Pathogenesis, Treatment and Prevention of Respiratory Viral Infections

A special issue of Pathogens (ISSN 2076-0817). This special issue belongs to the section "Viral Pathogens".

Deadline for manuscript submissions: closed (25 September 2023) | Viewed by 1922

Special Issue Editors


E-Mail Website
Guest Editor
Division of Infectious Diseases, University of Rochester Medical Center, Rochester, NY 14642, USA
Interests: respiratory viruses; vaccines; molecular diagnostics

E-Mail Website
Guest Editor
School of Medicine and Dentistry, University of Rochester Medical Center, 601 Elmwood Ave, P.O. Box 609, Rochester, NY 14642, USA
Interests: strategies for engineering new antivirals and improving vaccines

Special Issue Information

Dear Colleagues,

Acute respiratory infections and pneumonia are important causes of hospitalizations and mortality in children and adults and approximately one-third of cases are associated with viral infections. Therefore understanding the pathogenesis of influenza, SARS-CoV-2, respiratory syncytial virus (RSV) and other respiratory viruses is important to public health as well as the development of better vaccines and effective treatment strategies.

There are certain well-recognized risk factors such as extremes of age, pregnancy, and underlying cardiopulmonary conditions that have been shown to predispose individuals infected with viruses to have more severe and complicated outcomes. Yet, the severity of these illnesses can be influenced by many factors including the virus itself and host responses to infection. A common pathogenic mechanism for many respiratory viruses is disruption of the epithelial barrier by pro-inflammatory mediators such as IL6, IL-8, tumor necrosis factor-α (TNF-α), and interferon-γ. Cytokine storms and exaggerated respiratory tract inflammation have been postulated to contribute to disease severity. There is also increasing evidence in the literature for the importance of polymicrobial infections, with studies demonstrating greater rates of hospitalization and the need for ICU care in patients with viral-viral or viral-bacterial coinfections. RSV, human metapneumovirus (HMPV), RSV and human rhinovirus (HRV) infection increases adherence of colonizing bacteria to nasal epithelial cells and influenza suppresses or depletes macrophages and neutrophils. 

Understanding these mechanisms of pathogenesis continues to be the basis for the development of new therapies and vaccines, the field of which has expanded significantly in the last decade and even more rapidly during the SARS-CoV-2 pandemic.  Here we propose to comprehensively review the basic virology, the pathogenesis of the disease, epidemiology, and current methods of treatment and prevention for respiratory viruses which cause acute illnesses and carry a risk of severe outcomes in pediatric and adult populations.

Dr. Angela Branche
Prof. Dr. David J. Topham
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Pathogens is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • respiratory viruses
  • pathogenesis
  • treatment
  • prevention
  • epidemiology

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

13 pages, 1729 KiB  
Article
TLR Responses in Preterm and Term Infant Cord Blood Mononuclear Cells
by Jeremy Anderson, Georgia Bender, Cao Minh Thang, Le Quang Thanh, Vo Thi Trang Dai, Phan Van Thanh, Bui Thi Hong Nhu, Do Ngoc Xuan Trang, Phan Thi Phuong Trinh, Nguyen Vu Thuong, Nguyen Trong Toan, Kim Mulholland, Daniel G. Pellicci, Lien Anh Ha Do and Paul V. Licciardi
Pathogens 2023, 12(4), 596; https://doi.org/10.3390/pathogens12040596 - 14 Apr 2023
Cited by 3 | Viewed by 1524
Abstract
Preterm infants are more susceptible to severe bacterial and viral infectious diseases than their full-term counterparts. A major contributor to this increased susceptibility may be due to differences in their ability to respond to pathogens. While studies have demonstrated altered bacterial Toll-like receptor [...] Read more.
Preterm infants are more susceptible to severe bacterial and viral infectious diseases than their full-term counterparts. A major contributor to this increased susceptibility may be due to differences in their ability to respond to pathogens. While studies have demonstrated altered bacterial Toll-like receptor (TLR) responses, there is limited data on viral TLR responses in preterm infants. In this study, cord blood mononuclear cells (CBMCs) from 10 moderately preterm (30.4–34.1 wGA), 10 term (37–39.5 wGA) infants, and 5 adults were stimulated with TLR2 (lipoteichoic acid), TLR3 (poly I:C), TLR4 (lipopolysaccharide), TLR7/8 (R848), and TLR9 (CpG-ODN 2216) agonists. Following stimulation, the cellular response was measured by intracellular flow cytometry to detect cell-specific NF-κB (as a marker of the inflammatory response), and multiplex assays were used to measure the cytokine response. This study found that preterm and term infants exhibit very similar baseline TLR expression. In response to both bacterial and viral TLR agonists comparing cell-specific NF-κB activation, preterm infants exhibited increased monocyte activation following LTA stimulation; however, no other differences were observed. Similarly, no difference in cytokine response was observed following stimulation with TLRs. However, a stronger correlation between NF-κB activation and cytokine responses was observed in term infants following poly I:C and R848 stimulation compared to preterm infants. In contrast, despite similar TLR expression, adults produced higher levels of IFN-α following R848 stimulation compared to preterm and term infants. These findings suggest preterm and term infants have a similar capacity to respond to both bacterial and viral TLR agonists. As preterm infants are more likely to develop severe infections, further research is required to determine the immunological factors that may be driving this and develop better interventions for this highly vulnerable group. Full article
Show Figures

Figure 1

Back to TopTop