Abstract

Platelets transfusion is a safe process, but during or after the process, the recipient may experience an adverse reaction and occasionally a serious adverse reaction (SAR). In this review, we focus on the inflammatory potential of platelet components (PCs) and their involvement in SARs. Recent evidence has highlighted a central role for platelets in the host inflammatory and immune responses. Blood platelets are involved in inflammation and various other aspects of innate immunity through the release of a plethora of immunomodulatory cytokines, chemokines, and associated molecules, collectively termed biological response modifiers that behave like ligands for endothelial and leukocyte receptors and for platelets themselves. The involvement of PCs in SARs—particularly on a critically ill patient’s context—could be related, at least in part, to the inflammatory functions of platelets, acquired during storage lesions. Moreover, we focus on causal link between platelet activation and immune-mediated disorders (transfusion-associated immunomodulation, platelets, polyanions, and bacterial defense and alloimmunization). This is linked to the platelets’ propensity to be activated even in the absence of deliberate stimuli and to the occurrence of time-dependent storage lesions.

Highlights

  • Blood platelets are small anucleate cells essentially originating from megakaryocyte (MK) fragmentation

  • platelet components (PCs) are stored for a maximum of 5 days before being issued to a patient in need; prior to that, during their shelf life, platelets “spontaneously,” i.e., with no acknowledged exogeneous stimulus, release a number of CKs, soluble CD40L (sCD40L) [17, 30] in high enough quantities to exert functional activities on target cells possessing the ad hoc receptors. sCD40L was found to be consistently and significantly elevated in PCs that had led to serious adverse reaction (SAR) comprising various syndromes, including transfusion-related acute lung injury (TRALI) [30, 33]

  • In all cases investigated to date, either based on clinical observations or tested experimentally, biological response modifiers (BRMs) are found to be in close association

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Summary

INTRODUCTION

Blood platelets are small anucleate cells essentially originating from megakaryocyte (MK) fragmentation. These cells have a dense cytoskeleton that maintains their discoid shape in normal state and changes the platelets to a spherical form after their activation [1]. Platelets play a key role in vascular repair and maintenance of homeostasis, in primary hemostasis. Platelets play an important role in innate and adaptive immunity by interacting directly or indirectly with other immune cells to trigger or maintain the inflammatory response [1,2,3]. This review summarizes current information surrounding the association between inflammation and transfused platelets

A BRIEF OVERVIEW OF PLATELET FUNCTIONS
A BRIEF OVERVIEW OF PC TRANSFUSION
Findings
CONCLUSION
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