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无细胞Th2细胞产物介导的抗原特异性、MHC限制的B细胞活化。抗原特异性辅助因子与白细胞介素-4之间的协同作用。

Antigen-specific, MHC-restricted B cell activation by cell-free Th2 cell products. Synergy between antigen-specific helper factors and IL-4.

作者信息

Guy R, Hodes R J

机构信息

Experimental Immunology Branch, National Cancer Institute, Bethesda, MD 20892.

出版信息

J Immunol. 1989 Sep 1;143(5):1433-40.

PMID:2474597
Abstract

Ag-specific and MHC-restricted Th clones of different Ag specificities and MHC haplotypes were tested for their ability to produce soluble factors capable of providing the signals required for B cell activation and IgG antibody production. Each of five Th clones tested generated significant helper activity in supernatants derived from coculture of the T cell clone with specific Ag and syngeneic APC. The same helper activity was detected in supernatants of clones stimulated with immobilized anti-CD3 antibody in the absence of Ag or APC. The secreted helper activity resembled the activity of the intact Th cells in that it was Ag-specific, carrier-hapten-linked and MHC-restricted. These T cell products functioned to activate only those B cells expressing MHC products which corresponded to the specificity of each Th clone. Thus, the specificity of the cell-free T cell product mimicked precisely that expressed by the intact Th cell and presumably mediated by the cell surface TcR. In addition to the apparent presence of specific helper factor in Th clone supernatants, a role for nonspecific lymphokines was also identified in these preparations. Although recombinant or purified IL-4 alone was not sufficient to stimulate hapten-primed B cells to secrete hapten-specific IgG antibodies, mAb specific for IL-4 blocked the induction of antibody secretion by Th cell supernatant. These results indicate that stimulation of B cells to produce hapten-specific IgG antibody requires at least two distinct signals: an Ag-specific T cell signal which is restricted by MHC products expressed on the B cells, and a nonspecific signal mediated at least in part by the lymphokine IL-4.

摘要

对具有不同抗原特异性和MHC单倍型的抗原特异性且受MHC限制的Th克隆进行了测试,以检测它们产生可溶性因子的能力,这些可溶性因子能够提供B细胞活化和IgG抗体产生所需的信号。所测试的五个Th克隆中的每一个在T细胞克隆与特异性抗原和同基因抗原呈递细胞共培养产生的上清液中都产生了显著的辅助活性。在没有抗原或抗原呈递细胞的情况下,用固定化抗CD3抗体刺激的克隆上清液中也检测到了相同的辅助活性。分泌的辅助活性类似于完整Th细胞的活性,因为它是抗原特异性的、载体-半抗原连接的且受MHC限制的。这些T细胞产物仅作用于激活那些表达与每个Th克隆特异性相对应的MHC产物的B细胞。因此,无细胞T细胞产物的特异性精确地模拟了完整Th细胞所表达的特异性,并且推测是由细胞表面TCR介导的。除了Th克隆上清液中明显存在特异性辅助因子外,在这些制剂中还确定了非特异性淋巴细胞因子的作用。虽然单独的重组或纯化IL-4不足以刺激经半抗原致敏的B细胞分泌半抗原特异性IgG抗体,但针对IL-4的单克隆抗体阻断了Th细胞上清液诱导抗体分泌的过程。这些结果表明,刺激B细胞产生半抗原特异性IgG抗体至少需要两个不同的信号:一个受B细胞上表达的MHC产物限制的抗原特异性T细胞信号,以及一个至少部分由淋巴细胞因子IL-4介导的非特异性信号。

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