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新型辅助艾美耳球虫肌动蛋白结合蛋白复合物对肠道宿主针对活堆型艾美耳球虫攻击感染的免疫反应的评估。

Evaluation of novel adjuvant Eimeria profilin complex on intestinal host immune responses against live E. acervulina challenge infection.

作者信息

Lee Sung Hyen, Lillehoj Hyun S, Jang Seung I, Lee Kyung Woo, Kim Duk Kyung, Lillehoj Erik P, Yancey Robert J, Dominowski Paul J

机构信息

Animal and Natural Resources Institute, Agricultural Research Service-United States Department of Agriculture, Beltsville, MD 20705, USA.

出版信息

Avian Dis. 2012 Jun;56(2):402-5. doi: 10.1637/9906-082411-ResNote.1.

Abstract

The effects against avian coccidiosis of two novel adjuvants, Quil A/cholesterol/dimethyl dioctadecyl ammonium bromide/Carbopol (QCDC) and QCDC/Bay R1005 (R)/cytosine-phosphate-guanosine (CpG) oligodeoxynucleotides (CpG ODN [T]) (QCDCRT) emulsified with profilin, a conserved Eimeria recombinant protein, were determined in broiler chickens. Chickens were subcutaneously immunized with isotonic saline (control group), profilin (P), profilin emulsified with QCDC (P-Q), or profilin with QCDCRT (P-QR) at 2 and 9 days post-hatch and orally challenged with 1.0 x 10(4) sporulated oocysts of Eimeria acervulina (EA) at 7 days postimmunization. All profilin-immunized groups showed increased body weight gain when compared to the control group, and the P-QR group had significantly higher body weight gain than did those of the P and P-Q groups following EA challenge infection. All groups immunized with profilin showed significantly decreased intestinal lesions compared with the control group, with the P-QR group showing the lowest intestinal lesions among the profilin-treated groups. Finally, the P-QR group showed greater CD4+/CD8+ and TCR1+/TCR2+ splenocytes and higher antiprofilin serum antibody titers compared with the P and P-Q (or both) groups following EA challenge infection. These results further suggest that vaccination of chickens with profilin, in combination with the QCDCRT adjuvant, may provide a novel control strategy against EA infection in commercial flocks.

摘要

在肉鸡中测定了两种新型佐剂,即与保守的艾美耳球虫重组蛋白肌动蛋白结合蛋白乳化的Quil A/胆固醇/二甲基二十八烷基溴化铵/卡波姆(QCDC)和QCDC/ Bay R1005(R)/胞嘧啶-磷酸-鸟嘌呤(CpG)寡脱氧核苷酸(CpG ODN [T])(QCDCRT)对禽球虫病的影响。在孵化后第2天和第9天,用等渗盐水(对照组)、肌动蛋白结合蛋白(P)、与QCDC乳化的肌动蛋白结合蛋白(P-Q)或与QCDCRT的肌动蛋白结合蛋白(P-QR)对鸡进行皮下免疫,并在免疫后第7天用1.0×10⁴个堆型艾美耳球虫(EA)的孢子化卵囊进行口服攻毒。与对照组相比,所有用肌动蛋白结合蛋白免疫的组体重增加均有所增加,并且在EA攻毒感染后,P-QR组的体重增加显著高于P组和P-Q组。与对照组相比,所有用肌动蛋白结合蛋白免疫的组肠道病变均显著减少,在经肌动蛋白结合蛋白处理的组中,P-QR组的肠道病变最低。最后,在EA攻毒感染后,与P组和P-Q(或两者)组相比,P-QR组显示出更高的CD4⁺/CD8⁺和TCR1⁺/TCR2⁺脾细胞以及更高的抗肌动蛋白结合蛋白血清抗体滴度。这些结果进一步表明,用肌动蛋白结合蛋白联合QCDCRT佐剂对鸡进行疫苗接种可能为商业鸡群中预防EA感染提供一种新的控制策略。

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