Patent Application
20220177559
This invention generally relates to coronavirus and human immunodeficiency biology and biological therapeutics. In alternative embodiments, provided are compositions, including products of manufacture and kits, and methods, for inhibiting, or slowing the rate of, a viral infection, wherein optionally the viral infection is a coronavirus infection, optionally a COVID-19 infection, or a human immunodeficiency virus (HIV) infection, in vitro and in vitro.
Apolipoprotein A-I binding protein (AIBP) is a secreted protein involved in regulation of lipid rafts and cholesterol efflux. AIBP has been suggested to function as a protective factor in several pathological conditions associated with increased abundance of lipid rafts, such as atherosclerosis and acute lung injury.
HIV infection and HIV components modify host and bystander cell plasma membrane (specifically, lipid rafts) in a way that promotes new HIV-cell membrane fusion, propagation of infection and promotes HIV-associated co-morbidities.
COVID-19 is the biggest global pandemic of the 21st century and it may not be the last. Increased interactions of humans with animals amplifies chances of animal viruses “jumping” to humans, while increased density of human population and abundant international travel further contribute to the extremely fast spread of the infectious diseases around the globe. At the peak of a pandemic, public health measures provide the most effective protection against spread of the infection, but when the peak passes, it leaves behind important problems. First, it is now clear that the virus will continue to circulate in the population and mutate causing periodic outbreaks. Second, initial infection often causes an outbreak of various chronic diseases ensuing from the presence of a “suppressed” virus or as a long-term consequence of the initial exposure. Global immunization reduces the severity of the disease and frequency of outbrakes , but, as a rule, does not achieve full eradication of an infectious disease. Many viruses are resistant to vaccination through rapid mutagenesis, like influenza viruses (Altman et al., 2018), employing cell-to-cell transmission altogether bypassing exposure to antibodies, like HTLV (Omsland et al., 2018), gaining entry through the respiratory tract delaying the access of antibodies and T-cells to the site of infection, like coronaviruses (He et al., 2020), or a combination of these and yet unknown factors, such as with HIV and influenza. A solution is to develop an anti-viral medication. Ideally, such treatment should target an early stage of the viral lifecycle, be insensitive to frequent changes of viral phenotype due to mutagenesis (for example targeting host cell rather than the virus) and be safe. Preferably, this treatment should also target complications of the infection.
In alternative embodiments, provided are products of manufacture for inhibiting, or slowing the rate of, coronavirus (optionally COVID-19 or a variant thereof, such as for example a delta or omicron COVID variant strain) or HIV replication in vitro and in vitro.
In alternative embodiments, provided are methods for:
(a)
(i) providing or having provided a protein or a composition having Apolipoprotein A-I binding protein (AIBP) activity, and
(ii) administering to an individual in need thereof the protein or the composition having Apolipoprotein A-I binding protein (AIBP) activity; or
(b) administering to an individual in need thereof a protein or a composition having Apolipoprotein A-I binding protein (AIBP) activity.
In alternative embodiments, provided are a protein or a composition having Apolipoprotein A-I binding protein (AIBP) activity for use in:
In alternative embodiments, provided are uses of a protein or a composition having Apolipoprotein A-I binding protein (AIBP) activity in the manufacture of a medicament for:
In alternative embodiments, of the methods or uses as provided herein:
(a) for administration in vitro or in vivo;
(b) for enteral or parenteral administration;
(c) as a liposome, a nanoparticle, or a nanoliposome;
(d) as a tablet, a pill, a capsule, a gel, a hydrogel, a geltab, a liquid, a powder, an emulsion, a lotion, an aerosol, a spray, a lozenge, an aqueous or a sterile or an injectable solution, an eye drop, or an implant; or
(e) for intravenous injection, subcutaneous injection, intramuscular injection, inhalation, or intravitreal injection; or
In alternative embodiments, of the methods or uses as provided herein, the protein or the composition having Apolipoprotein A-I binding protein (AIBP) activity comprises a human AIBP protein, an active fragment thereof, or a nucleic acid acid encoding AIBP, or an active fragment thereof, for example, in alternative embodiments the protein or the composition having Apolipoprotein A-I binding protein (AIBP) activity comprises:
The details of one or more exemplary embodiments of the invention are set forth in the accompanying drawings and description below. Other features, objects, and advantages of the invention will be apparent from the figures (drawings), description, and from the claims.
All publications, patents, patent applications cited herein are hereby expressly incorporated by reference for all purposes.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
The drawings set forth herein are illustrative of exemplary embodiments provided herein and are not meant to limit the scope of the invention as encompassed by the claims.
FIG. lA-B illustrate data showing that AIBP inhibits HIV-1 replication:
as further discussed in Example 1, below.
as further discussed in Example 1, below.
as further discussed in Example 1, below.
as further discussed in Example 1, below.
as further discussed in Example 1, below.
Like reference symbols in the various drawings indicate like elements.
In alternative embodiments, provided are compositions, including products of manufacture and kits, and methods, for inhibiting, or slowing the rate of, coronavirus (optionally COVID-19 or variant thereof, such as for example a delta or omicron COVID variant strain) or HIV replication in vitro and in vitro.
In alternative embodiments, provided are compositions and methods using AIBP to potently inhibit coronavirus (optionally COVID-19 or variant thereof, such as for example a delta or omicron COVID variant strain) or HIV replication in vitro and in vitro.
It was demonstrated that AIBP can potently inhibit HIV replication in vitro in HIV-infected humanized mice. AIBP inhibited virus-cell fusion, and this effect depended on lipid raft activation by Nef. Cells from donors with the HLA-B*35 genotype, associated with rapid progression of HIV disease, bound less AIBP than the cells from slow progressing HLA-B*57 donors, and were not protected by AIBP from rapid HIV replication. These results demonstrate that AIBP is an anti-HIV factor that can be used a potential anti-HIV biologic agent.
We have discovered that AIBP selectively targets cells affected by a coronavirus or an HIV or HIV-associated proteins and reverses pathological changes, thereby preventing spread of a coronavirus, or an HIV infection, and coronavirus- and/or HIV-comorbidities.
As described in Example 1, below, we investigated whether the dependence of HIV on lipid rafts and the ability of AIBP to reduce the abundance of lipid rafts translates into inhibition of HIV replication. We found that AIBP inhibits HIV replication both in vitro and in vivo and reverses the pro-infectious effects of Nef-containing extracellular vesicles. New therapeutic approaches aimed at inhibition of HIV infection and HIV-associated co-morbidities via stimulation of AIBP production are provided herein.
In alternative embodiments, provided are pharmaceutical formulations or compositions comprising a protein or a composition having Apolipoprotein A-I binding protein (AIBP) activity. In alternative embodiments, provided are pharmaceutical formulations or compositions for use in in vivo, in vitro or ex vivo methods to treat, prevent, reverse and/or ameliorate coronavirus (optionally COVID-19 or variant thereof, such as for example a delta or omicron COVID variant strain) or HIV.
In alternative embodiments, the pharmaceutical compositions used to practice methods as provided herein can be administered parenterally, topically, orally or by local administration, such as by aerosol or transdermally. These pharmaceutical compositions can be formulated in any way and can be administered in a variety of unit dosage forms depending upon the condition or disease and the degree of illness, the general medical condition of each patient, the resulting preferred method of administration and the like. Details on techniques for formulation and administration are well described in the scientific and patent literature, see, for example, the latest edition of Remington's Pharmaceutical Sciences, Maack Publishing Co., Easton PA (“Remington's”). For example, in alternative embodiments, compositions used to practice methods as provided herein (comprising, for example, AIBP polypeptides) are formulated in a buffer, in a saline solution, in a powder, an emulsion, in a vesicle, in a liposome, in a nanoparticle, in a nanolipoparticle and the like. In alternative embodiments, the compositions can be formulated in any way and can be applied in a variety of concentrations and forms depending on the desired in vivo, in vitro or ex vivo conditions, a desired in vivo, in vitro or ex vivo method of administration and the like. Details on techniques for in vivo, in vitro or ex vivo formulations and administrations are well described in the scientific and patent literature. Formulations and/or carriers used to practice methods as provided herein can be in forms such as tablets, pills, powders, capsules, liquids, gels, syrups, slurries, suspensions, etc., suitable for in vivo, in vitro or ex vivo applications.
In alternative embodiment, compounds (for example, formulations) used to practice methods as provided herein can comprise a solution of compositions (which include peptidomimetics, racemic mixtures or racemates, isomers, stereoisomers, derivatives and/or analogs of compounds AIBP) disposed in or dissolved in a pharmaceutically acceptable carrier, for example, acceptable vehicles and solvents that can be employed include water and Ringer's solution, an isotonic sodium chloride. In addition, sterile fixed oils can be employed as a solvent or suspending medium. For this purpose any fixed oil can be employed including synthetic mono- or diglycerides, or fatty acids such as oleic acid. In one embodiment, solutions and formulations used to practice methods as provided herein are sterile and can be manufactured to be generally free of undesirable matter. In one embodiment, these solutions and formulations are sterilized by conventional, well known sterilization techniques.
The solutions and formulations used to practice methods as provided herein can comprise auxiliary substances as required to approximate physiological conditions such as pH adjusting and buffering agents, toxicity adjusting agents, for example, sodium acetate, sodium chloride, potassium chloride, calcium chloride, sodium lactate and the like. The concentration of active agent in these formulations can vary widely, and can be selected primarily based on fluid volumes, viscosities and the like, in accordance with the particular mode of in vivo, in vitro or ex vivo administration selected and the desired results.
The compositions and formulations used to practice methods as provided herein can be delivered by the use of liposomes. By using liposomes, particularly where the liposome surface carries ligands specific for target cells (for example, an injured or diseased neuronal cell or CNS tissue), or are otherwise preferentially directed to a specific tissue or organ type, one can focus the delivery of the active agent into a target cells in an in vivo, in vitro or ex vivo application.
Also provided are nanoparticles, nanolipoparticles, vesicles and liposomal membranes comprising compounds used to practice methods as provided herein.
Provided are multilayered liposomes comprising compounds used to practice methods as provided herein n, for example, as described in Park, et al., U.S. Pat. Pub. No. 20070082042. The multilayered liposomes can be prepared using a mixture of oil-phase components comprising squalane, sterols, ceramides, neutral lipids or oils, fatty acids and lecithins, to about 200 to 5000 nm in particle size, to entrap a composition used to practice methods as provided herein.
Liposomes can be made using any method, for example, as described in Park, et al., U.S. Pat. Pub. No. 20070042031, including method of producing a liposome by encapsulating an active agent (for example, APOA1BP nucleic acids and polypeptides), the method comprising providing an aqueous solution in a first reservoir; providing an organic lipid solution in a second reservoir, and then mixing the aqueous solution with the organic lipid solution in a first mixing region to produce a liposome solution, where the organic lipid solution mixes with the aqueous solution to substantially instantaneously produce a liposome encapsulating the active agent; and immediately then mixing the liposome solution with a buffer solution to produce a diluted liposome solution.
In one embodiment, liposome compositions used to practice methods as provided herein comprise a substituted ammonium and/or polyanions, for example, for targeting delivery of a compound (for example, a AIBP), as described for example, in U.S. Pat. Pub. No. 20070110798.
In alternative embodiments, also provided are nanoparticles comprising compounds (for example, AIBP polypeptides) used to practice methods as provided herein in the form of active agent-containing nanoparticles (for example, a secondary nanoparticle), as described, for example, in U.S. Pat. Pub. No. 20070077286. In one embodiment, provided are nanoparticles comprising a fat-soluble active agent of this invention or a fat-solubilized water-soluble active agent to act with a bivalent or trivalent metal salt.
In one embodiment, solid lipid suspensions can be used to formulate and to deliver compositions used to practice methods as provided herein to mammalian cells in vivo, in vitro or ex vivo, as described, for example, in U.S. Pat. Pub. No. 20050136121.
In alternative embodiments, any delivery vehicle can be used to practice the methods as provided herein, for example, to deliver compositions used to practice methods as provided herein (for example, AIBP polypeptides) to mammalian cells in vivo, in vitro or ex vivo. For example, delivery vehicles comprising polycations, cationic polymers and/or cationic peptides, such as polyethyleneimine derivatives, can be used for example as described, for example, in U.S. Pat. Pub. No. 20060083737.
In one embodiment, a dried polypeptide-surfactant complex is used to formulate a composition used to practice methods as provided herein, for example as described, for example, in U.S. Pat. Pub. No. 20040151766.
In one embodiment, a composition used to practice methods as provided herein can be applied to cells using vehicles with cell membrane-permeant peptide conjugates, for example, as described in U.S. Pat. Nos. 7,306,783; 6,589,503. In one aspect, the composition to be delivered is conjugated to a cell membrane-permeant peptide. In one embodiment, the composition to be delivered and/or the delivery vehicle are conjugated to a transport-mediating peptide, for example, as described in U.S. Pat. No. 5,846,743, describing transport-mediating peptides that are highly basic and bind to poly-phosphoinositides.
In one embodiment, electro-permeabilization is used as a primary or adjunctive means to deliver the composition to a cell, for example, using any electroporation system as described for example in U.S. Pat. Nos. 7,109,034; 6,261,815; 5,874,268.
The pharmaceutical compositions and formulations used to practice methods as provided herein can be administered for prophylactic and/or therapeutic treatments. In alternative embodiments, therapeutic applications, compositions are administered to a subject already suffering from a coronavirus infection (for example, COVID-19 or variant thereof), or an HIV infection (a “therapeutically effective amount”). For example, in alternative embodiments, polypeptides used to practice methods as provided herein are administered to an individual in need thereof in an amount sufficient to treat, prevent, reverse and/or ameliorate HIV or a coronavirus such as COVID-19 or a variant thereof, such as for example a delta or omicron COVID variant strain.
The amount of pharmaceutical composition adequate to accomplish this is defined as a “therapeutically effective dose.” The dosage schedule and amounts effective for this use, i.e., the “dosing regimen,” will depend upon a variety of factors, including the stage of the disease or condition, the severity of the disease or condition, the general state of the patient's health, the patient's physical status, age and the like. In calculating the dosage regimen for a patient, the mode of administration also is taken into consideration.
The dosage regimen also takes into consideration pharmacokinetics parameters well known in the art, i.e., the active agents' rate of absorption, bioavailability, metabolism, clearance, and the like (see, for example, Hidalgo-Aragones (1996) J. Steroid Biochem. Mol. Biol. 58:611-617; Groning (1996) Pharmazie 51:337-341; Fotherby (1996) Contraception 54:59-69; Johnson (1995) J. Pharm. Sci. 84:1144-1146; Rohatagi (1995) Pharmazie 50:610-613; Brophy (1983) Eur. J. Clin. Pharmacol. 24:103-108; the latest Remington's, supra). The state of the art allows the clinician to determine the dosage regimen for each individual patient, active agent and disease or condition treated. Guidelines provided for similar compositions used as pharmaceuticals can be used as guidance to determine the dosage regiment, i.e., dose schedule and dosage levels, administered practicing the methods as provided herein are correct and appropriate.
Single or multiple administrations of formulations can be given depending on the dosage and frequency as required and tolerated by the patient. The formulations should provide a sufficient quantity of active agent to effectively treat, prevent or ameliorate a conditions, diseases or symptoms as described herein. For example, alternative exemplary pharmaceutical formulations for enteral or parenteral (for example, IM, IV or oral) administration of compositions used to practice methods as provided herein are in a daily amount of between about 0.1 to 0.5 to about 20, 50, 100 or 1000 or more ug per kilogram of body weight per day. In an alternative embodiment, dosages are from about 1 mg to about 4 mg per kg of body weight per patient per day are used. Lower dosages can be used, in contrast to administration orally, into the blood stream, into a body cavity or into a lumen of an organ. Substantially higher dosages can be used in topical or oral administration or administering by powders, spray or inhalation. Actual methods for preparing parenterally or non-parenterally administrable formulations will be known or apparent to those skilled in the art and are described in more detail in such publications as Remington's, supra.
The methods as provided herein can further comprise co-administration with other drugs or pharmaceuticals, for example, compositions for treating any neurological or neuromuscular disease, condition, infection or injury, including related inflammatory and autoimmune diseases and conditions, and the like, associated with HIV. For example, compositions used to practice methods as provided herein can be co-formulated with and/or co-administered with, fluids, antibiotics, cytokines, immunoregulatory agents, anti-inflammatory agents, pain alleviating compounds, complement activating agents, such as peptides or proteins comprising collagen-like domains or fibrinogen-like domains (for example, a ficolin), carbohydrate-binding domains, and the like and combinations thereof.
In alternative embodiment, bioisosteres of compounds used to practice methods as provided herein, for example, polypeptides having a AIBP activity, are used. Bioisosteres used to practice methods as provided herein can comprise compounds, for example, AIBP polypeptides, comprising one or more substituent and/or group replacements with a substituent and/or group having substantially similar physical or chemical properties which produce substantially similar biological properties to compounds used to practice methods as provided herein. In one embodiment, the purpose of exchanging one bioisostere for another is to enhance the desired biological or physical properties of a compound without making significant changes in chemical structures.
For example, in one embodiment, one or more hydrogen atom(s) is replaced with one or more fluorine atom(s), for example, at a site of metabolic oxidation; this may prevent metabolism (catabolism) from taking place. Because the fluorine atom is similar in size to the hydrogen atom the overall topology of the molecule is not significantly affected, leaving the desired biological activity unaffected. However, with a blocked pathway for metabolism, the molecule may have a longer half-life or be less toxic, and the like.
Provided are products of manufacture and kits for practicing the methods as described herein, optionally also including instructions for practicing methods as provided herein. In alternative embodiments, provided are kits comprising a pharmaceutical, a formulation, an implant or a device, comprising a protein or a composition having Apolipoprotein A-I binding protein (AIBP) activity.
Any of the above aspects and embodiments can be combined with any other aspect or embodiment as disclosed here in the Summary, Figures and/or Detailed Description sections.
As used in this specification and the claims, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Unless specifically stated or obvious from context, as used herein, the term “or” is understood to be inclusive and covers both “or” and “and”.
Unless specifically stated or obvious from context, as used herein, the term “about” is understood as within a range of normal tolerance in the art, for example within 2 standard deviations of the mean. About (use of the term “about”) can be understood as within 20%, 19%, 18%, 17%, 16%, 15%, 14%, 13%, 12% 11%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of the stated value. Unless otherwise clear from the context, all numerical values provided herein are modified by the term “about.”
Unless specifically stated or obvious from context, as used herein, the terms “substantially all”, “substantially most of”, “substantially all of” or “majority of” encompass at least about 90%, 95%, 97%, 98%, 99% or 99.5%, or more of a referenced amount of a composition.
The entirety of each patent, patent application, publication and document referenced herein hereby is incorporated by reference. Citation of the above patents, patent applications, publications and documents is not an admission that any of the foregoing is pertinent prior art, nor does it constitute any admission as to the contents or date of these publications or documents. Incorporation by reference of these documents, standing alone, should not be construed as an assertion or admission that any portion of the contents of any document is considered to be essential material for satisfying any national or regional statutory disclosure requirement for patent applications. Notwithstanding, the right is reserved for relying upon any of such documents, where appropriate, for providing material deemed essential to the claimed subject matter by an examining authority or court.
Modifications may be made to the foregoing without departing from the basic aspects of the invention. Although the invention has been described in substantial detail with reference to one or more specific embodiments, those of ordinary skill in the art will recognize that changes may be made to the embodiments specifically disclosed in this application, and yet these modifications and improvements are within the scope and spirit of the invention. The invention illustratively described herein suitably may be practiced in the absence of any element(s) not specifically disclosed herein. Thus, for example, in each instance herein any of the terms “comprising”, “consisting essentially of”, and “consisting of” may be replaced with either of the other two terms. Thus, the terms and expressions which have been employed are used as terms of description and not of limitation, equivalents of the features shown and described, or portions thereof, are not excluded, and it is recognized that various modifications are possible within the scope of the invention. Embodiments of the invention are set forth in the following claims.
The invention will be further described with reference to the examples described herein; however, it is to be understood that the invention is not limited to such examples.
Unless stated otherwise in the Examples, all recombinant DNA techniques are carried out according to standard protocols, for example, as described in Sambrook et al. (2012) Molecular Cloning: A Laboratory Manual, 4th Edition, Cold Spring Harbor Laboratory Press, NY and in Volumes 1 and 2 of Ausubel et al. (1994) Current Protocols in Molecular Biology, Current Protocols, USA. Other references for standard molecular biology techniques include Sambrook and Russell (2001) Molecular Cloning: A Laboratory Manual, Third Edition, Cold Spring Harbor Laboratory Press, NY, Volumes I and II of Brown (1998) Molecular Biology LabFax, Second Edition, Academic Press (UK). Standard materials and methods for polymerase chain reactions can be found in Dieffenbach and Dveksler (1995) PCR Primer: A Laboratory Manual, Cold Spring Harbor Laboratory Press, and in McPherson at al. (2000) PCR - Basics: From Background to Bench, First Edition, Springer Verlag, Germany.
This example demonstrates that methods and compositions as provided herein using the exemplary embodiments are effective for treating HIV and other viral infections.
Apolipoprotein A-I binding protein (AIBP) is a recently identified innate anti-inflammatory factor. Here, we show that AIBP inhibited HIV replication by targeting lipid rafts and reducing virus-cell fusion. Importantly, AIBP selectively reduced rafts on cells stimulated by an inflammatory stimulus or treated with extracellular vesicles containing HIV-1 protein Nef, without affecting rafts on non-activated cells. Accordingly, fusion of monocyte-derived macrophages with HIV was sensitive to AIBP only in the presence of Nef. Silencing of endogenous AIBP significantly upregulated HIV-1 replication. Interestingly, HIV-1 replication in cells from donors with the HLA-B*35 genotype, associated with rapid progression of HIV disease, was not inhibited by AIBP. These results suggest that AIBP is an innate anti-HIV factor that targets virus-cell fusion.
Apolipoprotein A-I binding protein (AIBP) is a protein involved in regulation of lipid rafts and cholesterol efflux. AIBP has been suggested to function as a protective factor in several pathological conditions associated with increased abundance of lipid rafts, such as atherosclerosis and acute lung injury. Here, we show that exogenously added AIBP reduced the abundance of lipid rafts and inhibited HIV replication in vitro as well as in HIV-infected humanized mice, whereas knockdown of endogenous AIBP increased HIV replication. Endogenous AIBP was much more abundant in activated T cells than in monocyte-derived macrophages (MDM), and exogenous AIBP was much less effective in T cells than in MDM. AIBP inhibited virus-cell fusion, specifically targeting cells with lipid rafts mobilized by cell activation or Nef-containing exosomes. MDM-HIV fusion was sensitive to AIBP only in the presence of Nef provided by the virus or exosomes. Peripheral blood mononuclear cells from donors with the HLA-B*35 genotype, associated with rapid progression of HIV disease, bound less AIBP than the cells from donors with other HLA genotypes, and were not protected by AIBP from rapid HIV-1 replication. These results provide the first evidence for the role of Nef exosomes in regulating HIV-cell fusion by modifying lipid rafts and suggest that AIBP is an innate factor that restricts HIV replication by targeting lipid rafts.
Given the dependence of HIV on lipid rafts and the ability of AIBP to reduce the abundance of lipid rafts, in this study we investigated whether such activity of AIBP translates into inhibition of HIV replication. We found that AIBP inhibits HIV replication both in vitro and in vivo and reverses the pro-infectious effects of Nef-containing extracellular vesicles. New therapeutic approaches aimed at inhibition of
HIV infection and HIV-associated co-morbidities via stimulation of AIBP production are provided herein.
Peripheral blood mononuclear cells (PBMCs) were isolated from whole blood (purchased from NY Blood Bank) by Ficoll gradient centrifugation. Monocyte-derived macrophages (MDMs) were prepared from PBMCs by plastic adherence and differentiation for 7 days in the presence of 50 ng/ml M-CSF (Sigma) as previously described (29). HIV-1 ADA was used for infection of MDMs. Non-adherent cells (peripheral blood lymphocytes, PBLs) were activated or not with PHA (5 μg/ml) and IL-2 (20 U/ml) for 2 days prior to infection with HIV-1 LAI or primary transmitted/founder (T/F) virus, the CCRS-tropic strain pCH185.c/K3016 (30).
AIBP was produced in a baculovirus/insect cell system to allow for posttranslational modifications and to ensure endotoxin-free preparation. Human AIBP was cloned into a pAcHLT-C vector behind the polyhedrin promoter. The vector contains an N-terminal His-tag to enable purification and detection. Insect Sf9 cells were transfected with BD BaculoGold Baculovirus DNA and the AIBP vector to produce a baculovirus stock. Fresh Sf9 cells were infected with the AIBP producing baculovirus, cell pellets were collected after 3 days and His-AIBP was purified on Ni-NTA agarose column.
Protein was dialyzed against saline, and aliquots were stored at −80° C. AIBP was used at concentration of 0.2 μg/ml, unless indicated.
PBMC from donors with the following HLA-B genotypes were purchased from AllCells Inc.: B*35 positive (B*15:17:01/B*35:01:01, B*35:01:01/B*55:01:01, B*35:01:01/B*35:01:01, B*35:08:01/B*51:01:01); B*57 positive (B*07:02:01/B*57:01:01, B*51:01:01/B*57:01:01, B*40:01:02/B*57:01:01); non-B*35,B*57 (B*08:01:01/B*38:01:01, B*27:05:02/B*38:01:01, B*07:02:01/B*27:05:02, B*15:11:01/B*51:01:02). To analyze AIBP binding, PBMC were blocked with TBS containing 1% BSA for 30 min on ice and incubated with either 2 μg/ml BSA or recombinant His-tagged AIBP for 2 hours on ice. Cells were washed with PBS and incubated with 1 μg/ml FITC-conjugated anti-His polyclonal antibody (Abcam) and LIVE/DEAD Fixable Aqua Dead Cell Stain (Invitrogen) for 1 hour at 4° C. After washes with PBS, cells were analyzed by flow cytometry gating on live cells.
PBMCs from HLA-B*35 and HLA-B*57 donors were incubated with His-AIBP as above and stained for bound AIBP with FITC-conjugated anti-His polyclonal antibody (Abcam) and for lipid rafts with Alexa Fluor 555-conjugated Cholera Toxin B subunit (CT-B). Cells were then mounted on microscopic glass slides, fixed, permeabilized with Triton X-100, and nuclei were stained with DAPI. Imaging and analysis were performed on a Cell Observer Spinning Disk fluorescent microscope (Carl Zeiss) equipped with Yokogawa CSU X1 spinning disk and Evolve Delta EM CCD cameras (512×512, Photometrics). Plan Apochromat 63×/1.46 oil objective lens was used to visualize the optical section close to the center of the majority of the cells. The camera exposure time for each channel and the emission and excitation parameters were kept constant across the experiments. DAPI was excited with a 405 diode laser, and the emission was recorded with 450/50 bandpass filter. FITC was excited with a 488 diode laser, and emission was recorded with 535/30 bandpass filter. To record the CT-B immunolabeling, a 561 diode laser was used for excitation, and the emission was recorded with a 629/62 emission filter. Images were further enhanced using ZEN Microscope Software (Carl Zeiss). Again, an identical setting was used for all images. Final images were saved as TIFF files.
Mean fluorescence intensity (MFI) quantitation was performed on 108 individual cells with HLA-B*35 and 159 cells with HLA-B*57 genotype. To compute the cellular intensities for AIBP and CTB (lipid rafts), the original data stored as czi files (the Carl Zeiss Image Data file type) were used. In each image, taken with a 63× objective, every cell was evaluated using Volocity software. Individual cells were outlined using the freehand ROI tool and each cell's overall cellular fluorescent intensity was recorded for each channel. Mean fluorescence intensity (MFI) quantitation was performed on 108 individual cells with HLA-B*35 and 159 cells with HLA-B*57 genotype. To compute the cellular intensities for AIBP and CTB (lipid rafts), the original data stored as czi files (the Carl Zeiss Image Data file type) were used. In each image, taken with a 63× objective, every cell was evaluated using Volocity software. Individual cells were outlined using the freehand ROI tool and each cell's overall cellular fluorescent intensity was recorded for each channel. Outliers were removed using statistical software in the GraphPad Prism 8 program.”
Isolation and purification of exosomes
Forty eight hours post transfection of HEK293T cells (purchased from ATCC) with pcDNA3.1 vector expressing Nef of HIV-1 NL4-3 (to make exNef) or with empty vector (to make exCont), medium from cell culture was collected. Exosomes were isolated by differential centrifugation, as described (31). Briefly, culture supernatants were pre-clarified by centrifugation at 500×g for 10 min at 4° C. to remove cells and cellular debris, then clarified by spinning at 2,000×g for 30 min at 4° C. to remove remaining debris and large apoptotic bodies, and exosomes were pelleted by centrifugation at 100,000×g for 75 min at 4° C. The pellet was re-suspended in exosome-free medium and frozen at −70° C. Of note, the pellet contained a mixture of extracellular vesicles with sizes from 25 to over 150 nm (
Bradford assay after dilution in RIPA buffer and boiling for 3 minutes; 1 μg of exosomes was used to treat 1×106 cells.
The size and the concentration of exosomes were determined using a NanoSight NS300 (Malvern Instruments Ltd, Malvern, UK) based on Nanoparticle tracking analysis (NTA). NTA utilizes the properties of both light scattering and Brownian motion to obtain the particle size distribution of samples in liquid suspension. Briefly, exosome samples from Nef- and mock (empty vector)-transfected HEK293T cells were diluted 1:100 in PBS and exosomes were tracked on the NanoSight NS300. The samples were loaded by means of a constant pressure syringe pump controller. Videos were recorded for 60 seconds two times, at camera level 13, and analyzed with NTA software 3.0 (Malvern instruments Ltd, Malvern, UK).
The fluorescence HIV-1 virion-based assay was used as previously described (33). The CCF2 substrate was purchased from Life Technology and added to cells at a final concentration of 1 μM. CCR5-tropic viruses used for MDMs were: 1) pNL(AD8), which carries Env of AD8 strain (34), used at 1×106 cpm of RT activity per 106 cells; 2) pBRNL4.3_92BR020.4(R5)nef−_IRES_GFP and pBRNL4.3_92BR020.4(R5)nef+_IRES_GFP (35), the Nef-negative and Nef-positive recombinant constructs, respectively, both used at 2×106 cpm of RT activity per 106 cells. The CXCR4-tropic virus used for PBLs was pNL4-3 at 1×106 cpm of RT activity per 106 cells. Cells were analyzed by flow cytometry, percentage of cells showing fluorescence at 450 nm reflects the percentage of cells fused with HIV.
Abundance of lipid rafts was evaluated by binding of cholera toxin subunit B (CT-B), as previously described (17). Briefly, cells were incubated for 1 h at 4° C. in serum-containing medium with FITC-CT-B conjugate (Invitrogen) (final concentration 0.5 μg/ml), fixed with 5% formaldehyde and analyzed by flow cytometry gating on live cells revealed by LIVE/DEAD Fixable Aqua Dead Cell Stain kit (Invitrogen).
Murine AIBP was fused with fibronectin secretion sequence (FIB) at the N-terminus and 6×-His at the C-terminus (FIB-AIBP-His). FIB-AIBP-His was cloned into the pAAV-MCS vector (Agilent Technologies). AAV-293 cells (Agilent Technologies) were transfected with 20 μg each of pAAV-FIB-mAIBP-His, pAAV-DJ/8 (Cell Biolabs), and pHelper DNA (Cell Biolabs). Subsequent steps of virus harvest, purification and storage were according to published protocols (36). Viral DNA was extracted from purified virus and the number of gene copies (gc) was determined using qPCR with primers for the inverted terminal repeats (Takara Bio Inc).
AIBP silencing in PBLs
Silencing was performed using Accell SMARTpool siRNA (4 siRNAs) and delivery mix (Dharmacon) following the manufacturer's protocol. AIBP target sequences were CGAGUGUGUCUAUCGUCUG (SEQ ID NO:1), UGACGAUUGAUGAACUGUA (SEQ ID NO:2), CUACUGUCCUGGUCAUCUG (SEQ ID NO:3), UCAGCGUGGACCAACUUAU (SEQ ID NO:4).
Western blot analysis was performed on ProteinSimple Jess microfluidic capillary equipment, using manufacturer's software for band quantification. Unless indicated, loading control for quantification was total protein measured in the same capillary as the protein of interest, using ProteinSimple proprietary technology. Nef was detected using anti-Nef rabbit polyclonal antibody from NIH AIDS Reagent Program (37) followed by secondary goat anti-rabbit-Green (ProteinSimple), for p55 we used and anti-p24 mouse monoclonal (AG3.0) from NIH AIDS Reagent Program (38), followed by secondary goat anti-mouse-Red (PROTEINSIMPLET™). For AIBP detection, rabbit polyclonal anti-AIBP from Novus Biologics was used, followed by anti-rabbit-HRP from PROTEINSIMPLE™.
Cell metabolic activity was measured by the MTT Assay Kit (Abcam) following manufacturer's instructions.
Memory CD4+ T-cells were isolated from PBMCs (Peripheral Blood Leuko Pak, AllCells) by negative selection (EasySep Human Memory CD4+ T Cell Enrichment Kit, Stemcell Technologies) following the manufacturer's instructions. Isolated memory CD4+ T-cells were then engrafted into 7 to 9-week-old NOD.Cg-PrkdcscidIl/2rgtmlwjl/SzJ (NSG) mice (The Jackson Laboratory) at 107 cells per animal via tail vein injection. Peripheral blood was collected weekly post-engraftment by tail nick to assess human cell reconstitution by flow cytometry and to measure HIV viral load (see below). Two weeks after CD4+ T-cell engraftment, mice were intravenously injected with empty virus or AAV-AIBP at 1×1012 gc/mouse, and after two more weeks were infected with 70,000 TCID50/animal of HIV-1 ADA virus via intraperitoneal injection. Animals were sacrificed at the study conclusion, and liver samples and peripheral blood were collected.
Flow Cytometry of Cells from hu-mice
Peripheral blood cells from hu-mice were resuspended in a staining cocktail of anti-human CD27 (clone 0323, BioLegend), CD197 (clone G043H7, BioLegend), CD45RA (clone HI100, BD Biosciences), CD8a (clone RPA-T8, BioLegend), CD4 (clone RPA-T4, BD Biosciences), CD3 (clone SK7, BD Biosciences), and CountBright Absolute Counting Beads (for cell quantification, ThermoFisher). Red blood cells were lysed in RBC Lysis/Fixation Solution (BioLegend), and the remaining cells were fixed with 4% paraformaldehyde. Fixed cells were analyzed by flow cytometry on an LSRFortessa X-20 Cell Analyzer (BD).
Viral RNA was extracted from cell-free plasma using the QlAamp Viral RNA Mini Kit (Qiagen) following the manufacturer's instructions. HIV viral RNA was quantified by qRT-PCR using the integrase single-copy assay (iSCA) (39). Reactions were performed with the AgPath-ID One-Step RT-PCR kit (Applied Biosystems), using 400 nM primers (forward primer: 5′-TTTGGAAAGGACCAGCAAA-3′ (SEQ ID NO:5); reverse primer: 5′-CCTGCCATCTGTTTTCCA-3′) (SEQ ID NO:6) and 250 nM dual-labeled probe (probe: 5′-6FAM-AAAGGTGAAGGGGCAGTAGTAATACA-TAMRA-3′) (SEQ ID NO:7) targeting a highly conserved 127 base pair region of HIV integrase gene. Absolute quantifications were established by comparison to a standard curve of in vitro transcribed HIV-1 RNA standards generated by cloning the p31 region of pol from plasmid pNL4-3 containing an infectious clone of HIV-1 (GenBank ascension number: K02013). PCR was first used to generate a 418 base pair amplicon from pNL4-3 using 600 nM primers (forward primer: 5′-CCCTACAATCCCCAAAGTCA-3′ (SEQ ID NO:8); reverse primer: 5′-CACAATCATCACCTGCCATC-3′) (SEQ ID NO:9). The resulting amplicon was cloned into the pGEM T-Easy Vector (Promega) downstream of the T7 promoter. Plasmid containing the correct insert was linearized with Sad, and in vitro RNA synthesis was performed with a 4-hour incubation at 37° C. using the MEGAscript T7 Transcription Kit (ThermoFisher). Template DNA was degraded by treatment with RQ1 RNase-free DNase (Promega), and RNA was purified with the RNeasy Mini Kit (Qiagen) followed by dNTP removal (Qiagen). Purified RNA was quantified using spectrophotometry at 260 nm, diluted in 5 mM Tris, 1 μM DTT and 1,000 units/mL of recombinant RNasin ribonuclease inhibitor (Promega), and stored at -80° C. until use.
The experiments were conducted in triplicates and repeated 2-5 times. Statistical significance of the differences was assessed, unless indicated otherwise) by ordinary one-way ANOVA with Tukey adjustment for multiple comparisons (when 3 or more samples were compared), or by t-test with Bonferroni-Dunn adjustment for multiple comparisons (when repeated measures of 2 samples were compared) in GraphPad Prism 8 software package, p<0.05 was considered significant.
All animal procedures in this study were conducted under IACUC protocol A333 approved by The George Washington University in compliance with the Animal Welfare Act and in accordance with the principles set forth in the “Guide for the Care and Use of Laboratory Animals”.
AIBP Inhibits HIV Replication In Vitro
In previous studies, AIBP concentration of 0.2 μg/ml was found to be an effective dose for stimulation of cholesterol efflux from myeloid cells (5, 6, 8, 9). It is important to note that AIBP activity depends on the presence of apoA-I, so all experiments measuring functional activity of AIBP were done in the presence of 10% human serum as a source of apoA-I. To test the effect of AIBP on HIV replication, we first titrated the effect of baculovirus-expressed recombinant AIBP on MDM infection by HIV-1 ADA. Results in
Analysis of HIV replication kinetic in PBL and MDM cultures infected with X4 (LAI) or R5 (ADA) HIV-1 strains, respectively, demonstrated significant suppression by AIBP of HIV-1 replication in both PBLs and MDMs (
Laboratory-adapted HIV strains, such as R5-ADA and X4-LAI used above, are less predictive of in vivo outcomes than strains mediating transmission between HIV-positive individuals, also known as transmitted/founder (T/F) viruses, which consistently display CCR5 co-receptor tropism (40, 41). We thus tested the effect of AIBP on replication of the primary T/F virus, the CCR5-tropic strain pCH185.c/K3016 (30). This virus did not replicate in MDM, consistent with previous report (30) and ex vivo data showing that the primary targets of transmitted HIV-1 are CD4+ T cells and not macrophages (42). In PBLs, AIBP noticeably suppressed replication of pCH185.c/K3016 (
Given that AIBP reduces the abundance of lipid rafts (5), we hypothesized that the mechanism of HIV inhibition by AIBP might involve suppression of virus-cell fusion, which relies on rafts (43). Previous studies demonstrated that AIBP reduces lipid rafts on activated, but not on non-activated, macrophages, endothelial and glial cells (5, 7). Nothing has been reported about the effects of AIBP on T cells. Using fluorescently labeled cholera toxin B subunit (CTB), which specifically binds to the raft-associated ganglioside GM1 (44) and is commonly used to assess lipid raft abundance (45-47), we evaluated the effect of AIBP on lipid rafts of PBLs activated or not with PHA. In non-activated PBLs, the percentage of cells with high intensity signal was very small, suggesting a low abundance of lipid rafts (consistent with previously reported findings (48, 49)), and AIBP did not decrease the raft abundance (in fact, in this donor AIBP increased the rafts) (
Virus-cell fusion was analyzed by fluorescent HIV-1 virion-based assay (33). For the assay with PBLs, we used the CXCR4-tropic HIV-1 NL4.3 virus containing BlaM-Vpr. This analysis demonstrated that AIBP inhibits fusion between HIV-1 and PHA-activated PBLs (
To test the possibility that Nef makes MDM-HIV fusion susceptible to AIBP-mediated inhibition, we compared the effect of AIBP on fusion between MDM, exposed to exCont or exNef, and Nef-positive (HIV) or Nef-deficient (HIVANef) HIV-1 (
Taken together, these results indicate that AIBP inhibits HIV infection by suppressing virus-cell fusion.
To investigate the anti-HIV effects of AIBP in the in vivo setting, we used humanized mice. Immunodeficient mice were reconstituted with human CD4+ memory T lymphocytes (Table 1). One group of hu-mice (animals #1-6) was injected intravenously with non-replicating adeno-associated viral vector expressing His-tagged AIBP. As a control, another group (animals #7-12) was injected with empty AAV. Two weeks after AAV injection, all hu-mice were infected with HIV-1 ADA using intraperitoneal injection. We used the R5 HIV-1 strain here to mimic human infections, which are transmitted almost exclusively with CCR5-tropic viruses (59). Mice were maintained for 9 weeks after HIV infection, after that period, mice were sacrificed and AIBP expression was measured by Western blotting of the liver tissue (direct detection of AIBP in blood is challenging, likely due to rapid binding of AIBP to cells (5, 7, 8)). The timeline of the experiment is presented in
The impact of host genetic variation on susceptibility to HIV infection and progression of the disease has been well established (61). In particular, specific HLA alleles have been found to be the primary determinants of the rate of progression to AIDS (62-65). For example, the HLA-B*35 genotype has been associated with rapid progression of the disease (62), whereas the HLA-B*57 allele has been consistently associated with slower disease progression (66). This has been explained by differences between the alleles in antigenic peptide presentation (67). However, given association of MHC-I molecules with lipid rafts (68), which are regulated by AIBP, we hypothesized that HLA-B genotype may also influence HIV replication by altering the effect of AIBP. We infected PBMCs isolated from 3 donors with HLA-B*35, HLA-B*57, and non-B*35,57 genotypes with HIV-1 LAI and followed virus replication in the presence or absence of recombinant AIBP. As shown in
Accumulating evidence suggests a protective, and possibly a therapeutic, role of AIBP in human diseases associated with inflammation and impairment of cholesterol metabolism, in particular in atherosclerosis (6, 69). The main finding of this study is that AIBP also exerts an anti-HIV activity. Mechanistically, AIBP decreased the abundance of lipid rafts on activated cells, reducing virus-cell fusion. Importantly, no change in the abundance of lipid rafts or fusion was observed after incubation of non-activated cells with AIBP. This result is consistent with previously reported findings and suggests that AIBP specifically targets lipid rafts on cells subjected to an inflammatory or infectious agent or factors produced by infected cells (6, 7). One such ‘activating’ factor could be Nef-containing exosomes (exNef). Indeed, AIBP reversed the effect of exNef on the abundance of lipid rafts on MDM. Our results suggest that exNef, which are produced by HIV-infected cells even in the presence of suppressive ART (70, 71), may enhance HIV-associated pathology by manipulating lipid rafts on uninfected cells. Nef is considered the key pathogenic factor of HIV due to its profound effects on viral replication, immune system, and multiple tissues (72-74). Previous studies attributed pathogenic activity of Nef to its ability to suppress CTL response by downregulating MEW I (75), and to stimulate viral spread by downregulating CD4 (76) and SERINC3 and 5 in infected cells (77, 78). Our findings suggest another, previously unappreciated, activity of Nef: Nef exosomes increase the abundance of lipid rafts on macrophages stimulating HIV infection (this report) and potentiating lipid raft-dependent inflammatory responses (52).
Our finding that AIBP inhibits fusion of the Nef-positive virus, which does not incorporate SERINC (77, 78), but does not inhibit fusion of Nef-deficient virus, which incorporates SERINC, suggests that fusion of SERINC-positive HIV occurs via lipid rafts that are insensitive to AIBP. One suggested mechanism of SERINC5 anti-HIV activity is that it forms large oligomers, which harden the viral membrane, restrict lipid diffusion, slow the folding of the envelope for fusion, and decrease virus-cell fusion (79, 80). The slowed fusion of such virus may proceed via ‘normal’ lipid rafts, not affected by AIBP. However, treatment of MDM with exNef induces formation of ‘pathological’ rafts, increases fusion with Nef-deficient HIV, and makes fusion susceptible to AIBP inhibition. Interestingly, pre-treatment of macrophages with exNef, while increasing abundance of lipid rafts, did not increase MDM fusion with wild-type HIV, suggesting that Nef delivered by either virions or by virion-contaminating exosomes is sufficient to ensure maximal fusion. This effect of Nef on fusion contradicts conclusion of previous reports that Nef does not alter fusion (57, 58). The difference with those studies is that the effects reported here were observed with MDM, whereas cited above reports used T cell lines or PHA-activated CD4+ T cells. Our analysis demonstrated that activated T cells have high levels of lipid rafts (
In this study, we used a simplified model of humanized mice, immunodeficient mice reconstituted with human memory CD4+ T lymphocytes. This model allows to avoid graft versus host reaction (81) and maintains HIV replication for several months. Lack of human myeloid cells in this model is a limitation, especially in view of the role of these cells in HIV infection (82), and their sensitivity, relative to CD4+ T lymphocytes, to agents targeting cholesterol efflux (17, 27, 83). In vitro experiments with MDM performed in this study demonstrated that AIBP potently inhibits HIV replication in these cells, so we expect that AIBP will exert an even more pronounced anti-HIV activity in a model containing a full range of HIV-susceptible cells. AAV-delivered AIBP protein was detected in liver lysates (
The finding that HLA-B*35 genotype associated with reduced AIBP binding and decreased anti-HIV activity was serendipitous. Given that HLA association with lipid rafts has been previously suggested (68), it is likely that HLA-B*35-dependent modifications of lipid raft structure/composition may influence AIBP binding to cells, modulating its ability to reduce lipid rafts and inhibit virus-cell fusion. This may be a contributing factor to the known association of HLA-B*35 genotype with fast disease progression. This conclusion is supported by our finding that AIBP silencing did not affect HIV-1 replication in the cells with HLA-B*35 genotype, while significantly increasing virus replication in cells with other HLA genotypes. The HLA-B*35 genotype appears to stand out, as we did not find significant differences in AIBP binding or anti-HIV activity between cells of other genotypes tested in this study. It remains to be established whether other HLA genotypes associated with HIV susceptibility or control influence AIBP binding, before more elaborate mechanistic studies of HLA-mediated changes in lipid rafts are initiated. The mechanism of anti-HIV activity of AIBP is likely to involve its ability to reduce the abundance of lipid rafts. This conclusion is based on well-established capacity of
AIBP to disrupt lipid rafts (1, 5, 7, 8), and the role of rafts in HIV fusion (43); concurrent effect of AIBP on rafts and HIV fusion was demonstrated in several independent experimental systems throughout this study. The mechanism behind AIBP-mediated disruption of lipid rats was not investigated in this study, but previous reports suggested that AIBP stimulates cholesterol efflux depleting rafts of cholesterol (1, 5). It may also stabilize ABCA1 (9), providing additional capacity for cholesterol efflux.
Results of this study demonstrate that AIBP is an innate anti-HIV restriction factor. Although pathways regulating endogenous AIBP expression and secretion are not well understood, existing evidence points to spatiotemporal and/or regulated pattern of AIBP secretion (1, 5, 8). Described in this study low sensitivity to AIBP-mediated anti-HIV activity of cells from HLA-B*35 donors, which are susceptible to fast progression of HIV disease, suggests the role of AIBP in controlling natural HIV infection. In this work we sought to augment the benefit of an innate AIBP protective mechanism by delivering recombinant protein or AAV-expressed AIBP to target activated host cells and make them less susceptible to HIV infection. The anti-HIV effect of such treatment, while significant, was relatively small when compared to the effects of anti-retroviral drugs (for example T-20). One potential reason is that the effect was measured on the background of endogenous AIBP. PBLs are hard to transfect and the silencing approach we used produced only a 30-50% downregulation of endogenous AIBP. Future studies with engineered AIBP-deficient cells are likely to produce more impressive results. . Given that lipid rafts are used by many pathogens as an entry platform (84), AIBP may also protect against infection by other viruses and microbes. Overall, this study reveals a novel innate factor that inhibits HIV infection by targeting lipid rafts.
A—Quadruplicate wells of monocyte-derived macrophages (MDM) were infected with HIV-1ADA, and virus production was measured on day 12 post infection by RT activity in culture supernatant. Bars show mean±SD. Statistical analysis was done by Dunnett's multiple comparison test, **p=0.0013, ****p<0.0001. B—PHA-activated PBLs or MDM from one representative donor were infected in triplicate wells with HIV-1LA1 or HIV-1ADA strains, respectively, cultured in the presence or absence of recombinant AIBP (0.2 μg/ml), and HIV replication was followed by measuring p24 in culture supernatants. Holm-Sidak adjusted p values from multiple comparison test are shown. C—Experiment was performed as in B with PHA-activated PBL from 6 donors and MDM from 4 donors. Virus replication was followed by RT activity. Results are presented for each donor at the peak of infection as percent of RT activity in AIBP-negative (control) culture. Holm-Sidak adjusted p values are shown. D—PHA-activated PBLs were infected with T/F strain pCH185.c/K3016 and cultured in the presence or absence of 0.2 μg/ml recombinant AIBP (recombinant AFP was used as control). Virus replication was followed by RT activity. Results show mean±SD (n=4). Holm-Sidak adjusted p value is shown. E. PHA-activated PBLs and MDMs were exposed to indicated concentrations of recombinant AIBP for 3 days, and cytotoxic effect of AIBP was measured by MTT assay and presented as percent of metabolic activity of AIBP-negative (control) cultures. Bars show mean±SD (n=4). F—PHA-activated PBLs were treated with AIBP as in panel C and percentage of live cells was measured by flow cytometry using LIVE/DEAD Fixable Aqua kit (Invitrogen). Bars show mean±SD (n=3). G—PHA-activated PBLs were treated with AIBP-targeting or control Accell siRNA for 72 h. AIBP abundance was measured by
PROTEINSIMPLETM Western blotting (left panel), normalized against total protein, and presented relative to cells treated with siRNACont (right top panel). Cells were infected in 5 wells with HIV-1LAI, cultured for 3 days, and HIV production was measured by RT activity in culture supernatant (right bottom panel). P value was calculated by unpaired t test (n=5). H—PBLs and MDMs from the same donor were analyzed in triplicate for AIBP by PROTEINSIMPLE™ Western blotting (left panel). Relative abundance of AIBP normalized against total protein is shown in the right panel. P value was calculated by unpaired t test (n=3).
A—PBLs from a representative donor were stimulated or not with PHA, stained with fluorescently labeled cholera toxin B subunit, and analyzed by flow cytometry. B—Representative analysis of vesicle size and concentration in exosome samples from supernatants of HEK293 T cells transfected with Nef (exNef) or empty vector (exCont) by Nanosight (top panels). Mean±SEM of vesicle size (nm) and vesicle concentration (particles/mL) are shown in the bottom panel. C—Vesicles were analyzed by Western blotting for the exosomal marker Alix, tetraspanin CD63, cytosolic marker HSP70, and Nef. D—MDM from a representative donor were treated with exNef or exCont in the presence of AIBP or BSA, and lipid rafts were analyzed as in A. E—Lipid rafts were analyzed as in A and D. Results are presented for experiments with cells from 4 different donors. Left panel: *p=0.0088, unpaired t-test with Holm-Sidak adjustment, relative to activated PBL treated with BSA. Right panel: *p=0.0038 relative to cells treated with exCont and BSA, #p=0.0129 relative to MDM treated with exNef and BSA, ordinary one-way ANOVA with Tukey adjustment for multiple comparisons.
A—PBLs were activated with PHA for 48 h, treated with 0.2 μg/ml recombinant AIBP (or BSA as control) for another 48 h, and exposed to BlaM-Vpr carrying HIV-1NL4-3 in the presence or absence of recombinant AIBP. Percentage of fused cells (cleaved CCF-2) was determined by flow cytometry. B—Results of fusion analysis of PBLs from 4 donors (mean±SD) are presented relative to fusion of activated PBL treated with BSA, taken as 100%. P values were calculated by multiple t-test with Bonferroni-Dunn adjustment (BSA vs AIBP groups) or one-way ANOVA with Tukey adjustment (comparison of individual treatments); only significant values are shown. C—MDM were exposed to control (exCont) or Nef exosomes (exNef) for 48 h in the presence of 0.2 μg/ml recombinant AIBP (or BSA as control), and then infected with BlaM-Vpr carrying HIV-1NL(AD8) in the presence or absence of recombinant AIBP. Percentage of fused cells was determined as in A. D—Results of fusion analysis of MDMs from 3 donors (mean±SD) are presented relative to fusion of exCont exposed cells treated with BSA, taken as 100%. P values were calculated by multiple t-test with Bonferroni-Dunn adjustment for multiple comparisons. E—Western blot for Nef (green) and p55 (red) of HEK293T cells transfected with vectors expressing Nef-positive and Nef-negative HIV-1.F—MDM were exposed to exCont or exNef as in C and infected with BlaM-Vpr carrying Nef-positive or Nef-deficient HIV-1. Fusion was analyzed as in A. G—Experiment described in F was performed with MDM from 6 donors. Results are presented for each donor relative to fusion of exCont-treated MDM with HIVΔNef. P values were calculated by repeated measures ANOVA with Bonferroni correction for multiple comparisons.
AIBP (0.2 μg/ml). Total ABCA1 and K,Na ATPase (loading control) were assayed by Western blotting (left panel), and images from 6 independent experiments were quantified by ImageJ (right panel). Results present mean±SD. Significance was calculated by 1-way ANOVA with Tukey multiple comparisons adjustment.
A—PHA-activated PBMCs from donors with HLA-B*35, HLA-B*57, and non-B*35,B*57 genotypes were infected with HIV-ILA1 and incubated in the presence or absence of recombinant AIBP. Virus replication was followed by RT activity. Results are presented for donors B*35/55 (B*35), B*51/57 (B*57), and B*27/38 (non-B*35,B*57). Results are presented as mean±SD of 5 replicates, *−p=0.01, **−p<0.01, ***−p<0.001 by multiple comparisons tests with Holm adjustment. B—Experiment was performed as in A with cells from 3 donors of each genotype. Results (mean±SD) are presented relative to cells from non-B*35,57 donor (taken as 100%) at the time point corresponding to the peak of infection (day 5 p.i.). P values were calculated by ordinary one-way ANOVA with Tukey multiple comparisons adjustment. C—PHA-activated PBMCs from HLA-B*35 or non-B*35 donors were infected with T/F strain pCH185.c/K3016 and cultured in the presence or absence of 0.2 μg/ml recombinant AIBP or BSA. Virus replication was followed by RT activity. Results show mean±SD (n=4). Significance was calculated by multiple t-tests with Holm-Sidak correction for multiple comparisons. ***p<0.001. D—PHA-activated PBMCs from HLA-B*35 and non-B*35 donors were treated with AIBP-targeting (siRNAAIBP) or control (siRNACont) Accell siRNA. AIBP abundance was measured by PROTEINSIMPLE™ Western blotting (left panel), normalized against total protein, and presented relative to non-B*35 cells treated with siRNACont (right top panel). Cells were infected with HIV-1 LAI, and RT activity in culture supernatant was measured on day 4 post infection (right bottom panel). Results show mean±SD of 4 replicates. Ordinary one-way ANOVA with Tukey adjustment for multiple comparisons was used to calculate p values. E—Binding of recombinant AIBP to cells with different HLA-B genotype was analyzed by flow cytometry using anti-His antibody (top panel). Bottom panel—Quantitation of AIBP binding to cells from 4 different donors each of genotypes B*35 and non-B*35,B*57 and 3 donors of B*57 genotype. P values were calculated by multiple t tests, with post-hoc Holm adjustment for multiple comparisons. F—Binding of recombinant AIBP to cells with HLA-B*35 and HLA-B*57 genotype was analyzed by fluorescent microscopy using Alexa Fluor®555 conjugated CTB for lipid rafts (red), FITC-conjugated anti-His antibody for AIBP (green), and DAPI for nuclei (blue). G—Quantification of WI on 108 cells with HLA-B*35 and 159—with HLA-B*57 genotype using Volocity software. ****p<0.0001 calculated by ANOVA with Bonferroni correction for multiple comparisons.
This example demonstrates that methods and compositions as provided herein using the exemplary embodiments are effective for treating coronaviruses such as COVID-19 and other viral infections.
COVID-19 is a global pandemic currently in an acute phase of rapid expansion. While public health measures remain the most effective protection strategy at this stage, when the peak passes, it will leave in its wake important health problems. Historically, very few viruses have ever been eradicated. Instead, the virus may persist in communities causing recurrent local outbreaks of the acute infection as well as several chronic diseases that may arise from the presence of a “suppressed” virus or as a consequence of the initial exposure. An ideal solution would be an anti- viral medication that (i) targets an early stage of the viral lifecycle, (ii) is insensitive to frequent changes of viral phenotype due to mutagenesis, (iii) has broad spectrum, (iv) is safe and (v) also targets co-morbidities of the infection.
Provided herein is a therapeutic approach that uses “lipid raft therapy”. Lipid raft therapy is an approach aimed at reducing the abundance and structural modifications of host lipid rafts or at targeted delivery of therapeutics to the rafts. Lipid rafts are the sites of the initial binding, activation, internalization and cell-to-cell transmission of SARS-CoV-2. They also are key regulators of immune and inflammatory responses, dysregulation of which is characteristic to COVID-19 infection. Lipid raft therapy was successful in targeting many viral infections and inflammatory disorders and can be highly effective for treatment of COVID-19.
Lipid rafts are solid domains of plasma membrane embedded into predominantly fluid membrane (Lingwood and Simons, 2010). Proteins that work together (for example in multiunit receptors or endocytosis machinery) are usually located in lipid rafts preventing these molecules from drifting apart, instead keeping them in proximity to each other. Lipid rafts host many receptors involved in immune and inflammatory responses and play a key role in regulation of inflammation (Sorci-Thomas and Thomas, 2016), an important attribute given the role of unique pattern of immune and inflammatory responses in the clinical manifestations of COVID-19 (Giamarellos-Bourboulis et al., 2020; Ong et al., 2020). At the same time, numerous viruses, for example HIV and Influenza virus, use host lipid rafts as a “point of entry”, owing to rafts harboring high concentration of receptors utilized to bind and guide pathogen as well as affiliated endocytosis machinery ready to take an obligate intracellular parasite inside. Lipid rafts also serve as a platform for pathogen's assembly (for example HIV) and as a “point of exit” (Ebola virus, HIV and HBV (Bukrinsky et al., 2020). Furthermore, viruses often exploit host raft-associated pathways and modify lipid rafts through binding to rafts and/or releasing raft-modifying factors to further promote their infection cycle. The list of viruses where disruption of rafts was shown to inhibit virus infectivity is long and includes HIV, HCV, Influenza A, Ebola and Marburg and many other viruses (for review see (Bagam et al., 2017; Bukrinsky et al., 2020)). SARS-CoV-2 may also be one of such viruses.
Molecular pathogenesis of SARS-CoV-2 is schematically presented in
Targeting lipid rafts for treatment of various diseases, from neurodegeneration and neuropathic pain to cancer, infections and atherosclerosis, is a rapidly growing therapeutic approach, as described in detail in our recent review (Sviridov et al., 2020). Fundamentally, there are two ways to utilize lipid rafts for anti-viral therapy, either to directly disrupt these domains, or to use lipid raft for targeted delivery of anti-viral therapeutics. As only approaches involving lipid raft disruption have been investigated in the context of SARS-CoV-2 pathogenesis (
One approach is to reduce abundance of lipid rafts by depleting them of lipids responsible for their stability, cholesterol or sphingomyelin. For example, cholesterol can be physically removed from rafts by sequestrants, such as cyclodextrins. β-Cyclodextrin is used as a food additive and is proven to be safe for consumption (Mortensen et al., 2016), it inhibits entry of another enveloped virus, HIV, into host cells (Carter et al., 2009) and has anti-inflammatory properties (Zimmer et al., 2016). Another option is stimulation of physiological pathways responsible for the efflux of cholesterol, such as stimulation of the expression of ATP-binding cassette transporters A1 and G1, using LXR agonists or heterologous over-expression of these transporters. Further, elevation of the levels of natural acceptors of cholesterol, high-density lipoprotein (HDL) and apolipoprotein A-I (apoA-I), or infusion of HDL and apoA-I mimetics also reduces the abundance of lipid rafts. The third option is to reduce cholesterol and sphingolipid supply using inhibitors of their biosynthesis, for example statins and Miglustat, respectively. Given the proven safety record of statins, drugs widely used to treat hypercholesterolaemia, they are a good candidate for immediate testing for this application. Finally, recently discovered modulator of lipid rafts, apoA-I Binding Protein (AIBP), may be an especially beneficial “lipid raft therapy” compound to treat COVID-19. AIBP stimulates cholesterol efflux and reduces the abundance of lipid rafts in various tissues (Schneider et al., 2018; Woller et al., 2018; Fang and Miller, 2019), it effectively reduces inflammation (Fang and Miller, 2019) and was recently shown to have an anti-HIV activity (Dubrovsky et al., 2020).
Importantly, AIBP targets only cells activated with LPS, cholesterol-loaded or infected, reducing the abundance of lipid rafts to the “healthy level”, but not below (Woller et al., 2018; Dubrovsky et al., 2020), a selectivity beneficial for avoiding adverse side-effects. Another advantage of AIBP is that it remains active when administered directly to lungs via inhalation (Choi et al., 2018), an application especially relevant to COVID-19.
Second approach takes advantage of unique partitioning of various receptor assemblies to the lipid rafts allowing for an effective targeting of therapeutic agents specifically to these domains. Lipid-coated nanoparticles (Partlow et al., 2008) or liposomes carrying a vector (for example antibody to ACE2 or another raft protein) can carry anti-viral therapies, such as Irbesartan, an ACE2 antagonist, Camostat mesylate, a TMPRSS2 inhibitor, or heparin, which breaks down proteoglycans essential for the SARS-CoV-2 binding to the cell, thus increasing the treatment efficiency and reducing the effective drug concentration and toxicity. Finally, β-cyclodextrin (Lee et al., 2018) and synthetic HDL (Sabnis et al., 2017; Panja and Jana, 2020) particles can also be used to deliver to cells compounds with limited solubility, such as Remdesivir.
One of the puzzling features of COVID-19 infection is abnormal immune response (Giamarellos-Bourboulis et al., 2020) and severe inflammation resembling autoimmune vasculitis (Verdoni et al., 2020; Zhou et al., 2020) or sepsis (Li et al., 2020). The exact pathogenesis of dysregulation of the immune and inflammatory responses in COVID-19 is unknown and emergency response relies on general anti-inflammatory medications or inhibitors of inflammatory cytokines. These approaches in most cases are effective in mitigating the acute phase, but, if sepsis and autoimmune vasculitis are a guide, heightened chronic inflammation will persist for a long time causing multiple chronic co-morbidities. Lipid rafts play a key role in immunity and inflammation (Sorci-Thomas and Thomas, 2016) and targeting lipid rafts to reduce inflammation is a promising therapeutic approach that can reduce both acute and inflammatory responses (Sviridov et al., 2020). Another common co-morbidity of COVID-19 is coagulopathy (Miesbach and Makris, 2020). Lipid rafts are involved in regulation of platelet function, and lipid raft therapy was effective in attenuating platelet function (Calkin et al., 2009). Thus, therapeutic approaches targeting lipid rafts may mitigate both COVID-19 infection itself and its acute and chronic co-morbidities.
Use of “lipid raft therapy” approach has important advantages over other strategies. First, it targets the element of pathogenesis common to both acute and residual infection, as well as the most likely co-morbidities of COVID-19. Second, involvement of lipid rafts in pathogenesis of viral infection is common to many viruses and the proposed treatment may be applicable for both current and future pandemics. Third, it utilises medications that are currently used or being tested for treatment of other diseases, where therapeutic doses were proven to be safe and have high degree of hemocompatibility promising a rapid repurposing for treatment of COVID-19. Finally, it can be used both as a stand-alone therapy and in combination with other therapeutic approaches.
Lipid raft therapy also has some limitations. Agents of lipid raft therapy may induce immune response dangerously combining with the immune response to the SARS-CoV-2. Although no adverse immune reaction to any of the lipid raft therapy agents has been described so far (even to large multiprotein complexes such as HDL), such reaction in the context of COVID-19 infection cannot be a priori dismissed. Conversely, disruption of rafts reduces immune responses, which may have a negative effect on resistance to the virus. However, several lines of evidence suggest that suppressed immunity is not detrimental, but could be even beneficial for the anti-COVID-19 therapy. Immunosuppression and chemotherapy do not have a negative effect on severity of COVID-19 (Koker et al., 2020;Robilotti et al., 2020). Asymptomatic patients have lower level of virus-specific antibody than those with severe disease manifestation (Long et al., 2020). In humans, ACE2, a receptor for SARS-CoV-2, is stimulated by interferon, a key element of anti-viral immune response (Ziegler et al., 2020). Collectively, these findings suggest that SARS-CoV-2 is hijacking immune responses, and mitigation of immune response, perhaps counterintuitively, may be beneficial. Another limitation is that, given that lipid rafts are a central element of numerous signalling pathways, their disruption may have unintended negative consequences for functionality of these pathways. However, this complication is more of a theoretical nature: while phenotype of excessive raft abundance has well-described manifestations, very little is known of phenotype of lipid raft deficiency (Sviridov et al., 2020), most likely due to a high level of redundancy in regulation of lipid raft originating pathways. Furthermore, some therapeutic approaches, such as AIBP, allows “fine tuning” of the rafts, reducing the overabundant lipid rafts to the “normal” level, but not below (Woller et al., 2018;Dubrovsky et al., 2020). Finally, some agents of lipid raft therapy may have side-effects seemingly unrelated to their activity toward lipid rafts. For example, high doses of hydroxypropyl-β-cyclodextrin had unexpected impact on renal and systemic hemodynamics (Rosseels et al., 2013). These potential toxicities should be carefully considered when designing therapeutic regimens.
Figure legend Example 2:
SARS-CoV-2 docks onto ACE2, which is a lipid raft protein. After binding to ACE2 the S protein in the viral envelope undergoes enzymatic activation by TMPRSS2 or furin, which are likely located in lipid rafts. Subsequent endocytosis of SARS-CoV-2 occurs using raft-dependent endocytic pathway. After internalization SARS-CoV-2 undergoes intracellular trafficking within endosomes, fuses with mature lysosomes and releases its viral RNA genome into the host cytoplasm. One of the pathways of virus transmission, cell-to-cell transmission, occurs through formation of intercellular channels or syncytia and also requires intact lipid rafts. Thus, at least four stages of SARS-CoV-2 lifecycle, initial binding, activation, internalization and cell-to-cell transmission, require intact host rafts to proceed and, if other viruses are a guide, disruption of lipid rafts using lipid raft therapy mitigates the infection.
55. Arakelyan A, Fitzgerald W, Zicari S, Vanpouille C, Margolis L. 2017. Extracellular Vesicles Carry HIV Env and Facilitate Hiv Infection of Human Lymphoid Tissue. Sci Rep 7:1695.
A number of embodiments of the invention have been described. Nevertheless, it can be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.
This U.S. Utility Patent Application claims the benefit of priority under 35 U.S.C. § 119(e) of U.S. Provisional Application Ser. No. 63/122,203 filed Dec. 7, 2020. The aforementioned application is expressly incorporated herein by reference in its entirety and for all purposes.
This invention was made with government support under HL135737, HL131473, P30 AI117970, P30 AI055019, NS102432, HL136275, NS104769, awarded by the National Institutes of Health. The government has certain rights in the invention.
| Number | Date | Country | |
|---|---|---|---|
| 63122203 | Dec 2020 | US |
