Ricciardi-Castagnoli P, Robbiati F, Barbanti E, Colizzi V, Pini C, De Santis R, Doria G, Adorini L
Eur J Immunol. 1985 Apr;15(4):351-5. doi: 10.1002/eji.1830150409.
Polypeptides synthesized in a rabbit reticulocyte lysate system directed by mRNA from the T cell line LH8-105, obtained by radiation leukemia virus-induced transformation of hen egg-white lysozyme (HEL)-specific suppressor T lymphocytes, are able, when injected into mice, to specifically suppress the antibody response and delayed-type hypersensitivity to HEL. The suppressive activity exerted by in vitro translated proteins appears to be independent from post-translational modifications. These in vitro translated polypeptides display fine antigenic specificity in immunosuppression and bind to HEL but not to the closely related ring-necked pheasant egg-white lysozyme immunosorbents. Suppressive molecules obtained by cell-free translation of LH8-105 mRNA or by culture supernatant of LH8-105 cells display, by gel filtration, a similar molecular mass of about 82-90 kDa.
在兔网织红细胞裂解物系统中,由通过辐射白血病病毒诱导转化鸡卵清溶菌酶(HEL)特异性抑制性T淋巴细胞获得的T细胞系LH8-105的mRNA指导合成的多肽,当注射到小鼠体内时,能够特异性抑制对HEL的抗体反应和迟发型超敏反应。体外翻译的蛋白质所发挥的抑制活性似乎与翻译后修饰无关。这些体外翻译的多肽在免疫抑制中表现出良好的抗原特异性,与HEL结合,但不与密切相关的环颈雉卵清溶菌酶免疫吸附剂结合。通过LH8-105 mRNA的无细胞翻译或LH8-105细胞的培养上清液获得的抑制分子,经凝胶过滤显示,其分子量相似,约为82-90 kDa。