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新生儿及母亲体内缺乏前列腺素E2介导的单核细胞抑制活性。

Lack of prostaglandin E2-mediated monocyte suppressive activity in newborn and mothers.

作者信息

Fischer A, Durandy A, Mamas S, McCall E, Dray F, Griscelli C

出版信息

Clin Exp Immunol. 1982 Aug;49(2):377-85.

Abstract

An excess of adult blood adherent cells (monocytes) inhibits mitogen, antigen and allogeneic cell-induced lymphocyte proliferations. This inhibition is dependent on the number of the adherent monocytes in the cultures and is substantially reduced (by 60%) by indomethacin or anti-PGE2 antiserum. Newborn monocytes exert only a weak inhibitory effect and produce about eight times less PGE2 than adult monocytes. The production of PGE2 and the suppression can be induced by incubating newborn monocytes with mixed leucocyte culture supernatants. Both monocytes from mothers at the time of delivery and from newborn infants, usually exert a poor suppressive activity related to a low production of PGE2. We strongly suggest that the expression of the PGE2-mediated suppression by monocytes is under the control of activated short-lived suppressor lymphocytes.

摘要

过量的成人血液黏附细胞(单核细胞)会抑制有丝分裂原、抗原和同种异体细胞诱导的淋巴细胞增殖。这种抑制作用取决于培养物中黏附单核细胞的数量,吲哚美辛或抗PGE2抗血清可使其大幅降低(降低60%)。新生单核细胞仅产生微弱的抑制作用,其产生的PGE2比成人单核细胞少约八倍。将新生单核细胞与混合白细胞培养上清液一起孵育可诱导PGE2的产生和抑制作用。分娩时母亲的单核细胞和新生儿的单核细胞通常抑制活性较差,这与PGE2产生量低有关。我们强烈认为,单核细胞对PGE2介导的抑制作用的表达受活化的短期抑制性淋巴细胞的控制。

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