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Pd l1 ig

Manufactured by R&D Systems

PD-L1-Ig is a laboratory product that functions as a recombinant fusion protein composed of the extracellular domain of human PD-L1 and the Fc region of human IgG1. PD-L1-Ig can be used for research purposes.

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2 protocols using pd l1 ig

1

T Cell Polarization and Checkpoint Regulation

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Naïve CD4+CD25negCD62L+ T cells were isolated using CD4+ T cell isolation kit II (negative selection), CD25 microbead kit (negative selection), and CD62L microbeads (all from Miltenyi Biotec, Auburn, CA). Isolated CD4+CD25negCD62L+ T cells were plated in flasks coated with αCD3 (5 μg/ml) in the presence of αCD28 (5 μg/ml) and Th1-(10 ng/ml IL-12, 1 μg/ml αIL-4), Th2- (10 ng/ml IL-4, μg/ml αIFNγ), or Th17- (20 ng/ml IL-6, 5 ng/ml TGFβ1, 10 ng/ml IL-23, 1 μg/ml αIL-4, 1 μg/ml αIFNγ) skewing cytokines. Cells were cultured for 5 days. Cultures were skewed or stimulated in the presence of either plate bound IgG-Fc (5 μg/ml), or plate bound PD-L1-Ig (R&D Systems, Minneapolis, MN). Cells were rested overnight in the absence of stimulation, and then restimulated on plates coated with various concentrations of αCD3, IgG-Fc and PD-L1-Ig. Cytokine production was assessed by ELISA using eBioscience mAbs.
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2

Immunomodulatory Interventions in Murine Pregnancy

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A total of 50 female CBA/J, 20 male DBA/2 and 5 male BALB/c mice (age, 8–10 weeks; weight, 12–15 g) were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. The mice were maintained under controlled conditions at 19–23°C with 12-h light/dark cycles and 40–60% humidity, with free access to drinking water and food. Animal experiments were approved by the Institutional Animal Care and Use Committee of Kunming Medical University.
The mice were divided into the following five groups: the normal group (10 CBA/J mice), the spontaneous abortion group (10 CBA/J mice), the PD-L1 Ig group (0.1 mg/kg PD-L1 Ig; 10 CBA/J mice), the CD40L mAb group (0.2 mg/kg anti-CD40L mAbs; 10 CBA/J mice) and the PD-L1 Ig + CD40L mAb group (0.1 mg/kg PD-L1 Ig and 0.2 mg/kg anti-CD40L mAbs; 10 CBA/J mice). The normal group was mated with male BALB/c mice (n=5). The spontaneous abortion, PD-L1 Ig, CD40L mAb and PD-L1 Ig + CD40 mAb groups were mated with male DBA/J mice (n=5/group). The day the vaginal plug was observed was recorded as day 0 of gestation. PD-L1 Ig and/or anti-CD40L mAbs were injected intraperitoneally into CBA/J female mice at days 4, 6, 8, 10 and 12 of gestation. At day 14 of gestation, the CBA/J mice were euthanized with an overdose of sodium pentobarbital (150 mg/kg; intraperitoneally). PD-L1 Ig and anti-CD40L mAbs were purchased from R&D Systems.
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