In combat against viruses

Author(s):  
Irina Shirokova ◽  
◽  
Yuliya Prozherina ◽  

The late 20th century and the early 21st century have been marked by the explosive development of virology due to activation of viral infections. New mutations of the influenza virus, high incidence of persistent virus infections in humans, as well as respiratory viral diseases that have not yet been eradicated has boosted further development of this direction [1].

2021 ◽  
Vol 31 (1) ◽  
Author(s):  
Faruk Hadziselimovic

AbstractCryptorchidism is as common as type 2 diabetes or celiac disease. Boys with congenital cryptorchidism are at increased risk of infertility and testicular cancer. Zika syndrome, which affects pregnant women, is associated with a high incidence of undescended testes in the infant, accompanied by epididymal anomalies. Zika and influenza virus infections during pregnancy trigger a strong anti-inflammatory immune response and elevated estradiol levels. Elevated estradiol and α-fetoprotein in syncytiotrophoblasts from women who have given birth to cryptorchid boys are indicative of increased estradiol levels in the fetus. Here, I present a hypothesis that hypogonadotropic hypogonadism, cryptorchidism, and retarded epididymal development may be due to elevated fetal estradiol levels caused by viral infection during pregnancy.


2014 ◽  
Vol 5 (1) ◽  
pp. 23-27
Author(s):  
L. V. Yashchuk ◽  
N. V. Cherevach ◽  
A. I. Vinnikov

Cats and dogs kept at home, as well as other animals, are susceptible to infectious diseases caused by pathogenic microorganisms, including viruses. Viral infections in urban environments are extremely common and cause severe diseases in domestic animals which often lead to death, resulting in high material and moral damages to owners of animals. Therefore, investigation of the prevalence of pathogens of viral diseases is very important in our time. The aim of this work is to define the indicators of spreading viral diseases of animals in Dnipropetrovsk, to analyze the seasonal spread of viral infections in animals, and influence of sex and breed on the frequency of disease manifestations. Materials for research were obtained on the basis of three veterinary clinics in Dnipropetrovsk. During the study, we used serological methods of diagnostics of clinical materials, namely ELISA and IHA. Immunosorbent assay was performed using the thermostatic shaker ST-3 and strip immunoassay analyzer Stat Fax 303 Plus. Also we used commercial test systems VetExpert CAV Ag and Feline VacciCheck ImmunoComb®, based on the immuno-chromatographic method. During clinical studies of 491 animals (268 cats and 223 dogs) it was found that the most common respiratory viral infections in cats were calicivirus infection and rhinotracheitis, while in dogs there were viral diseases of gastrointestinal tract, i.e. enteritis and hepatitis. Using IHA method, we revealed the antibodies to respiratory viruses in the blood of deseased cats: to calicivirus – in 95 cats, to rhinotracheitis – in 60 cats; by ELISA method we identified antigens of parvovirus, enteritis pathogen, in biological material of 61 dogs, by IHA we found antibodies to virus of infectious hepatitis in 49 individuals. Based on these data, it has been revealed that during the winter months the animals suffered mostly the respiratory viral infections (60%), and in spring there were increased occur-rence of enteritis, observed in all age groups of animals. From May, hepatitis started to appear and prevailed for all summer months, mixed with enteritis (about 50% of total number of cases). Hepatitis was recorded both in cats and dogs. By the fall, recurrence was observed for calicivirus and herpes virus infections in cats, and the cases of enteritis decreased, while hepatitis was recorded until mid-October. Such statistics is kept relatively constant. The research results can be applied in the practice of veterinary laboratories for the development of diagnostic measures and prevention of viral diseases in domestic animals, as well as in the prediction of dissemination of viral infections in animals in the near future.


2008 ◽  
Vol 21 (2) ◽  
pp. 274-290 ◽  
Author(s):  
W. Garrett Nichols ◽  
Angela J. Peck Campbell ◽  
Michael Boeckh

SUMMARY Though several antivirals have been developed and marketed to treat influenza virus infections, the development of antiviral agents with clinical activity against other respiratory viruses has been more problematic. Here we review the epidemiology of respiratory viral infections in immunocompetent and immunocompromised hosts, examine the evidence surrounding the currently available antivirals for respiratory viral infections other than influenza, highlight those that are in the pipeline, and discuss the hurdles for development of such agents.


2019 ◽  
Vol 20 (13) ◽  
pp. 1108-1121 ◽  
Author(s):  
Miriam Dibo ◽  
Eduardo C. Battocchio ◽  
Lucas M. dos Santos Souza ◽  
Matheus D. Veloso da Silva ◽  
Bruna K. Banin-Hirata ◽  
...  

The epidemiological impact of viral diseases, combined with the emergence and reemergence of some viruses, and the difficulties in identifying effective therapies, have encouraged several studies to develop new therapeutic strategies for viral infections. In this context, the use of immunotherapy for the treatment of viral diseases is increasing. One of the strategies of immunotherapy is the use of antibodies, particularly the monoclonal antibodies (mAbs) and multi-specific antibodies, which bind directly to the viral antigen and bring about activation of the immune system. With current advancements in science and technology, several such antibodies are being tested, and some are already approved and are undergoing clinical trials. The present work aims to review the status of mAb development for the treatment of viral diseases.


2020 ◽  
Vol 20 (4) ◽  
pp. 423-432 ◽  
Author(s):  
Imre Kovesdi ◽  
Tibor Bakacs

: Viral interference, originally, referred to a state of temporary immunity, is a state whereby infection with a virus limits replication or production of a second infecting virus. However, replication of a second virus could also be dominant over the first virus. In fact, dominance can alternate between the two viruses. Expression of type I interferon genes is many times upregulated in infected epithelial cells. Since the interferon system can control most, if not all, virus infections in the absence of adaptive immunity, it was proposed that viral induction of a nonspecific localized temporary state of immunity may provide a strategy to control viral infections. Clinical observations also support such a theory, which gave credence to the development of superinfection therapy (SIT). SIT is an innovative therapeutic approach where a non-pathogenic virus is used to infect patients harboring a pathogenic virus. : For the functional cure of persistent viral infections and for the development of broad- spectrum antivirals against emerging viruses a paradigm shift was recently proposed. Instead of the virus, the therapy should be directed at the host. Such a host-directed-therapy (HDT) strategy could be the activation of endogenous innate immune response via toll-like receptors (TLRs). Superinfection therapy is such a host-directed-therapy, which has been validated in patients infected with two completely different viruses, the hepatitis B (DNA), and hepatitis C (RNA) viruses. SIT exerts post-infection interference via the constant presence of an attenuated non-pathogenic avian double- stranded (ds) RNA viral vector which boosts the endogenous innate (IFN) response. SIT could, therefore, be developed into a biological platform for a new “one drug, multiple bugs” broad-spectrum antiviral treatment approach.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
James D. Allen ◽  
Ted M. Ross

AbstractWhile vaccines remain the best tool for preventing influenza virus infections, they have demonstrated low to moderate effectiveness in recent years. Seasonal influenza vaccines typically consist of wild-type influenza A and B viruses that are limited in their ability to elicit protective immune responses against co-circulating influenza virus variant strains. Improved influenza virus vaccines need to elicit protective immune responses against multiple influenza virus drift variants within each season. Broadly reactive vaccine candidates potentially provide a solution to this problem, but their efficacy may begin to wane as influenza viruses naturally mutate through processes that mediates drift. Thus, it is necessary to develop a method that commercial vaccine manufacturers can use to update broadly reactive vaccine antigens to better protect against future and currently circulating viral variants. Building upon the COBRA technology, nine next-generation H3N2 influenza hemagglutinin (HA) vaccines were designed using a next generation algorithm and design methodology. These next-generation broadly reactive COBRA H3 HA vaccines were superior to wild-type HA vaccines at eliciting antibodies with high HAI activity against a panel of historical and co-circulating H3N2 influenza viruses isolated over the last 15 years, as well as the ability to neutralize future emerging H3N2 isolates.


2012 ◽  
Vol 87 (3) ◽  
pp. 1400-1410 ◽  
Author(s):  
Donald M. Carter ◽  
Chalise E. Bloom ◽  
Eduardo J. M. Nascimento ◽  
Ernesto T. A. Marques ◽  
Jodi K. Craigo ◽  
...  

ABSTRACTIndividuals <60 years of age had the lowest incidence of infection, with ∼25% of these people having preexisting, cross-reactive antibodies to novel 2009 H1N1 influenza. Many people >60 years old also had preexisting antibodies to novel H1N1. These observations are puzzling because the seasonal H1N1 viruses circulating during the last 60 years were not antigenically similar to novel H1N1. We therefore hypothesized that a sequence of exposures to antigenically different seasonal H1N1 viruses can elicit an antibody response that protects against novel 2009 H1N1. Ferrets were preinfected with seasonal H1N1 viruses and assessed for cross-reactive antibodies to novel H1N1. Serum from infected ferrets was assayed for cross-reactivity to both seasonal and novel 2009 H1N1 strains. These results were compared to those of ferrets that were sequentially infected with H1N1 viruses isolated prior to 1957 or more-recently isolated viruses. Following seroconversion, ferrets were challenged with novel H1N1 influenza virus and assessed for viral titers in the nasal wash, morbidity, and mortality. There was no hemagglutination inhibition (HAI) cross-reactivity in ferrets infected with any single seasonal H1N1 influenza viruses, with limited protection to challenge. However, sequential H1N1 influenza infections reduced the incidence of disease and elicited cross-reactive antibodies to novel H1N1 isolates. The amount and duration of virus shedding and the frequency of transmission following novel H1N1 challenge were reduced. Exposure to multiple seasonal H1N1 influenza viruses, and not to any single H1N1 influenza virus, elicits a breadth of antibodies that neutralize novel H1N1 even though the host was never exposed to the novel H1N1 influenza viruses.


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