Février M, Chen J, Duquenne C, Liacopoulos P
Ann Inst Pasteur Immunol (1985). 1986 May-Jun;137C(3):299-311. doi: 10.1016/s0771-050x(86)80048-1.
Mouse spleen cells cultured with muramyl dipeptide (MDP) release factors (SMF, or splenic macrophage factors) which enhance the in vitro plaque-forming cell (PFC) response to the T-dependent antigen SRBC (sheep red blood cells). The present study substantiates previous results and shows that T cells were the target cells of such conditioned medium. We investigated which T-cell subpopulations had their activities modified by these factors. In the presence of SMF, T cells educated in vivo elicited enhanced PFC responses to both specific educating antigen and an unrelated antigen (during a bystander response). This could indicate that SMF potentiates Th2-cell activity. Moreover, in vivo matured but unprimed thymocytes, which are unable to cooperate with virgin B cells in an in vitro T-dependent response, are able to do so when SMF is added in cooperative cultures. It is concluded that MDP-conditioned medium allows the maturation/differentiation of a subset of T cells to the point where they can be stimulated by the antigen.
用胞壁酰二肽(MDP)培养的小鼠脾细胞释放因子(SMF,即脾巨噬细胞因子),这些因子可增强体外对T细胞依赖性抗原绵羊红细胞(SRBC)的空斑形成细胞(PFC)反应。本研究证实了先前的结果,并表明T细胞是这种条件培养基的靶细胞。我们研究了哪些T细胞亚群的活性受到这些因子的影响。在存在SMF的情况下,体内受过诱导的T细胞对特异性诱导抗原和无关抗原均引发增强的PFC反应(在旁观者反应期间)。这可能表明SMF增强了Th2细胞的活性。此外,体内成熟但未致敏的胸腺细胞,在体外T细胞依赖性反应中无法与未致敏的B细胞协同作用,但在协同培养中加入SMF时则能够协同。得出的结论是,MDP条件培养基可使一部分T细胞成熟/分化到能够被抗原刺激的程度。