Showing posts with label influenza. Show all posts
Showing posts with label influenza. Show all posts

Friday, March 13, 2020

Q&A: Similarities and differences – COVID-19 and influenza 

As the COVID-19 outbreak continues to evolve, comparisons have been drawn to influenza. Both cause respiratory disease, yet there are important differences between the two viruses and how they spread. This has important implications for the public health measures that can be implemented to respond to each virus.

Q. How are COVID-19 and influenza viruses similar? Firstly, COVID-19 and influenza viruses have a similar disease presentation. That is, they both cause respiratory disease, which presents as a wide range of illness from asymptomatic or mild through to severe disease and death.

Secondly, both viruses are transmitted by contact, droplets and fomites. As a result, the same public health measures, such as hand hygiene and good respiratory etiquette (coughing into your elbow or into a tissue and immediately disposing of the tissue), are important actions all can take to prevent infection.

Q. How are COVID-19 and influenza viruses different? The speed of transmission is an important point of difference between the two viruses. Influenza has a shorter median incubation period (the time from infection to appearance of symptoms) and a shorter serial interval (the time between successive cases) than COVID-19 virus. The serial interval for COVID-19 virus is estimated to be 5-6 days, while for influenza virus, the serial interval is 3 days. This means that influenza can spread faster than COVID19.

Further, transmission in the first 3-5 days of illness, or potentially pre-symptomatic transmission –transmission of the virus before the appearance of symptoms – is a major driver of transmission for influenza. In contrast, while we are learning that there are people who can shed COVID-19 virus 24-48 hours prior to symptom onset, at present, this does not appear to be a major driver of transmission.

The reproductive number – the number of secondary infections generated from one infected individual – is understood to be between 2 and 2.5 for COVID-19 virus, higher than for influenza. However, estimates for both COVID-19 and influenza viruses are very context and time-specific, making direct comparisons more difficult.

Children are important drivers of influenza virus transmission in the community. For COVID-19 virus, initial data indicates that children are less affected than adults and that clinical attack rates in the 0-19 age group are low. Further preliminary data from household transmission studies in China suggest that children are infected from adults, rather than vice versa.

While the range of symptoms for the two viruses is similar, the fraction with severe disease appears to be different. For COVID-19, data to date suggest that 80% of infections are mild or asymptomatic, 15% are severe infection, requiring oxygen and 5% are critical infections, requiring ventilation. These fractions of severe and critical infection would be higher than what is observed for influenza infection.

Those most at risk for severe influenza infection are children, pregnant women, elderly, those with underlying chronic medical conditions and those who are immunosuppressed. For COVID-19, our current understanding is that older age and underlying conditions increase the risk for severe infection.

Mortality for COVID-19 appears higher than for influenza, especially seasonal influenza. While the true mortality of COVID-19 will take some time to fully understand, the data we have so far indicate that the crude mortality ratio (the number of reported deaths divided by the reported cases) is between 3-4%, the infection mortality rate (the number of reported deaths divided by the number of infections) will be lower. For seasonal influenza, mortality is usually well below 0.1%. However, mortality is to a large extent determined by access to and quality of health care. 

Q. What medical interventions are available for COVID-19 and influenza viruses? While there are a number of therapeutics currently in clinical trials in China and more than 20 vaccines in development for COVID-19, there are currently no licensed vaccines or therapeutics for COVID-19. In contrast, antivirals and vaccines available for influenza. While the influenza vaccine is not effective against COVID-19 virus, it is highly recommended to get vaccinated each year to prevent influenza infection.

https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200306-sitrep-46-covid-19.pdf?sfvrsn=96b04adf_2

Monday, July 1, 2013

Licorice Shown To Kill SARS And Other Lethal Viruses

Licorice has a rich and ancient history of use as a medicine, being rooted in Indian, Chinese, Greek and Egyptian traditions, alike. Technically a legume, related to beans and peas, its sweetness results from the presence of glycyrrhizin, a compound 30-50 times sweeter than sugar. This compound is what gave licorice its name, which derives from the Greek word γλυκύρριζα (glukurrhiza), meaning "sweet" (gluku)  "root" (rrhiza). But glycyrrhizin’s properties don’t end with its sweetness; it is also one of the most powerful antiviral compounds ever studied.

A study on glycyrrhizin’s inhibitory activity against SARS-associated coronovirus published in Lancet in June of 2003, received little mainstream media coverage, despite its profound importance to human health.  Mind you, only a few months before this the World Health Organization issued a press release (April 16, 2003) stating the recent outbreak of lethal Sudden Acute Respiratory Syndrome (SARS) in Asia was caused by the same coronoviruses used in this study. With the world still reeling from global SARS hysteria and "preparedness," i.e. stockpiling pharmaceuticals like Ribavirin despite their well-known lack of effectiveness, you would think more attention would have been paid to promising research of this kind...
In the groundbreaking Lancet study, titled "Glycyrrhizin, an active component of liquorice roots, and replication of SARS-associated coronavirus," German researchers summarized their intention in the following manner:
 
"The [recent] outbreak of SARS warrants the search for antiviral compounds to treat the disease. At present time, no specific treatment has been identified for SARS-associated coronavirus infection."
And here is what they found:
"We assessed the antiviral potential of ribavirin, 6-azauridine, pyrazofurin, mycophenolic acid, and glycyrrhizin against two clinical isolates of coronavirus (FFM-1 and FFM-2) from patients with SARS admitted to the clinical centre of Frankfurt University, Germany. Of all the compounds, glycyrrhizin was the most active in inhibiting replication of the SARS-associated virus. Our findings suggest that glycyrrhizin should be assessed for treatment of SARS." [emphasis added]

Licorice’s potent antiviral properties are not limited to SARS-associated coronaviruses, but have also been studied in connection with another epidemic/pandemic capable and potentially lethal virus:influenza.

In an animal study dating all the way back in 1997 and published in the journal Antibacterial Agents and Chemotherapy, titled: "Glycyrrhizin, an active component of licorice roots, reduces morbidity and mortality of mice infected with lethal doses of influenza virus," researchers found that when mice were administered glycyrrhizin at 10mg/kg body weight (the equivalent of 680 mg for a 150lb adult), they all survived a series of ten 50% lethal injections. The control group, on the other hand, only survived an average of 10.5 days, with no survivors by day 21, the end of the experiment.

Even more remarkable, when the splenic T cells from the glycyrrhizin-treated mice were transferred to mice exposed to the same lethal doses of influenza virus, 100% survived, compared to 0% for the control mice inoculated with naive T cells or splenic B cells and macrophages from glycyrrhizin-treated mice. The researchers discovered that glycyrrhizin’s powerful, life-sparing effects against lethal doses of influenza were a result of the compound increasing interferon gamma production by T cells.

In order to fully understand these findings, we must look at the question of safety first. Licorice is still commonly perceived as a "dangerous herb," due to its ability to stimulate blood pressure elevations in susceptible individuals when consumed excessively; but considering the relatively higher toxicity of most drugs, this perception must be taken with a grain of sea salt.  On the other hand, it is important to exercise caution when using licorice, or any herb, for medicinal purposes, and ideally obtaining the assistance of a medical herbalist who can work with conventional health practitioners, whenever possible.

In the United States glycyrrhizin is still classified as "Generally Recognized As Safe," when used as a flavoring agent, but not as a sweetener. It has also been removed from most "licorice" candies, substituted with with the similarly-tasting but taxonomically unrelated anise. In the European Union the recommendation is for people to consume no more than 100 mg a day, which is the equivalent of 50 grams of licorice sweets, and in Japan, where glycyrrhizin is often used as a sugar substitute, a recommended limit is set at 200 mg a day. This should give you a sense for what a commonly considered safe, daily dose is, and puts a 600 mg "therapeutic" dose in perspective.

Also, it is important to consider that even when the glycyrrhizin is isolated and concentrated pharmaceutically, its relative toxicity is extraordinarily low, when compared to antiviral drugs like Ribavirin.

According to the federally mandated Material Safety Data Sheets (MSDS) provided by the manufacturers on pharmaceutically extracted glycyrrhizin and the drug Ribavirin, the former is 30 times less toxic than the later (the mouse oral 50% lethal dose is 9818 mg/kg versus 300 mg/kg for Ribavirin).  It is important to understand, also, that when complexed in the whole root or powdered root form, glycyrrhizin will be treated differently by the body. It will be released slower, will have naturally occurring factors which may attenuate adverse effects, and therefore should be considered safer than the MSDS on isolated glycyrrhizin reflects.

Also consider that glycyrrhizin is much cheaper...

A 200 mg dose of Ribavirin from an online discount pharmacy costs approximately 4 dollars.
   
Let’s take a 1 pound bag of Frontier brand Licorice sticks, which costs $10, and which contains approximately 7% glycyrrhizin or the equivalent of 13,440 milligrams of glycyrrhizin per pound. This is also the equivalent of sixty-seven 200 mg servings.  If I bought sixty-seven 200mg pills of Ribavirinit would cost me 268 dollars. So, that’s 26.8 times the price of the glycyrrhizin found in licorice.  In both cases, the natural compound is approximately 30 times less toxic and less expensive, and let us not forget, in the SARS/licorice study, Ribavirin didn’t even work. So, it is potentially infinitely more effective. Hmmm. I wonder which I would choose if faced with an impending pandemic virus? A drug with low availability, exceedingly high costs and toxicity, and which doesn’t work, versus a time-tested, safe, affordable and highly effective herb?

The reason, of course, why licorice will never be used as an FDA-approved medicine is because it would take at least 800 million dollars of upfront capital to fund the preclinical and human clinical studies necessary to get it to that point.

In the meantime, I encourage everyone to immerse themselves in the first-hand research itself, which we have both lovingly and painstakingly gathered on your behalf. Visit the live reference page on Licorice (
http://www.greenmedinfo.com/substance/licoricehere, or skim through the remarkable research on Licorice’s potential value in 75 conditions below....
NameCumulative KnowledgeArticle CountFocus Articles
Hepatitis C314focus
Aphthous Ulcer303focus
Liver Cancer213focus
Duodenal Ulcer202focus
Polycystic Ovary Syndrome202focus
HIV Infections123focus
Pneumonia122focus
Cholesterol: Oxidation101focus
Cytomegalovirus Infections101focus
Familial Mediterranean Fever101focus
Gastroduodenal Ulcer101focus
Helicobacter Pylori Infection102focus
Hirsutism101focus
Rosacea101focus
Testosterone: Too High101focus
Abdominal Obesity (Midsection Fat)63focus
Prostate Cancer43focus
SARS43focus
Influenza A32focus
Bleeding: Excessive21focus
Breast Cancer22focus
Cervical Cancer22focus
Chemotherapy-Induced Toxicity: Cisplatin21focus
Chronic Obstructive Pulmonary Disease21focus
Diabetes Mellitus: Type 221focus
Epstein-Barr Virus Infections22focus
Hepatitis21focus
Hepatitis A22focus
Hepatitis B22focus
Hypercholesterolemia21focus
Hypertension21focus
Inflammation21focus
Lipopolysaccharide-Induced Toxicity21focus
Liver Disease21focus
Memory Disorders21focus
Metabolic Syndrome X21focus
Myocardial Infarction21focus
Obesity21focus
Pulmonary Inflammation21focus
Respiratory Syncytial Virus Infections22focus
Spinal Cord Injuries21focus
Surgery: Oral21focus
Trigeminal Neuralgia21focus
Tumors21focus
Acne11focus
Acquired Immunodeficiency Syndrome11focus
Candida Infection11focus
Candidiasis: Vulvovaginal11focus
Chemotherapy-Induced Toxicity: Doxorubicin11focus
DNA damage11focus
Encephalitis: Japanese11focus
Endometrial Cancer11focus
Endometriosis11focus
Estrogen Dominance11focus
Fibroid Tumor11focus
Fibroids: Uterine11focus
Gastric Ulcer11focus
Heavy Metal Toxicity11focus
Herpes Zoster11focus
Herpes: Kaposi-Associated11focus
Iron Overload11focus
Iron Poisoning11focus
Kaposi Disease11focus
Leiomyoma11focus
Lung Cancer11focus
Oxidative Stress11focus
Periodontitis11focus
Promyelocytic leukemia11focus
Rotavirus Infections11focus
Stomach Cancer11focus
Tuberculosis11focus
Gastric Cancer01focus
HIV: Opportunist Infection.01focus
Influenza: Human01focus
Preventing Cavities02focus
View the Evidence: Substances
Pubmed Data : Zhongguo Zhong Xi Yi Jie He Za Zhi. 2000 Apr;20(4):245-7. PMID: 11789257
Study Type : Human Study