Waldenström macroglobulinemia (WM) is a lymphoplasmacytic lymphoma characterized by monoclonal immunoglobulin M (IgM) overproduction, leading to hyperviscosity syndrome and microvascular complications. While increased plasma viscosity is a well-recognized feature of WM, the impact of extreme IgM elevation on intrinsic red blood cell (RBC) mechanical properties remain incompletely characterized. Here, we report a case of WM with markedly elevated IgM associated with profound impairment of RBC deformability. Therapeutic plasma exchange rapidly reduced serum IgM levels, accompanied by parallel and sustained improvement in RBC deformability. Given the importance of RBC deformability in microvascular blood flow, these findings highlight a reversible, IgM-mediated alteration in RBC mechanics and provide novel insights into microcirculatory dysfunction in WM.
Radiation-induced brain injury (RIBI), a common adverse effect of cranial radiotherapy for head malignancies, causes severe complications, including blood-brain barrier (BBB) disruption, neuroinflammation, cognitive decline, and radiation necrosis (RN) that impair patients’ quality of life. The pathophysiology of RIBI involves intricate crosstalk between various central nervous system (CNS) cell types, with astrocytes, the principal CNS glial cells, serving as key mediators. Under physiological conditions, they sustain brain homeostasis, but their transition to reactive phenotypes and subsequent dysfunction propel RIBI development. This review summarizes recent advances in astrocytes’ pathophysiological roles in RIBI, focusing on mechanisms like reactive astrocyte polarization, neuroinflammation, BBB impairment, radiation-induced senescence, astrocyte-mediated RN progression, and pathological crosstalk with other CNS cells. It also outlines astrocyte-targeted therapeutic strategies with preclinical efficacy, including anti-inflammatory therapies, anti-vascular endothelial growth factor A (VEGFA) interventions, TSPO ligands, RAS blockers, apolipoprotein E (ApoE) regulation, Δ133p53, and microRNAs (miRNAs), which alleviate RIBI by targeting these pathological processes. A comprehensive understanding of astrocyte-mediated mechanisms and preclinical evidence will lay the foundation for developing targeted, low-toxicity therapies to mitigate RIBI in cranial radiotherapy patients.
