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Biotech / Medical : HuMAB companies

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To: Icebrg who wrote (655)9/15/2004 2:46:37 PM
From: Icebrg   of 1022
 
InNexus 20-F Registration Cleared by SEC
Wednesday September 15, 9:36 am ET

VANCOUVER, BRITISH COLUMBIA--(CCNMatthews - Sept. 15, 2004) - InNexus Biotechnology, Inc. (the "Company") is pleased to announce that the Company's Registration Statement on Form 20-F, filed with the United States Securities and Exchange Commission under Section 12(g) of the Securities Exchange Act of 1934, has become effective today. The Registration Statement can be viewed at www.sec.gov.

About InNexus

InNexus is developing the next generation of therapeutic, monoclonal antibodies using its SuperAntibody Technology Platform. InNexus intends to apply this technology to improve the potency of existing antibody products while opening new markets and disease applications with other forms of SuperAntibodies. InNexus will develop the technology through partnerships with biotechnology and pharmaceutical companies while pursuing development of its own products for unmet medical needs. To learn more about InNexus please visit the Company's website: www.innexusbiotech.com.

Super-antibodies break the cell barrier

15:23 19 April 04

Super-antibodies that can bind to targets within cells, rather than on their surface, could lead to a new range of treatments for diseases, a biotech company claims.

"Most good targets for diseases are inside cells," says Charles Morgan, president of InNexus Biotechnology of Vancouver, Canada, which has developed the super-antibody technology.

Super-antibodies could be used to target bacteria and viruses (including HIV) inside cells, for instance, or abnormal proteins that turn cells cancerous. In theory, they could do everything that the small molecules of most conventional drugs do, and more.

The beauty of a cell-penetrating super-antibody is that it would be highly discriminating. Because antibodies can be far more specific than small-molecule drugs, and because they are not inherently toxic, they should have fewer side effects.

The big disadvantage is that antibodies have to be injected as they do not survive in the stomach.

Molecular ferries

Antibody-based treatments are already being used to treat diseases in several ways (see graphic). Over a dozen are now approved for use in people. However, like natural antibodies, all bind to molecules on the surface of cells or viruses.

Antibodies under development can ferry other substances into cells, such as the toxin ricin, and they are sometimes engulfed by a cell after binding to its surface proteins, but none can enter cells freely and target molecules inside them.

However, InNexus says a simple chemical modification enables any antibody to flit in and out of cells until it finds its target. The "key" that allows them to enter is a short protein segment called a membrane-translocating sequence (MTS), normally found in signalling proteins such as growth factors that can enter cells. Several groups worldwide have shown that attaching MTS segments to other proteins allows them to enter cells.

"We thought, can you do this with an antibody?" says Morgan, who presented the technology at a BioVentures biotech conference in London earlier in April. InNexus found a way to attach an MTS segment to a structure common to all antibodies. "And lo and behold, it worked," he says.

Experiments with a fluorescently labelled super-antibody show it enters all cells but accumulates only inside cells containing its target, Morgan says. He thinks the antibodies could last in the body for up to a month, entering and leaving cells until they find their target.

As a proof of principle, the company developed a super-antibody that binds to and blocks caspase-3, an enzyme inside cells that triggers cell suicide. The super-antibody stopped human white blood cells from killing themselves when they were exposed to actinomycin D, a drug that normally triggers cell suicide (Apoptosis, vol 8, p 631).

InNexus hopes a super-antibody of this kind can be developed to block cell death in people who have just had heart attacks or strokes.

Some researchers have their doubts. "A lot of work has been done trying to make antibodies that are stable in cells," says Andrew Bradbury of the Los Alamos National Laboratory in New Mexico. "But it's proved far more difficult than expected."

But Morgan says an antibody's stability depends on how it enters the cell. Those that are engulfed after binding to surface proteins end up in structures called endosomes, where they are likely to be destroyed. Super-antibodies, however, enter the normal, safe environment of the cell.

"There would definitely be loads of new targets if it worked," says Daniel Elger of biotech company Antisoma, based in London, UK, which has developed an anti-cancer antibody that carries an enzyme into cells after binding to a surface receptor.

But for purposes like blocking viral replication, the success of cell-penetrating super-antibodies will depend on the concentrations they reach inside cells. "It would be down to the practicality of whether you could get enough in," he says.

newscientist.com
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