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由包膜糖蛋白120 T辅助细胞位点和B细胞中和表位组成的多价人类免疫缺陷病毒合成免疫原。

Polyvalent human immunodeficiency virus synthetic immunogen comprised of envelope gp120 T helper cell sites and B cell neutralization epitopes.

作者信息

Palker T J, Matthews T J, Langlois A, Tanner M E, Martin M E, Scearce R M, Kim J E, Berzofsky J A, Bolognesi D P, Haynes B F

机构信息

Department of Medicine, Duke University Medical Center, Durham, NC 27710.

出版信息

J Immunol. 1989 May 15;142(10):3612-9.

PMID:2469721
Abstract

In previous studies, we have used antisera raised to envelope (env)-gene-encoded synthetic peptides to identify a region of (HIV) glycoprotein (gp) 120 env protein designated SP10 that contains a type-specific neutralizing determinant. To develop a polyvalent, synthetic peptide inoculum that can evoke both neutralizing antibodies and T cell proliferative responses to more than one HIV isolate, synthetic peptides containing type-specific neutralizing determinants of gp120 from HIV isolates HTLV-IIIB (IIIB), HTLV-IIIMN (MN) and HTLV-IIIRF (RF) were coupled to a 16 amino acid T cell epitope (T1) of HIV-IIIB gp120 and used to immunize goats. Goat antisera to each T1-SP10 peptide derived from the SP10 region of gp120 of IIIB, MN, and RF neutralized HIV isolates IIIB, MN and RF in a type-specific manner. Moreover, peripheral blood T cells from immunized goats also proliferated in a type-specific manner to peptides derived from gp120 of IIIB, MN, and RF. When combined in a trivalent inoculum, T1-SP10 peptides from HIV-1 isolates IIIB, MN, and RF evoked a high titered neutralizing antibody response to isolates IIIB, MN, and RF in goats and as well induced immune T cells to undergo blast transformation in the presence of peptides derived from gp120 of all three HIV isolates. The T1 portion of the T1-SP10 construct was shown to induce a B cell antibody response against determinants within the T1 peptide in addition to inducing T cell proliferative responses in immune goat T cells. Moreover, the SP10 portion of the T1-SP10 constructs not only induced B cell antibody production but also induced type-specific T cell proliferative responses localized to the C-terminal variable sequences of the SP10 peptides. Finally, the T1-SP10 peptide construct induced memory T cell proliferative responses to native gp120 env protein. Thus, combinations of homologous SP10 region synthetic peptides containing type-specific neutralizing determinants and T cell epitopes of HIV gp120 may be useful in man to elicit high titered neutralizing B cell responses and, as well, T cell responses to more than one HIV isolate.

摘要

在先前的研究中,我们使用针对包膜(env)基因编码的合成肽产生的抗血清,来鉴定HIV糖蛋白(gp)120 env蛋白的一个区域,命名为SP10,该区域包含一个型特异性中和决定簇。为了开发一种多价合成肽接种物,使其能够引发中和抗体以及对多种HIV分离株的T细胞增殖反应,将来自HIV分离株HTLV-IIIB(IIIB)、HTLV-IIIMN(MN)和HTLV-IIIRF(RF)的gp120型特异性中和决定簇的合成肽,与HIV-IIIB gp120的一个16氨基酸T细胞表位(T1)偶联,并用于免疫山羊。针对源自IIIB、MN和RF的gp120的SP10区域的每个T1-SP10肽的山羊抗血清,以型特异性方式中和HIV分离株IIIB、MN和RF。此外,来自免疫山羊的外周血T细胞也以型特异性方式对源自IIIB、MN和RF的gp120的肽发生增殖反应。当以三价接种物组合时,来自HIV-1分离株IIIB、MN和RF的T1-SP10肽在山羊中引发了针对分离株IIIB、MN和RF的高滴度中和抗体反应,并且在存在源自所有三种HIV分离株的gp120的肽的情况下,诱导免疫T细胞发生母细胞转化。T1-SP10构建体的T1部分除了在免疫山羊T细胞中诱导T细胞增殖反应外,还显示出诱导针对T1肽内决定簇的B细胞抗体反应。此外,T1-SP10构建体的SP10部分不仅诱导B细胞抗体产生,还诱导定位于SP10肽C末端可变序列的型特异性T细胞增殖反应。最后,T1-SP10肽构建体诱导对天然gp120 env蛋白的记忆T细胞增殖反应。因此,包含HIV gp120型特异性中和决定簇和T细胞表位的同源SP10区域合成肽的组合,可能对人类有用,以引发高滴度中和B细胞反应,以及对多种HIV分离株的T细胞反应。

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