Vaquer S, Salmerón I, Salmerón-B O, Moix P, Márquez J A, Moltó L, Alvarez de los Heros J I, Salmerón O, Alvarez-Mon M
Departamento de Medicina, Facultad de Medicina, Universidad de Alcalá de Henares, España.
Rev Esp Fisiol. 1989;45 Suppl:359-69.
Normal development of pregnancy requires maternal immune system tolerance towards the fetoplacental allograft. Natural Killer (NK) cells can display spontaneous lytic activity against tumoral, and poorly differentiated cells, without a prior sensitization. Moreover this cytotoxic activity is not restricted by the Major Histocompatibility Complex (MHC). We investigated the existence of modifications in the NK activity mediated by peripheral blood mononuclear cells (PBMC) from pregnant women. A significant depression was found in this activity from the first trimester to the puerperium that cannot be ascribed to a defective number of NK cells among pregnant's PBMC. However this impaired NK activity can be reconstituted in vitro by incubation of PBMC with interleukin 2 (IL 2). Pregnancy is also associated with an absence of effectors and/or precursors which mediate other cytotoxic non MHC-restricted activities after long term incubation with IL 2, the so called Lymphokine Activated Killer (LAK) cells.
正常妊娠的发展需要母体免疫系统对胎儿胎盘同种异体移植物产生耐受性。自然杀伤(NK)细胞可以对肿瘤细胞和低分化细胞表现出自发的裂解活性,且无需预先致敏。此外,这种细胞毒性活性不受主要组织相容性复合体(MHC)的限制。我们研究了孕妇外周血单个核细胞(PBMC)介导的NK活性是否存在变化。发现从妊娠早期到产褥期,这种活性显著降低,这不能归因于孕妇PBMC中NK细胞数量的缺陷。然而,通过将PBMC与白细胞介素2(IL-2)孵育,这种受损的NK活性可以在体外重建。妊娠还与缺乏效应细胞和/或前体细胞有关,这些细胞在与IL-2长期孵育后介导其他细胞毒性非MHC限制活性,即所谓的淋巴因子激活的杀伤(LAK)细胞。