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August 17, 2025Microorganisms14 citationsOpen Access

Immunomodulation in Respiratory Syncytial Virus Infection: Mechanisms, Therapeutic Targets, and Clinical Implications

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VGVasiliki GeorgakopoulouVPVassiliki Pitiriga

Key Points

  • Excessive cytokine production contributes to immunopathology and severe disease in respiratory syncytial virus infection.
  • Therapeutic options remain limited, with emerging immunomodulatory therapies targeting specific cytokines and immune pathways.
  • Dysregulated immune responses led by RSV perpetuate viral persistence and increased severity of infections, particularly in vulnerable populations.
  • Innovative treatments aim to restore immune balance, enhancing responses against respiratory syncytial virus to improve clinical outcomes.

Abstract

Respiratory syncytial virus (RSV) remains a leading cause of acute lower respiratory tract infections globally, particularly affecting infants, older adults, and immunocompromised individuals. While recent advances in prophylaxis, such as long-acting monoclonal antibodies and maternal immunization, offer promise for prevention, therapeutic options for active infection remain limited. Severe RSV disease is often driven not solely by viral replication but by dysregulated host immune responses, including excessive cytokine production, T helper type 2 (Th2) and T helper type 17 (Th17) cell polarization, and impaired interferon signaling. RSV has evolved sophisticated immune evasion strategies, such as inhibition of dendritic cell maturation, degradation of signal transducer and activator of transcription 2 (STAT2) via nonstructural proteins 1 and 2 (NS1/NS2), and interference with pattern recognition receptor signaling, particularly Toll-like receptors (TLRs) and retinoic acid-inducible gene I (RIG-I)-like receptors. These mechanisms result in attenuated innate immune responses and defective adaptive immunity, contributing to viral persistence, immunopathology, and recurrent infections. Moreover, age-dependent vulnerabilities, such as immune immaturity in infants and immunosenescence in older adults, exacerbate disease severity. Excessive immune activation leads to bronchiolitis, airway remodeling, and long-term sequelae including wheezing and asthma. Emerging immunomodulatory therapies aim to restore immune balance, targeting cytokines (e.g., interleukin-6 IL-6, interleukin-1 beta IL-1β), the Janus kinase–signal transducer and activator of the transcription (JAK-STAT) pathway, or inflammasome activity. Host-directed therapies and direct-acting antivirals are also under investigation. A better understanding of RSV–host immune interactions is critical for optimizing therapeutic strategies and designing effective vaccines. This review synthesizes current knowledge on RSV immunopathogenesis and highlights immunomodulation as a promising frontier for therapeutic intervention.

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Cite This Study

Georgakopoulou et al. (2025) studied this question.

synapsesocial.com/papers/68a36dd90a429f7973330f92https://doi.org/10.3390/microorganisms13081876
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