Induction of antibody synthesis in vitro by immunogenic RNA.

R Slomski, A Horst
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Abstract

Spleen cells (SpC) from nonimmunized CFW mice were converted into antibody plaque-forming cells (PFC) by incubation with RNA extracted from livers and spleens of immunized mice (4 days after a single intravenous injection of 0.2 ml of 5% sheep red blood cells (SRBC). RNA was extracted by the phenol-detergent procedure only when sensitization determined by the technique of Jerne showed at least one PFC per 1,500 SpC. Immunogenic activity of RNA from lives of immunized mice was identical with that of RNA from spleens. Immunogenic RNA was inactivated by RNase but not by DNase or pronase, indicating that induction of antibody synthesis requires intact RNA. Newly synthesized antibodies were specific for the SRBC injected antigen; plaques did not occur when other RBC were used in place of SRBC for the in vitro test. The influence of antibiotics on this phenomenon is also discussed.

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免疫原性RNA体外诱导抗体合成。
经单次静脉注射含5%羊红细胞0.2 ml后(4 d),将未免疫的CFW小鼠脾细胞(SpC)与免疫小鼠肝脏和脾脏提取的RNA孵育,转化为抗体斑块形成细胞(PFC)。只有当由Jerne技术确定的致敏性显示每1,500 SpC至少有一个PFC时,才通过苯酚洗涤剂程序提取RNA。免疫小鼠活体RNA的免疫原性活性与脾脏RNA的免疫原性活性相同。免疫原性RNA可以被RNase灭活,而不能被DNase或pronase灭活,这表明诱导抗体合成需要完整的RNA。新合成的抗体对SRBC注射抗原具有特异性;当使用其他红细胞代替SRBC进行体外试验时,斑块不会发生。并讨论了抗生素对这一现象的影响。
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