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Breakthrough: HIV Vaccine Triggers Strong Antibody Formation

HIV Vaccine Triggers Strong Antibody Formation

United States: A vaccination must produce antibodies in the immunized that are ready to neutralize future invaders in order for it to be effective. A vaccine must be safe for the great majority of people without causing any significant adverse effects or responses.

In early-stage clinical trials, a novel HIV vaccine candidate is meeting well-known obstacles while also experiencing some success in one area and some difficulties in another.

Addressing Safety Concerns

Though its creators have redesigned the vaccine to increase safety in upcoming research, it’s still early in the process. Their most recent findings demonstrate how the vaccination successfully produces broadly neutralizing antibodies in a tiny percentage of recipients.
In certain HIV-positive individuals, broadly neutralizing antibodies (bnAbs) targeting the virus were found in the early 1990s, during the height of the HIV/AIDS epidemic.

The potential of bnAbs was instantly apparent: they had the ability to identify and kill many strains of HIV, a genetically diverse virus that changes its form to elude immune recognition.

However, despite almost forty years of research, there is still no vaccine for HIV that can produce bnAbs in humans, let alone one that works.


We can see how hard it is to persuade the immune system to produce these powerful antibodies from natural infections: bnAbs only appear in 10–25 percent of HIV-positive individuals and can take years to develop.

It is encouraging to learn that a vaccine candidate studied in a short clinical study produced bnAbs in multiple subjects after two doses.

Leading the study was immunologist Wilton Williams of the Duke Human Vaccine Institute (DHVI). “It was very exciting to see that, with this vaccine molecule, we could actually get neutralizing antibodies to emerge within weeks,” Williams says.

The most prevalent form of HIV, HIV-1, is the target of the vaccine candidate. More precisely, it targets a stable portion of the virus’s outer envelope that holds steady despite mutations.

Clinical Trials: Results and Adjustments

24 healthy volunteers were enlisted in the phase I clinical trial, which started in 2019, 4 of whom received a placebo. However, the experiment was stopped when a single participant experienced a severe allergic reaction to polyethylene glycol (PEG), a vaccine component used to stabilize the formulation, following their third dose.


Five participants received three of the four scheduled doses, while fifteen more received just two, prior to the trial’s termination.

Since then, a PEG-free version of the vaccine has been developed, allowing the trial to continue evaluating it. Williams and associates, in the meantime, examined the information at hand and discovered that the vaccine, following two doses, produced a potent immunological response.



Producing Potent Antibodies


Two of the five individuals who received three shots prior to the trial’s termination also produced the highly sought-after elite neutralizers, bnAbs. In cell studies, the most effective of those antibodies killed 15 to 35 percent of HIV strains.

“This work is a major step forward as it shows the feasibility of inducing antibodies with immunizations that neutralize the most difficult strains of HIV,” Barton Haynes, an immunologist at DHVI,

In order to stop the virus from escaping, our next course of action is to produce stronger neutralizing antibodies against additional HIV locations. Although we haven’t arrived yet, the path ahead is now much more apparent.”

Overcoming Development Challenges


Having options is undoubtedly beneficial, even in the early phases of development. The failure of other promising approaches to create vaccines that work against many HIV strains in late-stage clinical trials serves as a “harsh reminder” of the difficulties involved in creating an HIV vaccine.

Still, when possible vaccines fail, other treatments are working. A seminal research conducted in December 2023 demonstrated that regular use of preventive treatment lowered HIV infection risk by 86 percent.

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