HIV/AIDS and the Perth Group. Was:"AIDS Treatment News"...

f.raaphorst at worldonline.nl f.raaphorst at worldonline.nl
Sat Oct 3 10:56:31 EST 1998


In article <361626C9.1FF8 at ix.netcom.com>,
  todd33 at ix.netcom.com wrote:
> fm.raaphorst at azvu.nl wrote:
> >
> > In article <3614289A.5A26 at ix.netcom.com>,
> >   todd33 at ix.netcom.com wrote:
>
> > > How could he claim that the antibodies from the rabbit were
> > > specific for "HIV" given that the antigen could not possibly
> > > have been pure "HIV" and that apparently, at that time, no one
> > > had really investigated methods of trying to further purfiy
> > > "HIV"?
> > >
> >
> > It doesn't matter at all whether the vaccination happens with a pure
> > isolate - it all depends on the selection method that's used to
> > characterize the resulting antibodies.
>
> There was no information about this in the Gallo papers, but I
> agree this is one way to deal with the problem.
>
> > Immunization with something that 'is at best half "HIV"', and the
> > rest consisting of cellular material from a human cell line, will
> > work just fine. Of course you'll generate a lot of B-cell lines
> > producing antibodies specific for common, cellular, proteins. But
> > in addition there will be B-cell lines that produce an antibody
> > against HIV-proteins. Even if these proteins haven't been
> > characterized by molecular cloning, you can identify the antibodies
> > that recognize them. For instance, you screen the collection of
> > antibodies you generated against uninfected cells and infected
> > cells. Immunofluorescence will do the trick. Antibodies specific
> > for common cellular antigens will bind to both infected and
> > uninfected cell lines. Antibodies specific for an HIV-encoded
> > protein, for instance the envelope proteins, will only bind to
> > the infected cell lines.
>
> This could be done, although some experiments would have to be
> performed to show that antigens unique to the infected cell line
> were truly viral, and not some endogenous protein induced by the
> experiment/infection.

Granted, but we're not talking about a single protein here. Would you really
expect an epidemic of people mounting an immunological response to a
multitude of 'self' antigens? I think the size of the response, and the
repeated isolation of typical retroviral genes and proteins points to an
infection with a retrovirus.

I guess there are also methods to use such
> Western blots preparatively, so that the antibodies binding to
> specifically induced antigens could be purified.  The following
> link shows the proteins that are purified from 2 different lines
> of infected cells (lanes B and C), compared to uninfected cells
> (lane A).  I wouldn't want the task of trying to purify polyclonal
> antibodies from a rabbit that were specific for "infected" vs
> "uninfected" cells in this situation.

Why not? It's quite simple if the pathogen has been isolated and its genes
have been cloned (which to my mind has been done). One way to screen the
antibodies would be through phage-display libraries, and even such
experiments have been done.

Gallo does show the
> blots for uninfected vs infected, but selects only serum that
> was shown to be "positive" on infected at a 1:100 dilution,
> and then instead uses a 1:500 dilution for the blots with
> infected and uninfected extracts.  Frankly, even in the original
> _Science_ paper, it is extremely difficult to see anything,
> probably because of the highly diluted antibody.
>
> http://www.virusmyth.com/aids/perthgroup/geneva/slide23.htm
>
> Thanks for your response Frank.
>
> Todd Miller

I still fail to grasp why the shortcomings of the original Gallo paper refute
the current results from independent labs all over the world.

have a good weekend,

Frank

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