Key result
Symptomatic CMV infection in immunocompetent adults was not associated with variations in TLR2, 3, 4, 7, and 9 genes, but induced a skewed pro-inflammatory TLR-mediated cytokine response.
Why the study?
Limited data are available on the role of innate immunity receptors, such as toll-like receptors, in contributing to antiviral responses and inflammation during human cytomegalovirus infection.
Are TLR gene polymorphisms or functional TLR-mediated cytokine responses associated with symptomatic CMV mononucleosis in immunocompetent adults?
Case-Control (n=164)
Yes
Are TLR gene polymorphisms or functional TLR-mediated cytokine responses associated with symptomatic CMV mononucleosis in immunocompetent adults?
Symptomatic CMV mononucleosis in immunocompetent adults is associated with a skewed pro-inflammatory TLR-mediated response, but not with specific TLR gene polymorphisms.
Answers are grounded in this paper and cite their sources.
Skewed TLR cytokine response in symptomatic CMV warrants caution in immunocompetent adults; hypothesis-generating for immunomodulation, larger studies needed.
Background. Human cytomegalovirus (CMV) modulates both innate and adaptive immune responses. However, limited data are available on the role of receptors of innate immunity, such as toll-like receptors (TLR) in contributing to antiviral responses and inflammation. Objectives. The aim of this translational study was to characterize TLR responses in immunocompetent patients with primary and symptomatic CMV infection. Study Design. The study population consisted of 40 patients suffering of CMV mononucleosis and 124 blood donors included as controls. We evaluated the association between TLR2, 3, 4, 7 and 9 gene single nucleotide polymorphism (SNP) and susceptibility to symptomatic CMV infection in immunocompetent adults. Additionally, functional TLR-mediated cytokine responses in supernatants of short-term cultures of whole blood from patients with CMV mononucleosis and blood donors were evaluated. Results. TLR2 and TLR7/8 responses were altered in CMV infected patients as compared to healthy donors and were associated to release of higher levels of pro-inflammatory, but not anti-inflammatory mediators. The analysis on the TLRs SNP indicated no difference between patients with CMV infection and the control group. Conclusions. No variation in the TLR2,3,4,7 and 9 genes was associated to the development of symptomatic CMV infection in immunocompetent adults. Nevertheless, TLR-mediated responses in CMV-infected patients appeared to be skewed towards a pro-inflammatory profile, which may contribute to the development of inflammatory symptoms during the CMV mononucleotic syndrome.
No takes yet. Share an insight, caveat, or question.
Frascaroli et al. (2020) conducted a case-control in CMV mononucleosis (n=164). Symptomatic CMV infection vs. Healthy blood donors was evaluated on Association of TLR2, 3, 4, 7, and 9 gene single nucleotide polymorphisms with symptomatic CMV infection. Symptomatic CMV infection in immunocompetent adults was not associated with variations in TLR2, 3, 4, 7, and 9 genes, but induced a skewed pro-inflammatory TLR-mediated cytokine response.
Synapse has enriched 10 related papers. Consider them for comparative context: