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与肺炎支原体感染相关的神经系统疾病。PCR证据反驳直接侵袭机制。

Neurological disease associated with Mycoplasma pneumoniae infection. PCR evidence against a direct invasive mechanism.

作者信息

Fink C G, Sillis M, Read S J, Butler L, Pike M

机构信息

Department of Clinical Virology, John Radcliffe Hospital, Oxford OX3 9DU.

出版信息

Clin Mol Pathol. 1995 Feb;48(1):M51-4. doi: 10.1136/mp.48.1.m51.

Abstract

Aims-To investigate the pathology in patients presenting with sudden onset neurological illnesses associated with Mycoplasma pneumoniae infection.Methods-M pneumoniae infection was diagnosed by a highly rigorous interpretation of serological markers initially using complement fixation, agglutination and IgM antibodies. Confirmation of the serological diagnosis was achieved using indirect immunofluorescence for IgM, IgA, and IgG. Serum and cerebrospinal fluid (CSF) samples from these patients were examined using the polymerase chain reaction to look for evidence of M pneumoniae DNA.Results-No M pneumoniae DNA was found in any serum or CSF samples. Diagnosis of M pneumoniae infection by agglutination and complement fixation antibodies was not always confirmed by indirect immunofluorescence.Conclusion-The neurological lesions in these patients do not appear to be caused by the direct invasion of M pneumoniae into the nervous system. The lesions may be an immune response to infection. Serological diagnosis of M pneumoniae continues to be a laboratory problem.

摘要

目的——调查患有与肺炎支原体感染相关的突发神经系统疾病患者的病理学情况。

方法——通过对血清学标志物进行高度严格的解读来诊断肺炎支原体感染,最初使用补体结合试验、凝集试验和IgM抗体。使用针对IgM、IgA和IgG的间接免疫荧光法对血清学诊断进行确认。对这些患者的血清和脑脊液(CSF)样本进行聚合酶链反应检测,以寻找肺炎支原体DNA的证据。

结果——在任何血清或脑脊液样本中均未发现肺炎支原体DNA。通过凝集试验和补体结合抗体对肺炎支原体感染的诊断并非总能通过间接免疫荧光法得到证实。

结论——这些患者的神经病变似乎并非由肺炎支原体直接侵入神经系统所致。这些病变可能是对感染的免疫反应。肺炎支原体的血清学诊断仍然是一个实验室难题。

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Fulminant Mycoplasma pneumoniae infection. Report of a fatal case, and a review of the literature.
Am Rev Respir Dis. 1980 Sep;122(3):491-6. doi: 10.1164/arrd.1980.122.3.491.
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[Demonstration of mycoplasma pneumoniae in cerebrospinal fluid in acute polyneuritis].
Dtsch Med Wochenschr. 1972 Apr 28;97(17):678-82. doi: 10.1055/s-0028-1107421.
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Lancet. 1967 Nov 25;2(7526):1116-8. doi: 10.1016/s0140-6736(67)90620-4.

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