Khalifian Saami, Raimondi Giorgio, Lee Wp Andrew, Brandacher Gerald
Department of Plastic and Reconstructive Surgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Immunotherapy. 2014;6(5):637-53. doi: 10.2217/imt.14.25.
Transplantation tolerance remains an elusive goal, partly due to limitations in our understanding of the interplay between inflammatory mediators and their role in the activation and regulation of T lymphocytes. Although multiple mechanisms acting both centrally and peripherally are responsible for tolerance induction, the signaling pathways leading to activation or regulation of adaptive immunity are often complex, branched, redundant and modulated by the microenvironment's inflammatory milieu. Accumulating evidence clearly indicates that inflammatory cytokines limit the tolerogenic potential of immunomodulatory protocols by supporting priming of the immune system and counteracting regulatory mechanisms, ultimately promoting rejection. In this review, we summarize recent progress in the development of novel therapeutics to manipulate this inflammatory environment and achievements in targeted inhibition of inflammatory cytokine signaling. Ultimately, robust transplant tolerance induction will probably require a multifaceted, holistic approach that integrates the various mechanisms of tolerance induction, incorporates the dynamic alterations in costimulatory requirements of alloreactive T cells, while maintaining endogenous mechanisms of immune regulation.
移植耐受仍然是一个难以实现的目标,部分原因在于我们对炎症介质之间相互作用及其在T淋巴细胞激活和调节中的作用的理解存在局限性。尽管中枢和外周起作用的多种机制都负责诱导耐受,但导致适应性免疫激活或调节的信号通路通常很复杂、分支众多、冗余且受微环境炎症环境的调节。越来越多的证据清楚地表明,炎症细胞因子通过支持免疫系统的启动和对抗调节机制来限制免疫调节方案的致耐受潜力,最终促进排斥反应。在本综述中,我们总结了操纵这种炎症环境的新型疗法开发的最新进展以及炎症细胞因子信号靶向抑制方面的成果。最终,强大的移植耐受诱导可能需要一种多方面、整体的方法,该方法整合了耐受诱导的各种机制,纳入同种异体反应性T细胞共刺激需求的动态变化,同时维持免疫调节的内源性机制。