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由无载体或佐剂的合成链球菌抗原引发的表位特异性免疫。

Epitope specific immunity elicited by a synthetic streptococcal antigen without carrier or adjuvant.

作者信息

Jolivet M, Audibert F, Beachey E H, Tartar A, Gras-Masse H, Chedid L

出版信息

Biochem Biophys Res Commun. 1983 Dec 16;117(2):359-66. doi: 10.1016/0006-291x(83)91208-1.

Abstract

A polypeptide fragment of type 24 streptococcal M protein (pep M24) has been shown to raise protective anti-streptococcal antibodies in rabbits and humans when administered with adjuvants. More recently, such protective antibodies were shown to be evoked by a synthesized 35-residue sub-peptide fragment (S-CB7 synthetic cyanogen bromide fragment 7) of pep M24. We now show that the weak pep M24 immunogen induces high titers of long lasting antibodies when associated with murabutide, a synthetic derivative of MDP (NAcMur-L-Ala-D-Gln-n-butyl-ester) which is currently undergoing clinical trials. We demonstrate also that the polymerized synthetic S-CB7 administered without adjuvant or carrier evokes a strong epitope specific, protective immune response in mice primed with the parent pep M24. A booster dose of polymerized S-CB7 induced antibodies directed specifically against the S-CB7 structure whereas a booster dose of pep M24 evoked antibodies recognizing additional determinants of the whole pep M24 molecule.

摘要

已证明,24型链球菌M蛋白的多肽片段(pep M24)与佐剂一起给药时,可在兔和人体内产生保护性抗链球菌抗体。最近发现,pep M24的一个合成的35个残基的亚肽片段(S-CB7合成溴化氰片段7)也能诱发此类保护性抗体。我们现在发现,当与murabutide(MDP的一种合成衍生物,NAcMur-L-Ala-D-Gln-n-丁酯,目前正在进行临床试验)结合时,弱免疫原性的pep M24能诱导产生高滴度的持久抗体。我们还证明,在未用佐剂或载体的情况下给予聚合的合成S-CB7,能在以亲本pep M24免疫的小鼠中引发强烈的表位特异性保护性免疫反应。一剂加强剂量的聚合S-CB7可诱导产生特异性针对S-CB7结构的抗体,而一剂加强剂量的pep M24则引发能识别整个pep M24分子其他决定簇的抗体。

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