PRIORITY
EQUITABLE CANDIDATES AND AFFLICTION
1.
Zoonotic viruses
2.
Synthetic viruses/bioweapons
3.
Bacterial infections
4.
Crimean-Congo hemorrhagic fever
5.
Ebola virus disease and Marburg virus
disease
6.
Lassa fever
7.
Middle East respiratory syndrome corona
virus(MERS-CoV) and Severe Acute Respiratory Syndrome(SARS)
8.
Nipah and henipaviral diseases
9.
Rift valley fever
10.
Zika
11.
“Disease X”(MAJOR PANDEMIC)
Disease X is implicit to be a major outbreak. This is a placeholder name that was adopted by the World Health Organization (WHO) in February 2018 on their shortlist of blueprint priority disease given to the very grave threat that unknown viruses the pretense to human health. Each year the WHO updates the list with guidance from experts in all fields of the scientific study of which pathogens pose the most the threat of causing the next global pandemic.
WHY THIS NAME?
WHO
adopted this name to guarantee that their planning was sufficiently flexible to
adapt to an unknown pathogen (eg.broader vaccines and manufacturing
facilities). Disease X is caused by Pathogen X, an infectious agent that is not
currently known to cause human disease, but an etiologic agent of a future
outbreak with epidemic or pandemic potential.Director of the National Institute
of Allergy and Infectious Diseases
Anthony Fauci stated that the concept of Disease X would encourage WHO projects
to focus their research efforts on entire classes of viruses(eg.flaviviruses)
instead of just individual strains (Zika virus), thus improving WHO capability
to respond to unforeseen strains. In 2020, it was speculated, including among
some of the WHO’s own expert advisors, that COVID -19, caused by SARS Co –V-2
Virus strain, Met the necessities to be the first Disease X.
X SPOTLIGHT ON VIRUSES
It is a big query that why X focus is on viruses and why all these viruses appear new. The theory o “new” is very implicit. The viruses included in the Blueprint list are called emerging because they were identified only recently, after having caused diseases in humans. However, these viruses existed in nature for a very long time, in animal reservoirs. The Nature journal estimated that, if all viruses present on the planet were aligned, they would cover a distance of 100 million light-years. A rough estimation based on a study in bats suggests that at least 3,20,000 viruses can infect mammals and that all species of vertebrates together could host at least 3 million and a half different viruses.
SUMMONS VS ADVANCES IN DRUG DEVELOPMENT
The
product development cycle remains lengthy for de novo medical counter
measures: diagnostic tests normally take 2-5 yrs to develop and 5-10 years of
their completion before procurement can be initiated. The timeline for vaccines
development is even longer since it requires human Safety and efficacy data.
Technological
opportunities speed up discovery and translation of new products. This lead to the discovery of effective antiviral drugs which extend to
papillomavirus, enteroviruses, Hepatitis C virus over the next 5-10
years. Currently,18 specific antiviral drugs (excluding interferon)are licensed
in the UK, with more in phase 3 clinical
trials or available on expended access. Cloning and sequencing have provided
tools to identify viral enzymes and have brought the day of the “designer drug” nearer to reality. At the
other end of the spectrum of drug discovery, huge numbers of compounds for
screening can now be generated by combinatorial chemistry. The thrust to find
drugs effective against HIV has also stimulated research into novel treatments
for other virus infections including herpes virus, respiratory infections, and
Hepatitis B and C viruses.
Is
the apocalypse really upon us? Well maybe…but our greatest good and what we
least can spare is hope itself.
Good work.πππ
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