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母体对鼠类胚胎的同种免疫反应及移植物抗宿主反应(GVHR)。II. 胎盘提取物对致敏的抑制作用。

Maternal alloimmune reactions towards the murine conceptus and graft-versus-host reaction (GVHR). II. Inhibition of priming by placental extracts.

作者信息

Voisin J E, Kinsky R G, Voisin G A

出版信息

J Reprod Immunol. 1986 Jul;9(2):85-94. doi: 10.1016/0165-0378(86)90002-1.

DOI:10.1016/0165-0378(86)90002-1
PMID:3746778
Abstract

Gestation can induce a priming for a GVHR towards paternal strain antigens, although this priming is significantly lower than the one induced by experimental immunization. A role has been sought for placental substances in decreasing this priming through immunomodulation. BALB/c (H-2d) spleen cells do not usually induce a systemic, lethal GVHR in DBA/2 (H-2d) newborn mice except when the donors are preimmunized with DBA/2 cells. Placental extracts (as well as RPMI medium or liver extracts used as controls) were added to DBA/2 cells injected into BALB/c mice used as cell donors for GVH induction. The latter's spleen cells, harvested on day 6 after immunization, were used for systemic and local GVHR. In the systemic assay (lethal effect on DBA/2 newborn mice injected i.v. with BALB/c spleen cells) a significant protection was observed. In the local assay (popliteal lymph node assay in F1 hybrids injected with BALB/c spleen cells into the foot-pad) a highly significant inhibition of priming was detected in recipients injected with spleen cells from placental extract-treated donors. The stimulation index was even lower than that obtained with unprimed BALB/c spleen cells. The same type of local GVHR in (CBA/Ca X A/J) F1 hybrids injected with CBA cells led to similar results. In both situations (systemic and local GVHR) the observed inhibition was found to be specific to the priming cell strain. These results support the working hypothesis that placental substances are able to modify the systemic response of an organism towards both H-2 and non-H-2 alloantigens.

摘要

妊娠可诱导对父系菌株抗原的移植物抗宿主反应(GVHR)致敏,尽管这种致敏程度明显低于实验性免疫诱导的致敏。人们一直在寻找胎盘物质在通过免疫调节降低这种致敏方面的作用。BALB/c(H-2d)脾细胞通常不会在DBA/2(H-2d)新生小鼠中诱导全身性致死性GVHR,除非供体预先用DBA/2细胞免疫。将胎盘提取物(以及用作对照的RPMI培养基或肝脏提取物)添加到注入BALB/c小鼠的DBA/2细胞中,这些BALB/c小鼠用作GVH诱导的细胞供体。在免疫后第6天收获后者的脾细胞,用于全身性和局部GVHR。在全身性试验(对静脉注射BALB/c脾细胞的DBA/2新生小鼠的致死作用)中观察到显著的保护作用。在局部试验(将BALB/c脾细胞注射到足垫的F1杂种中的腘窝淋巴结试验)中,在注射了经胎盘提取物处理的供体脾细胞的受体中检测到对致敏的高度显著抑制。刺激指数甚至低于未致敏的BALB/c脾细胞所获得的刺激指数。在注射CBA细胞的(CBA/Ca×A/J)F1杂种中进行的相同类型的局部GVHR导致了类似的结果。在两种情况(全身性和局部GVHR)下,观察到的抑制作用被发现对致敏细胞株具有特异性。这些结果支持了胎盘物质能够改变生物体对H-2和非H-2同种异体抗原的全身性反应这一工作假设。

相似文献

1
Maternal alloimmune reactions towards the murine conceptus and graft-versus-host reaction (GVHR). II. Inhibition of priming by placental extracts.母体对鼠类胚胎的同种免疫反应及移植物抗宿主反应(GVHR)。II. 胎盘提取物对致敏的抑制作用。
J Reprod Immunol. 1986 Jul;9(2):85-94. doi: 10.1016/0165-0378(86)90002-1.
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Maternal alloimmune reactions towards the murine conceptus and graft-versus-host reaction (GVHR). I. Priming for anti-paternal GVHR by gestation.母体对小鼠胚胎的同种免疫反应及移植物抗宿主反应(GVHR)。I. 妊娠引发针对父系的GVHR。
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Specific depletion of graft-versus-host activity of normal or allosensitized parental spleen cells.正常或同种异体致敏亲代脾细胞移植物抗宿主活性的特异性耗竭。
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Attempts at standardization of lupus-like graft-vs-host disease: inadvertent repopulation by DBA/2 spleen cells of H-2-different nonirradiated F1 mice.狼疮样移植物抗宿主病标准化的尝试:H-2不同的未受照射F1小鼠被DBA/2脾细胞意外重新定植。
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Modulation of F1 cytotoxic potentials by GvHR. Host- and donor-derived cytotoxic lymphocytes arise in the unirradiated F1 host spleens under the condition of GvHR-associated immunosuppression.移植物抗宿主反应对F1细胞毒性潜能的调节。在移植物抗宿主反应相关免疫抑制条件下,宿主和供体来源的细胞毒性淋巴细胞在未受照射的F1宿主脾脏中产生。
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Modulation of F1 cytotoxic potentials by GvHR: role and mode of action of non-MHC genes that determine the hybrid resistance to GvHR-associated suppression of F1 cytotoxic potential.移植物抗宿主反应对F1细胞毒性潜能的调节:决定杂种对移植物抗宿主反应相关的F1细胞毒性潜能抑制的杂种抗性的非主要组织相容性复合体基因的作用及作用方式
J Immunol. 1984 May;132(5):2218-25.

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Expression of H-2 class I genes in murine extra-embryonic tissues.H-2 I类基因在小鼠胚外组织中的表达。
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