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April 19, 2026Science Immunology1 citations

Gene delivery of immunomodulatory cytokines to the lung preserves respiratory function during inflammatory challenge

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NMNtombizodwa MakuyanaLSLaura SeldeslachtsLMLauren Michiels

Key Points

  • The research aims to develop a gene delivery method for expressing anti-inflammatory cytokines in the lung to restore immune balance during infections.
  • Development of gene delivery system using AAV6.2-CC10 vector.
  • Induction of interleukin-2, IL-1 receptor antagonist, and IL-10 in lung tissue.
  • Assessment of immune responses in the lung and peripheral immune system in response to gene delivery.
  • Successfully expressed IL-2, IL-1RA, and IL-10 in the lung without affecting systemic immunity.
  • Reduced respiratory pathology associated with influenza-related pulmonary infections.
  • Achieved local immune homeostasis without systemic side effects.

Abstract

Respiratory infections that result in severe and life-threatening immune-mediated respiratory decline are a major public health issue. Controlling local respiratory immune reactions without the use of systemic immunosuppressants remains an unmet clinical challenge. We developed a gene delivery system to express anti-inflammatory cytokines in the lung, which reestablishes local immune homeostasis without triggering systemic effects. Using an adeno-associated vector cargo system (AAV6.2- CC10 ), we induced production of interleukin-2 (IL-2), IL-1 receptor antagonist (IL-1RA), and IL-10 in situ in the lung microenvironment, with no detectable expression or immunological deviation in the peripheral immune system. We demonstrate the effective potential of IL-2, IL-1RA, and IL-10 as immunomodulatory cargos in severe infectious challenge, which reduced respiratory pathology after influenza-associated pulmonary aspergillosis. Thus, the AAV6.2- CC10 platform enables targeted delivery of biologics to the lung, modulates the lung environment, and improves pathology without inducing systemic immune reactions.

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Cite This Study

Makuyana et al. (2026) studied this question.

synapsesocial.com/papers/69e4734c010ef96374d8f274https://doi.org/10.1126/sciimmunol.adv7969
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