VACCINE-INDUCED DISEASE EPIDEMIC OUTBREAKS

(V.I.D.E.O.s)
The Engineering of “Pandemics”
By A. True Ott, PhD, ND

The year was 1921. America was entering a decade of robust prosperity. Later called
“The Roaring Twenties”, it was a time of unparalleled economic expansion. Debt
money from Wall Street banks was plentiful and easy to obtain. The “Great War” was
over. America was flexing her industrial muscles. Factories were being built and
expanded in every major city. Automobiles began rolling off Detroit assembly lines in
record numbers. The stock market began making millionaires. People were HEALTHY
and HAPPY – largely because the dreaded “world mystery disease” (which decades
later became known as the “1918 Flu Pandemic”) had disappeared. Two entire years
had passed with no dreaded “mystery deaths” being reported. America had cause to
celebrate, and celebrate they did!

As a matter of fact, the American Public in general was so optimistic and HAPPY in
1921, that relatively few people were unhealthy as well. For the first time in decades,
hospital beds were empty. The fledgling American Medical Association, formed by John
D. Rockefeller just a few years earlier, was worried. Business was sagging. Profits
from vaccines and drugs were spiraling. Something had to be done, and done
immediately. False, faux epidemics of smallpox were created to solve the problem, and
keep the Medical Mafia’s cash registers ringing.

We know this dastardly plan actually happened, thanks to a citizen’s WATCHDOG

GROUP in Kansas City, Missouri named “The Advertiser’s Protective Bureau”, who
filed, and successfully prosecuted criminal charges against the Missouri state chapter of
the AMA – the Jackson Medical Society. The ‘Protective Bureau’s” official report of this
cold-blooded plot reads as follows:

“In the Fall of 1921, the health of the city was unusually good, but slow for the
doctors. So the Jackson Medical Society met and resolved to make an epidemic in the
city. According to the minutes of this meeting: ‘MOTION WAS MADE AND SECONDED,
THAT A RECOMMENDATION BE MADE BY THE COMMITTEE, TO THE BOARD OF
HEALTH, THAT AN EPIDEMIC OF SMALLPOX BE DECLARED IN THE CITY.
(Investigation later revealed that there was NO SIGN OF AN EPIDEMIC at the time, in
the city, or anywhere in the state or region!)
‘It was moved and seconded that a day be set aside, termed VACCINATION DAY, on
which physicians would be stationed at ALL SCHOOLS, clinics, public buildings and
hospitals to vaccinate “free of charge”. (Vaccinations are never “free”. The taxpayers
are always forced to pay for every one of the “free” vaccines.)
“IT IS FURTHER RECOMMENDED THAT WIDE PUBLICITY BE GIVEN, STATING
THAT VACCINATION IS A PREVENTIVE OF SMALLPOX, AND URGING THE
ABSOLUTE NECESSITY OF VACCINATION FOR EVERY MAN, WOMAN, AND
CHILD IN THE CITY.”
 The Protective Bureau proved in court that there WAS NO EPIDEMIC before the
vaccinations!! The court records show that the Medical Society manufactured vast
amounts of posters, fliers, newspaper stories and ads featuring horrific and lurid
pictures of diseased children covered with massive smallpox sores and open wounds.
Some pictures actually showed children’s corpses covered with the same ugly sores.
The PANIC-DRIVEN message was clear --- VACCINATE EVERYONE, or face a deadly
public disease. There was a “sweeping epidemic” in the city; the disease was “highly
contagious” and would “strike anyone who was not vaccinated” was the bill of goods
sold! (Does this sound at all familiar today – 88 years later??)

The Medical Mafia’s propaganda blitz was successful, and over a million previously
healthy and happy American citizens were hypnotized and terrorized into placing the
vaccine toxins into their bloodstreams. All public school children in the region were
vaccinated while at school! Parents who dared question the vaccination of their children
were ostracized and publicly vilified.

THE COURT RECORD ON THIS CASE IS VERY CLEAR. In the weeks and months
following the “mass vaccinations” – the area’s hospital beds were filled to over-flowing
with VACCINE-INDUCED SMALLPOX CASES! Tens of thousands of people became
ill, and many hundreds of innocents died, and many more were permanently crippled!
Of course, THE NEWSPAPERS THEN TRUMPETED HOW WISE THE MEDICAL
ESTABLISHMENT WAS TO PROMOTE THE VACCINES – stating how much worse
the death toll would have been without the vaccination campaign!! Untold MILLIONS
OF DOLLARS of profit was generated by this massive “medical” fraud.

Thanks to the ADVERTISER’S PROTECTIVE BUREAU, however; the massive fraud

was exposed and criminally prosecuted to a successful conviction. During the trial,
three amazing facts were proven beyond any “reasonable doubt”.

Fact 1: The poster and advertising pictures showing the diseased and dying children
used so successfully by the “doctors”, WERE NOT EVEN CASES OF LOCAL
SMALLPOX CASES AS THEY WERE BILLED TO BE! The Protective Bureau
documented that they were pictures of ENGLISH CHILDREN who were victims of
“court-proven” cases of SMALLPOX VACCINE POISONING!! One of the pictures was
of a 5-week-old baby named Mona Stevenson, of Humphrey Street, Burnley, England.
A previously healthy and happy baby, Little Mona had been vaccinated for smallpox at 5
weeks of age. Four weeks later, her pox-ridden little body was placed in a tiny coffin
and buried. The horrific photos of Little Mona and others in England had previously
been published in British newspapers where details of the resulting CRIMINAL TRIALS
were also given. The full details of the trials, as well as the pictures, were also included
in a comprehensively large medical boot titled “THE HISTORY AND PATHOLOGY OF
VACCINATION” by Edgar M Crookshank, MD – professor of Bacteriology at the ultra-
elite Kings College, London England.
Fact 2: Vaccines containing LIVE VIRUSES, weakened (i.e. attenuated) or otherwise
universally causes more diseases than the vaccine ever could prevent.

Fact 3: Vaccine-Induced-Disease (VID) is an extremely effective socio-economic tool.

It has the potential to generate BILLIONS OF DOLLARS OF WINDFALL PROFITS,
while permanently changing the social structures of large groups of people.

While the Protective Bureau won the criminal court case – the American People lost.
The case should have made front-page headlines around the nation, showing the
Modus Operandi of certain corrupt “medical practitioners”. How, by means of fraud,
treachery, and trickery, they made millions of dollars in windfall profits while thousands
of innocent, trusting, and naïve Americans suffered and died. The entire sordid affair,
with all its damning details, was kept out of the American Press. John D. Rockefeller’s
AMA, with its millions of dollars of influence – made sure of that!

Amazingly, even though thousands of people had died or become crippled by this
managed manslaughter, the doctors involved were only given a light penalty in the form
of a token fine. The medical establishment as a whole was not upset in the least by the
exposure – and has continued on unabated perpetuating the same crimes against
humanity – creating vaccine-induced-diseases while fleecing the people continually until
this present day.

It is a proven (albeit little-known) fact, EPIDEMIC/PANDEMIC MANUFACTURING IS

STANDARD PRACTICE with the world-wide “Medical Mafia” circles. In order to
maximize profits and re-shape geographical regions, they often manufacture a false-flag
“emergency”. If there is an outbreak of mild seasonal virus, they call it an influenza
pandemic, give it a fancy new name, and then actually CREATE THE PANDEMIC by
means of mass vaccinations using ATTENUATED, or LIVE VIRUSES!! Remember the
shocking words of the AMA’s Dr. Simon Louis Katzoff who said: “ DOCTORS LIVE BY
DISEASE, SO THE PUBLIC CAN EXPECT THE SUPPLY OF DISEASE TO MEET THE
DEMANDS OF THE MEDICAL PROFESSION.”

OTHER DOCUMENTED CASES OF V.I.D.E.O.s (Vaccine Induced Disease Epidemic

Outbreaks.)

Case 1: Following the lead of their colleagues in Kansas City, the exact same events
occurred in Pittsburgh, PA under the direction of Pittsburgh’s “Health Director”, Dr. C.J.
Voux in the autumn of 1924. As in Kansas City, a group of public watchdogs brought
suit against Voux and his vaccine-promoters. As in Kansas City, the vaccine promoters
were found guilty. The case documented that over 1,000,000 vaccine shots were “sold”
to the residents of Pennsylvania, even though there had been ZERO documented cases
of smallpox in the region. It was successfully proven that ONLY AFTER the million
shots had been given, that a smallpox epidemic began. This vaccine-induced,
manmade “epidemic” resulted in 330 deaths and at least 1,680 cases of severe
smallpox that caused permanent, crippling damage to the survivors. Moreover, it cost
the city a total monetary loss of $3,069,616; although Dr. Voux and his accomplices had
collected more than $10 million in hospital and related care revenues – they were not
forced to pay for damages or reparations. As in the Kansas City trial, a small,
insignificant fine was levied, and the case was not widely publicized.

Case 2: The initial batches of Dr. Jonas Salk’s polio vaccine produced thousands of
cases of poliomyelitis in vaccinated individuals. This was due to an unsafe amount of
LIVE VIRUSES in the vaccine itself. Dr. Sabin then introduced his “improved” vaccine
with “attenuated” or “weakened’ live viruses in 1958, and the following year his vaccine
was made to be compulsory (mandatory) in all school-age children in a number of
states. As a result, polio increased a whopping 300% in these states. For example,
Tennessee reported 119 polio cases in 1958, after “vaccination” this total increased to
386 cases in 1959, Ohio – 17 cases in 1958, 52 cases in 1959, Connecticut – 45 cases
in 1958, 123 cases in 1959, and North Carolina: 78 cases in 1958 compared to 312
cases in 1959 AFTER forcing compulsory shots in school children. The modern record
is equally damning. The ONLY cases of recorded polio in the modern era is
immediately following vaccinations. Poliomyelitis, you see, is a water-borne virus and is
caused by drinking contaminated water. During the early 60’s, water-treatment facilities
became standardized across America – small amounts of CHLORINATION effectively
wiped out polio viruses. The conquering of polio had NOTHING TO DO with the
vaccine needles and swallowing sugar cubes. In fact, as author Ed Haslem documents
so well in his book, Dr. Mary’s Monkey, the Sabin vaccines were actually contaminated
with mutated GREEN MONKEY VIRUSES (SV-40 viruses to be specific) which has
caused untold millions of SOFT-TISSUE CANCERS and deaths worldwide. (The
cancer “industry” has reaped BILLIONS of dollars from this “contamination” over the
years, of course.) Dr. Maurice Hilleman has actually confessed as being a part of this
very activity.

Case 3: Knowingly added to “hepatitis” vaccines, HIV viruses were inoculated into
thousands of homosexual men and intravenous drug users in America’s inner cities
resulting in the “AIDS epidemic” in the 80’s. Purposefully placed in SMALLPOX
VACCINE SYRINGES, HIV was also introduced into African nations as a tool of ethnic
cleansing and GENOCIDE. The covert development and weaponization of the
HIV/AIDS virus and its monkey-virus origins, along with the amazing story of how the
scientists involved are tied to President Kennedy’s assassination is well documented in
Dr. Mary’s Monkey. The covert biological experimentation labs responsible for this
mayhem are today consolidated into the NIH, the NAIDS, the National Cancer Institute,
and Ft. Detrick, Maryland. The Centers for Disease Control (CDC) in Atlanta became
the centralized hub of pandemic and epidemic creations and propagation.

Case 4: The 1976 “Swine Flu” Fiasco and Fraud is perpetrated. A solitary soldier at Ft.
Dix collapses and dies following a reaction to an “experimental” vaccine while
completing an intense physical “forced march” exercise at Ft. Dix. Immediately, the
CDC swings into action, declaring a nationwide SWINE FLU PANDEMIC is pending.
Providentially, of course, the CDC just happens to have 200+MILLION DOSES of Swine
Flu vaccine already stockpiled, prepared with ATTENUATED (live, yet weakened)
viruses and experimental ADJUVANTS. President Gerald Ford, (with proven ties to Big
Pharma and Nixon’s covert viral weapons labs – also a key member of the “Warren
Commission’s” obfuscation of the JFK murder) rolls up his sleeves on national TV and
dutifully takes the vaccine. 40 million vaccines are given to naïve American human
guinea pigs. A rash of auto-immune disorders (Guillan-Barre Syndrome GBS, and
lupus) as well as a large number of deaths is immediately attributed to the vaccine, and
the mass vaccination campaign is halted. (What happened to the other 140 million
vaccines, one may ask?) In 1979, the television news magazine 60 Minutes did a
documentary investigation on this travesty-for-money scandal. Against all odds and the
threats of Big Pharma, the OBJECTIVELY FAIR 60 Minutes program aired ONE TIME.
There was no follow-up story, No criminal indictments were ever issued. There was no
MASS- MURDER-FOR-HIRE trial. As a result, America has largely forgotten the 1976
SWINE FLU SCANDAL! Click here for Part I of the 60 Minutes story; and Part II.

Case 5: During the first Gulf War – Operation Desert Storm, an experimental anthrax
vaccine was forcibly given to 140,000 rear-echelon support troops. This experimental
vaccine included an oil-in-water adjuvant called squalene (aka MF-59 made by
NOVARTIS). Despite voluminous studies showing dangerous toxicity factors conducted
on “oil-in-water” adjuvants at such prestigious research labs as UCLA – the U.S. Military
brass consented to the experimental injections. As a result, ALL 140,000 troops
developed a condition subsequently named “Gulf War Syndrome”. This sordid tale is
explained in a very honest and credible book by Gary Matsumoto, called, Vaccine-A.

ALL MODERN “PANDEMICS” ARE CAUSED BY VACCINE NEEDLES

As this author has repeatedly declared during many public radio interviews, the deadly
1918 Influenza Pandemic was the direct result of live-virus-contaminated Typhus Fever
Vaccines mandatorily given to U.S. and Allied military personnel during World War I.
During that era, viruses were not yet discovered and diseases were thought to be
bacterial only. These deadly typhus fever vaccines were manufactured by John D.
Rockefeller’s research labs and Chinese pharma factories. The vaccine “seed stock”
consisted of viruses harvested from human typhoid fever patients, cross-injected into
swine herds to create increased “seed stock”, and then injected into chicken and turkey
eggs for further incubation of the pathogens. The final, harvested “vaccine material”
then was injected into HUNDREDS OF MILLIONS OF HUMAN VEINS. The result was
a massive ‘pandemic’ that claimed the lives of as many as 50 million people worldwide.

In 1918, the viral pandemic was an honest mistake – the result of a combination of a
very bad vaccine and gross ignorance about viruses and the diseases they cause.
However, the continued denial of these FACTS, and the subsequent REVERSE
ENGINEERING OF THE KILLER VIRUS in Ft. Detrick labs (1997-2003) is inexcusable
and constitutes a veritable crime against humanity.

Moreover, the ONLY WAY a modern “SWINE FLU PANDEMIC” can actually materialize
is by injection of certain LIVE VIRUSES via vaccine needles. Make no mistake, the
world is NOT experiencing a true pandemic explosion at this time – but it most
assuredly WILL when and if the planned mass influenza vaccinations are completed
worldwide.

THE DANGERS INHERENT IN “DUPLEX” VACCINES FROM DESIGNER VIRUSES

“Modern Medical Practitioners”, including some well-meaning “osteopaths”, would have

the world believe the MYTH that vaccines containing attenuated (weakened) live viruses
cannot cause the viral disease conditions they are targeting. This is a most dangerous
misconception for the following SCIENTIFIC reasons.

Traditional “common” vaccines targeting measles, mumps and rubella for instance,
contain small amounts of “attenuated” live viruses which have been “weakened” but not
100% killed outright. Research has shown that these weakened “live” viruses create a
very mild form of the disease in the human that has been vaccinated, which in turn
creates a cellular immunity from that pathogen. The science behind this is correct, and
valid for the most part. To keep the targeted viral pathogen in a perpetually weakened
state, specific amounts of formaldehyde and ether are typically added, and in some
formulations, mercury in the form of thimerasol is added as a preservative to keep the
egg albumin cells from decaying and dying prematurely. The established theory behind
all of this ‘vaccination’ is the “protect the herd” theory which originated with Pasteur in
the late 19th century. As in all vaccines, a certain small percentage of the herd will
develop severe, ‘full blown’ disease states CAUSED by the attenuated viruses in the
vaccine itself, and another percentage will exhibit side effects from the chemicals added
to the vaccine – but if the vast majority of the herd is “protected” from the disease
condition – the vaccine is approved and stamped “safe and effective”.

Science has also proven that each viral pathogen has its own unique characteristics
that produce its own set of symptoms in the human hosts. Thus, each viral pathogen
has its own unique fingerprints of replication and reproduction as well. Each virus also
has a different level of effectiveness in its attenuated (weakened) state. Moreover,
some viruses have shown the ability to “drift” and acquire additional genetic alterations
over time. THIS IS ESPECIALLY TRUE OF THE SO-CALLED “NOVEL”
RECOMBINATION VIRUSES that have been “reverse engineered” in the world’s
weapons laboratories! When the RNA of the virus is spliced with other viral genes, the
resulting “Franken-virus” is very unpredictable. Studies conducted (yet currently
unpublished) by Terrence Tumpey, Jeffrey Taubenberger, and others at the NIH and
CDC show that these ‘resurrected pandemic viruses’ do not exhibit the NORMAL
tendencies of traditional, NATURAL influenza viruses such as seasonal H3N2 human
strains. They are best described as “Viral Wild Cards”.

This is just one problem with the headlong, mad rush to vaccinate Americans with a
series of reverse-engineered lab-created viruses, attenuated or otherwise, in an
UNTESTED, UNTRIED, EXPERIMENTAL VACCINE that has not been subjected to
LONG-TERM CLINICAL TRIALS TO DETERMINE THE LEVELS OF “DRIFT” or even
ATTENUATED TENDENCIES OVER TIME.
To supposedly minimize this “safety” issue, the CDC is now recommending a DUPLEX
vaccination, of all things. A “duplex” vaccination basically involves a two-shot series.
The first shot consists of a VERY WEAK, HIGHLY ATTENUTATED dose of the live
virus. This is intended to create an initial immune response patterning the specific virus
injected. Within a couple of weeks of the 1st shot, a BOOSTER SHOT is given. The
booster shot has only lightly attenuated, or even FULL STRENGTH VIRUSES in the
injection. This 2nd shot is then intended to create a full-strength immune system
response in the human subject.

This is, at the very least, BAD SCIENCE and borders on insanity for self-evident and
fairly obvious reasons. By their own admissions, the NIH scientists in their various
writings have declared that the level of potency of these REVERSE ENGINEERED
VIRUSES show abnormal, almost RANDOM tendencies in their attenuated states.
Nobody really knows what will happen over time as the inevitable “genetic drifts” occur.
It is a literal crap shoot. It is highly probable that even the HIGHLY ATTENUATED
FRANKEN-VIRUSES can swiftly regain their FULL POTENCY even in the presence of
ether and formaldehyde. (See Addendum Below) Secondly, the full-strength BOOSTER
shot viruses could just as easily “DRIFT” into something much more deadly than the
“original’ recombinant virus that it is targeting.

I submit that the scientists responsible for this “pandemic” are not stupid. They have to
know these facts as well as I do.

Therefore, I can only conclude that this entire affair is following the Modus Operandi of
the medical elite since the 1920 engineered smallpox epidemics. It is all being
ORCHESTRATED first and foremost for MONEY, and secondly, for social and
geographical restructuring of the “human herd”.

Also, it must be understood that this “Novel 2009 Influenza” is not easily nor readily
transmissible between humans. (See published study in the addendum). If this report
is accurate, how then did the “Pandemic” begin, and why the need for mass
vaccinations at all?? Like the “study” shows, the only way the test ferrets could contract
or transmit the 2009 “Novel Swine Flu” was by and through INOCULATION OF THE
DISEASE!! Humanity demands an answer, and demands it NOW!!!

A.True Ott, Phd, ND

Those who cannot remember the past are condemned to repeat it.
George Santayana
Those who are ignorant of the past, cannot be expected to remember it.
A. True Ott, PhD, ND
 ADDENDUM

ABSTRACTS FROM SELECTED FRANKEN-VIRUS STUDIES

http://www.ncbi.nlm.nih.gov/pubmed/11226311?ordinalpos=70&itool=EntrezSystem2.PEntrez.Pubmed
.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum

Feb. 27, 2001

Sequence of the 1918 pandemic influenza virus

nonstructural gene (NS) segment and characterization of
recombinant viruses bearing the 1918 NS genes.
Basler CF, Reid AH, Dybing JK, Janczewski TA, Fanning TG, Zheng H, Salvatore M,
Perdue ML, Swayne DE, García-Sastre A, Palese P, Taubenberger JK.

Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029, USA.

The influenza A virus pandemic of 1918-1919 resulted in an estimated 20-40 million deaths
worldwide. The hemagglutinin and neuraminidase sequences of the 1918 virus were previously
determined. We here report the sequence of the A/Brevig Mission/1/18 (H1N1) virus
nonstructural (NS) segment encoding two proteins, NS1 and nuclear export protein.
Phylogenetically, these genes appear to be close to the common ancestor of subsequent human
and classical swine strain NS genes. Recently, the influenza A virus NS1 protein was shown to
be a type I IFN antagonist that plays an important role in viral pathogenesis. By using the
recently developed technique of generating influenza A viruses entirely from cloned
cDNAs, the hypothesis that the 1918 virus NS1 gene played a role in virulence was tested in
a mouse model. In a BSL3+ laboratory, viruses were generated that possessed either the
1918 NS1 gene alone or the entire 1918 NS segment in a background of influenza
A/WSN/33 (H1N1), a mouse-adapted virus derived from a human influenza strain first
isolated in 1933. These 1918 NS viruses replicated well in tissue culture but were attenuated in
mice as compared with the isogenic control viruses. This attenuation in mice may be related to
the human origin of the 1918 NS1 gene. These results suggest that interaction of the NS1 protein
with host-cell factors plays a significant role in viral pathogenesis.

I FIRST READ THIS FOLLOWING REPORT (No Laughing Matter) BACK IN 2004. IT
HAS SINCE BEEN REMOVED FORM THE CDC DATABASE. IT IS
TAUBENBERGER’S DECLARATION THAT THE “HEMAGLUTININ CLEAVAGE” OF
THE “NOVEL” VIRUSES REACTS MUCH DIFFERENTLY THAN NORMAL VIRUSES
– IT MAY “DRIFT” AND CAUSE VERY DANGEROUS MUTATIONS. --- Ott
http://www.ncbi.nlm.nih.gov/pubmed/9707539?ordinalpos=90&itool=EntrezSystem2.PEntrez.P
ubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum&log$=freejrp
mc

Aug. 18, 1998

Influenza virus hemagglutinin cleavage into HA1, HA2: no

laughing matter.
Taubenberger JK.

Division of Molecular Pathology, Department of Cellular Pathology, Armed Forces Institute of

Pathology, Washington, DC 20306-6000, USA. taubenbe@afip.osd.mil

http://www.ncbi.nlm.nih.gov/pubmed/19574347?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubm
ed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum

July 24, 2009

Transmission and pathogenesis of swine-origin 2009

A(H1N1) influenza viruses in ferrets and mice.
Maines TR, Jayaraman A, Belser JA, Wadford DA, Pappas C, Zeng H, Gustin KM, Pearce
MB, Viswanathan K, Shriver ZH, Raman R, Cox NJ, Sasisekharan R, Katz JM, Tumpey
TM.

Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for
Disease Control and Prevention, Atlanta, GA 30333, USA.

Recent reports of mild to severe influenza-like illness in humans caused by a novel swine-origin
2009 A(H1N1) influenza virus underscore the need to better understand the pathogenesis and
transmission of these viruses in mammals. In this study, selected 2009 A(H1N1) influenza
isolates were assessed for their ability to cause disease in mice and ferrets and compared with a
contemporary seasonal H1N1 virus for their ability to transmit to naïve ferrets through
respiratory droplets. In contrast to seasonal influenza H1N1 virus, 2009 A(H1N1) influenza
viruses caused increased morbidity, replicated to higher titers in lung tissue, and were recovered
from the intestinal tract of intranasally inoculated ferrets. The 2009 A(H1N1) influenza viruses
exhibited less efficient respiratory droplet transmission in ferrets in comparison with the
highly transmissible phenotype of a seasonal H1N1 virus. Transmission of the 2009
A(H1N1) influenza viruses was further corroborated by characterizing the binding
specificity of the viral hemagglutinin to the sialylated glycan receptors (in the human host)
by use of dose-dependent direct receptor-binding and human lung tissue-binding assays.