The Combination of Nirmatrelvir and Ivermectin Exerts Strongly Synergistic Antiviral and Anti-Inflammatory Effects Against Murine Coronavirus Infection of Macrophages

How et al., International Journal of Molecular Sciences, doi:10.3390/ijms27167316, Aug 2026
In vitro study showing strong synergistic antiviral and anti-inflammatory effects with the combination of ivermectin and nirmatrelvir for RAW264.7 murine macrophages infected with murine hepatitis virus (MHV).
The combination achieved at least 5-6 log10 reduction in live virus titer and 3 log10 reduction in viral RNA load at concentrations lower than either monotherapy, with a Bliss synergy score of 9.95 for live virus titer.
The combination also markedly suppressed key pro-inflammatory cytokines implicated in cytokine storm, including IL-6 (reduced to undetectable levels), TNFα (7.5-fold reduction), IL-1β (9.3-fold reduction), and MCP-1 (3-fold reduction).
Authors hypothesize that the benefit comes from complementary host-targeting mechanisms, potentially including importin-mediated nuclear transport inhibition and STAT3-mediated IL-6 suppression.
Nirmatrelvir combined with azithromycin or doxycycline showed only additive or mildly additive antiviral effects (Bliss scores of 3.79 and 0.66, respectively) with limited immunomodulatory activity.
This study uses a murine coronavirus model rather than SARS-CoV-2 directly. The results are reasonably likely to generalize qualitatively to SARS-CoV-2, although the magnitude of the effect and degree of synergy may differ. MHV and SARS-CoV-2 are both betacoronaviruses with conserved replication machinery, nirmatrelvir directly targets the conserved coronavirus main protease, and prior ivermectin-remdesivir synergy has been observed in both MHV and SARS-CoV-2 models. The study uses murine RAW264.7 macrophages rather than human airway cells, so species- and cell-type-specific factors may alter the observed synergy.
Study covers ivermectin and paxlovid.
How et al., 16 Aug 2026, Singapore, peer-reviewed, 3 authors. Contact: micctk@nus.edu.sg (corresponding author), wilsonhzy@gmail.com, lexin.teh02@gmail.com.
In vitro studies are an important part of preclinical research, however results may be very different in vivo.
Abstract: Article The Combination of Nirmatrelvir and Ivermectin Exerts Strongly Synergistic Antiviral and Anti-Inflammatory Effects Against Murine Coronavirus Infection of Macrophages Wilson Z. Y. How 1 , Le Xin Teh 1 and Vincent T. K. Chow 1,2, * - 1 Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Kent Ridge, Singapore 117545, Singapore; wilsonhzy@gmail.com (W.Z.Y.H.); lexin.teh02@gmail.com (L.X.T.) - 2 Infectious Diseases Translational Research Program, Yong Loo Lin School of Medicine, National University of Singapore, Kent Ridge, Singapore 117545, Singapore * Correspondence: micctk@nus.edu.sg Abstract The emergence of SARS-CoV-2 variants and antiviral resistance highlights the need for improved therapeutic strategies against COVID-19 and other coronavirus infections. By pairing direct-acting antivirals with repurposed host-modulating drugs, combination therapy approaches may enhance antiviral efficacy while mitigating inflammation. In this study, we evaluated the effects of combining Nirmatrelvir (a SARS-CoV-2 main protease inhibitor) with Ivermectin, Azithromycin or Doxycycline-using a murine hepatitis virus (MHV) infection model of RAW264.7 macrophages. Checkerboard assays demonstrated that the Nirmatrelvir-Ivermectin combination exhibited strongly synergistic antiviral activity. This combination achieved potent inhibition of live virus titer of at least 5 to 6 log10 and reduction in viral RNA load of 3 log10, at drug concentrations much lower than the respective monotherapies. The Nirmatrelvir-Ivermectin combination treatment affected the coronavirus replication cycle at the same time-point of 8 h as Nirmatrelvir monotherapy. Moreover, multiplex cytokine protein profiling revealed that Nirmatrelvir-Ivermectin markedly suppressed key pro-inflammatory cytokines and chemokines associated with the cytokine storm, including IL-6, TNFα , IL-1 β , and MCP-1. Conversely, the combinations of Nirmatrelvir with Azithromycin or Doxycycline exhibited only additive or mildly additive effects, with alterations in certain cytokine levels. These findings support the potential of Nirmatrelvir-Ivermectin as a promising novel combination therapy with both antiviral and anti-inflammatory benefits, warranting further in vivo validation and clinical investigation. Keywords: Nirmatrelvir; Ivermectin; Azithromycin; Doxycycline; antiviral; anti-inflammatory; combination therapy; repurposed drugs; murine hepatitis virus; coronavirus
DOI record: { "DOI": "10.3390/ijms27167316", "ISSN": [ "1422-0067" ], "URL": "http://dx.doi.org/10.3390/ijms27167316", "abstract": "<jats:p>The emergence of SARS-CoV-2 variants and antiviral resistance highlights the need for improved therapeutic strategies against COVID-19 and other coronavirus infections. By pairing direct-acting antivirals with repurposed host-modulating drugs, combination therapy approaches may enhance antiviral efficacy while mitigating inflammation. In this study, we evaluated the effects of combining Nirmatrelvir (a SARS-CoV-2 main protease inhibitor) with Ivermectin, Azithromycin or Doxycycline—using a murine hepatitis virus (MHV) infection model of RAW264.7 macrophages. Checkerboard assays demonstrated that the Nirmatrelvir–Ivermectin combination exhibited strongly synergistic antiviral activity. This combination achieved potent inhibition of live virus titer of at least 5 to 6 log10 and reduction in viral RNA load of 3 log10, at drug concentrations much lower than the respective monotherapies. The Nirmatrelvir–Ivermectin combination treatment affected the coronavirus replication cycle at the same time-point of 8 h as Nirmatrelvir monotherapy. Moreover, multiplex cytokine protein profiling revealed that Nirmatrelvir–Ivermectin markedly suppressed key pro-inflammatory cytokines and chemokines associated with the cytokine storm, including IL-6, TNF-α, IL-1β, and MCP-1. Conversely, the combinations of Nirmatrelvir with Azithromycin or Doxycycline exhibited only additive or mildly additive effects, with alterations in certain cytokine levels. 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