Patent Application
20130302362
The present disclosure relates to immunomodulatory compositions methods, systems, compositions, and in particular vaccines that comprise immunogenic fragments of ApoB100 are suitable for the treatment or prevention of conditions such as atherosclerosis, aneurysms, hypertension and/or of a condition associated thereto.
Immunogenic fragments of ApoB100 have been associated with treatment and/or prevention to various conditions in an individual.
In particular, certain immunogenic fragments of ApoB100 have been associated with treatment of atherosclerosis in individuals.
Provided herein are compositions, methods and systems that allow in several embodiments treatment and/or prevention of various conditions treated with immunogenic fragments of ApoB100 in a human individual.
According to a first aspect, a method to treat and/or prevent a condition in a human individual, is described the condition treatable and/or preventable by administering one or more immunogenic fragments of ApoB100 or an immunogenically active portion thereof. The method comprises administering to an individual the one or more immunogenic fragment of apoB-100 or the immunogenically active portion thereof at a concentration of less than 1 mg.
According to a second aspect, a pharmaceutical composition comprising less than 1 mg of one or more immunogenic fragments of ApoB100 or an immunogenically active portion thereof and a pharmaceutically acceptable vehicle.
The compositions, methods and systems herein described can be used in connection with applications wherein treatment of a condition treatable and/or preventable by administering one or more immunogenic fragments of ApoB100 or an immunogenically active portion thereof in a human individual is desired.
The details of one or more embodiments of the disclosure are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.
The accompanying drawings, which are incorporated into and constitute a part of this specification, illustrate one or more embodiments of the present disclosure and, together with the detailed description and the examples, serve to explain the principles and implementations of the disclosure.
Methods and systems are herein described that allow in several embodiments, treatment and/or prevention of various conditions in a human individual.
The term “treat,” or “treating” or “treatment” as used herein indicates any activity that is part of a medical care for, or that deals with, a condition medically or surgically. The term “preventing” or “prevention” as used herein indicates any activity, which reduces the burden of mortality or morbidity from a condition in an individual. This takes place at primary, secondary and tertiary prevention levels, wherein: a) primary prevention avoids the development of a disease; b) secondary prevention activities are aimed at early disease treatment, thereby increasing opportunities for interventions to prevent progression of the disease and emergence of symptoms; and c) tertiary prevention reduces the negative impact of an already established disease by restoring function and reducing disease-related complications.
The term “condition” as used herein indicates the physical status of the body of an individual (as a whole or of one or more of its parts) that does not conform to a physical status of the individual (as a whole or of one or more of its parts) that is associated with a state of complete physical, mental and possibly social well-being. Conditions herein described include but are not limited to disorders and diseases wherein the term “disorder” indicates a condition of the living individual that is associated to a functional abnormality of the body or of any of its parts, and the term “disease” indicates a condition of the living individual that impairs normal functioning of the body or of any of its parts and is typically manifested by distinguishing signs and symptoms. Exemplary conditions include but are not limited to injuries, disabilities, disorders (including mental and physical disorders), syndromes, infections, deviant behaviours of the individual and atypical variations of structure and functions of the body of an individual or parts thereof.
In some embodiments, treatment and/or prevention of various conditions can be provided by administering to a human individual an effective amount of one or more immunogenic fragments of ApoB100 or an immunogenically active portion thereof, wherein the effective amount is less than 1 mg.
The term “administer” or “administering” or “administration” as used herein means any method of providing an individual with a substance in any fashion including, but not limited to, those discussed herein.
The term “individual” or “individuals” as used herein indicates a single biological organism such as higher animals and in particular vertebrates such as mammals and more particularly human beings. In some embodiments, the individual has been previously identified as having an increased risk of aneurysm based on the detection of conditions typically associated with an increased risk of aneurysm (e.g. higher blood pressure, atherosclerosis). In some embodiments, the individual has not been identified as having an increased risk of aneurysm. In some embodiments, no investigation as to the risk for aneurysm in the individual has been performed.
The term “immunogenic fragment” or “antigenic fragment” as used herein indicates a portion of a polypeptide of any length capable of generating an immune response, such as an antigen. An antigen is a molecule recognized by the immune system. An antigenic fragment of ApoB100 is accordingly a portion of ApoB-100 that presents antigenic properties. The ability of a fragment or other molecule to generate an immune response and in particular a cellular and/or humoral response can be detected with techniques and procedures identifiable by a skilled person.
The term fragment in the sense of the present disclosure comprises not only fragments of any length from ApoB100, but also peptides produced by genetic recombination or chemically synthesized. The term “immunogenic fragments” in the sense of the present disclosure further comprise also derivative of any fragment, such as oxidative derivative and/or peptide treated with MDA or copper, which maintain a detectable antigenic property of the original fragment.
The term “derivative” as used herein with reference to a first peptide (e.g., an immunogenic fragment), indicates a second peptide that is structurally related to the first polypeptide and is derivable from the first polypeptide by a modification that introduces a feature that is not present in the first peptide while retaining functional properties of the first peptide. Accordingly, a derivative peptide of an immunogenic fragment, or of any portion thereof, e.g. an epitope thereof, usually differs from the original an immunogenic fragment or portion thereof by modification of the amino acidic sequence that might or might not be associated with an additional function not present in the original peptide or portion thereof. A derivative peptide of an immunogenic fragment or of any portion thereof retains however one or more of the immunogenic activities that are herein described in connection with an immunogenic fragment or portion thereof. The antigenic properties can be verified with methods and systems such as the ones already described for the immunogenic fragments and additional methods and systems identifiable to a skilled person. Typically, a derivative of an immunogenic fragment comprises at least one epitope of the immunogenic fragment.
The term immunogenically active portion in the sense of the present disclosure indicates any part of a reference antigen that can elicit specific immune response. Exemplary immunogenically active portions are the epitopes formed by 5 or more residues comprised within an immunogenic fragment. In some embodiments, epitopes within one fragment can overlap.
Immunogenic fragments can be expressed by recombinant technology, such as a fusion with an affinity or epitope tag, chemical synthesis of an oligopeptide, either free or conjugated to carrier proteins, or any other methods known in the art to express the ApoB-100 peptides.
Exemplary fragments of ApoB100 are peptides each comprising one of the sequences listed in the Sequence Listing as SEQ ID NO: 1 to SEQ ID NO: 302 described in further detail in the Examples section. Methods and systems suitable to identify an immunogenic fragment in the sense of the present are described in WO 02/080954, hereby incorporated by reference. Additional methods are exemplified in the Examples section (see e.g. Example 1). The term “protein” or “polypeptide” or “peptide” as used herein indicates an organic polymer composed of two or more amino acid monomers and/or analogs thereof. The term “polypeptide” includes amino acid polymers of any length including full length proteins and peptides, as well as analogs and fragments thereof. A polypeptide of three or more amino acids is also called an oligopeptide. As used herein the term “amino acid”, “amino acidic monomer”, or “amino acid residue” refers to any of the twenty naturally occurring amino acids including synthetic amino acids with unnatural side chains and including both D and L optical isomers. The term “amino acid analog” refers to an amino acid in which one or more individual atoms have been replaced, either with a different atom, isotope, or with a different functional group but is otherwise identical to its natural amino acid analog. In some embodiments, the one or more immunogenic fragments of ApoB100 is associated to atherosclerosis reduction.
Methods to identify a molecule associated with atherosclerosis reduction are identifiable by a skilled person and include the exemplary procedures described in WO 02/080954 herein incorporated by reference in its entirety. In particular, the ability of a molecule to reduce atherosclerosis can be tested in an animal model following administration of the molecule in a suitable amount using procedure identifiable by a skilled person. For example following subcutaneous administration of a molecule herein described the ability of the molecule to affect atherosclerosis can be tested in mice as illustrated in the Examples sections. A skilled person will be able to identify additional procedure, schedule of administration and dosages upon reading of the present disclosure.
Accordingly in an exemplary embodiment, immunogenic molecule associated with atherosclerosis reduction can be identified by identifying a candidate immunogenic molecule able to provide a cellular and/or humoral response in the individual of interest; and testing the candidate immunogenic molecule for an ability to reduce atherosclerosis, to select the candidate immunogenic molecule associated with atherosclerosis reduction.
In particular, in some embodiments, immunogenic fragments of ApoB100 are immunogenic fragments producing an immune response associated to atherosclerosis reduction in the individual or in an animal model. In some of those embodiments, a percentage atherosclerosis reduction is at least about 20%, or at least about 30%, from about 40% to about 60% or about 50% to about 80%.
In some embodiments, the immunogenic fragment comprises at least one of peptide, each comprising p1 (SEQ ID NO: 1), p2 (SEQ ID NO: 2), p 11 (SEQ ID NO:11), p25 (SEQ ID NO:25), p45 (SEQ ID NO:45), p74 (SEQ ID NO:74), p99 (SEQ ID NO:99), p100 (SEQ ID NO:100), p102 (SEQ ID NO:102), p103 (SEQ ID NO: 103), p105 (SEQ ID NO:105), p129 (SEQ ID NO:129), p143 (SEQ ID NO:143), p148 (SEQ ID NO:148), p210 (SEQ ID NO:210), or p301 (SEQ ID NO:301).
In an embodiment, the one or more immunogenic fragments comprise one or more peptides each comprising p2 (SEQ ID NO:2), p 11 (SEQ ID NO:11), p45 (SEQ ID NO: 45), p74 (SEQ ID NO: 74), p102 (SEQ ID NO: 102), p148 (SEQ ID NO:148), or p210 (SEQ ID NO:210).
In an embodiment, the one or more immunogenic fragments comprise two peptides each comprising p143 (SEQ ID NO: 143), or p210 (SEQ ID NO:210). In an embodiment, the one or more immunogenic fragments associated to atherosclerosis reduction comprises three peptides each comprising, one of p 11 (SEQ ID NO:11), p25 (SEQ ID NO: 25), or p74 (SEQ ID NO:74). In an embodiment, the one or more immunogenic fragments associated to atherosclerosis reduction comprises five peptides each comprising one of p99 (SEQ ID NO: 99), p100 (SEQ ID NO: 100), p102 (SEQ ID NO: 102), p103 (SEQ ID NO: 103), and p105 (SEQ ID NO: 105).
In an embodiment, the one or more immunogenic fragments comprise one or more peptides each comprising p2 (SEQ ID NO: 2), p45 (SEQ ID NO: 45), p74 (SEQ ID NO: 74), p102 (SEQ ID NO: 102), or p210 (SEQ ID NO:210).
In an embodiment, the one or more immunogenic fragments comprise a peptide comprising amino acids 16-35 of human apoB-100 (p2; SEQ ID NO:2).
In an embodiment the one or more immunogenic fragments comprise a peptide comprising amino acids 661-680 of human apoB-100 (p45; SEQ ID NO:45).
In an embodiment, the one or more immunogenic fragments comprise a peptide comprising amino acids 3136-3155 of human apoB-100 (P210; SEQ ID NO: 210).
In an embodiment, the one or more immunogenic fragments comprise a peptide comprising amino acids 4502-4521 of human apoB-100 (P301; SEQ ID NO: 301).
In an embodiment, the one or more immunogenic fragments comprise a peptide comprising amino acids 1-20 of human apoB-100 (P1; SEQ ID NO: 1).
Exemplary data showing association of the above peptides to atherosclerosis reduction are shown in Example 5 of the present disclosure and in International application WO 02/080954, herein incorporated by reference in its entirety (see in particular Table 1, Table 2, Table A and Table B). In particular for some of those peptides or combination thereof a percentage reduction of 64.6% (p143 and p210), 59.6% (p11, p25 and p174), 56.8% (p129, p148, and p167), p67.7 (p2), 57.9% (p210), 55.2% (p301), 47.4% (p45), 31% (p1) has been detected (see W0/02080954 incorporated herein by reference in its entirety, and in particular Table B).
Immunogenic peptides comprising any of the sequences herein described or immunogenically active portions of those peptides are identifiable by a skilled person using in silico and/or in vitro approaches. For example, in silico methods can be used to identify any of said epitopes or immunogenic peptides based on any of the sequences herein described. Reference is made for example, to the papers [44] to [51] each of which are incorporated herein by reference in its entirety.
Such papers describe various algorithms such as Tepitope (Radrizzani et al 2000), Adept (Maksuytov et al 1993), antigenic index (Jameson et al 1988) and others which can be used to identify the immunogenic molecules comprising the sequences at issue or any relevant epitopes.
Additional tests and laboratory procedures in vitro and/or in vivo suitable to be used alone or in connection with the identification in silico (e.g. ELISA, antigen-specific T cell proliferation assay, ELISPOT, antibody measurement) are identifiable by a skilled person that can be used by a skilled person to verify the in silico data and/or identify immunologically active molecules comprising any of the sequences herein described or immunologically active portions of those sequences.
Accordingly, in an exemplary embodiments, immunogenic peptides, herein described, immunogenically active portions thereof as well as derivative thereof can be identified by identifying candidate peptides, candidate active portion and/or candidate derivative by in silico analysis of any one of the sequences herein described, and by identifying the immunogenic peptides, immunogenically active portions and/or derivative by in vitro and/or in vivo testing of the candidate peptides, candidate active portion and/or candidate derivative. In particular, the in silico analysis can be performed by analyzing the sequence of the candidate with algorithm suitable to identify immunogenicity of a molecule or portion thereof. Similarly, the in vitro and/or in vivo testing comprises methods directed to identify immunogenicity of the candidate peptide, candidate active portion and/or derivative as well as effects of those molecules on aneurysm, with particular reference to formation or regression. Suitable methods and techniques are identifiable by a skilled person upon reading of the present disclosure.
In several embodiments, the immunogenic peptides, active portions thereof and derivative thereof are expected to include a sequence of at least about 5 amino acids, consistently with the typical length of epitopes as indicated in WO 02/080954 herein incorporated by reference in its entirety.
Additional conditions treatable with immunogenic fragments or an immunogenically active portion thereof herein described comprise aneurysmand hypertension.
The term “aneurysm” as used herein indicates a localized blood filled dilation of a blood vessel or of a portion thereof. In particular, an aneurysm can be an abnormal widening or ballooning of a portion of an artery due to weakness in the wall of the blood vessel, and can occur within any vasculature in the body. Aneurysms can be “true” in which the inner layers of a blood vessel bulges outside the outer layer of the vessel, or “false,” which is a collection of blood leaking out of an artery or vein. Aneurysms commonly occur, but are not limited to, in arteries at the base of the brain or aortic in the main artery carrying blood from the left ventricle of the heart. In particular, with reference to the aorta, aneurysms can occur at different segments of the aorta including, but not limited to, the beginning of the arch, the end of the arch, the apex, between segments 3 and 5, the supra renal segment, the infra renal segment, before bifurcation, and between the renal artery. Symptoms of aneurysms include pain, peripheral embolization, bleeding and additional symptoms identifiable by a skilled person.
In an embodiment, immunization with one or more of the immunogenic molecules herein described reduces the incidence of experiencing aortic aneurysm rupture (e.g. Examples 2 and 11).
In an embodiment, immunization with one or more of the immunogenic molecules herein described reduces the aortic aneurysmal segment formation. In particular, some of those embodiments, reduction of aneurysms can occur at different segments of the aorta including, but not limited to, the beginning of the arch, the end of the arch, the apex, between segments 3 and 5, the supra renal segment, the infra renal segment, before bifurcation, and between the renal arteries (se e.g. Example 3). The expected reduction of aneurysm after immunization is at least about 20%, and in particular about 20-80% when compared to a control measurement.
In an embodiment, immunization with one or more of the immunogenic molecules herein described reduces mortality associated with aortic aneurysmal rupture (see e.g. Examples 4 and 11).
In an embodiment, immunization with one or more of the immunogenic molecules herein described is associated with a reduction in hypertension.
The term “hypertension” as used herein refers to high blood pressure. In particular, hypertension (HTN) or high blood pressure is a chronic medical condition in which the systemic arterial blood pressure is elevated. It is the opposite of hypotension. It is classified as either primary (essential) or secondary. About 90-95% of cases are termed “primary hypertension”, which refers to high blood pressure for which no medical cause can be found. The remaining 5-10% of cases (Secondary hypertension) is caused by other conditions that affect the kidneys, arteries, heart, or endocrine system.
In an embodiment, immunization with one or more of the immunogenic molecules herein described reduces the incidence of blood pressure (e.g. Examples 10 and 11).
The expected reduction of blood pressure after immunization is at least about 10%, when compared to a control measurement and in particular from about 10% to an amount determined by a physician based on the condition and the individual to be immunized (e.g. Examples 10 and 11).
The term “effective amount” as used herein is meant to describe that amount of antigen, e.g. p210, which induces an antigen-specific immune response.
Effective amounts of an immunogenic fragment and of one or more of the immunogenic molecules herein described to treat and/or prevent a condition will depend on the individual wherein the activation is performed and will be identifiable by a skilled person upon reading of the present disclosure For example in an embodiment a desired effect can be achieved in mice with an effective amount of from about 100 μg to less than about 1000 μg immunogenic fragment or immunogenically active portion thereof.
It has now unexpectedly found that treatment of human individuals with concentration similar to the ones used in mice are particularly effective for all the applications wherein one or more immunogenic fragments of ApoB100 (which include any derivative thereof see related WO 02/080954, PCT application Ser. No. ______ entitled “Immunomodulatory Methods and Systems for Treatment and/or Prevention of Aneurysms” filed on Nov. 11, 2011 with docket number P686-PCT, and to PCT application Ser. No. ______ entitled “Immunomodulatory Methods and Systems for Treatment and/or Prevention of Hypertension” filed on Nov. 11, 2011 with attorney docket P694-PCT each of which is herein incorporated by reference in its entirety), or an immunogenic portion thereof, are administered to humans.
In an embodiment, an effective amount for the treatment or prevention can be about 100 μg or more. In particular, treatment with about 100 μg is expected to prevent aneurysm rupture in humans (see e.g. Example 2).
A greater concentration can be used in some embodiments depending on the desired effect as illustrated in the present disclosure. For example, in embodiments wherein treatment of a condition is expected to be performed with an effective amount be 250 μg or more and in particular with about 500 μg. In another example, an effective amount to treat the condition is expected to be 250 μg or 500 μg or higher is also expected to be effective also depending on other factors affecting the pharmacological activity of the molecule in an individual.
According to the same data, treatment or prevention of a condition can be performed in humans with an effective amount of from about 0.1 to about 100 mg immunogenic fragment or immunogenically active portion thereof.
In particular, the effective amount is expected to vary depending on the number and combination of peptides utilized for each particular vaccine, and specific characteristic and conditions of the individual treated (e.g. immune system, diet and general health and additional factors identifiable by a skilled person). More particular, lower or higher amounts within the defined range are expected to be effective in an individual depending on factors such as weight, age, gender of the individual as well as additional factors identifiable by a skilled person.
There are several well established methods for extrapolating a human equivalent dose (HED) from a dose that is effective in animals. One popular approach is to convert dose per body weight and another is to use an allometric conversion which takes into account body surface area. These approaches are most reliable for small molecules for which the typical sigmoidal dose-response relationship exists. Dose-response relationships for immune modulating therapies are atypical and often unpredictable. This situation is further complicated by the differences in the immune systems of animals and of humans (see attached). Furthermore, the dose that will work in humans need not be an “n” times greater multiple of the dose that worked in animals. It could be the same or even less. There are some in silico (EpiVax) and in vitro (Vax Design, Probiogen) tools that have recently become available that can be used to more accurately predict what formulations/doses will and will not work in humans.
The effective amount is also expected to vary depending on the number and combination of peptides utilized for each particular vaccine, and specific characteristic and conditions of the individual treated (e.g. immune system, diet and general health and additional factors identifiable by a skilled person). More particular, lower or higher amounts within the defined range are expected to be effective in an individual depending on factors such as weight, age, gender of the individual as well as additional factors identifiable by a skilled person. In some embodiments, the immunogenic peptides herein described or related immunogenically active portions can be administered in combination with an adjuvant or other carrier suitable to affect and in particular increase immunogenicity of the peptide o active portion thereof. In particular, in some embodiments, the immunogenic peptide or active portion thereof can be conjugated to the adjuvant or carrier according to procedures identifiable to a skilled person. Suitable carriers comprise BSA, and in particular, cationized BSA, aluminum salts such as aluminum phosphate and aluminum hydroxide and additional carriers identifiable by a skilled person.
In some embodiments, immunogenic molecules herein described can be administered in ratios of immunogenic molecule to carrier to aluminum of about: 1:2:35, 1:2:20.6, 1:2:7.7, 1:2:3.3, 1:1:13.8 weight to weight ratios. In particular, in some embodiments, ratios can be provided wherein the number of peptides conjugated to each carrier molecule while minimizing the amount of aluminum (adjuvant). In particular in one embodiment, ratio can be provided that result in a concentration up to 2.7 mg conjugate/mL.
The route of immunization can vary depending on the purposes of immunization described herein. For example, successful prevention and treatment of aneurysms in mice occurred by subcutaneous route of administration of immunization (Examples 2, 3, and 4). The type of immune response triggered is largely determined by the route of immunization. Various routes can be used comprising subcutaneous, parenteral, and systemic among the others. In particular, the mucosal linings of airways and intestines contain lymphatic tissue that, when exposed to antigen, elicits anti-inflammatory, immunosuppressive responses. Distinct immunological features of the respiratory and intestinal mucosa lead to partly different types of protective immunity upon antigen exposure by the nasal or oral route.
In some embodiments the immunogenic molecules herein described can be administered according to a schedule of administration devised in view of the amount of time required by the adaptive immune system of an individual to mount a response to the initial exposure to an immunogen. Typically, the response is expected to plateau at 2-3 weeks after exposure. Subsequent exposures often elicit a more rapid response. In various embodiments, the following schedules and manner of administration can be followed: (1) single administration, (2) two administrations 2-3 weeks apart, (3) three weekly administrations, (4) up to 6 administrations on a 1 every 3 week schedule. The vaccines have been administered by: (1) subcutaneous injection; (2) intraperitoneal injection; (3)nasal installation; (4) subcutaneous infusion.
In particular, an embodiment, administering one or more immunogenic fragment or an immunogenically active portion thereof can be performed subcutaneously or intramuscularly.
In some embodiments, disclosed are pharmaceutical compositions which contain at least one the immunogenic fragments, active portions thereof, herein described as herein described, in combination with one or more compatible and pharmaceutically acceptable vehicles, and in particular with pharmaceutically acceptable diluents or excipients. In those pharmaceutical compositions the immunogenic fragments, active portions thereof, herein described can be administered as an active ingredient for treatment or prevention of a condition in an individual.
The term “excipient” as used herein indicates an inactive substance used as a carrier for the active ingredients of a medication. Suitable excipients for the pharmaceutical compositions herein disclosed include any substance that enhances the ability of the body of an individual to absorb an immunogenic fragment, active portions thereof herein described. Suitable excipients also include any substance that can be used to bulk up formulations with the immunogenic fragments, active portions thereof, herein described to allow for convenient and accurate dosage. In addition to their use in the single-dosage quantity, excipients can be used in the manufacturing process to aid in the handling of the immunogenic fragments, active portions thereof, herein described. Depending on the route of administration, and form of medication, different excipients can be used. Exemplary excipients include but are not limited to antiadherents, binders, coatings disintegrants, fillers, flavors (such as sweeteners) and colors, glidants, lubricants, preservatives, sorbents.
The term “diluent” as used herein indicates a diluting agent which is issued to dilute or carry an active ingredient of a composition. Suitable diluent include any substance that can decrease the viscosity of a medicinal preparation.
In some embodiments, pharmaceutical composition can include (1) a peptide or other immunogenic molecule herein described administered alone, (2) a peptide or other immunogenic molecule herein described +carrier(s); (3) a peptide or other immunogenic molecule herein described +adjuvant; (4) a peptide or other immunogenic molecule herein described +carrier +adjuvant. In particular, the carriers for each of the exemplary composition (1) to (4) can comprise: (1) cBSA, (2) rHSA, (3) KLH, (4) cholera toxin subunit B, respectively, each of which can be mineral salt-based. Other carriers, known to those skilled in the art, are expected to be suitable as well as will be identified by a skilled person. Examples of those adjuvants comprise adjuvants having Th2 effects, carriers having adjuvant properties, e.g., diphtheria toxoid, and adjuvants able to function as carriers, e.g., oil-water emulsions. In some embodiments, a necessary, and under certain conditions sufficient, component for the pharmaceutical composition is the immunogenic peptides. Additional components of the composition can be selected to modulate the immunological impact of the peptides or other immunogenic molecule herein described as will be understood by a skilled person.
In an embodiment, any of the immunogenic molecules herein described can be used to specifically activate T cell, and in particular CD8(+) T cells which can be activated using one or more immunogenic fragments of ApoB100 or an immunogenically active portion thereof.
The term “T cells” as used herein indicates T lymphocytes belonging to a group of white blood cells known as lymphocytes, and participate in humoral or cell-mediated immunity. T cells can be distinguished from other lymphocyte types, such as B cells and natural killer cells (NK cells) by the presence of special markers on their cell surface such as T cell receptors (TCR). Additional markers identifying T cell include CD1a, CD3, or additional markers possibly associated to a T cell state and/or functionality as will be understood by a skilled person.
The term “CD8(+) T cells” indicates T cells expressing the CD8 glycoprotein at their surface, wherein the CD8 (cluster of differentiation 8) glycoprotein is a transmembrane glycoprotein that serves as a co-receptor for the T cell receptor (TCR). Similarly to the TCR, CD8 binds to a major histocompatibility complex (MHC) molecule, but is specific for the class I MHC protein. Exemplary CD8 T cells comprise cytotoxic memory CD8 T cells, regulatory CD8 T cells, cytotoxic effector CD8 T-cells and additional cells identifiable by a skilled person. There are two isoforms of the protein, alpha and beta, each encoded by a different gene. In humans, both genes are located on chromosome 2 in position 2p12.
The term “activated” and activation as used herein indicate the process by which a T cells interacts with an antigen presenting cell which presents a specific antigen for a time and under condition resulting in a T cell having a preassigned immunological role (e.g. cytotoxicity) within the immune system. The term “antigen-presenting cell” (APC) indicates a cell that displays antigen complex with major histocompatibility complex (MHC) on its surface. T-cells recognize this complex using their T-cell receptor (TCR). Exemplary APCs comprise dendritic cells (DCs) which are known to play an important role in linking innate and acquired immunity, see references (3) (4), and both immune responses participate in atherogenesis, see references (5) (6).
Detection of T cells and in particular, CD8(+) T cells, can be performed by detection of markers such as CD8, alone or in combination with TCR and additional markers identifiable by a skilled person. Detection of activated CD8(+) T cells can be performed by detection of T cells markers and in particular of markers such as CD25, CD44, CD62 and additional markers identifiable by a skilled person using process and techniques suitable for detecting surface markers.
The terms “detect” or “detection” as used herein indicates the determination of the existence, presence or fact of a molecule or cell in a limited portion of space, including but not limited to a sample, a reaction mixture, a molecular complex and a substrate. The “detect” or “detection” as used herein can comprise determination of chemical and/or biological properties of the target, including but not limited to ability to interact, and in particular bind, other compounds, ability to activate another compound and additional properties identifiable by a skilled person upon reading of the present disclosure. The detection can be quantitative or qualitative. A detection is “quantitative” when it refers, relates to, or involves the measurement of quantity or amount of the target or signal (also referred as quantitation), which includes but is not limited to any analysis designed to determine the amounts or proportions of the target or signal. A detection is “qualitative” when it refers, relates to, or involves identification of a quality or kind of the target or signal in terms of relative abundance to another target or signal, which is not quantified.
Exemplary techniques suitable for detecting T cell markers comprise use of suitable monoclonal or polyclonal antibodies or antigen-specific HLA or MHC pentamers or hexamers labeled with an appropriate molecule allowing detection as well as additional methods and techniques identifiable by a skilled person. In an exemplary approach T cell markers are identified by flow cytometric analysis as described in the Examples section. Exemplary techniques suitable for detecting T cell markers comprise use of suitable monoclonal or polyclonal antibodies or antigen-specific HLA or MHC pentamers or hexamers labeled with an appropriate molecule allowing detection as well as additional methods and techniques identifiable by a skilled person. In an exemplary approach T cell markers are identified by flow cytometric analysis as described in the Examples section.
In particular, in some embodiments, an effective amount of immunogenic molecules herein described from about 100 μg to less than about 1000 μg is associated with CD8+ Tcell activation that is specific for the activating immunogenic molecule. (see e.g. Example 12).
Additional effective concentrations of immunogenic fragment or immunogenically active portion thereof for specific CD8+ T cell activation comprise concentration from 100 μg to 250 μg and from 250 μg to about 500 μg and from about 0.1 to about 100 mg.
In particular, T cell activation can be performed using any of the molecules herein described administered in vivo in an amount suitable to treat or prevent aneurysms, (see e.g. Example section). Activation of T cell can also be performed in vitro using methods and procedures such as the ones described in ref [52] as well as additional procedures identifiable by a skilled person. Further advantages and characteristics of the present disclosure will become more apparent hereinafter from the following detailed disclosure by way of illustration only with reference to an experimental section.
In some embodiments, activated CD8(+) T cells herein described are expected to be effective in treatment and/or prevention of a condition treatable with the corresponding activating immunogenic molecule herein described. In particular, in some embodiments, activate CD8(+) T cells herein described are expected to be effective according to a schedule of administration wherein those cells are administered to an individual daily (for up to 21 days) and on an every 10 day schedule (days 0, 10, 20). Additional schedules expected to be effective can be identified by a skilled person based on cell treatments of conditions such as HIV and/or cancer.
Further advantages and characteristics of the present disclosure will become more apparent hereinafter from the following detailed disclosure by way of illustration only with reference to an experimental section.
The compositions, methods system herein described are further illustrated in the following examples, which are provided by way of illustration and are not intended to be limiting.
In particular, the following examples illustrate exemplary immunogenic fragments and methods using fragment p210. A person skilled in the art will appreciate the applicability and the necessary modifications to adapt the features described in detail in the present section, to additional immunogenic fragments, administered subcutaneously or using other routes of administration in vivo or in vitro according to embodiments of the present disclosure.
Unless otherwise indicated the following material and methods were followed in the Examples reported below.
Selection of peptides and their preparation for immunization The establishment and screening of human apoB-100 peptides has been reported (8). Based on Applicants pilot experiments and prior reports, see references (9),(10) Applicants selected peptide 210 (p210, KTTKQ SFDLS VKAQY KKNKH—SEQ ID NO: 210) as a candidate immunogen. Native p210 peptide (Euro-Diagnostica AB, Sweden) was conjugated to cationic bovine serum albumin (cBSA) as carrier using a method described previously see references (3), (4) Alum was used as adjuvant and mixed with peptide/cBSA conjugate with 1:1 ratio in volume. Peptide conjugation and mixing with alum were prepared fresh prior to each immunization.
Immunization Protocols
Male apoE (−/−) mice (Jackson Laboratories) were housed in an animal facility accredited by the American Association of Accreditation of Laboratory Animal Care and kept on a 12-hour day/night cycle with unrestricted access to water and food. The Institutional Animal Care and Use Committee of Cedars-Sinai Medical Center approved the experimental protocols. In a pilot experiment, p210 immunization using 100 μg dose conferred optimum athero-reduction compared to 25 or 50 μg dose. Hence 100 μg dose was used for all subsequent experiments. Mice, maintained on normal chow diet, received subcutaneous primary immunization in the dorsal area between scapulas at 6-7 weeks of age, followed by a booster at 9 and 12 weeks of age. One week after last booster, diet was switched to high cholesterol chow (TD 88137, Harlan-Teklad) and continued until euthanasia at the age of 25 weeks. Separate groups of mice receiving PBS or cBSA/alum at the same immunization time-points served as control. Some mice were sacrificed at 8 or 13 weeks of age to assess immune response against p210.
Tissue Harvesting and Preparation
At euthanasia the hearts were harvested and embedded in OCT compound (Tissue-Tek) for cryo-section. Whole aortas were cleaned, processed and stained with Oil Red 0 to assess the extent of atherosclerosis en face with computer-assisted histomorphometry, see references (3),(4).
Immunohistochemistry and Histomorphometry
The sections from aortic sinus were stained with MOMA-2 (Serotec), or CD11c (eBioscience) antibody to identify macrophages or dendritic cells immunohistochemically using standard protocol. Oil-Red-O stain for plaque size was done using standard protocol. Computer-assisted morphometric analysis was performed to assess histomorphometry as described previously, see references (3),(4).
Serum ELISA
Flat-bottomed 96-well polystyrene plates (MaxiSorp, Germany) were pre-coated with 100 ul (20 μg/ml) p210, KLH, TNP-KLH (Biosearch Technologies T-5060) or BSA (2 μg/ml for IgG or 10 μg/ml for IgM) respectively by incubation overnight at 4° C. to assess antibodies levels using standard protocol. The coating concentration was optimized in pilot experiments. Goat anti-mouse HRP-IgG (Pierce 31437) or IgM (Southern Biotech) were used as detecting antibodies and the bound antibodies were detected by developing in ABTS (Southern Biotech) as substrate and optical density values were recorded at 405 nm.
Flow Cytometric Analysis
Flow cytometric analysis was performed using standard protocols with antibodies listed in Table 1 below and a FACScan (Becton Dickinson) or a CyAn ADP analyzer (Beckman Coulter). For intracellular cytokine staining, Brefeldin A (3 μg/ml) was added to the cultured cells for 2 hours before cells subject to staining procedure. Cell membranes were permeabilized for staining intracellular molecules.
Adoptive Transfer Experiment
Male apoE (−/−) mice on regular chow received subcutaneous immunization as described in previous paragraph and were sacrificed at 13 weeks of age as donors. Splenocytes from the same treatment group were pooled before cell isolation. Donor CD8(+) T-cells, CD4(+)CD25(+) T-cells or B-cells were isolated using Dynabeads FlowComp (Invitrogen) according to the manufacturer's protocols. CD4(+) T-cells were negatively selected from the splenocytes followed by positive selection of CD4(+)CD25(+) cells. B cells were negatively isolated whereas CD8(+) T-cells were positively isolated first and released from beads. The purity of pooled CD8(+) T-cells, CD4(+)CD25(+) T-cells and B-cells was 90%, 80% and 70%, respectively. The isolated CD8(+) T-cells (1×106 cells/mouse), CD4(+)CD25(+) T-cells (1×105 or 3×105 cells/mouse) or B-cells (2×107 cells/mouse) were then adoptively transferred to naïve male apoE (−/−) recipient mice at 6-7 weeks of age via tail vein injection. In the published literatures of vascular biology, the number of adoptively transferred lymphocytes varied greatly. For B-cells transfer, the number of 2×107 cells/mouse was chosen based on two prior reports, see references (11),(12). For CD4(+)CD25(+) T-cells transfer, the number of cells transferred ranged from 5×104 cells/mouse to 1×106 cells/mouse in the published literature see references (13),(14),(15). Hence we chose 2 intermediate doses for our experiment. As to CD8(+) T-cells, 1×106 cells was chosen based on a report from the field of autoimmune disease see ref (16). Applicants did not adoptively transferred CD4(+) T-cells because naïve or antigen-primed CD4(+) T-cells are known to be pro-atherogenic see references (17),(18) Recipient mice were fed normal chow until 13 weeks of age when chow was switched to high cholesterol diet until euthanasia at 25 weeks of age. Aortas were harvested to assess the extent of atherosclerosis.
KLH or Trinitrophenyl-Lipopolysaccharide (TNP-LPS) Immunization
Applicants also tested if p210 immunization affected the efficacy of subsequent immunization with other antigens. KLH was chosen as a prototypical T-cell dependent and TNP as a T-cell independent antigen. Male C57/BL6 mice on regular chow received subcutaneous immunization with p210 conjugate or adjuvant control as described in previous paragraphs for apoE (−/−) mice. At 13 and 15 weeks of age mice were subcutaneously immunized with 100 μg KLH (with alum as adjuvant) at injection sites away from p210 sites or injected intraperitoneally with 100 μg TNP-LPS (Sigma). KLH or TNP immunization was done in separate groups of mice. Blood was collected via retro-orbital puncture at euthanasia (16 weeks of age).
In Vitro Generation of BM-Derived Dendritic Cells (BMDCs)
The method for generating BMDC with GM-CSF was adapted from previous publication with modification see reference (19). Briefly, bone marrow cells from femurs and tibiae of male apoE−/− mice were plated into 10 cm culture plates (Falcon) with 20 ml complete RPMI-1640 containing 10 ng/ml GM-CSF (R&D Systems) and 10 ng/ml IL-4 (Invitrogen). Cells were washed and fed on day 3 and day 5 by removing the old medium followed by replenishing with fresh culture medium with GM-CSF and IL-4. On day 8, the immature DC appeared as non-adherent cells under the microscope and harvested by vigorous pipetting and subcultured into new culture plates with 2×105 DCs in 1.5 ml medium.
In Vitro CD8(+) T-Cells Isolation and Co-Culture with Dendritic Cells
Donor mice [male apoE (−/−) mice] for CD8(+) T-cells were immunized with PBS, cBSA/Alum, or cBSA/Alum/P210 according to the schedule described in earlier paragraphs and splenocytes were harvested at 13 weeks of age. CD8(+) T-cells were negatively isolated using a CD8 selection Dynabeads kit (Invitrogen) per manufacturer's protocol. The selected CD8(+) T-cells were then co-culture with DCs in a CD8:DC ratio of 3:1. A series of pilot studies has been performed to determine the optimal CD8:DC ratio for this assay. After co-culture for 4 hours, cells were collected and processed for flow cytometric determination of CD11c and 7-AAD by LSR II flow cytometer (BD Biosciences) and data was analyzed with Summit V4.3 software. Dendritic cell death without CD8(+) T-cells in the co-culture was used as baseline and percentage of specific lysis of cells was calculated using a method described previously, see reference (20).
Statistics
Data are presented as mean+Std. Number of animals in each group is listed in text or description of the figures. Data were analyzed by ANOVA followed by Newman-Keuls multiple group comparison, or by t-test when appropriate. P<0.05 was considered as statistically significant and horizontal bars in each figure indicated statistically significant difference between groups.
Specific immunogenic epitopes by focusing on the single protein found in LDL, apolipoprotein B-100 (apo B) were characterized. A peptide library comprised of 302 peptides, 20 amino acid residues in length, covering the complete 4563 amino acid sequence of human apo B was produced. The peptides were produced with a 5 amino acid overlap to cover all sequences at break points. Peptides were numbered 1-302 starting at the N-terminal of apo B as indicated in Table 1 below.
The full length sequence of ApoB100 can be found in various publications such as San-Hwan Chen et al The complete cDNA and amino acid sequence of Human Apolipoprotein B100 Journal of Biological Chemistry 1986 Vol. 261No 28, Issue of October 5, 12918-12921 (see in particular
Male apoE KO mice were subcutaneously immunized at 7, 10, and 12 weeks of age with either Group 1: P210/cBSA conjugate using alum as adjuvant (100 μg P210); Group 2: control-100 μg of cBSA/alum (cBSA); Group 3: control PBS (PBS). Fourteen P210, 17 cBSA, 16 PBS, and 8 Saline injected mice were examined.
AngII (1000 ng/Kg/min) was delivered by a subcutaneous osmotic pump implanted at 10 weeks of age for 4 weeks to cause aneurysms in all three groups. Saline was delivered to the control group. Mice were sacrificed at 14 weeks of age of age. The mice were fed normal chow for the duration of experiment.
Aneurysm formation (including rupture) and incidence were investigated. The results are illustrated in Table 3A and Table 3B below.
As illustrated in the above Tables, P210 immunization reduced rupture incidence. Immunization with apoB-100 related peptide P210 reduced rupture incidence 7.1% from 17.7% with cBSA as a control and 31.3% using PBS as a control.
A possible mechanism of action provided herein for guidance purposes only and not intended to be limiting is that p210 immunization reduces BP; 2. Effect of p210 immunization is mediated by CD8 to a same or comparable extent detected for reduction of atherosclerosis illustrated in the following examples. Accordingly, ability to elicit a T cell response is specific for p210 (antigen specificity) and other apoB-100 peptides are expected to show similar antigen-specific CD8 effect.
Male apoE KO mice were subcutaneously immunized at 7, 10, and 12 weeks of age with either Group 1: P210/cBSA conjugate using alum as adjuvant (100 μg P210); Group 2: control-100 μg of cBSA/alum (cBSA); Group 3: control PBS (PBS). 42 P210, 46 cBSA, 37 PBS, and 8 Saline injected mice were examined.
AngII (1000 ng/Kg/min) was delivered by a subcutaneous osmotic pump implanted at 10 weeks of age for 4 weeks to cause aneurysms in all three groups. Saline was delivered to the control group. Mice were sacrificed at 14 weeks of age of age. The male apoE KO mice were fed normal chow for the duration of experiment.
The measurement of the aorta was taken at 8 segments: 1) beginning of arch, 2) end of arch, 3) apex level, 4) between 3 & 5, 5) supra renal, 6) infra renal, 7) before bifurcation, and 8) between renal arteries (see schematic illustration of
The average diameters of each segment illustrated in
A further elaboration of the data of Table 4, illustrated in Table 5 below suggests that P210 immunization significantly reduces aneurysmal section formation. Whereas the aneurysmal segment/total segment percentage is 29.6% for cBSA controls and 23.4% for PBS controls, P210 immunization reduced the aneurysmal segment/total segment percentage to 14.3%.
Male apoE KO mice were subcutaneously immunized at 7, 10, and 12 weeks of age with either Group 1: P210/cBSA conjugate using alum as adjuvant (100 μg P210); Group 2: control-100 μg of cBSA/alum (cBSA); Group 3: control PBS (PBS). 42 P210, 46 cBSA, 37 PBS, and 8 Saline injected mice were examined.
AngII (1000 ng/Kg/min) was delivered by a subcutaneous osmotic pump implanted at 10 weeks of age for 4 weeks to cause aneurysms in all three groups. Saline was delivered to the control group. Mice were sacrificed at 14 weeks of age of age. 42 P210, 46 cBSA, 37 PBS, and 8 Saline injected mice were examined. Mice were sacrificed at 14 weeks of age. The male apoE KO mice were fed normal chow for the duration of experiment.
The results are illustrated in the chart of
The vaccine preparation consisted of the p210 peptide (Euro-Diagnostica AB, Sweden) conjugated to cationic bovine serum albumin (cBSA) as carrier using a method described previously3;4. Alum was used as adjuvant and mixed with peptide/cBSA conjugated with 1:1 ratio in volume. Peptide conjugation was performed on the day of immunization and freshly mixed with alum just prior to each immunization. Mice fed normal chow diet received subcutaneous primary immunization in the dorsal area between scapulas at 6-7 weeks of age, followed by a booster at 10 and 12 weeks of age. One week after the last booster, diet was switched to high cholesterol chow (TD 88137, Harlan-Teklad) and continued until euthanasia at the age of 25 weeks.
Immunization with p210 reduced aortic atherosclerosis by 57% and 50% compared to PBS and cBSA/Alum group, respectively (
The aortic sinus plaques from p210/cBSA/alum group contained significantly reduced macrophage and DC immuno-reactivity assessed by MOMA-2 and CD11c immuno-staining, respectively (
Since DCs are the major cell type upstream to both cellular and humoral immune responses, Applicants determined if these cells were affected by the immunization strategy. Cells from the subcutaneous immunization sites were isolated for flow cytometric analysis one week after primary immunization. The PBS group could not be included in this analysis because mice receiving PBS injection did not develop swelling or cell accumulation at the injection site.
There were significantly fewer CD11c(+) and CD11c(+)CD86(+) cells in p210/cBSA/alum group compared to cBSA/alum group at the immunization site (
Applicants next assessed antibody response to define the humoral immune response against p210. Before immunization all 3 groups of mice had low levels of IgG titers against p210. At euthanasia, the IgG titer against p210 remained low in the PBS group but was significantly increased in cBSA/alum group. Immunization with p210/cBSA/alum resulted in increased p210 IgG titer compared with PBS group but was significantly reduced compared with cBSA/alum group (
The IL-2Rcc (CD25) is a well-defined lymphocyte activation marker. Applicants therefore analyzed the expression of CD25 on CD4(+) or CD8(+) T-cells from superficial cervical and axillary lymph nodes (LN) from mice one week after primary immunization to assess the T-cell immune response. CD8(+)CD25(+) T-cell population in the lymph nodes was significantly higher in p210/cBSA/alum group when compared to that of PBS or cBSA/alum groups (
There was a significantly larger population of splenic CD8(+)CD25(+)IL-10(+) T-cells in p210/cBSA/alum group when compared to PBS or cBS A/alum groups (
Donor apoE(−/−) mice were subjected to the same immunization protocol with the same groupings, namely: PBS, cBSA/alum, or p210/cBSA/alum. Recipient naïve male apoE(−/−) mice were injected with donor cells at 6-7 weeks of age and were fed normal chow until 13 weeks of age when chow was switched to high cholesterol diet until euthanasia at 25 weeks of age.
At euthanasia, the recipient mice injected with CD8(+) T-cells from p210/cBSA/alum group developed significantly less atherosclerotic lesions in aorta compared to the recipient mice injected with CD8(+) T-cells from PBS or cBSA/alum groups, strongly suggesting that the effector T cell induced by the vaccine are CD8+ and is mechanistically involved (
This reduction of aortic lesions was coupled with decreased splenic CD11c(+) DCs (PBS group: 4.3±1.7%; cBSA/alum group: 3.4±0.3%; p210/cBSA/alum group: 1.5±0.3%; n=5 each group, p<0.05 p210/cBSA/alum group vs. PBS or cBSA/alum group by ANOVA) with no difference in circulating levels of total cholesterol among 3 groups (PBS group: 1083±296 mg/dl; cBSA/alum group: 975±401 mg/dl; p210/cBSA/alum group: 1098±379 mg/dl).
Adoptive transfer of B cells isolated from the spleens of p210 immunized donor mice did not affect atherosclerosis in recipient mice compared to mice receiving B cells from other donors (
To rule out CD4(+)CD25(+) T-cells as possible athero-protective mediators induced by sub-cutaneous p210 immunization, Applicants adoptively transferred CD4(+)CD25(+)T-cells at a dose of 1×105 cells/mouse into naïve recipient apoE−/− mice. There was no difference in lesion size among the 3 groups of CD4(+)CD25(+)T-cell recipients. Depletion of CD25+ cells from the pool of CD8+ T cells abrogated the reduction in atherosclerosis observed in the p210/cBSA/alum recipient mice, further supporting the notion that CD8+ CD25+ T cells are mechanistically involved in the protective effects of the vaccine against atherosclerosis (
Given the observation that p210 immunization reduced DCs in the immunization sites and atherosclerotic plaques and adoptive transfer of CD8(+) T-cells from p210 immunized donors rendered a decrease of splenic DCs in the recipients, Applicants hypothesized that DCs could be a potential target of CD8(+) T-cells.
To test this, Applicants co-cultured bone marrow derived DCs with CD8(+) T-cells from various immunized groups. CD8(+) T-cells from p210 immunized mice significantly increased the percentage of DC death when compared to those from PBS or BSA/alum groups (
Given the observations that p210 immunization decreased CD11c(+) DCs and reduced adaptive IgG response to p210, Applicants next tested if such modulation of DCs by p210 immunization would alter the host immune response to other antigens.
Applicants first immunized mice with p210 as described in previous sections followed by two separate subcutaneous KLH immunizations or intra-peritoneal injection of TNP-LPS. Using the KLH- or TNP-IgG titer as a surrogate for the efficacy of individual immunization, Applicants found that there was no difference in KLH- or TNP-IgG titers between p210 immunized mice and the titers from mice of PBS or cBSA/alum groups (
Male apoE KO mice were subcutaneously immunized at 7, 10, and 12 weeks of age with 100 μg of either Group 1: P210/cBSA conjugate using alum as adjuvant (P210); Group 2: control-100 μg of cBSA/alum (cBSA); Group 3: control PBS (PBS). 14 P210, 17 cBSA, 16 PBS, and 8 Saline injected mice were examined.
AngII (1000 ng/Kg/min) was delivered by a subcutaneous osmotic pump implanted at 10 weeks of age for 4 weeks to cause an increase in blood pressure in all three groups. Saline was delivered to the control group. Mice were sacrificed at 14 weeks of age of age. The mice were fed normal chow for the duration of the experiment.
According to the above data it is expected that a p210 vaccine can prevent HTN.
A possible mechanism of action provided herein for guidance purposes only and not intended to be limiting is that p210 immunization reduces BP; and that the effect of p210 immunization is mediated by CD8 to a same or comparable extent detected for reduction of atherosclerosis illustrated in the following examples. Accordingly, ability to elicit a T cell response is specific for p210 (antigen specificity) and other apoB-100 peptides are expected to show similar antigen-specific CD8 effect.
A further possible mechanism of action provided herein for guidance purposes only and not intended to be limiting is that p210 action is performed also through modulation of angiotensin expression. Based on published anti-HTN vaccine literature, an anti-angiotensin vaccine can treat HTN. As a consequence, based on anti-angiotensin vaccine, multiple administration can be desired in certain condition and for certain types of individuals.
ApoE (−/−) mice were immunized with p210/cBSA/Alum (p210; 100 μg) at 7, 10, and 12 weeks of age. Mice receiving PBS or cBSA/Alum (cBSA) served as controls. At 10 weeks of age, mice were subcutaneously implanted with an osmotic pump which released AngII (1 mg/Kg/min), and were euthanized 4 weeks later. The aorta, spleen, and lymph nodes (LN) were harvested. The p210 vaccine significantly reduced mortality due to AA rupture compared to controls (see
Flow cytometric analysis of dendritic cells (DCs) in LNs and spleen showed intracellular IFN-γ expression was upregulated in the p210 group. Aortic superoxide production measured by in situ dihydroethidine method and aortic AT1 receptor (AT1R) expression measured by Western blot were significantly decreased in p210 group. The p210 vaccine significantly decreased mean arterial BP at 13 weeks of age (see Table 7).
Mortality from AngII induced AA rupture was significantly reduced by the p210 vaccine. This protective effect was associated with upregulation of IFN-γ expression in DCs and decreased arterial BP, AT1R expression, and superoxide production in aorta. The vaccine may be a promising new non-invasive treatment for AA.
Applicants have shown that immunization with apoB-100 related-peptide p210 significantly reduces atherosclerosis and decreases intra-plaque CD11c+ dendritic cells (DCs) in apoE−/− mice. Adoptive transfer experiments showed that athero-protection was mediated by CD8+ T cells. Because apoB-100 is found on the LDL fraction of serum lipids, Applicants assessed the CD8+ T cell cytolytic activity of p210 immunized mice specific to lipid-associated antigens presented by DCs.
ApoE−/− mice were immunized at 7, 9, and 12 weeks of age with p210/cBSA/alum, cBSA/alum, or PBS. One week after the third immunization, mice were euthanized to collect spleen CD8+ T cells. Bone-marrow derived DCs were differentiated from naïve apoE−/− mice and used as target cells. A four-hour lytic assay was performed using a CD8-to-DC ratio of 3:1 in culture medium with 10% FBS. The cells were then collected and stained for CD11c to identify DCs and 7-AAD to assess cell lysis using flow cytometry. There was significantly more lytic activity by CD8+ T cells from p210/cBSA/alum immunized mice compared to cBSA/alum and PBS (Table). When the assay was performed in media with delipidated FBS, the lytic activity specific to CD8+ T cells from p210/cBSA/alum immunized mice was abrogated (Table 8), suggesting that the lipid fraction of FBS in the culture media provided a source of antigen. Loading of DCs with FITC-labeled p210 24 hours prior to the lytic assay demonstrated antigen uptake and specificity of the lytic activity of CD8+ T cells from p210/cBSA/alum immunized mice (see Table 8).
These results show that the cytolytic function of CD8+ T cells targeting DCs are specific to lipid-associated antigens, specifically the p210 fragment of apoB-100, and this may underly the protective effects of p210 immunization.
Antibody titers to p210 was low prior to immunization. At euthanasia at 25 weeks of age, there was a significant increase in p210 IgM titer in all groups (
T cells from superficial cervical and axillary lymph nodes (LN) from mice one week after primary immunization were collected to assess the T cell immune response. CD4+ CD25+ T cells in the lymph nodes (Table 1) did not differ among 3 groups. Splenic CD4+ CD25+IL-10+ T cell population significantly increased in the cBSA/alum group. However, this increased response was significantly attenuated by the p210/cBSA/alum immunization (Table 9). Interestingly, splenic CD4+ CD62L+ T cell (Table 1) population was lower in cBSA/alum group.
One week after primary immunization, the CD8+ CD25+ T cell population in the lymph nodes was significantly higher in p210/cBSA/alum group when compared to that of PBS or cBSA/alum groups (Table 2). There was a significantly larger population of splenic CD8+ CD25+IL-10+ T cells in p210/cBSA/alum group when compared to PBS or cBSA/alum groups (Table 2). The splenic CD8+ CD62L+ T cell population was significantly higher in p210/cBSA/alum group when compared to that of PBS or cBSA/alum groups (Table 9). The T cell profile at other time points were not significantly different between groups.
The vaccine reduced DC presence in the plaques (
CD8+ T cells from p210 immunized mice significantly increased the percentage of DC lysis when compared to those from PBS or cBSA/alum groups (
Peptide loading on BMDCs was defined using p210 labeled with FITC (FITC conjugating kit from Pierce). The presence of FITC fluorescence in the dendritic cells indicated uptake of p210 by dendritic cells (
The p210 peptide contains the proteoglycan binding site of the apoB-100 molecule. This peptide is a cell-penetrating peptide capable of efficiently delivering antigens for cross-presentation to cytotoxic CD8+ T cells.53 Applicants therefore assessed activation of CD8+ CD25− T cells co-cultured with DCs loaded with p210 and matured with LPS. There was significantly increased CD8+ CD25+ T cells 48 hours after co-culture with p210-loaded DCs treated with LPS compared to untreated, or LPS only treated co-cultures (
The results shown above in Example 17 support the notion that p210 is presented by DCs to CD8+ T cells. It remained unclear if the lytic activity against DCs was specific to the p210 antigen. Applicants therefore repeated the lytic assay using FITC-labeled p210 loaded BMDC as targets. Lytic activity against FITC DCs was significantly increased in CD8+ T cells from the p210/cBSA/alum mice (
In summary, in several embodiments herein described are immunostimulatory agents, T cell, compositions, methods and systems for treating and/or preventing various conditions in a individual and in particular in a human individual.
The examples set forth above are provided to give those of ordinary skill in the art a complete disclosure and description of how to make and use the embodiments of the molecules, compositions, systems and methods of the disclosure, and are not intended to limit the scope of what the inventors regard as their disclosure. All patents and publications mentioned in the specification are indicative of the levels of skill of those skilled in the art to which the disclosure pertains.
The entire disclosure of each document cited (including patents, patent applications, journal articles, abstracts, laboratory manuals, books, or other disclosures) in the Background, Summary, Detailed Description, and Examples is hereby incorporated herein by reference. All references cited in this disclosure are incorporated by reference to the same extent as if each reference had been incorporated by reference in its entirety individually. However, if any inconsistency arises between a cited reference and the present disclosure, the present disclosure takes precedence. Further, the sequence listing submitted herewith in the txt file “P700-PCT-2011-11-11-Sequence Listing_ST25” created on Nov. 11, 2011 forms an integral part of the present application and is incorporated herein by reference in its entirety.
The terms and expressions which have been employed herein are used as terms of description and not of limitation, and there is no intention in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the disclosure claimed Thus, it should be understood that although the disclosure has been specifically disclosed by preferred embodiments, exemplary embodiments and optional features, modification and variation of the concepts herein disclosed can be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this disclosure as defined by the appended claims.
It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting. As used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the content clearly dictates otherwise. The term “plurality” includes two or more referents unless the content clearly dictates otherwise. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the disclosure pertains.
When a Markush group or other grouping is used herein, all individual members of the group and all combinations and possible subcombinations of the group are intended to be individually included in the disclosure. Every combination of components or materials described or exemplified herein can be used to practice the disclosure, unless otherwise stated. One of ordinary skill in the art will appreciate that methods, device elements, and materials other than those specifically exemplified can be employed in the practice of the disclosure without resort to undue experimentation. All art-known functional equivalents, of any such methods, device elements, and materials are intended to be included in this disclosure. Whenever a range is given in the specification, for example, a temperature range, a frequency range, a time range, or a composition range, all intermediate ranges and all subranges, as well as, all individual values included in the ranges given are intended to be included in the disclosure. Any one or more individual members of a range or group disclosed herein can be excluded from a claim of this disclosure. The disclosure illustratively described herein suitably can be practiced in the absence of any element or elements, limitation or limitations which is not specifically disclosed herein.
A number of embodiments of the disclosure have been described. The specific embodiments provided herein are examples of useful embodiments of the disclosure and it will be apparent to one skilled in the art that the disclosure can be carried out using a large number of variations of the devices, device components, methods steps set forth in the present description. As will be obvious to one of skill in the art, methods and devices useful for the present methods can include a large number of optional composition and processing elements and steps.
In particular, it will be understood that various modifications may be made without departing from the spirit and scope of the present disclosure. Accordingly, other embodiments are within the scope of the following claims.
The present application claims priority to U.S. Provisional Application Ser. No. 61/413,378 entitled “Immunomodulatory Compositions, Methods and Systems Comprising Immunogenic Fragments of Apob100” filed on Nov. 12, 2010, with docket number P700-USP, which is herein incorporated by reference in its entirety. The present application is also related to PCT application WO 02/080954 filed on Apr. 5, 2002, to PCT application Ser. No. ______ entitled “Immunomodulatory Methods and Systems for Treatment and/or Prevention of Aneurysms” filed on Nov. 11, 2011 with docket number P686-PCT, and to PCT application Ser. No. ______ entitled “Immunomodulatory Methods and Systems for Treatment and/or Prevention of Hypertension” filed on Nov. 11, 2011 with attorney docket P694-PCT, each of which is herein incorporated by reference in its entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US11/60483 | 11/11/2011 | WO | 00 | 5/10/2013 |
| Number | Date | Country | |
|---|---|---|---|
| 61413378 | Nov 2010 | US |
