We demonstrate that a peptoid composed of five monomers and attached via a maleimide linker to a carrier protein elicits anti-peptoid, anti-linker and anti-carrier antibodies in rabbits. Specific anti-peptoid antibodies were affinity purified and used to reproducibly retrieve three specific peptoid-coupled beads from 20,000 irrelevant peptoid-beads using magnetic screening.

Peptoids are synthetic molecules that share structure with peptides, but bear side groups on the backbone nitrogen. They are protease resistant and relatively cheap to synthesize. Since many amines can form peptoid side groups, peptoids are more diverse than peptides and can take on various shapes, making them good B cell epitopes or haptens. We aim to develop peptoid-based vaccines by screening on-bead peptoid libraries we have made with broadly neutralizing monoclonal antibodies against pathogens. Resulting peptoids can be attached to carrier proteins (which provide T cell epitopes) to elicit antibodies that should mimic the screening antibody. To test the immunogenicity of peptoid haptens, we generated the first affinity-purified anti-peptoid antibody by immunizing rabbits with a peptoid linked to a carrier and adsorbed to an adjuvant, alum. Antibodies were produced against the hapten, carrier and linker. After affinity purification, an enzyme-linked immunosorbent assay demonstrated a robust, specific response against the peptoid. This vaccine platform will now be applied using broadly neutralizing monoclonal antibodies against West Nile and hepatitis C viruses, mouse norovirus-1 and HIV. Candidate peptoids will be tested for the ability to induce neutralizing antibodies against the pathogen. If successful, this platform could be applied to any pathogen for which a broadly neutralizing monoclonal antibody is available, without structural knowledge of the native epitope.

The aim of this research is to generate vaccine candidates for any virus for which a neutralizing monoclonal antibody exists without prior knowledge of the protective epitope. We have developed a platform to generate such vaccine candidates and are working on a device to automate their identification. The platform consists of libraries of B cell epitopes prepared by displaying peptoid sequences on beads, screening with neutralizing monoclonal antibodies to select peptoids bound by the antigen binding site of the monoclonal antibody, and retaining the antibody-bound peptoids with protein G dynabeads and a magnet. Peptoids are similar to peptides but with the R group attached to the nitrogen instead of the carbon. They are haptens that can be attached to protein carriers to elicit anti-peptoid antibody responses. We have conducted platform optimization and proof-of-principle testing using FLAG peptide and anti-FLAG monoclonal antibody. We then applied the optimized platform to screen peptoid libraries with monoclonal anti-FLAG and identified two potential mimetics. Mice immunized with the peptoids have made FLAG peptide-reactive antibodies, thereby demonstrating proof of concept. Implementation of this platform with neutralizing monoclonal antibodies we have in hand against HIV, West Nile virus and hepatitis C virus can identify potential mimetic vaccine candidates without prior knowledge of important epitopes, and could represent an entirely new way to generate safe vaccines.

ABSTRACT There is no FDA-approved vaccine for the potent plant toxin ricin. We have developed a recombinant ricin vaccine, RiVax. Without adjuvant it is safe and immunogenic in mice, rabbits, and humans. Based on our studies in mice, we now report the results of a small clinical trial with Alhydrogel-adsorbed RiVax.

In this chapter we discuss vaccines to protect against the highly toxic plant-derived toxin, ricin. Due to its prevalence, ease of use, and stability it has been used in sporadic incidents of espionage. There is also concern that it will be used as an agent of bioterrorism. As a result there has been a great deal of interest in developing a safe vaccine or antidote to protect humans, and in particular soldiers and first responders. Although multiple types of vaccines have been tested, at this time two recombinant vaccines are the leading candidates for the national vaccine stockpile. In terms of passive post-exposure protection, monoclonal neutralizing antibodies that passively protect animals are also under development. These vaccines and antibodies are discussed in the context of the toxicity and structure of ricin.

RiVax is a recombinant protein that is currently under clinical development as part of a human vaccine to protect against ricin poisoning. RiVax includes ricin A-chain (RTA) residues 1-267 with two intentional amino-acid substitutions, V76M and Y80A, aimed at reducing toxicity. Here, the crystal structure of RiVax was solved to 2.1 angstrom resolution and it was shown that it is superposable with that of the ricin toxin A-chain from Ricinus communis with a root-mean-square deviation of 0.6 angstrom over 258 C(alpha) atoms. The RiVax structure is also compared with the recently determined structure of another potential ricin-vaccine immunogen, RTA 1-33/44-198 R48C/T77C. Finally, the locations and solvent-exposure of two toxin-neutralizing B-cell epitopes were examined and it was found that these epitopes are within or near regions predicted to be involved in catalysis. The results demonstrate the composition of the RiVax clinical material and will guide ongoing protein-engineering strategies to develop improved immunogens.

Ricin toxin (RT) is derived from castor beans, produced by the plant Ricinus communis. RT and its toxic A chain (RTA) have been used therapeutically to arm ligands that target disease-causing cells. In most cases these ligands are cell-binding monoclonal antibodies (MAbs). These ligand-toxin conjugates or immunotoxins (ITs) have shown success in clinical trials [1]. Ricin is also of concern in biodefense and has been classified by the CDC as a Class B biothreat. Virtually all reports of RT poisoning have been due to ingestion of castor beans, since they grow abundantly throughout the world and are readily available. RT is easily purified and stable, and is not difficult to weaponize. RT must be considered during any "white powder" incident and there have been documented cases of its use in espionage [2,3]. The clinical syndrome resulting from ricin intoxication is dependent upon the route of exposure. Countermeasures to prevent ricin poisoning are being developed and their use will depend upon whether military or civilian populations are at risk of exposure. In this review we will discuss ricin toxin, its cellular mode of action, the clinical syndromes that occur following exposure and the development of pre- and post-exposure approaches to prevent of intoxication.

Ricin is a CDC level B biothreat. Our recombinant ricin A chain vaccine (RiVax) contains two mutations, rendering it non-toxic at high doses. Frozen or alum formulations of RiVax protected mice against ricin administered by injection, gavage or aerosol. Without alum, RiVax was safe and immunogenic in rabbits and human volunteers. For military use, the predominant target group, it would be optimal not to require a cold chain for transport and storage. We have now developed a lyophilized formulation and demonstrated stability and efficacy for at least 1 year stored refrigerated or at room temperature administered with or without alum.

Ricin toxin is a CDC level B biothreat. We have developed a ricin vaccine, RiVax, which is a recombinant mutant of ricin A chain. RiVax is safe, immunogenic and protective in mice when administered intramuscularly (IM). We have now attempted to increase the utility and immunogenicity of RiVax by administering it intradermally (ID) with or without alum. Without alum, Rivax administered by the ID and IM routes was equally immunogenic and protective. With alum, ID vaccinations were more immunogenic and protective against both systemic and mucosal challenge with ricin and superior in protecting animals from ricin-induced lung damage.

We have recently reported a peptoid ( N -alkyl-oligoglycine) molecule that binds to the Vascular Endothelial Growth Factor Receptor 2 (VEGFR2) with high affinity and specificity. Moreover, this peptoid is capable of inhibiting VEGFR2 function in vivo (Udugamasooriya et al. J Am Chem Soc 130:5744–5745, 2008) and thus is a lead compound for anti-angiogenic agents. Moreover, the assay developed to identify this VEGFR2 inhibitor is likely to be a general route to peptoid antagonists or agonists of integral membrane receptors. Therefore, it is important to determine whether the VEGFR2-targeted peptoid, and indeed peptoids in general, are inherently immunogenic since an anti-peptoid immune response would significantly complicate their development as therapeutic candidates. In this study, the VEGFR2-targeted peptoid as well as other peptoids of varying lengths were injected into mice along with an immunostimulatory agent. We demonstrate that no significant anti-peptoid immune response is induced. It is further shown that this is not a trivial result of the lack of immunogenicity of a particular peptoid sequence, since conjugation of the peptoids to carrier proteins such as KLH prior to injection induces a robust anti-peptoid immune response. We conclude that free peptoid molecules are not immunogenic, probably due to a lack of T cell epitopes and that peptoid-based therapeutics are therefore not likely to be hindered by anti-peptoid antibody production in most cases.

903 A tetravalent chimeric anti-human CD22 antibody (cRFB4-TetraMAb) with improved anti-tumor activity has been developed. The DNA encoding the single chain Fv (scFv) was spliced to the Fc of human IgG1 and expressed in Chinese hamster ovary cells. The construct was purified on Sepharose- Protein G followed by HPLC. The characteristics of the cTetraMAb were analyzed and compared to its parental divalent MAb, RFB4. The TetraMAb bound to CD22+ Daudi cells as well as the divalent RFB4, but had a slower dissociation rate. Both the TetraMAb and the divalent RFB4 bound equally well to FcγR-positive human cells, to human C1q, and to recombinant human FcRn in vitro. It also had comparable ADCC activity when human effector cells were used. Despite its slightly larger size, the TetraMAb penetrated normal tissues in Swiss Webster mice as well as the divalent MAb. The TetraMAb had a longer half-life in both Swiss Webster mice and mFcRn-/hFcRn+ transgenic mice, and it showed improved anti-tumor activity in SCID mice xenografted with various CD22 positive human tumor cell lines. Moreover, the enhanced activity of the TetraMAb was dose-related. In conclusion, these data suggest that this tetravalent RFB4 antibody should be further developed for human use.

Ricin is a plant toxin that is a CDC level B biothreat. Our recombinant ricin A chain vaccine (RiVax), which contains mutations in both known toxic sites, has no residual toxicity at doses at least 800 times the immunogenic dose. RiVax without adjuvant given intramuscularly (i.m.) protected mice against intraperitoneally administered ricin. Furthermore the vaccine without alum was safe and immunogenic in human volunteers. Here we describe the development of gavage and aerosol ricin challenge models in mice and demonstrate that i.m. vaccination protects mice against ricin delivered by either route. Also RiVax protects against aerosol-induced lung damage as determined by histology and lung function tests.

UV3 is a monoclonal antibody that recognizes human CD54 (intercellular adhesion molecule-1), and it was generated for the therapy of human multiple myeloma. In a severe combined immunodeficient (SCID) xenograft model of human multiple myeloma.. UV3 significantly prolonged the survival of mice with either early or advanced stages of disease. However, the mechanism by which UV3 exerted its antitumor effect remained unknown. As reported previously UV3 could mediate antibody-dependent cell-mediated cytotoxicity or complement-dependent cytotoxicity in vitro. F(ab)'(2) fragments of UV3 had therapeutic efficacy in vivo, suggesting that effector functions were not critical. The purpose of this study was to further define the importance of the Fc portion of UV3 for its antitumor activitv in vivo. To this end, we examined the effect of an "ultrapure" preparation of UV3 F(ab)'2 to treat SCID mice xenografted with either ARH-77 cells, a human multiple myeloma cell line, or Daudi cells, a human Burkitt's lymphoma cell line. In addition, we evaluated different doses of UV3 immunoglobulin G (IgG) in these mice to determine the minimum amount of IgG that would produce a therapeutic effect. Data obtained from this study suggest that (1) the Fc portion of UV3 is critical for its antitumor activity in vivo, (2) low levels of UV3 IgG in a preparation of F(ab)'2 fragments account for all of its in vivo activity in multiple myeloma and most of its activity in lymphoma, and (3) UV3 IgG significantly prolongs the survival of SCID/ARH-77 mice as well as SCID/Daudi mice.

BIOPHYSICS. For the article ‘‘An allosteric model for heterogeneous receptor complexes: Understanding bacterial chemotaxis responses to multiple stimuli,’’ by Bernardo A. Mello and Yuhai Tu, which appeared in issue 48, November 29, 2005, of Proc. Natl. Acad. Sci. USA (102, 17354–17359; first published November 17, 2005; 10.1073 pnas.0506961102), the authors note that the citation given for ref. 24 [Ames, P. & Parkinson, J. S. (2004) Proc. Natl. Acad. Sci. USA 101, 2117–2122] was incorrect. The citation should have read as follows:

BIOPHYSICS. For the article ‘‘An allosteric model for heterogeneous receptor complexes: Understanding bacterial chemotaxis responses to multiple stimuli,’’ by Bernardo A. Mello and Yuhai Tu, which appeared in issue 48, November 29, 2005, of Proc. Natl. Acad. Sci. USA (102, 17354–17359; first published November 17, 2005; 10.1073 pnas.0506961102), the authors note that the citation given for ref. 24 [Ames, P. & Parkinson, J. S. (2004) Proc. Natl. Acad. Sci. USA 101, 2117–2122] was incorrect. The citation should have read as follows:

Ricin, a highly potent toxin produced by castor beans, is classified by the Centers for Disease Control and Prevention as a level B biothreat because it is easily produced, readily available, and highly stable. There have been > 750 cases of documented ricin intoxication in humans. There is no approved vaccine for ricin. Ricin contains a lectin-binding B chain and a ribotoxic A chain (RTA). In addition to its ribotoxic site, we have identified a separate site on RTA that is responsible for inducing vascular leak syndrome (VLS) in humans. We have generated a recombinant RTA with two amino acid substitutions that disrupt its ribotoxic site (Y80A) and its VLS-inducing site (V76M). This mutant recombinant RTA (named RiVax) was expressed and produced in Escherichia coli and purified. When RiVax was injected i.m. into mice it protected them against a ricin challenge of 10 LD50S. Preclinical studies in both mice and rabbits demonstrated that RiVax was safe. Based on these results, we have now conducted a pilot clinical trial in humans under an investigational new drug application submitted to the Food and Drug Administration. In this study, three groups of five normal volunteers were injected three times at monthly intervals with 10, 33, or 100 mu g of RiVax. The vaccine was safe and elicited ricin-neutralizing Abs in one of five individuals in the low-dose group, four of five in the intermediate-dose group, and five of five in the high-dose group. These results justify further development of the vaccine.

Ricin toxin is a plant-derived ribosome inactivating protein (RIP) of extraordinary toxicity. Vaccination using ricin toxoid or its A chain (RTA) is protective in animals but both vaccines have two potential toxicities, RIP and vascular leak syndrome (VLS). Previously we described three recombinant RTA constructs from which both toxicities were eliminated by site-specific mutations. One mutant, V76M/Y80A, RiVax, has now been further characterized for immunogenicity and toxicity in animals. We have found that RiVax is safe at doses of at least 8mg in mice, 800-fold higher than the protective dose, and induces neutralizing antibodies in both mice and rabbits.