Immunological Defects and Infectious Disease in Emergency

A special issue of Immuno (ISSN 2673-5601).

Deadline for manuscript submissions: closed (31 December 2023) | Viewed by 8208

Special Issue Editors


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Guest Editor
First Division of Infectious Diseases, Cotugno Hospital, 80131 Naples, Italy
Interests: novel coronavirus; infectious disease

Special Issue Information

Dear Colleagues,

Immunological defects and chronic inflammatory immunological diseases are able to induce different types of immunodeficiency that may predispose those suffering from them to several, sometimes severe, infections.

In these situations, infections almost always necessitate a visit to the emergency room; furthermore, infections are also frequent causes of clinical complications for inpatients that are hospitalized for other reasons.

The clinical outcome of this type of opportunistic infection is still a matter of discussion because septic shock and other life-threatening complications are not infrequent.

Yet another intriguing aspect of these disorders is related to immunosuppressive drugs used to treat systemic autoimmune diseases that represent a frequent reason for admission to emergency departments, along with the drug induced risk of developing a follow-up infection.

Therefore, we invite you to offer your experience in this field by sending your contribution in the form of a case report, case series, brief report, or regular clinical article to this Special Issue in the journal Immuno.

Dr. Alessandro Perrella
Dr. Novella Carannante
Guest Editors

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Keywords

  • immunological defects
  • infectious diseases
  • chronic inflammatory immunological diseases

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Published Papers (1 paper)

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22 pages, 2046 KiB  
Review
Immunopathogenesis of Nipah Virus Infection and Associated Immune Responses
by Brent Brown, Tanya Gravier, Ingo Fricke, Suhaila A. Al-Sheboul, Theodor-Nicolae Carp, Chiuan Yee Leow, Chinua Imarogbe and Javad Arabpour
Immuno 2023, 3(2), 160-181; https://doi.org/10.3390/immuno3020011 - 27 Apr 2023
Cited by 8 | Viewed by 7362
Abstract
Pandemics in the last two centuries have been initiated by causal pathogens that include Severe Acute Coronavirus 2 (SARS-CoV-2) and Influenza (e.g., the H1N1 pandemic of 2009). The latter is considered to have initiated two prior pandemics in 1918 and 1977, known as [...] Read more.
Pandemics in the last two centuries have been initiated by causal pathogens that include Severe Acute Coronavirus 2 (SARS-CoV-2) and Influenza (e.g., the H1N1 pandemic of 2009). The latter is considered to have initiated two prior pandemics in 1918 and 1977, known as the “Spanish Flu” and “Russian Flu”, respectively. Here, we discuss other emerging infections that could be potential public health threats. These include Henipaviruses, which are members of the family Paramyxoviridae that infect bats and other mammals. Paramyxoviridae also include Parainfluenza and Mumps viruses (Rubulavirus) but also Respiratory Syncytial virus (RSV) (Pneumovirus). Additionally included is the Measles virus, recorded for the first time in writing in 1657 (Morbillivirus). In humans and animals, these may cause encephalitis or respiratory diseases. Recently, two more highly pathogenic class 4 viral pathogens emerged. These were named Hendra Henipavirus (HeV) and Nipah Henipavirus (NiV). Nipah virus is a negative-sense single-stranded ribonucleic acid ((−) ssRNA) virus within the family Paramyxoviridae. There are currently no known therapeutics or treatment regimens licensed as effective in humans, with development ongoing. Nipah virus is a lethal emerging zoonotic disease that has been neglected since its characterization in 1999 until recently. Nipah virus infection occurs predominantly in isolated regions of Malaysia, Bangladesh, and India in small outbreaks. Factors that affect animal–human disease transmission include viral mutation, direct contact, amplifying reservoirs, food, close contact, and host cell mutations. There are different strains of Nipah virus, and small outbreaks in humans limit known research and surveillance on this pathogen. The small size of outbreaks in rural areas is suggestive of low transmission. Person-to-person transmission may occur. The role that zoonotic (animal–human) or host immune system cellular factors perform therefore requires analysis. Mortality estimates for NiV infection range from 38–100% (averaging 58.2% in early 2019). It is therefore critical to outline treatments and prevention for NiV disease in future research. The final stages of the disease severely affect key organ systems, particularly the central nervous system and brain. Therefore, here we clarify the pathogenesis, biochemical mechanisms, and all research in context with known immune cell proteins and genetic factors. Full article
(This article belongs to the Special Issue Immunological Defects and Infectious Disease in Emergency)
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