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在用紫外线照射处理过的表皮细胞免疫小鼠后,表皮中携带I-J的细胞负责产生可转移的抑制性细胞。

Epidermal I-J-bearing cells are responsible for transferable suppressor cell generation after immunization of mice with ultraviolet radiation-treated epidermal cells.

作者信息

Granstein R D

出版信息

J Invest Dermatol. 1985 Mar;84(3):206-9. doi: 10.1111/1523-1747.ep12265141.

Abstract

Subcutaneous immunization of mice with hapten-coupled, ultraviolet radiation (UVR)-treated epidermal cells (EC) results in a hyporesponsive delayed-type hypersensitivity (DTH) response associated with the appearance of afferent-acting, hapten-specific T suppressor (Ts) cells. Depletion of I-J-bearing cells from the EC population prior to UVR-exposure and hapten coupling prevents the appearance of these Ts cells. However, non-UVR-treated EC depleted of I-J-bearing cells and hapten-coupled are capable of immunizing mice for a DTH response. Therefore, the set of I-J-bearing EC appears to be distinct from classic Langerhans cells. A novel set of I-J-bearing EC appears to be responsible for Ts activation after subcutaneous immunization with hapten-coupled UVR-treated EC.

摘要

用半抗原偶联的、经紫外线辐射(UVR)处理的表皮细胞(EC)对小鼠进行皮下免疫,会导致迟发型超敏反应(DTH)反应低反应性,这与传入作用的、半抗原特异性T抑制(Ts)细胞的出现有关。在UVR照射和半抗原偶联之前,从EC群体中去除携带I-J的细胞可防止这些Ts细胞的出现。然而,去除携带I-J的细胞并进行半抗原偶联的未经UVR处理的EC能够使小鼠产生DTH反应。因此,携带I-J的EC群体似乎与经典的朗格汉斯细胞不同。一组新的携带I-J的EC似乎是在用半抗原偶联的UVR处理的EC进行皮下免疫后Ts激活的原因。

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