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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.

DOI:10.1111/1523-1747.ep12265141
PMID:2579166
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。

相似文献

1
Epidermal I-J-bearing cells are responsible for transferable suppressor cell generation after immunization of mice with ultraviolet radiation-treated epidermal cells.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。
J Invest Dermatol. 1985 Mar;84(3):206-9. doi: 10.1111/1523-1747.ep12265141.
2
Epidermal cells in activation of suppressor lymphocytes: further characterization.
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Splenic I-J-bearing antigen-presenting cells in activation of suppression: further characterization.
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Ocular immune responses. II. Priming of A/J mice in the vitreous induces either enhancement of or suppression of subsequent hapten-specific DTH responses.眼部免疫反应。II. 在玻璃体中对A/J小鼠进行致敏可诱导随后的半抗原特异性迟发型超敏反应增强或抑制。
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Antigen- and receptor-driven regulatory mechanisms. X. The induction and suppression of hapten-specific granulomas.抗原和受体驱动的调节机制。十、半抗原特异性肉芽肿的诱导与抑制。
Am J Pathol. 1982 Mar;106(3):421-31.
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Suppression of hapten-specific delayed-type hypersensitivity responses in mice by idiotype-specific suppressor T cells after administration of anti-idiotypic antibodies.给予抗独特型抗体后,独特型特异性抑制性T细胞对小鼠中半抗原特异性迟发型超敏反应的抑制作用。
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TNP-specific Lyt-2+ cytolytic T cell clones preferentially respond to TNP-conjugated epidermal cells.针对三硝基苯(TNP)的Lyt-2+细胞毒性T细胞克隆优先对三硝基苯偶联的表皮细胞产生反应。
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Suppressive effect of ultraviolet-B-irradiation of epidermal cells on the induction of contact sensitivity.
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引用本文的文献

1
Role of phagocytic macrophages in induction of contact hypersensitivity and tolerance by hapten applied to normal and ultraviolet B-irradiated skin.吞噬性巨噬细胞在通过应用于正常皮肤和紫外线B照射皮肤的半抗原诱导接触性超敏反应和耐受性中的作用。
Immunology. 1994 Oct;83(2):281-7.
2
Suppression of pathogenesis in cutaneous leishmaniasis by UV irradiation.紫外线照射对皮肤利什曼病发病机制的抑制作用。
Infect Immun. 1986 Mar;51(3):838-43. doi: 10.1128/iai.51.3.838-843.1986.
3
The effect of ultraviolet radiation-induced suppressor cells on T-cell activity.
紫外线辐射诱导的抑制细胞对T细胞活性的影响。
Immunology. 1987 Mar;60(3):353-60.
4
Effector and suppressor circuits of the immune response are activated in vivo by different mechanisms.免疫反应的效应和抑制回路在体内通过不同机制被激活。
Proc Natl Acad Sci U S A. 1987 Jun;84(11):3841-5. doi: 10.1073/pnas.84.11.3841.
5
Presentation of antigen to suppressor cells by a dimethylbenz (a) anthracene-resistant, Ia-positive, Thy-1-negative, I-J-restricted epidermal cell.由一种抗二甲基苯并(a)蒽、Ia阳性、Thy-1阴性、I-J受限的表皮细胞将抗原呈递给抑制细胞。
Immunology. 1990 Jan;69(1):97-103.
6
Control of Langerhans' cell density by a skin tumour-derived cytokine.一种皮肤肿瘤衍生细胞因子对朗格汉斯细胞密度的调控
Immunology. 1992 Sep;77(1):13-8.