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使用抗CD5免疫结合物治疗类风湿关节炎期间的免疫评估

Immunologic assessment during treatment of rheumatoid arthritis with anti-CD5 immunoconjugate.

作者信息

Cannon G W, Marble D A, Griffiths M M, Cole B C, McCall S, Schulman S F, Strand V

机构信息

Salt Lake City Veterans Affairs Medical Center, Department of Medicine, Utah 84148, USA.

出版信息

J Rheumatol. 1995 Feb;22(2):207-13.

PMID:7537827
Abstract

OBJECTIVE

To determine if sustained immunologic effects occurred after treatment of patients with rheumatoid arthritis (RA) with an immunoconjugate of murine anti-CD5 monoclonal antibody with ricin A chain (anti-CD5).

METHODS

We measured lymphocyte populations, mitogen induced peripheral blood mononuclear cell (PBMC) stimulation, cytokine levels, immunoglobulin levels, in vivo immune function, and clinical outcomes in 9 patients with RA treated with anti-CD5.

RESULTS

The treatment of patients with RA with anti-CD5 was associated with marked acute depletion of peripheral blood lymphocytes (p < 0.01) during and immediately after treatment. A sustained decrease in the number of CD3, CD4, CD5, and CD8 bearing lymphocytes persisted for 2 months after treatment (p < 0.05). After 3 months a mild decrease in the number of these lymphocyte populations persisted, but when compared to baseline values, the differences were not found to be statistically significant. Phytohemagglutinin induced PBMC proliferation was decreased at the 3-month followup (p < 0.05). Evaluations of mitogen induced cytokine and immunoglobulin production, immunoglobulin level, autoantibody, and in vivo antibody response to tetanus toxoid did not show any consistent change from baseline.

CONCLUSION

Anti-CD5 treatment of RA appears to be associated with a decrease in the population of cells bearing CD5, but does not appear to induce any persistent immunologic abnormalities.

摘要

目的

确定用鼠抗CD5单克隆抗体与蓖麻毒素A链的免疫偶联物(抗CD5)治疗类风湿关节炎(RA)患者后是否会产生持续的免疫效应。

方法

我们检测了9例接受抗CD5治疗的RA患者的淋巴细胞群体、丝裂原诱导的外周血单个核细胞(PBMC)刺激、细胞因子水平、免疫球蛋白水平、体内免疫功能和临床结局。

结果

用抗CD5治疗RA患者与治疗期间及治疗后即刻外周血淋巴细胞的显著急性耗竭相关(p<0.01)。治疗后2个月,携带CD3、CD4、CD5和CD8的淋巴细胞数量持续减少(p<0.05)。3个月后,这些淋巴细胞群体的数量仍有轻度减少,但与基线值相比,差异无统计学意义。在3个月的随访中,植物血凝素诱导的PBMC增殖减少(p<0.05)。对丝裂原诱导的细胞因子和免疫球蛋白产生、免疫球蛋白水平、自身抗体以及对破伤风类毒素的体内抗体反应的评估未显示与基线相比有任何一致的变化。

结论

抗CD5治疗RA似乎与携带CD5的细胞群体减少有关,但似乎不会诱导任何持续的免疫异常。

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