Ninio Jacques, Amigorena Sebastian
Laboratoire de Physique Statistique, Ecole Normale Supérieure, 24 rue Lhomond, 75231 Paris cedex 05, France.
J Theor Biol. 2004 Dec 7;231(3):309-17. doi: 10.1016/j.jtbi.2004.06.026.
The specificity of the immunological responses is achieved through the cooperation of three classes of cells: B and T lymphocytes, and dendritic cells (DCs). A critical, intensely studied interaction is that between DCs and T cells, during which the DC presents MHC-bound antigenic fragments to the T cell receptor (TCR). There has been recent excitement about the possibility of increasing the signal-to-noise ratio in the detection of cognate antigen-TCR couples, by the use of kinetic proofreading mechanisms. We examine here the signal-to-noise problem in a broader perspective, and in particular, address the question of possible "antigen purification" mechanisms, prior to their presentation to the T cells. Ways in which the DCs might concentrate, purify and preserve their load of captured antigens are considered: (i) If antigens can be transferred from one DC to another, in such a way that the richer a DC in antigen, the more it captures antigens from other DCs, the antigens may end up concentrated in a small subset of DCs, (ii) antigen purification may be achieved through recycling interactions between DCs and B cells. A DC would transmit to a B cell antigen mixtures, and the DC would recapture only the antigens which can bind to the B cell's antibodies and (iii) dendrites, when they are present, may play an essential role in recapturing the antigens that were used in interactions of DCs with T cells, B cells, or other DCs, thereby reducing antigen losses. More generally, we provide a personal interpretation of cell-to-cell antigen transfers, in terms of a strategy in which there is a progressive emergence, through multiple interactions, of subsets of cells of each type better and better prepared for the subsequent rounds of interactions.
B淋巴细胞、T淋巴细胞和树突状细胞(DCs)。一种关键且被深入研究的相互作用是DCs与T细胞之间的相互作用,在此过程中,DC将与主要组织相容性复合体(MHC)结合的抗原片段呈递给T细胞受体(TCR)。最近,人们对利用动力学校对机制提高同源抗原 - TCR偶联检测中的信噪比的可能性感到兴奋。我们在此从更广泛的角度审视信噪比问题,特别是探讨在将抗原呈递给T细胞之前可能存在的“抗原纯化”机制问题。我们考虑了DCs集中、纯化和保存其捕获抗原负载的方式:(i)如果抗原可以从一个DC转移到另一个DC,使得抗原含量越丰富的DC从其他DC捕获的抗原越多,那么抗原最终可能集中在一小部分DC中;(ii)抗原纯化可以通过DCs与B细胞之间的循环相互作用来实现。DC会将抗原混合物传递给B细胞,然后DC只会重新捕获那些能与B细胞抗体结合的抗原;(iii)当存在树突时,它们可能在重新捕获DC与T细胞、B细胞或其他DC相互作用中使用过的抗原方面发挥重要作用,从而减少抗原损失。更一般地说,我们从一种策略的角度对细胞间抗原转移进行了个人解读,即通过多次相互作用,每种类型的细胞亚群会逐渐出现,并且为后续轮次的相互作用做好越来越好的准备。