SUPPRESSION BY HUMAN PLACENTAL PROTEIN-14 OF NATURAL-KILLER-CELL ACTIVITY

被引:208
作者
OKAMOTO, N
UCHIDA, A
TAKAKURA, K
KARIYA, Y
KANZAKI, H
RIITTINEN, L
KOISTINEN, R
SEPPALA, M
MORI, T
机构
[1] KYOTO UNIV, CTR RADIAT BIOL, DEPT LATE EFFECT STUDIES, KYOTO 606, JAPAN
[2] UNIV HELSINKI, CENT HOSP, DEPT OBSTET & GYNECOL 1, SF-00100 HELSINKI 10, FINLAND
关键词
PLACENTAL PROTEIN-14 (PP14); PLACENTAL PROTEIN-12 (PP12); LARGE GRANULAR LYMPHOCYTE (LGL); NATURAL KILLER (NK) CELL;
D O I
10.1111/j.1600-0897.1991.tb00713.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human decidua of early pregnancy contains considerable numbers of CD3-CD56+ natural killer (NK) cells. In this study, two major protein products of the decidua, placental protein 14 (PP14) and placental protein 12 (PP12), were tested for the ability to regulate human NK cell activity. In vitro overnight exposure to PP14 of blood lymphocytes or purified large granular lymphocytes (LGL) resulted in suppression of cytotoxicity against K562 target cells in a 4-h Cr-51 release assay. The NK inhibition was dependent on concentrations of PP14, being detectable at 5-mu-g/ml and reaching maximum at 50-mu-g/ml. Manifestation of PP14-induced NK suppression required 18-h contact with NK cells. The suppression of NK activity by PP14 was not abolished by indomethacin. In a target binding assay the number of PP14-treated LGL binding to K562 was comparable to that of untreated ones. By contrast with PP14, PP12 produced no effects on NK cells. These results indicate that PP14 suppresses the function of NK cells, which might be involved in prevention of maternal immune rejection of fetus at the fetomaternal interface.
引用
收藏
页码:137 / 142
页数:6
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