在同种异体移植中，沿着移植骨看不到膜内新骨，实际上显示为一层抑制骨形成的纤维组织。
In the allografts, no intramembranous new bone was seen along the shaft of the graft, and in fact it, appeared that there was a layer of fibrous tissue inhibiting such bone.
其能够抑制同种异体的T细胞的应答和修饰抗原呈递细胞的成熟。
They are able to suppress allogenic T-cell response and modify maturation of antigen-presenting cells.
目的评价非糖皮质激素的免疫抑制方案防止大鼠同种异体胰岛移植排斥反应的效果。
Objective To evaluate the effect of anti-rejection of glucocorticoid-free immunosuppressive regimen on allogenic islet transplantation.
目的探讨FK506滴眼液对同种异体角膜缘移植术后的免疫抑制作用。
Objective To discuss the effects of the immunosuppression of FK506 eye drops on limbal allograft transplantation.
近年来，调节性T细胞在自身耐受和抑制同种异体排斥反应中的作用受到越来越多的重视。
Recently, accumulating evidences have shown that regulatory t cells play a key role both in maintenance of self tolerance and tolerance to allograft.
结论：未应用免疫抑制剂的条件下，吻合血管的颌下腺同种异体移植存在急性排斥反应。
Conclusion: Without using immunosuppressant, acute rejections exist in the allotransplantation of submandibular glands with blood vessel anastomosis.
免疫抑制剂FK506能有效地抑制周围神经同种异体和异种移植中的排斥反应。
FK506 can suppress the rejection of xenoma and xenograft effectively in the peripheral nerve.
在现代免疫抑制治疗下，急性排斥降到最低；然而，病人和长期的同种异体移植物生存并没有同时得到改善。
Acute rejection has been minimised under modern immunosuppression; however, patient and long-term allograft outcomes have not improved concurrently.
目的探讨同种异体肢体(手)移植术后免疫抑制剂的临床应用剂量的规律及疗效。
The rules and treatment results of the amount of the dosage of Immunosuppressive agents in these cases were analyzed and summed up in this study.
补充外源性IL- 10并联合应用低剂量免疫抑制药物方案对同种异体移植肝长期存活是有用的。
Supplementary exogenous IL-10 administration combined with low-dose immunosuppressive drug may be a useful strategy to induce long-term liver allograft survival.
结果自体角质形成细胞可抑制淋巴细胞对同种异体抗原的增殖。
Methods The mixed epidermal cell and lymphocyte culture (MELC) was established, in which auto-keratinocytes were added to mimic the effect exerted by the auto-islets in vivo.
选择在移植时同时抑制CD4和CD 8依赖的免疫途径的特异性免疫保护胰岛同种异体移植物，从早期和晚期的免疫损害。
Selection of specific immunotherapy to suppress both CD4 - and CD8-dependent immune pathways at the time of transplant protects islet allografts from both early and late immune damage.
选择在移植时同时抑制CD4和CD 8依赖的免疫途径的特异性免疫保护胰岛同种异体移植物，从早期和晚期的免疫损害。
Selection of specific immunotherapy to suppress both CD4 - and CD8-dependent immune pathways at the time of transplant protects islet allografts from both early and late immune damage.
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