This research aims to examine the efficacy of melatonin as an adjuvant therapeutic agent for COVID-19 patients in the intensive care unit.
Methods
A randomized, double-blind, placebo-controlled investigation was conducted on a group of hospitalized COVID-19 patients. Individuals were allocated into 2 groups: one group received a combination of 18 mg of melatonin and standard treatment for 14 days; the other group received a placebo in addition to standard treatment. Patients were evaluated at the beginning of the study as well as the 7th and 15th days to analyze changes in clinical symptoms, P/F ratio, and inflammatory markers.
Results
The study included patients with an average age of 57.80 ± 17.96 years, with an equal gender representation. The average length of hospital stay was 19.83 ± 4.45 days. Hypertension and diabetes were commonly observed comorbidities. There were no significant differences in the demographic characteristics between the 2 groups (P > .05). Additionally, there were no significant distinctions between the 2 groups in terms of clinical symptom improvement, mortality rate, adverse effects, and various blood markers (P > .05).
Conclusion
Our study's findings suggested that melatonin is unlikely to significantly affect the clinical status of COVID-19 patients.
{"title":"Evaluation of the effect of melatonin on patients with COVID-19 admitted to ICU: A double-blind randomized clinical trial","authors":"Mahmoud Ganjifard , Shokouh Ghafari , Adeleh Sahebnasagh , Mahboubeh Esmaeili , Ali Reza Amirabadizadeh , Azadeh Ebrahimzadeh , Parvin Askari , Razieh Avan","doi":"10.1016/j.vacune.2025.100377","DOIUrl":"10.1016/j.vacune.2025.100377","url":null,"abstract":"<div><h3>Introduction and objectives</h3><div>This research aims to examine the efficacy of melatonin as an adjuvant therapeutic agent for COVID-19 patients in the intensive care unit.</div></div><div><h3>Methods</h3><div>A randomized, double-blind, placebo-controlled investigation was conducted on a group of hospitalized COVID-19 patients. Individuals were allocated into 2 groups: one group received a combination of 18 mg of melatonin and standard treatment for 14 days; the other group received a placebo in addition to standard treatment. Patients were evaluated at the beginning of the study as well as the 7th and 15th days to analyze changes in clinical symptoms, P/F ratio, and inflammatory markers.</div></div><div><h3>Results</h3><div>The study included patients with an average age of 57.80<!--> <!-->±<!--> <!-->17.96 years, with an equal gender representation. The average length of hospital stay was 19.83<!--> <!-->±<!--> <!-->4.45 days. Hypertension and diabetes were commonly observed comorbidities. There were no significant differences in the demographic characteristics between the 2 groups (<em>P</em> <!-->><!--> <!-->.05). Additionally, there were no significant distinctions between the 2 groups in terms of clinical symptom improvement, mortality rate, adverse effects, and various blood markers (<em>P</em> <!-->><!--> <!-->.05).</div></div><div><h3>Conclusion</h3><div>Our study's findings suggested that melatonin is unlikely to significantly affect the clinical status of COVID-19 patients.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"26 1","pages":"Article 100377"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143739601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The growing threat of monkeypox and the urgent need for vaccination in Pakistan","authors":"Alisha Saleem , Ashar Masood Khan , Danish Faheem , Bina Fawad","doi":"10.1016/j.vacune.2025.100378","DOIUrl":"10.1016/j.vacune.2025.100378","url":null,"abstract":"","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"26 1","pages":"Article 100378"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143739513","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01Epub Date: 2025-03-18DOI: 10.1016/j.vacune.2025.100381
Jordi Reina , Julia Viana-Ramírez
There are two types of vaccines available against polio virus: the inactivated (Salk, IPV) and the oral/attenuated (Sabin, OPV). Live vaccines are highly effective in inducing protective immunity against certain infections, also favoring the cessation of their epidemic spread. There are three wild serotypes of the polio virus, however currently two of them, serotype 2 and 3, are considered eradicated so that the only one that still circulates in endemic countries is serotype 1. One of the problems of OPV, which cannot occur with IPV, is its possible reversion to the wild form, circulating as vaccinal poliovirus (cOPV) and its transmission to unvaccinated people, giving rise to paralytic processes associated with the vaccine. To avoid this phenomenon, new oral polio vaccines (nOPV-c1) with greater safety and less reversion have been developed by modifying and introducing a series of genetic modifications in the RNA of the virus. Different studies have shown that children who received OPV2-c1 presented a higher degree of attenuation and thermostability and a highly significant decrease in the ability to affect the nervous system and develop severe neurovirulence and possible post-vaccination polio. These studies establish the pathogenic and molecular bases in the most vulnerable child population that allowed the use of this new genetically attenuated vaccine in population vaccination campaigns.
{"title":"The new genetically attenuated vaccines against poliomyelitis virus","authors":"Jordi Reina , Julia Viana-Ramírez","doi":"10.1016/j.vacune.2025.100381","DOIUrl":"10.1016/j.vacune.2025.100381","url":null,"abstract":"<div><div>There are two types of vaccines available against polio virus: the inactivated (Salk, IPV) and the oral/attenuated (Sabin, OPV). Live vaccines are highly effective in inducing protective immunity against certain infections, also favoring the cessation of their epidemic spread. There are three wild serotypes of the polio virus, however currently two of them, serotype 2 and 3, are considered eradicated so that the only one that still circulates in endemic countries is serotype 1. One of the problems of OPV, which cannot occur with IPV, is its possible reversion to the wild form, circulating as vaccinal poliovirus (cOPV) and its transmission to unvaccinated people, giving rise to paralytic processes associated with the vaccine. To avoid this phenomenon, new oral polio vaccines (nOPV-c1) with greater safety and less reversion have been developed by modifying and introducing a series of genetic modifications in the RNA of the virus. Different studies have shown that children who received OPV2-c1 presented a higher degree of attenuation and thermostability and a highly significant decrease in the ability to affect the nervous system and develop severe neurovirulence and possible post-vaccination polio. These studies establish the pathogenic and molecular bases in the most vulnerable child population that allowed the use of this new genetically attenuated vaccine in population vaccination campaigns.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"26 1","pages":"Article 100381"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143739511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study aimed to investigate the prevalence of HBV infection and its associated risk factors in the elderly in Birjand.
Materials and methods
The present study was a part of the community-based prospective cohort study. Subjects over 60 years of age were assessed using standard questionnaires and blood factors. The samples were tested for HBsAg by enzyme-linked immunosorbent assay.
Results
Of 542 elderly people living in Birjand, 11 cases (2.03%) were positive. The median age of patients with HBsAg positive and negative was 69 (IQR: 63–77) years and 67 (IQR: 63–74) years, respectively. The results of the multiple logistic regression model showed that fatty liver disease was significantly associated with having hepatitis B (AOR (95% CI)=5.50 (1.16, 25.88)) (p < .05). However, there was no significant relationship found between variables age, sex, marital status, years of study, underlying diseases, body mass index, smoking, and blood factors with having hepatitis B (p > .05).
Conclusions
Even though there were only a few positive cases, leading to a non-significant report, it is crucial to emphasize the clinical significance and health and well-being of elderly individuals contracting hepatitis B. This information can be valuable in devising suitable disease management strategies for this age group.
{"title":"Monitoring of hepatitis B infection in the elderly population of eastern Iran","authors":"Abdol Sattar Pagheh , Effat Alemzadeh , Eisa Nazar , Mitra Moodi , Farshad Sharifi , Ebrahim Miri-Moghaddam , Mohamad Taghi Rahimi , Soroush Mohammadi , Masood Ziaee","doi":"10.1016/j.vacune.2025.100373","DOIUrl":"10.1016/j.vacune.2025.100373","url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to investigate the prevalence of HBV infection and its associated risk factors in the elderly in Birjand.</div></div><div><h3>Materials and methods</h3><div>The present study was a part of the community-based prospective cohort study. Subjects over 60 years of age were assessed using standard questionnaires and blood factors. The samples were tested for HBsAg by enzyme-linked immunosorbent assay.</div></div><div><h3>Results</h3><div>Of 542 elderly people living in Birjand, 11 cases (2.03%) were positive. The median age of patients with HBsAg positive and negative was 69 (IQR: 63–77) years and 67 (IQR: 63–74) years, respectively. The results of the multiple logistic regression model showed that fatty liver disease was significantly associated with having hepatitis B (AOR (95% CI)=5.50 (1.16, 25.88)) (<em>p</em> <!--><<!--> <!-->.05). However, there was no significant relationship found between variables age, sex, marital status, years of study, underlying diseases, body mass index, smoking, and blood factors with having hepatitis B (<em>p</em> <!-->><!--> <!-->.05).</div></div><div><h3>Conclusions</h3><div>Even though there were only a few positive cases, leading to a non-significant report, it is crucial to emphasize the clinical significance and health and well-being of elderly individuals contracting hepatitis B. This information can be valuable in devising suitable disease management strategies for this age group.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"26 1","pages":"Article 100373"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143739600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01Epub Date: 2025-03-20DOI: 10.1016/j.vacune.2025.100379
Ana María Haro Pérez , Mar Jiménez Rodríguez , Saray Martín Monteagudo , Nieves Gutiérrez Zufiaurre
Objetives
Describe the evolution and characteristics of confirmed pertussis cases during the last 5 years, detect possible underreporting, study the burden of the pertussis on healthcare system at the current time and assess the effect of vaccination.
Material and methods
Retrospective observational study of pertussis cases reported in the province of Salamanca and patients diagnosed with pertussis by PCR by the Microbiology of the reference hospital, from January 2018 to March 2024.
Results
A total of 58 cases of pertussis were detected, 42 correspond to the period November 2023 – March 2024. Thirty-five (60.3%) were reported as EDO. A total of 48% were not vaccinated, and the average time from the last dose of the vaccine to diagnóstico in vaccinated people was 136.3 days (SD 40) in children under 1 year of age and 605.3 days (SD 407) in the 1–4 year-old group. Twelve cases (20.7%) required hospitalization (3 under 1 year old, 1 under 2 years old, 1 under 7 years old, 2 between 34 and 64 years old and 5 over 65 years old), of which 7 (58.3%) were not vaccinated.
Conclusions
The epidemiological evolution of pertussis shows a significant increase in 2023–2024, both in childhood and in adulthood, despite detecting underreporting. Vaccination is one of the fundamental strategies for the prevention of pertussis, the risk of which increases with the time elapsed since the last dose of vaccine, so vaccination coverage should be promoted in all age groups and in specific groups of risk, with the introduction of diphtheria-tetanus-pertussis in booster doses.
{"title":"Pertussis as a re-emerging disease. Epidemiological situation in the province of Salamanca","authors":"Ana María Haro Pérez , Mar Jiménez Rodríguez , Saray Martín Monteagudo , Nieves Gutiérrez Zufiaurre","doi":"10.1016/j.vacune.2025.100379","DOIUrl":"10.1016/j.vacune.2025.100379","url":null,"abstract":"<div><h3>Objetives</h3><div>Describe the evolution and characteristics of confirmed pertussis cases during the last 5 years, detect possible underreporting, study the burden of the pertussis on healthcare system at the current time and assess the effect of vaccination.</div></div><div><h3>Material and methods</h3><div>Retrospective observational study of pertussis cases reported in the province of Salamanca and patients diagnosed with pertussis by PCR by the Microbiology of the reference hospital, from January 2018 to March 2024.</div></div><div><h3>Results</h3><div>A total of 58 cases of pertussis were detected, 42 correspond to the period November 2023 – March 2024. Thirty-five (60.3%) were reported as EDO. A total of 48% were not vaccinated, and the average time from the last dose of the vaccine to diagnóstico in vaccinated people was 136.3 days (SD 40) in children under 1 year of age and 605.3 days (SD 407) in the 1–4 year-old group. Twelve cases (20.7%) required hospitalization (3 under 1 year old, 1 under 2 years old, 1 under 7 years old, 2 between 34 and 64 years old and 5 over 65 years old), of which 7 (58.3%) were not vaccinated.</div></div><div><h3>Conclusions</h3><div>The epidemiological evolution of pertussis shows a significant increase in 2023–2024, both in childhood and in adulthood, despite detecting underreporting. Vaccination is one of the fundamental strategies for the prevention of pertussis, the risk of which increases with the time elapsed since the last dose of vaccine, so vaccination coverage should be promoted in all age groups and in specific groups of risk, with the introduction of diphtheria-tetanus-pertussis in booster doses.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"26 1","pages":"Article 100379"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143739603","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01Epub Date: 2025-03-31DOI: 10.1016/j.vacune.2025.100380
Ali Mohammed Ashraf , Marwan Y. Al-Maqtoofi , Ahmed A. Burghal
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the pandemic of the coronavirus disease 2019 (COVID-19) that emerged in December 2019 in Wuhan city, China. Understanding the SARS-CoV-2 entry, invasion and infection mechanism is crucial for vaccine development. The immune system is divided into 2 parts: the innate immune system and the adaptive immune system, and they work in essential and powerful ways for SARS-CoV-2 managing and reducing COVID-19 infections. Spike proteins (S) of SARS-CoV-2 are a pivotal key during the viral invasion of the host cells. Cell surface receptors facilitate binding and then membrane fusion for virus endocytosis and causing infection. Host cells are covered with receptors for viral S proteins binding, such as the human angiotensin-converting enzyme 2 receptor. The innate immune responses initiate after viral antigen detection via a set of pathogen recognition receptors, including the Toll-like receptors (TLRs) family. TLRs are largely inducible in most body cell types. After SARS-CoV-2 antigen recognition, cellular sensors stimulate the production of interferons and inflammatory cytokines, which are crucial for controlling viral replication and dissemination. The cellular and humoral responses of the adaptive immune system antibody-producing B-cells, CD4 + T-cells to evoke the immune response, and CD8 + T-cells to kill infected cells. This review outlines the process of virus entry and detection by pattern recognition receptors and antiviral defence by both innate immunity and adaptive immunity for developing immunological memory that can help in vaccines and understanding the immune response to SARS-CoV-2.
{"title":"COVID-19 story: Entry and immune response","authors":"Ali Mohammed Ashraf , Marwan Y. Al-Maqtoofi , Ahmed A. Burghal","doi":"10.1016/j.vacune.2025.100380","DOIUrl":"10.1016/j.vacune.2025.100380","url":null,"abstract":"<div><div>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the pandemic of the coronavirus disease 2019 (COVID-19) that emerged in December 2019 in Wuhan city, China. Understanding the SARS-CoV-2 entry, invasion and infection mechanism is crucial for vaccine development. The immune system is divided into 2 parts: the innate immune system and the adaptive immune system, and they work in essential and powerful ways for SARS-CoV-2 managing and reducing COVID-19 infections. Spike proteins (S) of SARS-CoV-2 are a pivotal key during the viral invasion of the host cells. Cell surface receptors facilitate binding and then membrane fusion for virus endocytosis and causing infection. Host cells are covered with receptors for viral S proteins binding, such as the human angiotensin-converting enzyme 2 receptor. The innate immune responses initiate after viral antigen detection via a set of pathogen recognition receptors, including the Toll-like receptors (TLRs) family. TLRs are largely inducible in most body cell types. After SARS-CoV-2 antigen recognition, cellular sensors stimulate the production of interferons and inflammatory cytokines, which are crucial for controlling viral replication and dissemination. The cellular and humoral responses of the adaptive immune system antibody-producing B-cells, CD4<!--> <!-->+ T-cells to evoke the immune response, and CD8<!--> <!-->+ T-cells to kill infected cells. This review outlines the process of virus entry and detection by pattern recognition receptors and antiviral defence by both innate immunity and adaptive immunity for developing immunological memory that can help in vaccines and understanding the immune response to SARS-CoV-2.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"26 1","pages":"Article 100380"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143739604","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-01Epub Date: 2024-11-14DOI: 10.1016/j.vacune.2024.10.009
Ali Adel Dawood
The development of a conventional vaccine against gonococci has been difficult since there are no precise correlates of immune protection and the mechanisms of protective immunity are not yet understood. However, the drop in gonorrhea infections might be attributed to the development of vaccines based on Neisseria meningitidis' outer membrane. The goal of this research was to develop a multi-epitope vaccination utilizing proteins from N. meningitidis and Neisseria gonorrhoeae. A Neisseria Multi-Epitope Vaccine (NMEV), containing Opa, ProA, ProB, RmpM, and BamD, was developed using immunophysicochemical informatics techniques. The vaccine consists of 297 amino acids. Antigenicity and sensitivity to NMEV were evaluated. NMEV generates a substantial amount of immune cells and cytokines. The total quality factor of the NMEV 2D structure is around 91%. The vaccine's safety, effectiveness, and other properties make it an attractive option for in vitro and in vivo testing. The suggested NMEV subunit vaccine has the potential to elicit a strong immune response, necessitating additional in vitro and in vivo studies to eliminate Neisseria infections.
{"title":"Designing an immuno-epitope candidate vaccine from (Opa, ProA, ProB, RmpM and BamD) proteins against Neisseria gonorrhoeae and Neisseria meningitides","authors":"Ali Adel Dawood","doi":"10.1016/j.vacune.2024.10.009","DOIUrl":"10.1016/j.vacune.2024.10.009","url":null,"abstract":"<div><div>The development of a conventional vaccine against gonococci has been difficult since there are no precise correlates of immune protection and the mechanisms of protective immunity are not yet understood. However, the drop in gonorrhea infections might be attributed to the development of vaccines based on <em>Neisseria meningitidis</em>' outer membrane. The goal of this research was to develop a multi-epitope vaccination utilizing proteins from <em>N. meningitidis</em> and <em>Neisseria gonorrhoeae</em>. A <em>Neisseria</em> Multi-Epitope Vaccine (NMEV), containing Opa, ProA, ProB, RmpM, and BamD, was developed using immunophysicochemical informatics techniques. The vaccine consists of 297 amino acids. Antigenicity and sensitivity to NMEV were evaluated. NMEV generates a substantial amount of immune cells and cytokines. The total quality factor of the NMEV 2D structure is around 91%. The vaccine's safety, effectiveness, and other properties make it an attractive option for in vitro and in vivo testing. The suggested NMEV subunit vaccine has the potential to elicit a strong immune response, necessitating additional in vitro and in vivo studies to eliminate Neisseria infections.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"25 4","pages":"Pages 481-491"},"PeriodicalIF":0.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142664176","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Arboviral infections are predominantly transmitted by arthropods causing significant mortality, morbidity, and represent a major global health concern. These infections pose significant economic burdens especially in endemic regions. Dengue, chikungunya, yellow fever, and zika are the most common arboviral diseases spread by Aedes mosquitoes. Extensive research has been conducted on vector surveillance and vector control strategies to limit the arboviral transmission. However, vaccines remain the most powerful tool in the fight against infectious diseases. Over the years, significant progress has been made in developing vaccines against several infectious diseases. The global disease burden has been drastically reduced due to effective vaccination. The continual threat of arboviral outbreaks necessitates the need for effective vaccine and therapeutic development. For most arboviral diseases, vaccines are not available. Recently, plant-based vaccine development represents a promising platform for the rapid supply of antigens and antibodies for developing diagnostic kits or vaccines against pathogens. The concept of producing pharmaceutically significant and commercially viable therapeutic proteins in plants is defined as molecular farming. Substantial efforts have been made in this field, with improved expression strategies, refinement of downstream processing, and sufficient evidence showing the immunogenicity and efficacy of plant-produced recombinant proteins. Currently, few plant-produced vaccine antigens have reached the clinical trials. Notably, the plant-produced COVID-19 vaccine, Covifenz has been approved by Canada, and plant-produced influenza candidates showed safety and efficacy in clinical trials. In this review, we briefly summarize the potential of plant-derived vaccines in the fight against arboviral infections.
{"title":"Plant system as a versatile and robust platform for the development of vaccines against arboviral infections","authors":"Balamurugan Shanmugaraj , Nivetha Loganathan , Harish Mani Chandra","doi":"10.1016/j.vacune.2024.10.010","DOIUrl":"10.1016/j.vacune.2024.10.010","url":null,"abstract":"<div><div>Arboviral infections are predominantly transmitted by arthropods causing significant mortality, morbidity, and represent a major global health concern. These infections pose significant economic burdens especially in endemic regions. Dengue, chikungunya, yellow fever, and zika are the most common arboviral diseases spread by <em>Aedes</em> mosquitoes. Extensive research has been conducted on vector surveillance and vector control strategies to limit the arboviral transmission. However, vaccines remain the most powerful tool in the fight against infectious diseases. Over the years, significant progress has been made in developing vaccines against several infectious diseases. The global disease burden has been drastically reduced due to effective vaccination. The continual threat of arboviral outbreaks necessitates the need for effective vaccine and therapeutic development. For most arboviral diseases, vaccines are not available. Recently, plant-based vaccine development represents a promising platform for the rapid supply of antigens and antibodies for developing diagnostic kits or vaccines against pathogens. The concept of producing pharmaceutically significant and commercially viable therapeutic proteins in plants is defined as molecular farming. Substantial efforts have been made in this field, with improved expression strategies, refinement of downstream processing, and sufficient evidence showing the immunogenicity and efficacy of plant-produced recombinant proteins. Currently, few plant-produced vaccine antigens have reached the clinical trials. Notably, the plant-produced COVID-19 vaccine, Covifenz has been approved by Canada, and plant-produced influenza candidates showed safety and efficacy in clinical trials. In this review, we briefly summarize the potential of plant-derived vaccines in the fight against arboviral infections.</div></div>","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"25 4","pages":"Pages 492-501"},"PeriodicalIF":0.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142664185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-01Epub Date: 2024-10-29DOI: 10.1016/j.vacune.2024.10.002
Fernando Moraga-Llop , Magda Campins-Martí
{"title":"Measles eradication: Still a long and winding road","authors":"Fernando Moraga-Llop , Magda Campins-Martí","doi":"10.1016/j.vacune.2024.10.002","DOIUrl":"10.1016/j.vacune.2024.10.002","url":null,"abstract":"","PeriodicalId":101272,"journal":{"name":"Vacunas (English Edition)","volume":"25 4","pages":"Pages 431-435"},"PeriodicalIF":0.0,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142664142","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}