Agents and compositions and methods utilizing same useful in diagnosing and/or treating or preventing plaque forming

Abstract

A method of immunizing against plaque forming diseases using display technology is provided. The method utilize novel agents, or pharmaceutical compositions for vaccination against plaque forming diseases which rely upon presentation of an antigen or epitope on a display vehicle. The method further includes agents, or pharmaceutical compositions for vaccination against plaque forming diseases, which rely upon presentation of an antibody, or an active portion thereof, on a display vehicle. Whether antigens or antibodies are employed, disaggregation of plaques results from the immunization.

Description

[0001] The present application is a continuation of U.S. application Ser. No. 09 / 629,971, filed Jul. 31, 2000, which is a continuation-in-part of U.S. application Ser. No. 09 / 473,653, filed Dec. 29, 1999, which is a continuation-in-part of U.S. provisional application 60 / 152,417, filed Sep. 3, 1999, the entire contents of each being incorporated herein by reference.FIELD AND BACKGROUND OF THE INVENTION[0002] The present invention relates to agents and compositions and to methods of utilizing same for treating plaque-forming diseases. More particularly, the methods according to the present invention involve the use of (i) plaque derived antigens cloned and displayed on the surface of a display vehicle for in vivo elicitation of antibodies capable of preventing plaque formation and of disaggregating existing plaques; and (ii) antibodies raised against plaque derived antigens, at least an immunologic portion of which is cloned and displayed on a display vehicle, which immunologic porti...

AI Technical Summary

Problems solved by technology

This rearrangement is associated with abnormal physiochemical properties, including insolubility in non-denaturing detergents and partial resistance to proteolysis.

In both types of the disease, the pathology is similar, but the abnormalities tend to be more severe and widespread in cases beginning at an earlier age.

In addition, these teachings do not provide means with which to enable the penetration of such antibodies into the brain through the blood brain barrier (BBB).

Furthermore, this patent fails to teach the use of phage display technology as a delivery method for antigens or antibodies.

Yet furthermore, no experimental results demonstrating the in vivo effectiveness of such antibodies are demonstrated by U.S. Pat. No. 5,688,561.

Because this proposed dosage would barely alter the level of endogenous circulating beta-amyloid and because EP 526511 does not recommend the use of an adjuvant, it seems implausible that any therapeutic benefit would result therefrom.

These findings suggest that the teachings of Schenk and colleagues are inefficient at best.

Since, as has already been mentioned hereinabove, the normal concentration of beta-amyloid in human serum is 50-200 pg / ml, immunization with that peptide could be expected to produce either low antibody titers or high toxicity if strong adjuvants are used and as such it is not applicable for therapy.

However, they fail to teach use of an antigen so displayed to effect immunization.

In addition, delivery of antibody displayed on a display vehicle is not taught by Schenk or Schenk et al. altogether.

Collectively, the prior art fails to teach means with which an effective titer of anti-aggregation antibodies can be generated in vivo in a short time and / or be introduced into the brains of patients suffering a plaque-forming diseases.

In addition, the persistence of titers generated via prior art teachings has not been established.

This passive immunity may be of exceptionally long duration if the display vehicle employed is capable of replicating within the recipient.

Use of beta amyloid peptide antigens in conjunction with adjuvants to effect immunization has previously been difficult due to a combination of high toxicity and low titers which result.

For example, injection of A.beta.-KLH or A.beta.-fibril leads to very slow immune response (Anavi, S., 1998, M. Sc. thesis from the Department of Molecular Microbiology and Biotechnology of the Tel-Aviv University) and many efforts have been made to circumvent low affinity response, with limited success.

Previous experience has shown that standard production of polyclonal antibodies is not the method of choice for preparation of disaggregating antibodies for plaque forming peptides due to problems of poor titer and toxicity.

Images