AI Article Synopsis
- Cytomegalovirus (CMV) infection in solid-organ transplant (SOT) patients is associated with weakened immune responses, making them more vulnerable to other infections.
- The study found that patients infected with CMV had reduced cytokine production in response to various bacterial, fungal, and viral triggers, indicating a blunted inflammatory response.
- Additionally, even before acquiring CMV, some patients showed inherently lower immune responses, suggesting that other underlying patient factors also contribute to their increased susceptibility to infections.
Article Abstract
Cytomegalovirus (CMV) is an immunomodulatory virus that indirectly increases the risk for bacterial, fungal, and viral infections. However, the pathogenesis of this phenomenon is poorly understood. We determined whether inflammatory responses to different Toll-like receptor (TLR) ligands are blunted during CMV infection in solid-organ transplant (SOT) patients. Peripheral blood mononuclear cells from 38 SOT patients with and without CMV were incubated in the presence of various viral, fungal, and bacterial TLR ligands. Cytokines were measured in the supernatant by multiplex enzyme-linked immunosorbent assay. Patients had blunted cytokine responses to bacterial, fungal, and viral ligands during CMV infection when compared to the absence of CMV infection. This was independent of viral load, clinical presentation of CMV infection or immunosuppression, supporting the clinical observation in SOT recipients that CMV infection increases susceptibility to bacterial, fungal, and other viral infections. Moreover, in the absence of CMV infection, patients with subsequent CMV infection had lower cytokines in response to TLR ligands compared to those without subsequent CMV infection, suggesting that inherent differences in patients not directly related to CMV also contribute to this increased susceptibility. In summary, these data provide novel ex vivo evidence to support indirect effects of CMV.
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| http://dx.doi.org/10.1111/ajt.15371 | DOI Listing |
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