By Phill Wilson, Blackaids.org
The other day, I got a comment from Jane. She was concerned that some of the people who volunteered for the Merck vaccine trial might be at greater risk for HIV infection as a result of having participated.
I think this is a very important question. It is been reported that blacks are more distrustful of medical trials, because of historical precedent.

So I asked my friend Steve Wakefield (pictured above), the HIV Vaccine Trials Network Legacy Project Director, who works to increase the participation of Blacks and Latinos in clinical research.
Here's what Steve had to say:
"Jane was right to highlight the news that Merck's preventive HIV vaccine did not protect against HIV infection or disease. This is the process of clinical trials; we test concepts until we develop products that work. Thanks to this process there were three new drugs licensed last year that are part of the arsenal to fight HIV infection. We will all be better off when someone -- any individual or collection of researchers and community volunteers -- help us to identify a vaccine that will prevent more people from becoming infected. That was the goal of the Merck Study.
But there is never a guarantee that a product in a clinical trial will actually work. That is why there is a need to do clinical trials. Unfortunately, the Merck product did not work. That does not mean that the clinical trial did not work.
Every time there is a clinical trial we learn something that helps us toward the development of a successful product.
There are many steps that go into a clinical trial. In the case of the Merck vaccine, there was promising data in the early test tube and animal trials. Early safety studies, conducted with participants at low risk for HIV, provided data indicating it was OK to move forward with testing. As a result, many of us were hopeful that the Merck vaccine could potentially protect against HIV infection, or prevent disease by lowering the amount of HIV in the blood of people who became infected.
In the end, this vaccine did not work. It did not prevent HIV infection.
It also did not reduce the amount of virus in those study participants who became infected with HIV during the trial. As a matter of fact it looks like some who got the vaccine may have been more susceptible to HIV infection. There is still much to learn over the next several weeks and months about why the vaccine didn't work. There is always some risks involved in clinical trials. That is why every person who volunteers to be in a clinical trial is offered and required to go thru an informed consent process.
The reality is that developing vaccines is a time intensive process.
Ten years before the polio vaccine was licensed, a leading polio researcher publicly voiced doubt as to whether we would ever find a polio vaccine. It is with this thought in mind that I believe that we must continue our search for an HIV vaccine. Had researchers given up hope for a polio vaccine simply because the process took longer than expected, the world we live in today might be quite different.
Advocacy, fundraising and U.S. media coverage of HIV/AIDS has waned as the population infected has increasingly been Black and Brown, poor, women and young gay men. We owe it to our sisters and brothers, both here and in Africa, to make sure the resources that helped develop treatments for other communities continue to be available now that we are the ones most at risk. Education of trial participants and the cry for continued testing of new vaccines must be part of Black America's agenda to fight the virus."
For more information about vaccine trials or research in general, go to www.hvtn.org
Phill Wilson is the founder and CEO of the Black AIDS Institute in Los Angeles . He has been living with HIV for 26 years and full blown AIDS for 15 years.
Comments: (16)
Add a comment
By: Cecil Jones on 1/28/2008 4:57AM
Anyone that tries to tell you that vaccine trials aren't dangerous is a liar. This is as close to being a "Human Guinea Pig" as the law allows. People with nothing to lose should volunteer for these programs because it could save their life. Medicine is a "practice" until trial and error gets it right. This was an easy article to address. Somebody's got to do it, but I don't need to volunteer to be the first for a vaccine? Exposure to the key agent that leads to HIV could cause HIV. There is always some risks, but are they willing to go first? Why? Always ask why.
Reply to this Comment | Report This
By: Lise on 1/28/2008 10:07AM
Mr. Wakefield, there is one single sentence in your long winded plug for Merck and vaccine trials that deals with the actual question. Here it is:
"As a matter of fact it looks like some who got the vaccine may have been more susceptible to HIV infection."
Would you care to expand a little on that whenever you're done singing the praises of Merck and its trials?
How is it a vaccine that seemed "ok" all of a sudden crashed and burned?
Why are there no reliable animal models of HIV/AIDS, making human guinea pigs are all the more necessary?
When did Merck and HVTN become aware that the vaccine vector - an Adeno-virus carrier into which snippets of HIV genes were inserted - increases the risk of AIDS? Why did none of Merck's "promising data" from animal and test tube studies reveal information like this:
"Harmful HIV Carrier
Tracy Hampton, PhD
JAMA. 2008;299(1):29.
Vectors used to create experimental HIV vaccines could do patients more harm than good by dampening the immune response to a natural infection, according to animal studies performed at the Wistar Institute in
Philadelphia (Lin SW et al. J Clin Invest. 2007;117[12]:3958-3970).
The findings suggest that recombinant adeno-associated virus (rAAV) may undermine the immune system and should not be used for vaccine development.
Specifically, while rAAV properly induces HIV-specific T cells of the immune system, those cells are functionally impaired.
In studies conducted in mice, HIV-specific T cells induced by the rAAV vector only poorly protected animals from subsequent infection, failed to secrete adequate levels of immune system–activating cytokines, and displayed a severely impaired ability to proliferate.
The study may help explain why HIV clinical trials with rAAV vectors have yielded disappointing results. The authors suggest that rAAV may be detrimental to patients with HIV by increasing a vaccine recipient's
susceptibility to progress more rapidly to AIDS."
Mr. Wakefield, can you explain the rationale behind trying to persuade the participants in Merck's STEP trial to stay in the study and stay blinded?
Staying in the failed STEP study means the participants cannot enroll in other more promising studies that may save their lives.
Staying blinded means the participants will not be told if they have received the dangerous immune system undermining vaccine or not.
Mr. Wakefield, can you explain the ethics behind even entertaining these ideas? Can you explain why you are offering none of this information in your answer to Jane?
Reply to this Comment | Report This
By: Lise on 1/28/2008 10:17AM
Mr. Wakefield, there is one single sentence in your long winded plug for Merck and vaccine trials that deals with the actual question. Here it is:
"As a matter of fact it looks like some who got the vaccine may have been more susceptible to HIV infection."
Would you care to expand a little on that whenever you're done singing the praises of Merck and its trials?
How is it a vaccine that seemed "ok" all of a sudden crashed and burned?
Why are there no reliable animal models of HIV/AIDS, making human guinea pigs are all the more necessary?
When did Merck and HVTN become aware that the vaccine vector - an Adeno-virus carrier into which snippets of HIV genes were inserted - increases the risk of AIDS? Why did none of Merck's "promising data" from animal and test tube studies reveal information like this:
"Harmful HIV Carrier
Tracy Hampton, PhD
JAMA. 2008;299(1):29.
Vectors used to create experimental HIV vaccines could do patients more harm than good by dampening the immune response to a natural infection, according to animal studies performed at the Wistar Institute in
Philadelphia (Lin SW et al. J Clin Invest. 2007;117[12]:3958-3970).
The findings suggest that recombinant adeno-associated virus (rAAV) may undermine the immune system and should not be used for vaccine development.
Specifically, while rAAV properly induces HIV-specific T cells of the immune system, those cells are functionally impaired.
In studies conducted in mice, HIV-specific T cells induced by the rAAV vector only poorly protected animals from subsequent infection, failed to secrete adequate levels of immune system–activating cytokines, and displayed a severely impaired ability to proliferate.
The study may help explain why HIV clinical trials with rAAV vectors have yielded disappointing results. The authors suggest that rAAV may be detrimental to patients with HIV by increasing a vaccine recipient's
susceptibility to progress more rapidly to AIDS."
Mr. Wakefield, can you explain the rationale behind trying to persuade the participants in Merck's STEP trial to stay in the study and stay blinded?
Staying in the failed STEP study means the participants cannot enroll in other more promising studies that may save their lives.
Staying blinded means the participants will not be told if they have received the dangerous immune system undermining vaccine or not.
Mr. Wakefield, can you explain the ethics behind even entertaining these ideas? Can you explain why you are offering none of this information in your answer to Jane?
Reply to this Comment | Report This
By: Lise on 1/28/2008 10:24AM
Mr. Wakefield, there is one single sentence in your long winded plug for Merck and vaccine trials that deals with the actual question. Here it is:
"As a matter of fact it looks like some who got the vaccine may have been more susceptible to HIV infection."
Would you care to expand a little on that whenever you're done singing the praises of Merck and its trials?
How is it a vaccine that seemed "ok" all of a sudden crashed and burned?
Why are there no reliable animal models of HIV/AIDS, making human guinea pigs are all the more necessary?
When did Merck and HVTN become aware that the vaccine vector - an Adeno-virus carrier into which snippets of HIV genes were inserted - increases the risk of AIDS? Why did none of Merck's "promising data" from animal and test tube studies reveal information like this:
"Harmful HIV Carrier
Tracy Hampton, PhD
JAMA. 2008;299(1):29.
Vectors used to create experimental HIV vaccines could do patients more harm than good by dampening the immune response to a natural infection, according to animal studies performed at the Wistar Institute in
Philadelphia (Lin SW et al. J Clin Invest. 2007;117[12]:3958-3970).
The findings suggest that recombinant adeno-associated virus (rAAV) may undermine the immune system and should not be used for vaccine development.
Specifically, while rAAV properly induces HIV-specific T cells of the immune system, those cells are functionally impaired.
In studies conducted in mice, HIV-specific T cells induced by the rAAV vector only poorly protected animals from subsequent infection, failed to secrete adequate levels of immune system–activating cytokines, and displayed a severely impaired ability to proliferate.
The study may help explain why HIV clinical trials with rAAV vectors have yielded disappointing results. The authors suggest that rAAV may be detrimental to patients with HIV by increasing a vaccine recipient's
susceptibility to progress more rapidly to AIDS."
Mr. Wakefield, can you explain the rationale behind trying to persuade the participants in Merck's STEP trial to stay in the study and stay blinded?
Staying in the failed STEP study means the participants cannot enroll in other more promising studies that may save their lives.
Staying blinded means the participants will not be told if they have received the dangerous immune system undermining vaccine or not.
Mr. Wakefield, can you explain the ethics behind even entertaining these ideas? Can you explain why you are offering none of this information in your answer to Jane?
Reply to this Comment | Report This
By: mo power to the people on 1/28/2008 10:57AM
Not as much as the fags that introduce the disease to the black community in the first place.
Reply to this Comment | Report This
By: Scott on 2/01/2008 1:33AM
The study may help explain why HIV clinical trials with rAAV vectors have yielded disappointing results. The authors suggest that rAAV may be detrimental to patients with HIV by increasing a vaccine recipient's
susceptibility to progress more rapidly to AIDS.
###############################
I'm Charlotte, was once lonely and devasted due to aids even all the
guys said I am so hot. It was changed since I joined the trusted and
anonymous hiv/aids personal and support community $$ pozgroup.com $$ I
started my hot blog, upload my wonderful photos,made many friends....
Catch me by WildOne.
Reply to this Comment | Report This
By: van on 2/01/2008 8:48PM
hello
all trials are dangerous...that's why they call them trails...Now in order to save more lives
willingness to particapte is necessary.
I am a 20 year {hetro/male} survior HIV+/AIDS,I and my friends some of whom are gay participate
and take the risk...and put it in Gods hands
faith and god 's will be done
a leap of faith...how is yours?
Reply to this Comment | Report This
By: Prince Moses on 2/02/2008 4:14AM
Blacks like to make fun of White people in Appalachian Mtns..When they should compare the aids rate in appalchia compared to Africa.Their are more black aids spreaders.
Reply to this Comment | Report This
By: Renee on 2/02/2008 8:45AM
In reference to Prince Moses, When you refer to Niggers you mean yourself included right, cause only an ignorant Ass wipe would say something like that. No one knows who atarted the spread of HIV/AIDS, or where it came from, and right now that's not a big issue. The issue at hand is finding a cure, not finding Idiots like yourself to make stupid unnecessary coments. Knowledge is power, go back to school and expand your mind not your ignorance.
Reply to this Comment | Report This
By: JC on 2/02/2008 6:51PM
Medical Clinical Trials Usually Involve Some Risks. The Question Is: Does The Benefit To Mankind Outweigh The Risk? Furthermore, Whom Amongst Us Is Willing To Take That Risk? Merck Is A Global Leader Is The Development Of Drugs To Combat HIV/AIDS. "Intelligence Shall Prevail, While Ignorance Suffers A Violent Death".
Instantly Turn your Computer into a Super TV!
http://www.television-on-internet.com/
Reply to this Comment | Report This