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Science Forum Index » Medicine - Nutrition Forum » anti-bodies - sign of infection or immunity?
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Message |
| TC |
Posted: Thu Feb 22, 2007 2:01 pm |
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Guest
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http://www.labtestsonline.org/understanding/analytes/hiv_antibody/test.html
Antibodies to the HIV virus can be detected by a screening test called
an ELISA. The ELISA test is repeated if positive.
OR
http://content.nejm.org/cgi/content/full/351/22/2286
Intradermal administration of antigens is expected to facilitate their
exposure to antigen-presenting cells, such as macrophages and
dendritic cells, which are present at higher levels in skin than in
muscle.1 Therefore, as compared with intramuscular vaccination,
intradermal vaccination may induce similar serum antibody responses
with a smaller quantity of antigen. The intradermal route has been
evaluated for influenza, rabies, and hepatitis B virus vaccines.
2,3,4,5 Brown et al. found that the intradermal administration of one
fifth of the standard dose of A/Swine/NJ/76 influenza vaccine produced
antibody titers similar to those elicited by the standard
intramuscular dose in healthy adults and resulted in fewer systemic
reactions.6 We evaluated the safety and immunogenicity of the
intradermal injection of a candidate influenza vaccine containing 6 µg
of hemagglutinin antigen per strain in two groups of adults, one 18 to
60 years of age and the other over 60 years of age. A U.S.-licensed
influenza vaccine administered intramuscularly at the standard dose
was used as the reference vaccine.
****
So.....
If you have HIV antibodies, you are a pervert, you have AIDS and will
die a miserable death.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
TC |
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| TC |
Posted: Thu Feb 22, 2007 3:07 pm |
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Guest
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On Feb 22, 12:01 pm, "TC" <tunder...@hotmail.com> wrote:
Quote: http://www.labtestsonline.org/understanding/analytes/hiv_antibody/tes...
Antibodies to the HIV virus can be detected by a screening test called
an ELISA. The ELISA test is repeated if positive.
OR
http://content.nejm.org/cgi/content/full/351/22/2286
Intradermal administration of antigens is expected to facilitate their
exposure to antigen-presenting cells, such as macrophages and
dendritic cells, which are present at higher levels in skin than in
muscle.1 Therefore, as compared with intramuscular vaccination,
intradermal vaccination may induce similar serum antibody responses
with a smaller quantity of antigen. The intradermal route has been
evaluated for influenza, rabies, and hepatitis B virus vaccines.
2,3,4,5 Brown et al. found that the intradermal administration of one
fifth of the standard dose of A/Swine/NJ/76 influenza vaccine produced
antibody titers similar to those elicited by the standard
intramuscular dose in healthy adults and resulted in fewer systemic
reactions.6 We evaluated the safety and immunogenicity of the
intradermal injection of a candidate influenza vaccine containing 6 µg
of hemagglutinin antigen per strain in two groups of adults, one 18 to
60 years of age and the other over 60 years of age. A U.S.-licensed
influenza vaccine administered intramuscularly at the standard dose
was used as the reference vaccine.
****
So.....
If you have HIV antibodies, you are a pervert, you have AIDS and will
die a miserable death.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
TC
http://hivinsite.ucsf.edu/InSite?page=kb-02-02-01#S5.2X
During acute HIV infection, prior to the appearance of antibody
(window period or pre-seroconversion), HIV infection can be confirmed
only by the demonstration of circulating p24 antigen, or by the
presence of viral RNA or DNA. Although highly sensitive antibody
assays exist to detect very low levels of HIV antibody in blood, the
window period prior to appearance of antibody rarely can be shortened
to less than 3 weeks. Once antibody has appeared, titers progressively
increase during 3-5 months until levels peak, at which time they
remain fairly constant throughout the remainder of infection. Also,
antibodies during early infection usually are of low avidity, but
avidity increases as infection progresses. Therefore, HIV infection
can be divided into categories of recent or established infection,
depending on the quantity of antibody present or their avidities.
These parameters can be exploited as tools in order to estimate the
relative time that HIV infection occurred. For example, if antibody
titers or antibody avidity is low, it is likely that infection
occurred within the past 4 months; conversely, high-titer or high-
avidity antibodies signal an established infection that has been
present for longer than 4 months. Several epidemiological studies have
used the S/LS testing strategy to predict incidence in San Francisco
and in Rio de Janeiro, Brazil.(6-8)
****
HIV Antibodies = infection and certain death
OR
****
http://content.nejm.org/cgi/content/full/351/22/2286
Therefore, as compared with intramuscular vaccination,
intradermal vaccination may induce similar serum antibody responses
with a smaller quantity of antigen. The intradermal route has been
evaluated for influenza, rabies, and hepatitis B virus vaccines.
2,3,4,5 Brown et al. found that the intradermal administration of one
fifth of the standard dose of A/Swine/NJ/76 influenza vaccine
produced
antibody titers similar to those elicited by the standard
intramuscular dose in healthy adults and resulted in fewer systemic
reactions.
***
Influenza antibodies = successful vaccination and long healthy life
***
Is black white or is white black? Or is all a uniform grey and they
decide whether it is white or black depending on whether pharma can
make money on it or not.
TC |
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Posted: Thu Feb 22, 2007 5:47 pm |
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"During acute HIV infection, prior to the appearance of antibody
(window period or pre-seroconversion), HIV infection can be confirmed
only by the demonstration of circulating p24 antigen, or by the
presence of viral RNA or DNA..."
This is ludicrous. "Viral RNA" is smaller than the virus itself, but
no matter what has been tried, there has never been more than a couple
of particles found (which can be found in other conditions as well),
and they don't even have the characteristics ascribed to "HIV" in the
textbooks. Do you realize this is a total phantom "disease," in terms
of it being caused by a "germ?" It's like saying that a bunch of
people are inside an apartment building busy doing different tasks,
but whenever you lift the roof off (as in a child's play house), all
you find are things like teeth and fingernails. In this case, these
pieces of protein or genetic material are not specific to any virus,
let alone "HIV," whatever that is supposed to be at any given time. |
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| Jeff |
Posted: Thu Feb 22, 2007 11:08 pm |
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Guest
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"TC" <tunderbar@hotmail.com> wrote in message
news:1172167281.238073.207900@t69g2000cwt.googlegroups.com...
<...>
Quote: If you have HIV antibodies, you are a pervert, you have AIDS and will
die a miserable death.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
If you have antibodies to any virus, that means that the body has been
exposed to either the virus or a protein that is present on the virus. In
the case of HIV, anitbodies against HIV usually indicates infection.
People who have HIV often live many years without advancing to AIDS. And
many people who have HIV infection are kids, were raped or got it through
adult heterosexual behavior. Having HIV doesn't make one a pervert. Some
people even got it from blood transfusions (very rare now). Having HIV
doesn't necessarily mean a miserable death.
Influenza antibodies indicate that the body has been exposed to the viruses
that cause influenza. This can be from vacciantion or from infection. Having
antibodies doesn't mean that one will have a healthy life. It may indicate
that one is immune from influenza or may be related to an impending death
from respiratory arrest.
Have a lovely day.
Jeff
> TC |
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| GMCarter |
Posted: Fri Feb 23, 2007 6:34 am |
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On 22 Feb 2007 10:01:21 -0800, "TC" <tunderbar@hotmail.com> wrote:
Quote: http://www.labtestsonline.org/understanding/analytes/hiv_antibody/test.html
Antibodies to the HIV virus can be detected by a screening test called
an ELISA. The ELISA test is repeated if positive.
OR
http://content.nejm.org/cgi/content/full/351/22/2286
Intradermal administration of antigens is expected to facilitate their
exposure to antigen-presenting cells, such as macrophages and
dendritic cells, which are present at higher levels in skin than in
muscle.1 Therefore, as compared with intramuscular vaccination,
intradermal vaccination may induce similar serum antibody responses
with a smaller quantity of antigen. The intradermal route has been
evaluated for influenza, rabies, and hepatitis B virus vaccines.
2,3,4,5 Brown et al. found that the intradermal administration of one
fifth of the standard dose of A/Swine/NJ/76 influenza vaccine produced
antibody titers similar to those elicited by the standard
intramuscular dose in healthy adults and resulted in fewer systemic
reactions.6 We evaluated the safety and immunogenicity of the
intradermal injection of a candidate influenza vaccine containing 6 µg
of hemagglutinin antigen per strain in two groups of adults, one 18 to
60 years of age and the other over 60 years of age. A U.S.-licensed
influenza vaccine administered intramuscularly at the standard dose
was used as the reference vaccine.
****
So.....
If you have HIV antibodies, you are a pervert, you have AIDS and will
die a miserable death.
Wrong. Numerous infections may elicit an antibody response that is
ineffective in clearing that infection. In the case of an acute
infection, this can result in massive inflammatory responses and
death.
In the case of HIV, like hepatitis B, hepatitis C, TB and other
infections, the antibody response does not control the infection. The
body mounts a response that can be deleterious.
In the case of HIV, this response results in a chronic, sustained
decline of CD+ T cells. This is AIDS.
And I have watched WAY too many friends die of AIDS.
You have NO fucking idea what you're babbling about with this
bullshit.
Quote: If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
That's right, dearie. A vaccine that is EFFECTIVE stimulates immunity
so that the presence of the actual infecting agent is thwarted before
it gets a start. Undoubtedly, there is more to effective vaccination
than a humoral response and cell-mediated immune responses are also
key.
George M. Carter |
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| GMCarter |
Posted: Fri Feb 23, 2007 6:35 am |
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Guest
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On 22 Feb 2007 13:47:33 -0800, monty1945@lycos.com wrote:
Quote: "During acute HIV infection, prior to the appearance of antibody
(window period or pre-seroconversion), HIV infection can be confirmed
only by the demonstration of circulating p24 antigen, or by the
presence of viral RNA or DNA..."
This is ludicrous. "Viral RNA" is smaller than the virus itself, but
no matter what has been tried, there has never been more than a couple
of particles found (which can be found in other conditions as well),
The first part is true (so what?) but the next part is unsupported
bullshit. |
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| Jeff |
Posted: Fri Feb 23, 2007 9:10 am |
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Guest
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"GMCarter" <fiar@verizon.net> wrote in message
news:ijgtt2ddqrjia32mmtue2pivok288856ri@4ax.com...
<...>
Quote: In the case of HIV, like hepatitis B, hepatitis C, TB and other
infections, the antibody response does not control the infection. The
body mounts a response that can be deleterious.
Hepatitis B infection can be cleared. When it isn't cleared, it becomes
chronic hepatitis B. Infection results in chronic hepatitis B in 90% of kids
who get it at birth and 6% of people over 5. Hepatitis C results in chronic
infection about 3/4 of the time (CDC says 55%-85%).
Quote: In the case of HIV, this response results in a chronic, sustained
decline of CD+ T cells. This is AIDS.
Not necessarily. There are rare cases of HIV infection where the body is
able to beat it. With proper treatment, people are able to have 10+ disease
free years.
AIDS is an HIV infection that has advanced. If someone has a CD4 count of
200 or less or one of 26 conditions along with HIV infection, then he or she
has AIDS.
Quote: And I have watched WAY too many friends die of AIDS.
You have NO fucking idea what you're babbling about with this
bullshit.
You've nailed this one.
Quote: If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
That's right, dearie. A vaccine that is EFFECTIVE stimulates immunity
so that the presence of the actual infecting agent is thwarted before
it gets a start. Undoubtedly, there is more to effective vaccination
than a humoral response and cell-mediated immune responses are also
key.
George M. Carter
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| TC |
Posted: Fri Feb 23, 2007 12:42 pm |
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Guest
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On Feb 22, 9:08 pm, "Jeff" <n...@googlemail.com> wrote:
Quote: "TC" <tunder...@hotmail.com> wrote in message
news:1172167281.238073.207900@t69g2000cwt.googlegroups.com...
...
If you have HIV antibodies, you are a pervert, you have AIDS and will
die a miserable death.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
If you have antibodies to any virus, that means that the body has been
exposed to either the virus or a protein that is present on the virus. In
the case of HIV, anitbodies against HIV usually indicates infection.
People who have HIV often live many years without advancing to AIDS. And
many people who have HIV infection are kids, were raped or got it through
adult heterosexual behavior. Having HIV doesn't make one a pervert. Some
people even got it from blood transfusions (very rare now). Having HIV
doesn't necessarily mean a miserable death.
Influenza antibodies indicate that the body has been exposed to the viruses
that cause influenza. This can be from vacciantion or from infection. Having
antibodies doesn't mean that one will have a healthy life. It may indicate
that one is immune from influenza or may be related to an impending death
from respiratory arrest.
Have a lovely day.
Jeff
You are debating the wrong issues. The comments on pervert and dieing
a miserable death, etc, weren't the main points. I was being
sarcastic. But your comments about rape and blood transfusions, etc,
were pretty funny, especially since you were serious about it.
The point was: Why is it that if you have HIV antibodies, you are
considered infected and potentially diseased and when you have
influenza antibodies you are considered immunized and in a strong
position health-wise?
Here is another question. HIV is transmissible by blood products after
the blood products have been chilled, separated, frozen, thawed, etc.
and eventually, sometimes months later, introduced into a foreign live
immune system. Then HIV survives the new hosts inherent immune
response. But HIV can't be isolated because the virus can't survive
the simple isolation and filtration process intact. And HIV is so
delicate that it is almost impossible to grow in vitro.
How can such a delicate retrovirus that can't survive in vitro, or
thru the simple process of isolation, survive to infect thru the
gruelling blood product processing process?
TC |
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Posted: Fri Feb 23, 2007 6:13 pm |
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TC:
People who are more likely to have immune system problems are those
who do have a lot of antibodies. The test are non-specific, so that
"positive" results make sense, but not for the phantom "HIV." Such
people have exposed themselves to many foreign antigens and also
oxidized "normal" molecules that are then attacked (and antibodies
creatted), leading to the characteristic Th1 to Th2 shift very common
in "AIDS" patients.
Go to: http://groups.msn.com/aidsmythexposed/general.msnw
if you want to see "HIV" evidence analysis. You can also ask
questions on the forum there. People like Mr. Carter don't seem to
realize that the person making the claim must put forth a formal
hypothesis and then follow the scientific method. I can "cure" "HIV/
AIDS" if give the opportunity, and I would be willing to put up a
substantial amount of money, but "the other side" would have to put up
the same amount, and the "loser" would have to give that money to the
other person, minus expenses. The expenses would come from finding
"HIV infected," but otherwise healthy volunteers, and then having them
follow my protocols, with strict supervision to make sure that they
are not exposing themselves to stressors that do cause serious immune
system problems. Of course, the "HIV" advocate would have to claim
exactly what is supposed to happen to an "HIV infected" person who is
apparently in great health and who did not take the "AIDS cocktail
medication." Otherwise, it woiuld be impossible to use the scientific
method, because there would be no way to know what the effect that
"HIV" supposedly causes (in the absence of the "medicines") is, and
thus no way to judge the experiment. Once you take the ability of
these people to play their shell games away from them, they scamper
off like frightened rabbits, and I know how to do exactly that. In
fact, I has offered to become "HIV infected" with the "infectious
molecular clone" for years now, if they pay me the full retail cost of
thte "AIDS cocktail drug." If I die of "AIDS" within 12 years or so
(whatever their most recent claim is), I will give them all my money,
but if not, they keep paying me that amount for the rest of my life.
Of course, none of these people have any interest in this offer, even
though they criticize Peter Duesberg for not doing this (minus the
money aspect)! They are laughable, scientifically, but they do kill
people, because the "virus" nonsense has led them to give highly
toxic "medicines" instead of just telling people to avoid the
stressors that actually can compromise the immune system.
One thing you might hear is, "I can understand why IV drug users and
gay guys who took poppers and all kinds of other things go AIDS, but
what about the hemophiliacs?"
Just one study is needed to make it clear, though these patients are
usually in poor health, compared to "normal" controls:
QUOTE: Inhibitor antibodies directed against factor VIII or factor IX
present challenges to the clinician. Fortunately, several management
options are available, although each has disadvantages as well as
advantages. Alloantibodies against factor VIII (which develop in 25 to
50% of children with severe hemophilia A, as well as in a small
percentage of children with mild or moderate hemophilia A) may be low
titer and transient or may be high titer. Most patients with high-
titer problematic inhibitors now try to eliminate the inhibitor by
using one of several immune tolerance induction (ITI) regimens. For
treatment of bleeding episodes in patients who have high-titer (≥ 5
Bethesda units) inhibitors, one can use a prothrombin complex
concentrate (PCC) (preferably an activated PCC [APCC]), recombinant
(r) factor VIIa, or porcine factor VIII. The choice of product is
generally dependent on the type and severity of the patient's
bleeding, degree of cross-reactivity of the patient's inhibitor with
porcine factor VIII, physician familiarity with the product, product
availability, and cost. In persons with hemophilia B, alloantibodies
occur in only 1 to 3% of severely affected individuals. However, in
roughly half of those who develop inhibitors, anaphylaxis or severe
allergic reactions occur on infusion of any type of factor IX-
containing product. This phenomenon usually develops after relatively
few exposures to factor IX; thus it is recommended that the first 10
to 20 infusions of factor IX given to children with severe hemophilia
B be given in a setting equipped for treatment of shock. For treatment
of bleeding episodes in patients with severe allergic reactions, rF
VIIa is the treatment of choice. ITI has been less successful in
hemophilia B patients with inhibitors than in those with hemophilia A,
and in a subgroup of patients with severe allergic reactions who were
desensitized to factor IX and then tried on ITI, results were even
poorer. Additionally, several developed nephrotic syndrome while on
ITI. For hemophilia B patients with inhibitors who do not have
allergic reactions to factor IX, bleeding episodes can be treated with
PCC or APCC or with rF VIIa. Autoantibodies directed against factor
VIII are rare but can occur in a variety of settings. They occur
mainly in adults, and bleeding is often severe and life threatening.
Although some factor VIII autoantibodies disappear spontaneously, most
require immunosuppression. Corticosteroids and cyclophosphamide are
generally recommended. For treatment of bleeding, therapeutic options
include (human) factor VIII concentrates, porcine factor VIII, APCC,
and rFVIIa. The choice of product is generally determined by the
consulting hematologist's familiarity with the product, product
availability and cost, as well as response to treatment. UNQUOTE.
Source: http://cat.inist.fr/?aModele=afficheN&cpsidt=1444604 |
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| GMCarter |
Posted: Sat Feb 24, 2007 8:52 am |
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On 23 Feb 2007 08:42:12 -0800, "TC" <tunderbar@hotmail.com> wrote:
snip
Quote:
The point was: Why is it that if you have HIV antibodies, you are
considered infected and potentially diseased and when you have
influenza antibodies you are considered immunized and in a strong
position health-wise?
Then your point reveals significant ignorance of immunology. When our
bodies face a disease or infection, several systems kick in. The
innate immune response followed sometimes by the specific cellular and
humoral (antibody) generating responses. With good luck, they work to
eliminate or at least contain the infection.
Some infections don't work like that. An antibody response does not
guarantee infection is resolved.
Quote: Here is another question. HIV is transmissible by blood products after
the blood products have been chilled, separated, frozen, thawed, etc.
and eventually, sometimes months later, introduced into a foreign live
immune system. Then HIV survives the new hosts inherent immune
response. But HIV can't be isolated because the virus can't survive
the simple isolation and filtration process intact. And HIV is so
delicate that it is almost impossible to grow in vitro.
Ah, that's based on a lot of faulty premises. HIV has been isolated.
Duesberg even recognizes that. HIV in plasma or serum as infected
cells can survive quite nicely.
Quote: How can such a delicate retrovirus that can't survive in vitro, or
thru the simple process of isolation, survive to infect thru the
gruelling blood product processing process?
Because it has ways of "wearing coats" to protect itself, like a
lymphocyte or dendritic cell. Cell-free virus doesn't survive as well.
No more than would you standing naked in the Antarctice for a couple
of hours. Does that mean humans don't exist?
George M. Carter |
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| GMCarter |
Posted: Sat Feb 24, 2007 8:54 am |
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On 23 Feb 2007 14:13:07 -0800, monty1945@lycos.com wrote:
Quote: TC:
People who are more likely to have immune system problems are those
who do have a lot of antibodies. The test are non-specific, so that
"positive" results make sense, but not for the phantom "HIV."
That's a completely ridiculous statement.
These claims have been refuted or at least placed in a proper context.
SOME infectious diseases can cause a false antibody test in SOME small
percent of cases. This does not invalidate the HIV antibody test--it
merely indicates a limitation which is quite well characterized, your
conspiracy crazy nonsense notwithstanding.
George M. Carter |
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| GMCarter |
Posted: Sat Feb 24, 2007 8:57 am |
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Guest
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On Fri, 23 Feb 2007 13:10:45 GMT, "Jeff" <news@googlemail.com> wrote:
Quote:
"GMCarter" <fiar@verizon.net> wrote in message
news:ijgtt2ddqrjia32mmtue2pivok288856ri@4ax.com...
...
In the case of HIV, like hepatitis B, hepatitis C, TB and other
infections, the antibody response does not control the infection. The
body mounts a response that can be deleterious.
Hepatitis B infection can be cleared. When it isn't cleared, it becomes
chronic hepatitis B. Infection results in chronic hepatitis B in 90% of kids
who get it at birth and 6% of people over 5. Hepatitis C results in chronic
infection about 3/4 of the time (CDC says 55%-85%).
That's right. I should have said "does not necessarily" control
infection.
Quote: In the case of HIV, this response results in a chronic, sustained
decline of CD+ T cells. This is AIDS.
Not necessarily. There are rare cases of HIV infection where the body is
able to beat it. With proper treatment, people are able to have 10+ disease
free years.
Also an important point--long term non-progressors who maintain high
CD4 counts and low viral loads I think constitute about ONLY 6-8% of
HIV infected individuals. That's one of the things that makes it so
horrifying; even Ebola doesn't kill that many (though it does it so
much faster).
Quote: AIDS is an HIV infection that has advanced. If someone has a CD4 count of
200 or less or one of 26 conditions along with HIV infection, then he or she
has AIDS.
Correct.
Thanks for the additional thoughts and corrections!
George M. Carter
Quote: And I have watched WAY too many friends die of AIDS.
You have NO fucking idea what you're babbling about with this
bullshit.
You've nailed this one.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
That's right, dearie. A vaccine that is EFFECTIVE stimulates immunity
so that the presence of the actual infecting agent is thwarted before
it gets a start. Undoubtedly, there is more to effective vaccination
than a humoral response and cell-mediated immune responses are also
key.
George M. Carter
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| TC |
Posted: Sat Feb 24, 2007 11:18 pm |
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Guest
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On Feb 23, 4:34 am, GMCarter <f...@verizon.net> wrote:
Quote: On 22 Feb 2007 10:01:21 -0800, "TC" <tunder...@hotmail.com> wrote:
http://www.labtestsonline.org/understanding/analytes/hiv_antibody/tes...
Antibodies to the HIV virus can be detected by a screening test called
an ELISA. The ELISA test is repeated if positive.
OR
http://content.nejm.org/cgi/content/full/351/22/2286
Intradermal administration of antigens is expected to facilitate their
exposure to antigen-presenting cells, such as macrophages and
dendritic cells, which are present at higher levels in skin than in
muscle.1 Therefore, as compared with intramuscular vaccination,
intradermal vaccination may induce similar serum antibody responses
with a smaller quantity of antigen. The intradermal route has been
evaluated for influenza, rabies, and hepatitis B virus vaccines.
2,3,4,5 Brown et al. found that the intradermal administration of one
fifth of the standard dose of A/Swine/NJ/76 influenza vaccine produced
antibody titers similar to those elicited by the standard
intramuscular dose in healthy adults and resulted in fewer systemic
reactions.6 We evaluated the safety and immunogenicity of the
intradermal injection of a candidate influenza vaccine containing 6 µg
of hemagglutinin antigen per strain in two groups of adults, one 18 to
60 years of age and the other over 60 years of age. A U.S.-licensed
influenza vaccine administered intramuscularly at the standard dose
was used as the reference vaccine.
****
So.....
If you have HIV antibodies, you are a pervert, you have AIDS and will
die a miserable death.
Wrong. Numerous infections may elicit an antibody response that is
ineffective in clearing that infection. In the case of an acute
infection, this can result in massive inflammatory responses and
death.
In the case of HIV, like hepatitis B, hepatitis C, TB and other
infections, the antibody response does not control the infection. The
body mounts a response that can be deleterious.
In the case of HIV, this response results in a chronic, sustained
decline of CD+ T cells. This is AIDS.
And I have watched WAY too many friends die of AIDS.
You have NO fucking idea what you're babbling about with this
bullshit.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
That's right, dearie. A vaccine that is EFFECTIVE stimulates immunity
so that the presence of the actual infecting agent is thwarted before
it gets a start. Undoubtedly, there is more to effective vaccination
than a humoral response and cell-mediated immune responses are also
key.
George M. Carter- Hide quoted text -
- Show quoted text -
Hey DEARIE, I don't give a fuck how many of your bosom buddies died
from AIDS, it doen't make you right. Not by a long shot. You believe
the propaganda. Thats makes you a fool.
TC |
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| TC |
Posted: Sat Feb 24, 2007 11:22 pm |
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Guest
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On Feb 24, 6:54 am, GMCarter <f...@verizon.net> wrote:
Quote: On 23 Feb 2007 14:13:07 -0800, monty1...@lycos.com wrote:
TC:
People who are more likely to have immune system problems are those
who do have a lot of antibodies. The test are non-specific, so that
"positive" results make sense, but not for the phantom "HIV."
That's a completely ridiculous statement.
Nope, it is based on fact. Not faith, as you seem to base your beliefs
on.
Quote:
These claims have been refuted or at least placed in a proper context.
SOME infectious diseases can cause a false antibody test in SOME small
percent of cases. This does not invalidate the HIV antibody test--it
merely indicates a limitation which is quite well characterized, your
conspiracy crazy nonsense notwithstanding.
George M. Carter
The HIV tests are invalidated on more than just that. HIV tests are
non-specific to the point of being useless.
TC |
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Posted: Mon Feb 26, 2007 11:24 am |
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On Feb 24, 6:57 am, GMCarter <f...@verizon.net> wrote:
Quote: On Fri, 23 Feb 2007 13:10:45 GMT, "Jeff" <n...@googlemail.com> wrote:
"GMCarter" <f...@verizon.net> wrote in message
news:ijgtt2ddqrjia32mmtue2pivok288856ri@4ax.com...
...
In the case of HIV, like hepatitis B, hepatitis C, TB and other
infections, the antibody response does not control the infection. The
body mounts a response that can be deleterious.
Hepatitis B infection can be cleared. When it isn't cleared, it becomes
chronic hepatitis B. Infection results in chronic hepatitis B in 90% of kids
who get it at birth and 6% of people over 5. Hepatitis C results in chronic
infection about 3/4 of the time (CDC says 55%-85%).
That's right. I should have said "does not necessarily" control
infection.
In the case of HIV, this response results in a chronic, sustained
decline of CD+ T cells. This is AIDS.
Not necessarily. There are rare cases of HIV infection where the body is
able to beat it. With proper treatment, people are able to have 10+ disease
free years.
Also an important point--long term non-progressors who maintain high
"Non-progressors". That term refers to people with a positive HIV test
and no symptoms of AIDS for some extended period of time.
That should be a hint. A big fucking hint at that.
First they said that once you get the virus, you will be develop AIDS
symptoms within months. Then AIDS symptoms failed to occur for some
time for many HIV positive people.
So how do you explain away a virus that does not lead to the symptoms
of disease as predicted by basic virological principals? You come up
with a term that is completely new and unheard of in the field of
virology: "non-progressors".
First the latency period, ie. the period between infection of HIV and
the appearance of visible signs of disease, was measured in months.
Then, when non-progressors appeared, the latency period was extended
to years instead of months. Then more longer-term "non-progessors"
appeared. The latency period was extended to a decade and a half. Now
the latency period is in the single to multiple DECADES range.
In fact many of these non-progressors failed to progress to AIDS until
they started taking drugs like AZT. Then they quickly succeeded in
progressing to the AIDS symptoms that were predicted in the first
place.
Hey. When you test positive for a virus that is supposed to cause a
disease, it should cause the disease in all cases. And if you develop
the disease without the virus that is supposed to cause the disease,
then there is a problem with the theory of the cause of the disease.
It is simple. All HIV positive should develop the disease. All without
HIV should not develop the disease. That is the way this is supposed
to work by definition. The Human immunodeficiency virus should cause
the disease in all cases and the disease cannot manifest itself
without the Human immunodeficiency virus. But we all know that that is
not the case.
Either the virus does not cause the disease or the tests are wrong in
many cases. Which is it? Is it the tests or the theory?
TC
Quote: CD4 counts and low viral loads I think constitute about ONLY 6-8% of
HIV infected individuals. That's one of the things that makes it so
horrifying; even Ebola doesn't kill that many (though it does it so
much faster).
AIDS is an HIV infection that has advanced. If someone has a CD4 count of
200 or less or one of 26 conditions along with HIV infection, then he or she
has AIDS.
Correct.
Thanks for the additional thoughts and corrections!
George M. Carter
And I have watched WAY too many friends die of AIDS.
You have NO fucking idea what you're babbling about with this
bullshit.
You've nailed this one.
If you have influenza antibodies, that is a sign of immunity conferred
by a vaccination, given by a health professional, and you will live a
healthy life.
That's right, dearie. A vaccine that is EFFECTIVE stimulates immunity
so that the presence of the actual infecting agent is thwarted before
it gets a start. Undoubtedly, there is more to effective vaccination
than a humoral response and cell-mediated immune responses are also
key.
George M. Carter- Hide quoted text -
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