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疫苗接种与血小板生物学:揭示免疫止血相互作用

Vaccination and Platelet Biology: Unraveling the Immuno-Hemostatic Interplay.

作者信息

Ratnapriya Sneha, Yabaji Shivraj M

机构信息

Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

The National Emerging Infectious Diseases Laboratory, Boston University, Boston, MA 02215, USA.

出版信息

Vaccines (Basel). 2025 Apr 13;13(4):403. doi: 10.3390/vaccines13040403.

Abstract

Platelets, which have been traditionally associated with hemostasis and thrombosis functions, now receive attention for their role in immune responses that may affect vaccine development and effectiveness. Through their interactions with immune cells and modulation of inflammation alongside their role in antigen presentation, platelets become integral components of both innate and adaptive immune systems. New research shows platelets can improve vaccine effectiveness while reducing adverse side effects. During vaccine administration, platelets release cytokines and chemokines, which attract and stimulate immune cells to the injection site. Platelets work together with dendritic cells and T cells to support antigen processing and presentation, which leads to strong immune activation. Platelets' pro-inflammatory mediators strengthen local immune responses to boost protective immunity generation. Significant attention has been given to platelet involvement in vaccine-related thrombotic events, including vaccine-induced immune thrombotic thrombocytopenia (VITT). The rarity and severity of these events demonstrate the need to investigate the complex interplay between vaccine mechanisms and platelet activation. Exploration of the platelet-immune axis can lead to new methods for improving both the effectiveness and safety of vaccines. Researchers are working on creating innovative approaches for treatments that target platelet receptors and thrombosis pathways without interfering with the regular hemostatic functions of platelets. New vaccine development methods and personalized immunization strategies can emerge from targeting platelets with adjuvants and immune modulators.

摘要

血小板传统上与止血和血栓形成功能相关,现在因其在免疫反应中的作用而受到关注,这可能会影响疫苗的开发和效果。通过与免疫细胞的相互作用以及对炎症的调节,以及它们在抗原呈递中的作用,血小板成为先天免疫系统和适应性免疫系统的重要组成部分。新研究表明,血小板可以提高疫苗效果,同时减少不良副作用。在疫苗接种过程中,血小板会释放细胞因子和趋化因子,吸引并刺激免疫细胞到达注射部位。血小板与树突状细胞和T细胞协同作用,支持抗原处理和呈递,从而导致强烈的免疫激活。血小板的促炎介质会加强局部免疫反应,以促进保护性免疫的产生。血小板参与疫苗相关血栓事件,包括疫苗诱导的免疫性血栓性血小板减少症(VITT),已受到广泛关注。这些事件的罕见性和严重性表明,有必要研究疫苗机制与血小板激活之间的复杂相互作用。对血小板-免疫轴的探索可以带来提高疫苗有效性和安全性的新方法。研究人员正在致力于创造创新方法,以靶向血小板受体和血栓形成途径进行治疗,同时不干扰血小板的正常止血功能。通过用佐剂和免疫调节剂靶向血小板,可以出现新的疫苗开发方法和个性化免疫策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/078e/12031077/c49c86acb710/vaccines-13-00403-g001.jpg

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