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September 20, 2025Frontiers in OncologyOpen Access

Treating and triggering hyperinflammation: tackling hemophagocytic lymphohistiocytosis and HLH-like syndromes in the pediatric cell therapy and critical care setting

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Authors

HWHolly WobmaLHLauren A. HendersonCDChristine Duncan

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Overview

Review highlights the role of HCT and new cell therapies in combating hyperinflammation in HLH patients.

Key Points

  • HCT is the only curative option for primary HLH, with ongoing challenges in managing associated hyperinflammation.
  • Secondary HLH can arise from various causes, requiring tailored approaches to manage inflammation and immune response.
  • New cellular therapies, like chimeric antigen receptor T cells, can provoke hyperinflammatory complications and need careful monitoring.
  • Effective management of HLH hinges on a thorough understanding of its pathophysiology and evolving treatment options.

Cite This Study

Wobma et al. (2025) studied this question.

synapsesocial.com/papers/68d439fa713b0b5dfea79cd8https://doi.org/10.3389/fonc.2025.1631557
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Infection-associated hemophagocytic lymphohistiocytosis: A comprehensive review2025
  2. 2Hemophagocytic lymphohistiocytosis: an update in diagnostics, criteria, and treatment considerations2025 · 4 citations
  3. 3Hemophagocytic Lymphohistiocytosis: A Life-Threatening Hyperinflammatory Syndrome2025 · 1 citations
  4. 4Editorial: Refractory and relapsed hemophagocytic lymphohistiocytosis in pediatric population: targeted therapy2025
  5. 5Prelude to the perfect storm: the many triggers of secondary hemophagocytic lymphohistiocytosis2025