口服胸腺调节素对免疫缺陷大鼠肠绒毛中IgA B和T细胞的影响。

M G Márquez, G Pacheco, M E Roux
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引用次数: 0

摘要

先前关于在无蛋白日粮期间口服细菌免疫调节剂(1M-104和RN-301)影响的研究表明,肠道B细胞和T细胞再生增加,并伴有IgA抗体的产生。研究了免疫调节剂胸腺调节素(TmB)在蛋白质再饲喂期口服的有效性。TmB允许IgA B和CD5 T细胞恢复正常的肠道固有层再生,并降低活化的上皮内淋巴细胞(CD25+ T细胞亚群)的数量至控制值。因此,口服TmB可能是一种有用的治疗药物,因为它似乎可以改善具有免疫能力细胞的肠绒毛的再生。此外,它似乎在上皮水平上调节免疫监视,因为它增加了CD5+ T细胞,但减少了活化的T细胞。
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IgA B and T cells in the intestinal Villi of immunodeficient rats orally treated with thymomodulin.

Previous studies on the effect of the oral administration of bacterial immunomodulators (1M-104 and RN-301) during the protein free diet period, have shown an increase on B and T cell gut repopulation, accompanied by IgA antibody production. The usefulness of oral administration of the immunomodulator thymomodulin (TmB) during the protein refeeding period was investigated. TmB allowed the recovery of a normal repopulation of gut lamina propria with IgA B and CD5 T cells and decreases to control values the number of activated intraepithelial lymphocytes (CD25+ T cell subset). Therefore, the oral administration of TmB may be useful as a therapeutic agent as it seems to improve the repopulation of intestinal villi with immunocompetent cells. Also, it seems to regulate the immunosurveillance at the epithelium level as it increases the CD5+ T cells but decreases the activated ones.

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