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[强直性脊柱炎的免疫学方面]

[Immunologic aspects of ankylosing spondylarthritis].

作者信息

Saliou P, Thabaut A, Durosoir J L, Pattin S, Doury P

出版信息

Rev Rhum Mal Osteoartic. 1982 Jan;49(1):23-8.

PMID:6978510
Abstract

The immunological profile of 63 men, 53 of whom were carriers of the HLA B27 antigen, and 10 of whom were not, all of whom suffered from ankylosing spondylarthritis (ASP) which was either quiescent or subject to exacerbations, were studied: lymphocytic colonies, quantity determination of serum proteins, investigations of auto-immune antibodies. Following a discussion of the techniques, the results are presented and compared with those obtained in healthy subjects. No significant difference was revealed between the averages obtained for the results on the patients and the controls, nor as regards the B and T lymphocytes, the IgG, IgA, IgM immunoglobulins, the C3 fraction of the complement, or orosomucoid. The haptoglobin and alpha-antitrypsin rates increased significantly in the patients. Tests for the auto-immune antibodies were always negative. The results are compared to other, often contradictory, studies which have already been published. These authors conclude that the ASP in question does not seem to be an immunological disease.

摘要

对63名男性进行了研究,其中53名是HLA B27抗原携带者,10名不是,他们均患有静止期或处于病情加重期的强直性脊柱炎(ASP):研究内容包括淋巴细胞集落、血清蛋白定量测定、自身免疫抗体检测。在讨论了相关技术之后,给出了研究结果,并与健康受试者的结果进行了比较。患者组和对照组在各项结果的平均值方面,以及在B淋巴细胞、T淋巴细胞、IgG、IgA、IgM免疫球蛋白、补体C3组分或类粘蛋白方面,均未发现显著差异。患者组的触珠蛋白和α-抗胰蛋白酶水平显著升高。自身免疫抗体检测结果始终为阴性。研究结果与其他已发表的、常常相互矛盾的研究进行了比较。这些作者得出结论,所研究的ASP似乎不是一种免疫性疾病。

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