Can the world be the same ever again?

A few small countries have claimed near normalcy while a few bigger ones have feigned the same by unmasking, even-though the infection has not really abated. As per WHO guidelines, a country is considered infection free only when, no single case of new infection is reported for two incubation periods. That is, zero case for a month or so. This must be when no external constraints are in force for mobility and social gatherings. It doesn’t appear so anywhere in the near future.

Festivals, travels and elections are common activities of any free country in today’s world. Majority of the population engage in these activities in normal life, but these routines do not appear to be in the horizon.

For example, consider some of the recent election exercises: US had one to choose its president in the fag end of 2020. Neither the pandemic nor elections deter with the presence of each other. USA never had a relapse from infection ever since its onset in early 2020 is another story. Elections too were held in the four major states in the more populous India in April 2021. While the numbers in India were indeed quite low in March 2021- real bottom of the wave at less than 10000 cases a day, 10% of the September, 2021 peak! TPR, the test positivity rate, also was quite low, at less than a few percentage. In April 2021, it had a phenomenal raise during the busy the multiphase schedule. The election mela ended in 2nd May; the peak of the second wave in the country was on 13th May, after a typical ten day incubation period of this virus. Look at the numbers today when many states are still under lockdown: 70% of the daily infection of the country’s 220 K, is from six states, three of the four states that had elections are in the list. Only Karnataka, Maharashtra and AP being outliers – Have they paid the price for being close neighbours?

Now take the case of festivals: How come the kumbmela states, UP, Uttarakhand are out of the woods so quickly ? The congregation should have contributed to the infection as much as election bound states – but didn’t.. why? would it have been the large scale testing that could have led to scuttling of the menace? could be! UP tests over 3.2 lakhs a day even today and it’s positivity (TPR) is less than just 1%. Even at its peak of infection the TPR was not above 18%. Uttarakhand Could keep its positivity at its peak below 24%; today it is at less than 8%. Both the states had peaks around 10 days after the festival time.

Why the election bound states could not manage well? Poor testing? For strange reasons, the authorities did not comply to the warnings to ramp up the testing in TN, Kerala, WB and are paying a heavy price now. TPRs were all above 25% and sometimes dangerously even close to 30%? WB even today continues to be well above 25% while others are just less than 20%!

Conclusion is any congregation would contribute to a wave; no doubt! As long as there is any remnant of live virus around, there is a looming threat! From the experience of Mar-May 2021 period, it can be safely concluded that even a TPR of less than 1% in random testing would not guarantee a threat free world! Till immunisation of the whole public is done like in small pox, the threat would continue: virus would not only thrive, but mutate and can potentially become resistant to the existing immunity!

Universal vaccination policy of India

Kiran Majumdar, the chairperson of Biocon, tweeted, “The vaccine situation in India is like arranged marriage. First u r not ready, then u dont like any, then u dont get any”!!

Health minister Dr Harsh Vardhan, responded equally sportively, ‘everybody will get their match, soon’.

What is the ground reality?

Out of 35 crore Indian population in the 45+ segment, more than 11 crore have been already vaccinated at least once, which is a significant 30%! Assuming only 60% are either willing or targeted to get vaccinated, central government has to plan for another 11 to 12 crore which is quite doable in the next three months at best, considering the production capacities of Indian suppliers and the commitments by way of advance payments of purchase orders. This would largely protect the most vulnerable population in the quickest feasible time period. The increased gap between the jabs is a blessing in disguise.

This leaves 59 crore adult (18 to 44) population, that is left to the responsibility of states. The immunisation program for this section has taken off in a subdued way since the beginning of this month, and till now 50 lakh or less than 1% have taken the jabs, in the last 15 days. It is quite likely that a significant fraction would have already had asymptomatic infection and have antibodies, since they unmindfully venture out often even during lockout periods.

Though health is a state subject, centre has proactively pushed the vaccination program and has set in place a system. The state leaders who engage in slanging matches have the responsibility to vaccinate only this segment of population. With the liberalised policy, a fraction of this population would anyway get vaccinated by their employers and the affluent few who can afford can pay for the jabs in comfort. Those elites who have faiths only in the latest western technology as reliable and safe compared to the ‘under developed local varieties’ can prefer Pfizer or Modena at a cost! This apart from satisfying their ego would also relieve the states’ responsibility and burden to an extent.

This young adult population, being active in the social media, embarks itself into dictating terms with the ever willing anti-government bought out press, which is apparently irrational. There is no need to issue a global tender for foreign vaccines. The government can collectively bargain for the best reasonable price as these vaccines cannot be procured on lowest bidder basis!

The global tendering by some states is either ill-conceived or knee jerk reaction or playing to the gallery!

Would science thwart ‘curses’?

Could a cursed land that was destined to be a desert be transformed? Yes.. Technology and motivated leadership could!

The legend is as follows: Lord Krishna picked up Maata Rukmini from Avanti and on way to Dwarka on a Chariot, invited the ‘Angry’ Rishi Doorvasa to accompany them on the Rath and be their guest in Dwarka. Rishi Doorvas wanted Rukmini and Lord Krishna to pull the chariot instead of the Horses and then only he will come. Having agreed, they started pulling the chariot. In between Rukmini became thirsty and wanted water. Lord Krishna pressed his leg hard into the earth and water came oozing. Rukmini and Krishna drank the water and started the journey, Doorvas became angry since he was not offered water and gave curses (shaap), one of that was ‘The water the Dwarka Kingdom will be salty and not fit for drinking’.

To reverse the curse, Modi tirelessly struggled for over two decades to bring water to this parched Saurashtra region by implementing the Sardar Sarovar Narmada project. Some 3.77 lakh ha gets Narmada dam water, flowing directly to the farms through open canals.

SAUNI, the link project, fills the irrigation dams which already have canal networks to channel water to farms. Four trunk lines — Link I, II, III and IV — will take water to the 115 dams spread across all Saurashtra’s 11 districts. Pumping and piping networks are themselves engineering marvels, for example, two sets of pumps of 13 tmc per hour capacity at 30m head. Sourashtra region is 60m above Narmada valley!

Modi transformed Saurashtra in a decade.. More than being proud, I am envious of not having such a leadership in other states!

No fighting with the upper riparian states if you manage the water resources intelligently!

Salute to the great visionary……

Is legalising Immunisation, unethical?

Should refusal for getting immunised be made punishable? Yes? Those not opting for, can go to Mars!

In many countries, even strongly democratic, not wearing mask is an offence – penalty may be not just paying off fines but one may be put behind the bars even, like in ‘curtailed’ democracy like Singapore! Trump and his team were trolled for ridiculing Faucci and CDC for advising wearing mask in public. So also Jair Messias Bolsonaro, the president of Brazil for the same reason. Many European nations paid heavy penalty by not complying with the advices by epidemiologists. Indian PM, Modi is praised for nudging one sixth of the world population living in India to largely comply with his pleading of wearing face masks, which could be one of the reasons for India’s successful management of the pandemic. World has come far away from wearing mask with the infection spreading its tentacles far and wide. What is the strategy now? Can we say for certain we are seeing the light at the end of the tunnel, now that the infection seems to be receding in many countries? What has the humanity learnt from this ‘dark’ episode? Has the virus gone or is it going shortly?

What is the metric to judge the phase of infection: Trend of daily number of infections or deaths? Number of active cases? Positivities in testing? Or a combination of all these?

The first and foremost is the trend of daily deaths is definitely an indication.

The next could be the trend in the number of active cases either hospitalised or home quarantined. The daily mortalities would generally be a fraction of the number of active cases, depending upon the nature of the infectious disease. For COVID-19, it could be of the order of two weeks. The actual fraction would depend upon the type of medication and immunity of the cohort. The last one in the metric could be the trend and actual number of daily infections. This is an important metric even to understand the beginning of vicious cycle. If a society is able to prevent the contagion from spreading, the war is half won. One of the ways is to force the individuals to wear the mask apart from other interventions. The other is to test and quarantine those with positive infection. Obviously the effort would be exorbitant to test the whole population in one go. Not that it is impossible – China does that once a while when the authorities even sense infection in a district! Countries like India choose statistical sampling – test symptomatic individuals and their contacts – if the positivities exceed a certain guideline number, say 10%, widen the net to reach a figure of 5%.

With this strategy, the number of cases could reach an asymptotic value and never be close to zero. Even at 1% positivity with a sample size 0.1% a day, which is mind a boggling effort in a population of even 10 million, the daily infection can be safely assumed to be at 10,000 per million, though only 100 would be counted as daily infection, 9900 would be missed out – they would be either asymptomatic or mildly symptomatic but some of them could potentially be spreading the infection. No doubt, the number would be less than 10,000, but not insignificant! Unless the positivity goes down to an extremely low figure, we cannot take it for granted that the virus is gone. One has to ramp us testing many fold to reach that to reach very low positivities, very impractical! It is conservative to assume that the number of cases in the general public at the same positivity fraction.

The present strategy of statistical sampling and testing is cost effective, long term strategy. But, it is a pain on the health system, bleeding the public exchequer. With the present optimal viable strategy, the virus would continue to linger, mutate and resurge later. Is there a way out? Yes… vaccination

Vaccination has saved the humanity from many dreaded diseases, small pox, measles, polio, and many more. Some misguided public ‘opt’ out of the covid vaccination program. Should they be allowed to exercise this option? should they have any option at all in the first place?

Have we not learnt from the face mask experience? Whether this elixir to the humanity be shunned by some not only endangering others but also entailing unnecessary public expenditure on testing, quarantining, hospitalisation paraphernalia? Damocles’ sword would always be hanging above you and me as long as these half baked ‘illiterates’ who do not believe in science, cohabit with us in this planet. Such being the case, there is a strong reason to make it binding on everyone in the society to get vaccinated as and when called for.

Else they can go Mars!

Is Vaccine making a ‘rocket science?’

Why are many countries queuing up with a begging bowl to India for vaccines? Why are the developed countries running short of supplies? Why is the covid infection so high in Russia inspite of a ‘Sputnik’? Why is China on a lockdown again with a threatening outbreak, inspite of not only many vaccines at their disposal, but their regulatory clearances that permit quicker access?

Vaccine manufacture is a long process that typically requires complex stages of incubation in specialized facilities, and working with “living” bacteria or cell culture. They are attenuated or modified in their functionality so that they can help the immune system to recognize and fight the true pathogens. But the manufacturing facilities are not very difficult to set up.

But even then, there are shortages – why? The answer might lie in business opportunities! Vaccine is a low return, low volume enterprise. While epidemic is once in a while phenomenon, pandemics are extremely rare! Pharma companies always look beyond the horizon – they want a ‘kill’; they would grow only if investments are made in lifelong diseases like, diabetes, hypertension, anti cholesterol etc., and not in once in a lifetime risky proposals. Covid like viral infections may not be back for at least for another three or four decades. After this vaccination, there is absolutely no market for them. Even now, for the late entrants, the picture is extremely grim!

Governments should have funded not only in research but also in building production facilities, instead of waiting for some obscure companies (Moderna etc.,) to shore up. Even Pfizer would not invest heavily and if it does, would like the costing strategy such as to cover their return of investment in the first few supplies itself. That is why their vials are irrationally damn costly. Compare this in late 1930’s: USA took a bold decision during the II world war, of investing in the whole chain from research to production in ‘Manhattan Project’ – but Vannevar Bush and FDR were at the helm at that time and not Faucci and Trump! If you don’t compare Covid fight to the III world war, then you are way off the track!

Surprised why the socialist Chinese and Russian governments have not followed that Manhattan model! Even Russia is after Reddy labs to licence its production! Except SII all others in India are small business units – how they will sustain after the covid era would indeed be a million $ question!

Credits:

1. https://www.sanofi.com/en/media-room/articles/2017/understanding-the-complexity-of-vaccine-manufacturing

2. https://www.sartorius.com/download/525728/4/mrna-vaccines-biopharma-industry-white-paper-en-b-sartorius-data.pdf

Vaccine war hotting up?

There is now frantic search for vaccine supplies. Even countries like Brazil, that shunned vaccines earlier are now scouting to source the supplies. Are there enough? Even to inoculate half the world population, close to 8 billion doses may be required. There may be just enough capacities to meet that target.

Inoculation has just started world over but countries are struggling to inoculate their subjects; as of now only small countries such as Israel and Beharin seem capable of inoculating significant fraction soon; other countries are way behind the targets: even US and UK, though are getting ravaged, have inoculated just around 2% of the population; Russia is nowhere close to its vaccine production target. The reasons range from a shortage of vaccines to vials as well as manufacturing equipment to the difficulty of maintaining the right storage temperature.

India appears to be better placed in the vaccine war: Not only on the production capacity but also on the choice of the types; it could not only meet its own requirements but could also supply to others. It has as of now approved two types, one is the vector of virus protein developed by AstraZeneca-Oxford and the other, called Covaxin developed by Bharath Biotech -ICMR, attenuated whole corona virus. Both have large production capacities within the country;

With many types arriving in the market, there is competition for bigger pie.. to establish which one is better? Also there are lot of talks about the regulatory approval processes that are apparently accused of taking shortcuts – for example, one of the key parameters of evaluation, efficacy data either not available or not up to some mark like the ones by Pfizer and Moderna approved for emergency use by USA, UK, Canada, EU etc.,

What is efficacy of a vaccine?

It is evaluated in the large scale phase-3 double blind trials, wherein the volunteers are given either the vaccine or placebo – neither the volunteer nor the hospital that gives the shots is aware of who gets what. These volanteers do their normal social life, thereafter. These cohorts are followed up for infection; in due course when the number of infections reach a thresh hold number, the number of infection in the vaccinated and placebo are identified, say p and q respectively, for example; the efficacy is evaluated as q/(p+q), in percentage. All other numbers such as protection against symptoms severity, hospitalisation, mortalities are all derived from this trials.

Is it a deviation?

If the infection is not widely prevalent, it would take a lot of time to get naturally infected. Or if the infection is deadly, then also it would entail severe loss of life before even getting approvals. Then how to evaluate quickly, under ‘emergency use authorisation‘? It is done by testing the neutralising antibodies that are generated in animal and in human. For example, In 2009 H1N1 vaccines were cleared by Indian and other regulators under similar emergency use authorisation without phase 3 trials! It may not be out of place to mention that the practise of approval for the deadly Japanese encephalitis, rabies or even seasonal flu has always been to examine only the immunogenicity data! So, one need not have to treat the phase-3 trial efficacy data as an essential pre-requisite for approval.

But is it sacrosanct?

There is a recent trend in this breakneck competition to match or better the efficacy numbers. WHO prescribes 50% shall be the ballpark criterion. The early birds, Pfizer and moderna having reported 90+%, others also tend to make claims matching that, though it is not mandatory. For example, AstraZeneca-Oxford researchers have no clue about the 90% efficacy of lower first dose that was administered to some of the volanteers of UK ‘by mistake’, compared to the 60+% to those given the full first dose. The anomaly could also be statistical because of the low numbers involved. Or it could also be scientific? Many regulators world over would simply disallow such gross misadventures and any outcomes therefrom. Could it be the immune system reacting differently? They now propose increased spacing betweeen the two doses might do ‘wonders’.

The viral vector vaccines have a peculiar problem. If the immune system is familiar with the unrelated virus used as a courier, it will attack it.

To circumvent the problem of “anti-vector immunity” and it can make a vaccine less effective, AstraZeneca Researchers now contemplate use of hetero type vaccination for booster dose based on a different vector while vaccinating with adeno types (Oxford, Sputnik), instead of the same.

Attenuated types, on the other hand, should provide better immunity as body responds to many of the vectors in the virus simultaneously! Some of the Chinese vaccines are of this type.

Moderna and Pfizer vaccines are entirely of new types, hitherto not tested in humans so far but have set very high efficacy numbers over 90+! These types require deep refrigeration storage requirements such as -70 deg C, unlike others that demand only common refrigerator freezer conditions, 2 to 8 deg C. Thus there are variety of factors that go into the choice of a vaccine, especially for emergency. Rest assured all would work, generally with minimum side effects rarely with a very very low probability of anaphylactic reactions such as the one seen in penicillin injections.

In many countries such as US, EU, etc., the virus is raging with staggering mortalities. In September also, the situation in India was grim. Obviously, there is a rush in the west to get vaccinated, but may not be in India now.

Vaccine hesitancy on the raise….especially from the Indian healthcare professionals, where about a crore will be vaccinated soon on priority. Responses from participants in this segment, reflect their concerns about the efficacy of the vaccine and fear of side effects. A recent online survey shows that 59% preferred to defer vaccination. Another interesting finding is most of them want to do antibody serum test, and decide to take vaccines only if found negative! Vaccine hesitancy even in this group is worrisome, because it percolates down to the general population easily. If herd immunity does not develop quickly in the society, the fight would get prolonged……

To win the war against the dreaded virus not only should the right vaccine be available, but also there is a dire need to inoculate the media!

Credits:

1. https://timesofindia.indiatimes.com/india/how-the-immune-system-can-be-a-vaccines-enemy/articleshow/80109956.cms?utm_medium=referral&utm_campaign=iOSapp&utm_source=email

When would the Third World War end?

The moot question now is when would the pandemic come to an end? At this point of the pandemic, everyone is curious to know, Would the pandemic go? According World Health Organisation, for declaring such status, there shall not be any new infection for a period of two incubation periods, for this, there shall not be any single new infection for one full month! It appears to be a daunting task. Then, what would be a practical level of ‘considering it is contained‘ in reasonable time.

As all mathematical models so far have only led the planners and policy makers down, as they are studded with many underlying assumptions. Then, why not make a considered guess, based on the observation of trends. The real world trends depict the social behaviour and the complex interaction of the population to the infection nearly perfectly on real-time basis.

By now, it is clear that the daily discharges cannot be more than 7-10% active case loads as the incubation period for this virus is 10 to 14 days. Only if the daily new infections are less than, say, 8%, the discharges would exceed new infection and the number of active case loads would reduce.

On a closer scrutiny of the data from many Indian states, the number of daily new cases has already been seen to be just around 8-10% of the active case loads. It is seen that happening in larger states, like Bihar, Andhra and Telangana, where the active cases has tapering. This is evident, for example, in Orissa and Jharkhand: with nearly 44 and 37 million population respectively.the active case loads have stabilised at 2500 and 1500. The positivities are less than 2%! One could get still lower daily cases few days after ramping up the testing and isolation; but it is unviable and infeasible at such low positivity rates. Presently, sharp decreases are noticed prominently only in states with high case loads.

With this model, one can expect the active case numbers to reach an asymptotic value of something like 40 to 50 per million population for India in a reasonable time frame of say a couple of months or so. With this value, it would be approximately around 50-60k active case load for the whole country on an average. At that point of time, the daily infection rate would be 4-5K and daily mortality at around 30 – 50. Presently it is at 280K, 25K and a 250 respectively. Essentially it means, you have to be contended with one fifths of today’s figures when the virus can be assumed at reasonable control!

It is a Damocles sword with sporadic infection with a possibility of 4-5 in a million! Though it is a low risk scenario, the virologists would like nothing less than its eradication. These numbers would linger at that level whatever you do, until vaccination is done. So, don’t expect to get a ‘nil’ report! Until herd immunity with vaccination is reached, there is always a lurking danger of resurgence of this virus in some mutated form or the other! Those who don’t, are culpable of being not only hosts for the ‘demon‘ but also are facilitators of its mutation that cause immense havocs! It may not be even criminal to tag them ‘anti-socials‘!

Continuing present management measures seems to be the only viable solution as most of the larger states are already on the path of control, barring a few; While the late entrant Kerala, though has very low mortalities, has puzzled with its disproportionately high new infections. Only Maharashtra and WB are problem states. Relax while all these states reach their limiting numbers, it is only a question of time….

It may also be academically interesting if the government launches large scale sero surveys along side vaccination to understand the curious sharp fall in new infections! This would confirm the suspicion of the country having reached near herd immunity! There can’t be any other reason other than significant fraction already having got infected near the threshold herd immunity requirement. That is why Kerala reports now a large number of cases. But with uncertainties of the antibody counts that are monitored going down couple of months of infection, but immunity building up with T and B cells, that are not tested, one would not be able to draw any meaningful conclusion with such sero surveys. May be if they are also included in the testing strategy, it would be a very useful data for the future generation, as such infections are not going to be infrequent!

We have learnt many hard lessons in this nasty war: viruses can only be fought with cultural moderations of social interactions and non pharmaceutical interventions but not by allowing it to was through the community as that would entail many loss of loved ones; Vaccines would not take years to counter them. But one thing is certain, there is no end date fo this Third World War if many are unwilling to immunise!

The bottom line is, We are not that ignorant as we were once in ‘Spanish flu‘ times, also, neither the viruses are now, it is evolution!!

Shy of patting India?

Why not say ‘India has done better’ now at least?

It would be diabolic to giggle comparing the virus’ present western massacre especially when it is in the retreating phase in India. Western world never conceded that india could possibly face the wrath better, loaded with the pride of their immense infrastructure and technology! But facts are facts: In the beginning of the pandemic, when the mortalities were lower, they discounted to poor counting by this impoverished country; when the number of infections was low, it was lack of testing; when the cases were dropping, it was ‘hold on – the second wave is on the anvil’. Never accepted a possibility of better immunity or compliance to lockdown measures.

They not only refrained from taunting the rampant ‘protest marches for liberty’ in the west deaf to the words of wisdom and blind to the ‘Corona dance‘ in their midst, but even mimicked the modest calls of ‘diya and Thalia’ of Modi. More than the ‘western critics’, it was the bright immigrants of recent origin and the partisan Indian press, who were ever ready to turn their backs on the reality! For example, the Left leaning Karan Thapar and ‘renowned’ epidemiologist Ramanan Lakshminarayanan of Princeton University, repeatedly sounded bugle that India can’t do any better in this fight. Some of their interviews can’t be termed unbiased by any standards at all. One can re view them to confirm their predictions are all well off the mark.

Do you wish a country, that you orphaned for your selfish better pastures, perennially remain loser in any race? Have we lost our pride after being taught so by centuries’ of colonial rule? Is this a vulgar inferiority syndrome of the migrants, that they are more loyal to the country, they have recently adopted, than even the born natives there?

Still you are reluctant to accept the truth! Why not say now at least that ‘India has done better’ – even with a mumble ‘for reasons unknown’!

Crazy, but not Insane?

Oxford vaccine conundrum – in phase 2 studies, to assess the safety and immunology, studies were conducted with two different doses containing different quantity of virus particles of the vaccine[Low dose, LD: 2·2 × 10^10; Standard dose , SD: 3·5–6·5 × 10^10] to assess the immunological effectiveness of doses; the results indicated no strong difference between LD and SD. Also there was an increase in general in the antibody titres after the second dose [1]. Though they could have gone with LD itself, since even aged volunteers tolerated SD well, they decided to go with SD for phase 3 trials.

But, by mistake a significant number of people in a vaccine group were given LD as the initial dose. When they realised the mistake, they administered SD to the rest. The second dose, booster was SD for both all. Based on the infection data, it was surprisingly found [2], that efficacy is much higher in LD/SD group than the SD/SD.

LD/SD: efficacy estimated is 90·0% in a cohort size of 2741, (the infection in vaccinated is three vs 30 in the placebo group); SD/SD: efficacy estimated is 62% in a cohort size 8895, (infected in vaccine group against placebo group 27 vs 71);

The mistakenly delivered half-dose regimen appears to be more effective but was only given to ‌2,741‌ ‌subjects. Given the size of the group, differences between the demographics of the half- and full-dose cohorts and the lack of an accepted mechanistic explanation for the better efficacy, it is possible the 90% figure is an anomaly that will fail to stand up to a more rigorous assessment of the regimen.

In phase 2 studies, it may be seen that LD dose was not tested in older volunteers. So, to extend the results of LD/SD in the rest of the group to the aged is not a scientifically acceptable proposition. So, they have started a new phase- 3 trial in US with LD/SD regimen.

It is not just that: In this backdrop of Oxford vaccine’s curious contradiction of findings of higher effectiveness of LD/SD than the SD/SD regimen, scramble of permutation and combinations dominate the vaccine ‘science’. The crux is the ‘researchers’ don’t even have a ‘hypotheses’ leave alone established ‘theory’ to ‘explain’ a lower initial dose – higher booster dose effectiveness. But they also don’t want to discount the ‘findings of serendipity’ to possible statistical errors….

It is reasoned that possibly the first shot makes the second shot ineffective! Even this, still lacks the explanation – then why a lower first short could be more effective? The explanation apart, the vaccine researchers are trying to combine the different vaccines to boost the efficacy (may be mRNA’s magic 95% is the trigger, that makes them crazy to improve their numbers)!

In trying to pep up the AstraZeneca-Oxford University vaccine’s 62 percent efficacy found in the early analysis, a combination proposal from Russian authorities has been prompted [3]: The reason attributed to the lower immunity is that AstraZeneca uses the same Chimpanzee adenoviral vector for the two doses. In contrast, Sputnik V vaccine which claims 95 percent efficacy uses two different human adenoviral vectors for two shots, called as ‘heterogeneous boosting’. Russian researchers say by combining the vaccine with Sputnik V will further boost the efficacy of AstraZeneca-Oxford University‘s vaccine. The question now is, why at all to combine a vaccine having a much lower efficacy of 62%, with 95%! Though they have already started millions with Sputnik, Russian researchers probably want a foothold of acceptance by the west!

The UK government recently announced that it will begin a clinical trial combining the adenovirus vaccines with mRNA technology. AstraZeneca is also exploring heterogeneous combinations of different adenovirus vaccines.

If you wait a little longer, you may get a magic ‘concoction’ at the end… or a disgraceful acceptance of defeat by the Oxford researchers of their goof ups! Why not gracefully accept 62% figure and declare ‘take it or leave it‘! Unfortunately, the other vaccines have raised the expectation bar, which used to be only around 60% like other flu shots, to well over 90%!

Credits

1. https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)32466-1/fulltext

2. https://doi.org/10.1016/S0140-6736(20)32623-4

3. https://www.moneycontrol.com/news/business/companies/astrazeneca-to-initiate-human-testing-to-assess-its-covid-vaccine-with-russias-sputnik-v-6217451.html?fbclid=IwAR3F39TCzE1ZR6szsNYZtZKvq-cwtfupR6dNaovIsmSmv_TIgxA1IQvBqbc

Could Scientists ever become mightier than the Almighty?

Genes evolve over eons by natural selection. If one starts manipulating them, would nature not rebel? Is there a limit to exploit the knowledge of genes to suit the goals by those superior in the nature’s hierarchical ladder, the homosapens?

The major beneficial impact of genetic research was realised when Genentech announced the production of genetically engineered human insulin in 1978. The insulin produced by bacteria was approved for release by the Food and Drug Administration of USA in 1982. The prices of this life saving drug drastically reduced since then. Another breakthrough was in the drug research: Genetically modified mice are not aware opthe defacto standard for the study and modelling of cancer, obesity, heart disease, diabetes, arthritis, substance abuse, anxiety, aging and Parkinson disease. Also genetically modified pigs have been bred with the aim of increasing the success of pig to human organ transplantation.

Genetic research entered paradigm shift when Gene editing became a reality. The gene editing tool known as CRISPR catapulted into scientific laboratories and headlines only a few years ago. Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas systems are well-known acquired immunity systems that are widespread in archaea and bacteria. The RNA-guided nucleases from CRISPR-Cas systems are currently regarded as the most reliable tools for genome editing and engineering. The first hint of their existence came in 1987, when an unusual repetitive DNA sequence, which subsequently was defined as a CRISPR, was discovered in the Escherichia coli genome during an analysis of genes involved in phosphate metabolism.

This year’s chemistry Nobel was awarded to Emmanuelle Charpentier and Jennifer Doudna for their work on CRISPR, a method that can cut up DNA in an organism’s genome and edit its sequence, the genetic “instructions” that determine how an organism will develop. CRISPR is currently making a huge impact in health: There are clinical trials on its use for blood disorders such as sickle cell disease or beta-thalassemia, for the treatment of the most common cause of inherited childhood blindness and for cancer immunotherapy. It is literally a ‘cutting edge’ technology today.

The Regeneron cocktail that was recently administered to president Trump, has fully-human antibodies produced by the mice, which have been genetically modified to have a human immune system, as well as antibodies identified from humans who have recovered from COVID-19.

Fast on its heels of gene editing came the reemergence of a profoundly consequential controversy: Should these new techniques be used to engineer the traits of future children, who would pass their altered genes to all the generations that follow? This is not an entirely new question. The prospect of creating genetically modified humans was openly debated back in the late 1990s, more than a decade and a half before CRISPR came on the scene and several years before the human genome had been fully mapped.

The use of gene-editing in human cases following the first use by Chinese scientist He Jiankui, who made the first genome-edited human babies in 2018. He Jiankui and his colleagues were targeting a gene called CCR5, which is necessary for the HIV virus to enter into white blood cells (lymphocytes) and infect our body. The team wanted to recreate this mutation using CRISPR on human embryos, in a bid to render them resistant to HIV infection, the father being HIV positive. But this did not go as planned and they generated different mutations, of which the effects are unknown. The twin girls were delivered by the mother, may or may not have been conferred HIV resistance, and may or may not have other consequences.

Editing the genes of an embryo is not enough to create a designer baby. The embryo would need to be viable, and working with viable embryos — one that can actually develop into babies — is a whole new step that many countries would not allow. But if someone were to do this work on viable embryos, implant them in a hospitable womb in a fertility clinic, and let them be carried to term, that would effectively create a person with genetically modified DNA that they’d then be able to pass on.

During the same millennial shift, policymakers in dozens of countries came to a very different conclusion about the genetic possibilities on the horizon. They wholeheartedly supported gene therapies that scientists hoped (and are still hoping) can safely, effectively, and affordably target a wide a range of diseases. But they rejected human germline modification—using genetically altered embryos or gametes to produce a child—and in some 40 countries, passed laws against it. There are 29 countries had an outright legal ban on genetic editing. In China, India, Japan, and Ireland, bans existed but didn’t necessarily have legal enforcement mechanisms behind them. In the case of China, the group who announced their famous results in April was able to get permission to work with non-viable embryos that could never have been brought to term; that’s how they worked within China’s guidelines. The US a special case, where the NIH has a moratorium on this research. Other countries have ambiguous rules.

Direct genetic engineering in the food industry has been controversial ever since its introduction. The successful completion of two decades of commercial GM crop production (1996–2015) is underscored by the increasing rate of adoption of genetic engineering technology by farmers worldwide. With the advent of introduction of multiple traits stacked together in GM crops for combined herbicide tolerance, insect resistance, drought tolerance or disease resistance, the requirement of reliable and sensitive detection methods for tracing and labeling genetically modified organisms in the food/feed chain has become increasingly important. The most widely accepted genetically modified traits in GM crops are herbicide tolerance and insect resistance. GM soybean, maize, canola, and cotton are the most common examples of these crops in the market. Developing countries like India and China are the largest producers of genetically modified Bt cotton. The development of a newer dicamba and 2,4-D tolerant crops as an update of older version, exposes that despite contradicting the warnings of environmentalists, corporations were actively preparing for the emergence of superweeds. The introduction of these new herbicide tolerant crops is an admission of failure. It also represents a colossal failure of imagination in dealing with the cycle of problems in chemical-GM farming. The biotech industry is committed to addressing the problems that GM creates with new GM products rather than with actual solutions.

For 10 years, the company Oxitec has been testing whether genetically modified mosquitoes can suppress populations of their natural brethren, which carry devastating viruses such as Zika and dengue. Its strategy: Deploy (nonbiting) male Aedes aegypti mosquitoes bearing a gene that should doom most of their offspring before adulthood. Now, a team of independent researchers analyzing an early trial of Oxitec’s technology is raising alarm—and drawing fire from the firm—with a report that some offspring of the GM mosquitoes survived and produced offspring that also made it to sexual maturity. As a result, local mosquitoes inherited pieces of the genomes of the GM mosquitoes. There’s no evidence that these hybrids endanger humans more than the wild mosquitoes or that they’ll render Oxitec’s strategy ineffective. “The important thing is something unanticipated happened,” says population geneticist Jeffrey Powell of Yale University, who did the study with Brazilian researchers. “When people develop transgenic lines or anything to release, almost all of their information comes from laboratory studies. … Things don’t always work out the way you expect.”

Should the scientific pursuits and new knowledge frontiers not allow their exploitation for healthier life? Could the present day fertility clinics produce ‘designer babies’ in the future? Should it serve to increase the food production? Or Would it be construed as interfering with the God’s nature by the society?

So far this Million dollar question has not been answered yet, right?

Credits:

1. History of CRISPR-Cas from Encounter with a Mysterious Repeated Sequence to Genome Editing Technology: Yoshizumi Ishino, Mart Krupovic, Patrick Forterre

https://jb.asm.org/content/200/7/e00580-17