal Medicine II, Saarland University, Homburg/Saar, Germany.

出版信息

Gut. 2002 May;50(5):608-14. doi: 10.1136/gut.50.5.608.

Abstract

BACKGROUND

Little is known about secretory immunity-the major defence mechanism at mucosal surfaces-in human immunodeficiency virus (HIV) infected patients, especially in the early stages of the disease.

AIMS

The aim of the study was to analyse mucosal immunoglobulin production and simian immunodeficiency virus (SIV) specific antibody response in the intestinal mucosa during the course of SIV infection in comparison with serum and saliva.

ANIMALS AND METHODS

IgG, IgA, and IgM concentrations were determined in supernatants of short term cultured duodenal biopsies, serum, and saliva from SIV infected rhesus macaques (n=8) and controls (n=2) by ELISA at defined times before and after infection. Specific antibodies to SIV were detected by western blot and/or dot blot analysis. In addition, rectal swabs from two uninfected and 12 SIV infected rhesus macaques (seven without and five with enteritis) were analysed for albumin and IgG concentrations.

RESULTS

An increase in total intestinal IgG and a decrease in IgA were observed. SIV specific IgG or IgA responses were detectable as early as one week after SIV infection in the serum of seven of eight animals. In contrast, intestinal SIV specific IgG production was detected only four weeks after infection in six of eight animals, and intestinal SIV specific IgA was not produced in the intestine at any time point. In saliva, the secretory component on SIV specific IgA was only detected in one animal at week 24 after infection. Enteritis is frequent in SIV infected animals and results in a significant increase in albumin and IgG secretion into the intestinal lumen.

CONCLUSION

Despite modest quantitative changes in mucosal immunglobulin production there was a total lack of SIV specific IgA synthesis in the intestine during SIV infection. This lack or disturbed secretory SIV specific IgA response at mucosal surfaces may explain the rapid and high HIV/SIV replication in this compartment. In addition, our investigations indicate secretion of serum proteins into intestinal fluids during SIV infection. Previous investigations using intestinal secretions or swabs for analysing quantitative and specific immunglobulins therefore should be interpreted with caution.

摘要

背景

对于人类免疫缺陷病毒(HIV)感染患者,尤其是疾病早期阶段,关于黏膜表面主要防御机制——分泌性免疫,人们了解甚少。

目的

本研究旨在分析与血清和唾液相比,在猴免疫缺陷病毒(SIV)感染过程中,肠道黏膜内黏膜免疫球蛋白的产生及SIV特异性抗体反应。

动物与方法

通过酶联免疫吸附测定法(ELISA),在感染前后的特定时间,测定8只感染SIV的恒河猴(n = 8)和2只对照恒河猴(n = 2)的短期培养十二指肠活检组织、血清和唾液上清液中的IgG、IgA和IgM浓度。通过蛋白质印迹法和/或斑点印迹分析检测SIV特异性抗体。此外,分析了2只未感染和12只感染SIV的恒河猴(7只无肠炎,5只患有肠炎)的直肠拭子中的白蛋白和IgG浓度。

结果

观察到肠道总IgG增加,IgA减少。在8只动物中的7只动物的血清中,早在SIV感染后1周就可检测到SIV特异性IgG或IgA反应。相比之下,仅在8只动物中的6只动物感染后4周才在肠道中检测到SIV特异性IgG产生,并且在任何时间点肠道中均未产生SIV特异性IgA。在唾液中,仅在感染后第24周在1只动物中检测到SIV特异性IgA上的分泌成分。肠炎在感染SIV的动物中很常见,并导致白蛋白和IgG向肠腔的分泌显著增加。

结论

尽管黏膜免疫球蛋白产生存在适度的定量变化,但在SIV感染期间肠道中完全缺乏SIV特异性IgA合成。黏膜表面这种缺乏或受干扰的分泌性SIV特异性IgA反应可能解释了该区域中HIV/SIV的快速和大量复制。此外,我们的研究表明在SIV感染期间血清蛋白分泌到肠液中。因此,先前使用肠分泌物或拭子分析定量和特异性免疫球蛋白的研究应谨慎解释。

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