Topic Editors

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Northern Border University, Rafha, Saudi Arabia
Molecular Diagnostic Laboratory, Johns Hopkins Aramco Healthcare, Dhahran 31311, Saudi Arabia

Discovery and Development of Monkeypox Disease Treatments

Abstract submission deadline
31 May 2024
Manuscript submission deadline
31 August 2024
Viewed by
4791

Topic Information

Dear Colleagues,

Monkeypox disease (MPX) was first identified in monkeys in 1958. The first case of MPX in a human was reported in the Democratic Republic of Congo in 1971. Early outbreaks of MPX occurred in specific regions (Africa, United States, Singapore, United Kingdom, etc.); however, the MPX outbreak of 2022 is of global concern because it has spread to more than 105 countries. Unfortunately, MPX treatments (tecovirimat, brincidofovir, and cidofovir) and prophylactics (JYNNEOS vaccine) are limited. Monkeypox virus (MPXV) is an orthopoxvirus (OPXV). Various OPXVs (cowpox, vaccinia, smallpox, etc.) share similar genetic makeup. Accordingly, the drugs that are used to treat an OPXV disease may be useful in treating MPX. This Special Issue relates to the discovery and development of the treatment of OPXV-based diseases with a special emphasis on MPX. Submissions consisting of reviews, original articles, and communications based on the title theme are invited from experts around the globe. The scope of this Special Issue includes all aspects related to the drug discovery of treatments for OPXV-based diseases, including new targets, molecules, combinations, formulations, biopharmaceutical studies, natural products, biomedicines, vaccines, drug repurposing, pharmacovigilance, clinical reports, and patents. The content of this Special Issue will be of great value to the scientific community involved in the development of treatments for OPXV-based diseases.

Dr. Mohd Imran
Dr. Ali A. Rabaan
Topic Editors

Keywords

  • orthopoxvirus
  • monkeypox
  • treatment
  • drug discovery
  • drug development

Participating Journals

Journal Name Impact Factor CiteScore Launched Year First Decision (median) APC
Biomedicines
biomedicines
4.757 3.0 2013 17.4 Days 2200 CHF Submit
Journal of Clinical Medicine
jcm
4.964 4.4 2012 18 Days 2600 CHF Submit
Pathogens
pathogens
4.531 3.5 2012 15.9 Days 2200 CHF Submit
Vaccines
vaccines
4.961 4.5 2013 17.3 Days 2200 CHF Submit
Viruses
viruses
5.818 6.6 2009 15.6 Days 2600 CHF Submit

Preprints is a platform dedicated to making early versions of research outputs permanently available and citable. MDPI journals allow posting on preprint servers such as Preprints.org prior to publication. For more details about reprints, please visit https://www.preprints.org.

Published Papers (4 papers)

Order results
Result details
Journals
Select all
Export citation of selected articles as:
Review
VP37 Protein Inhibitors for Mpox Treatment: Highlights on Recent Advances, Patent Literature, and Future Directions
Biomedicines 2023, 11(4), 1106; https://doi.org/10.3390/biomedicines11041106 - 06 Apr 2023
Cited by 1 | Viewed by 673
Abstract
Monkeypox disease (Mpox) has threatened humankind worldwide since mid-2022. The Mpox virus (MpoxV) is an example of Orthopoxviruses (OPVs), which share similar genomic structures. A few treatments and vaccines are available for Mpox. OPV-specific VP37 protein (VP37P) is a target for developing drugs [...] Read more.
Monkeypox disease (Mpox) has threatened humankind worldwide since mid-2022. The Mpox virus (MpoxV) is an example of Orthopoxviruses (OPVs), which share similar genomic structures. A few treatments and vaccines are available for Mpox. OPV-specific VP37 protein (VP37P) is a target for developing drugs against Mpox and other OPV-induced infections such as smallpox. This review spotlights the existing and prospective VP37P inhibitors (VP37PIs) for Mpox. The non-patent literature was collected from PubMed, and the patent literature was gathered from free patent databases. Very little work has been carried out on developing VP37PIs. One VP37PI (tecovirimat) has already been approved in Europe to treat Mpox, while another drug, NIOCH-14, is under clinical trial. Developing tecovirimat/NIOCH-14-based combination therapies with clinically used drugs demonstrating activity against Mpox or other OPV infections (mitoxantrone, ofloxacin, enrofloxacin, novobiocin, cidofovir, brincidofovir, idoxuridine, trifluridine, vidarabine, fialuridine, adefovir, imatinib, and rifampicin), immunity boosters (vitamin C, zinc, thymoquinone, quercetin, ginseng, etc.), and vaccines may appear a promising strategy to fight against Mpox and other OPV infections. Drug repurposing is also a good approach for identifying clinically useful VP37PIs. The dearth in the discovery process of VP37PIs makes it an interesting area for further research. The development of the tecovirimat/NIOCH-14-based hybrid molecules with certain chemotherapeutic agents looks fruitful and can be explored to obtain new VP37PI. It would be interesting and challenging to develop an ideal VP37PI concerning its specificity, safety, and efficacy. Full article
(This article belongs to the Topic Discovery and Development of Monkeypox Disease Treatments)
Show Figures

Figure 1

Review
Monkeypox Virus in Animals: Current Knowledge of Viral Transmission and Pathogenesis in Wild Animal Reservoirs and Captive Animal Models
Viruses 2023, 15(4), 905; https://doi.org/10.3390/v15040905 - 31 Mar 2023
Cited by 1 | Viewed by 978
Abstract
Mpox, formerly called monkeypox, is now the most serious orthopoxvirus (OPXV) infection in humans. This zoonotic disease has been gradually re-emerging in humans with an increasing frequency of cases found in endemic areas, as well as an escalating frequency and size of epidemics [...] Read more.
Mpox, formerly called monkeypox, is now the most serious orthopoxvirus (OPXV) infection in humans. This zoonotic disease has been gradually re-emerging in humans with an increasing frequency of cases found in endemic areas, as well as an escalating frequency and size of epidemics outside of endemic areas in Africa. Currently, the largest known mpox epidemic is spreading throughout the world, with over 85,650 cases to date, mostly in Europe and North America. These increased endemic cases and epidemics are likely driven primarily by decreasing global immunity to OPXVs, along with other possible causes. The current unprecedented global outbreak of mpox has demonstrated higher numbers of human cases and greater human-to-human transmission than previously documented, necessitating an urgent need to better understand this disease in humans and animals. Monkeypox virus (MPXV) infections in animals, both naturally occurring and experimental, have provided critical information about the routes of transmission; the viral pathogenicity factors; the methods of control, such as vaccination and antivirals; the disease ecology in reservoir host species; and the conservation impacts on wildlife species. This review briefly described the epidemiology and transmission of MPXV between animals and humans and summarizes past studies on the ecology of MPXV in wild animals and experimental studies in captive animal models, with a focus on how animal infections have informed knowledge concerning various aspects of this pathogen. Knowledge gaps were highlighted in areas where future research, both in captive and free-ranging animals, could inform efforts to understand and control this disease in both humans and animals. Full article
(This article belongs to the Topic Discovery and Development of Monkeypox Disease Treatments)
Article
An Immunoinformatics Approach to Design Novel and Potent Multi-Epitope-Based Vaccine to Target Lumpy Skin Disease
Biomedicines 2023, 11(2), 398; https://doi.org/10.3390/biomedicines11020398 - 29 Jan 2023
Cited by 2 | Viewed by 975
Abstract
The lumpy skin disease (LSD) virus of the Poxviridae family is a serious threat that mostly affects cattle and causes significant economic loss. LSD has the potential to spread widely and its rapidly across borders. Despite the availability of information, there is still [...] Read more.
The lumpy skin disease (LSD) virus of the Poxviridae family is a serious threat that mostly affects cattle and causes significant economic loss. LSD has the potential to spread widely and its rapidly across borders. Despite the availability of information, there is still no competitive vaccine available for LSD. Therefore, the current study was conducted to develop an epitope-based LSD vaccine that is efficient, secure, and biocompatible and stimulates both innate and adaptive immune responses using immunoinformatics techniques. Initially, putative virion core proteins were manipulated; B-cell and T-cell epitopes have been predicted and connected with the help of adjuvants and linkers. Numerous bioinformatics methods, including antigenicity testing, transmembrane topology screening, allergenicity assessment, conservancy analysis, and toxicity evaluation, were employed to find superior epitopes. Based on promising vaccine candidates and immunogenic potential, the vaccine design was selected. Strong interactions between TLR4 and TLR9 and the anticipated vaccine design were revealed by molecular docking. Finally, based on the high docking score, computer simulations were performed in order to assess the stability, efficacy, and compactness of the constructed vaccine. The simulation outcomes showed that the polypeptide vaccine design was remarkably stable, with high expression, stability, immunogenic qualities, and considerable solubility. Additionally, computer-based research shows that the constructed vaccine provides adequate population coverage, making it a promising candidate for use in the design of vaccines against other viruses within the Poxviridae family and potentially other virus families as well. These outcomes suggest that the epitope-based vaccine developed in this study will be a significant candidate against LSD to control and prevent LSDV-related disorders if further investigated experimentally. Full article
(This article belongs to the Topic Discovery and Development of Monkeypox Disease Treatments)
Show Figures

Figure 1

Article
Monkeypox Cross-Sectional Survey of Knowledge, Attitudes, Practices, and Willingness to Vaccinate among University Students in Pakistan
Vaccines 2023, 11(1), 97; https://doi.org/10.3390/vaccines11010097 - 31 Dec 2022
Cited by 4 | Viewed by 1353
Abstract
This study aimed to explore knowledge, attitude, perceptions, and willingness regarding vaccination among university students in Pakistan. This cross-sectional study was carried out using an open online self-administered survey via Google Forms. The survey data were collected between the 15 to 30 of [...] Read more.
This study aimed to explore knowledge, attitude, perceptions, and willingness regarding vaccination among university students in Pakistan. This cross-sectional study was carried out using an open online self-administered survey via Google Forms. The survey data were collected between the 15 to 30 of October 2022. A total of 946 respondents participated in the study, of which the majority were female (514, 54.3%). Most students belonged to a medical background, specifically pharmaceutical sciences. Most of the respondents did not know about monkeypox before 2022 (646, 68.3%). Regarding overall knowledge of monkeypox, most of the respondents had average knowledge (726, 76.7%), with very few having good knowledge (60, 6.3%). Regarding overall attitudes towards monkeypox, most of the respondents had neutral attitudes (648, 68.5%). There was a significant association between knowledge of Monkeypox with the type of academic degree (p < 0.001), type of discipline (p < 0.001), and region of respondents (p < 0.001). The willingness to vaccinate among the population was (67.7%). The current study pointed out that the overall knowledge of monkeypox was average in most respondents, with considerable knowledge gaps in most aspects. The overall attitude towards monkeypox was neutral. Further, the knowledge about monkeypox was strongly associated with academic degree, study discipline, and region of respondents. Our findings emphasize the need to raise public awareness by educating students on the monkeypox virus. This will improve adherence to preventative recommendations. Full article
(This article belongs to the Topic Discovery and Development of Monkeypox Disease Treatments)
Show Figures

Figure 1

Back to TopTop