Bactericidal/permeability-increasing protein (BPI) deletion analogs

Abstract

Novel BPI deletion analogs are provided that consist of amino acid residues 10 through 193 of mature human BPI wherein the cysteine residue at BPI amino acid position 132 is replaced by another amino acid. Fusion proteins comprising these analogs are also provided, as are polynucleotides encoding these products, materials and methods for their recombinant production, compositions and medicaments of these products, and therapeutic uses for these products.

Description

BACKGROUND OF THE INVENTION

The present invention provides preparations of novel biologically active deletion analogs of bactericidal/permeability-increasing protein (BPI) characterized by improved stability and homogeneity as well as by enhanced in vivo activity, and pharmaceutical compositions containing the same.

BPI is a protein isolated from the granules of mammalian polymorphonuclear leukocytes (PMNs or neutrophils), which are blood cells essential in the defense against invading microorganisms. BPI is known to bind to lipopolysaccharide, a major component of the outer membrane of gram-negative bacteria that stimulates a potent inflammatory response which can lead to septic shock. Human BPI protein has been isolated from PMNs by acid extraction combined with either ion exchange chromatography [Elsbach, J. Biol. Chem., 254: 11000 (1979)] or E. coli affinity chromatography [Weiss, et al., Blood, 69: 652 (1987)]. BPI obtained in such a manner is referred to herein as natural BPI and has been shown to have potent bactericidal activity against a broad spectrum of gram-negative bacteria. The molecular weight of human BPI is approximately 55,000 daltons (55 kD). The amino acid sequence of the entire human BPI protein and the nucleic acid sequence of DNA encoding the protein have been reported in FIG. 1 of Gray et al., J. Biol. Chem., 264: 9505 (1989), incorporated herein by reference. The Gray et al. amino acid sequence is set out in SEQ ID NO: 1 hereto. U.S. Pat. No. 5,198,541, the disclosure of which is incorporated herein by reference, discloses recombinant genes encoding, and methods for expression of, BPI proteins including recombinant BPI holoprotein, referred to as rBPI, and recombinant fragments of BPI.

A proteolytic N-terminal fragment of BPI having a molecular weight of about 25 kD has an amphipathic character, containing alternating hydrophobic and hydrophilic regions. This N-terminal fragment of human BPI possesses the anti-bacterial activity of the naturally-derived 55 kD human BPI holoprotein. [Ooi et al., J. Bio. Chem., 262: 14891-14894 (1987)]. In contrast to the N-terminal portion, the C-terminal region of the isolated human BPI protein displays only slightly detectable anti-bacterial activity against gram-negative organisms. [Ooi et al., J. Exp. Med., 174: 649 (1991).] An N-terminal BPI fragment of approximately 23 kD, referred to as "rBPI.sub.23," has been produced by recombinant means and also retains anti-bacterial activity against gram-negative organisms. [Gazzano-Santoro et al., Infect. Immun. 60: 4754-4761 (1992).] An N-terminal analog of BPI, rBPI.sub.21, has been produced as described in Horwitz et al., Protein Expression Purification, 8: 28-40 (1996).

The bactericidal effect of BPI has been reported to be highly specific to gram-negative species, e.g., in Elsbach and Weiss, Inflammation: Basic Principles and Clinical Correlates, eds. Gallin et al., Chapter 30, Raven Press, Ltd. (1992). This reported target cell specificity was believed to be the result of the strong attraction of BPI for lipopolysaccharide (LPS), which is unique to the outer membrane (or envelope) of gram-negative organisms. Although BPI was commonly thought to be non-toxic for other microorganisms, including yeast, and for higher eukaryotic cells, it has recently been discovered, as discussed infra, that BPI protein products, exhibit activity against gram-positive bacteria, mycoplasma, mycobacteria, fungi, protozoa, and chlamydia.

The precise mechanism by which BPI kills gram-negative bacteria is not yet completely elucidated, but it is believed that BPI must first bind to the surface of the bacteria through electrostatic and hydrophobic interactions between the cationic BPI protein and negatively charged sites on LPS. LPS has been referred to as "endotoxin" because of the potent inflammatory response that it stimulates, i.e., the release of mediators by host inflammatory cells which may ultimately result in irreversible endotoxic shock. BPI binds to lipid A, reported to be the most toxic and most biologically active component of LPS.

In susceptible gram-negative bacteria, BPI binding is thought to disrupt LPS structure, leading to activation of bacterial enzymes that degrade phospholipids and peptidoglycans, altering the permeability of the cell's outer membrane, and initiating events that ultimately lead to cell death. [Elsbach and Weiss (1992), supra]. BPI is thought to act in two stages. The first is a sublethal stage that is characterized by immediate growth arrest, permeabilization of the outer membrane and selective activation of bacterial enzymes that hydrolyze phospholipids and peptidoglycans. Bacteria at this stage can be rescued by growth in serum albumin supplemented media [Mannion et al., J. Clin. Invest., 85: 853-860 (1990)]. The second stage, defmed by growth inhibition that cannot be reversed by serum albumin, occurs after prolonged exposure of the bacteria to BPI and is characterized by extensive physiologic and structural changes, including apparent damage to the inner cytoplasmic membrane.

Initial binding of BPI to LPS leads to organizational changes that probably result from binding to the anionic groups of LPS, which normally stabilize the outer membrane through binding of Mg.sup.++ and Ca.sup.++. Attachment of BPI to the outer membrane of gram-negative bacteria produces rapid permeabilization of the outer membrane to hydrophobic agents such as actinomycin D. Binding of BPI and subsequent gram-negative bacterial killing depends, at least in part, upon the LPS polysaccharide chain length, with long O-chain bearing, "smooth" organisms being more resistant to BPI bactericidal effects than short O-chain bearing, "rough" organisms [Weiss et al., J. Clin. Invest. 65: 619-628 (1980)]. This first stage of BPI action, permeabilization of the gram-negative outer envelope, is reversible upon dissociation of the BPI, a process requiring high concentrations of divalent cations and synthesis of new LPS [Weiss et al., J. Immunol. 132: 3109-3115 (1984)]. Loss of gram-negative bacterial viability, however, is not reversed by processes which restore the envelope integrity, suggesting that the bactericidal action is mediated by additional lesions induced in the target organism and which may be situated at the cytoplasmic membrane Mannion et al., J. Clin. Invest. 86: 631-641 (1990)). Specific investigation of this possibility has shown that on a molar basis BPI is at least as inhibitory of cytoplasmic membrane vesicle function as polymyxin B (In't Veld et al., Infection and Immunity 56: 1203-1208 (1988)) but the exact mechanism as well as the relevance of such vesicles to studies of intact organisms has not yet been elucidated.

BPI protein products (which include naturally and recombinantly produced BPI protein; natural, synthetic, and recombinant biologically active polypeptide fragments of BPI protein; biologically active polypeptide variants of BPI protein or fragments thereof, including hybrid fusion proteins and dimers; biologically active polypeptide analogs of BPI protein or fragments or variants thereof, including cysteine-substituted analogs; and BPI-derived peptides) have been demonstrated to have a variety of beneficial activities. BPI protein products are known to be bactericidal for gram-negative bacteria, as described in U.S. Pat. Nos. 5,198,541 and 5,523,288, both of which are incorporated herein by reference. BPI protein products are also known to enhance the effectiveness of antibiotic therapy in gram-negative bacterial infections, as described in U.S. Pat. No. 5,523,288 and corresponding International Publication No. WO 95/08344 (PCT/US94/11225), which are incorporated herein by reference. BPI protein products are also known to be bactericidal for gram-positive bacteria and mycoplasma, and to enhance the effectiveness of antibiotics in gram-positive bacterial infections, as described in U.S. Pat. No. 5,578,572 and corresponding International Publication No. WO 95/19180 (PCT/US95/00656), which are incorporated herein by reference. BPI protein products are further known to exhibit anti-fungal activity, and to enhance the activity of other anti-fungal agents, as described in U.S. Pat. No. 5,627,153 and corresponding International Publication No. WO 95/19179 (PCT/US95/00498), and further as described for anti-fungal peptides in U.S. Pat. No. 5,858,974, which is in turn a continuation-in-part of U.S. application Ser. No. 08/504,841 filed Jul. 20, 1994 and corresponding International Publication Nos. WO 96/08509 (PCT/US95/09262) and WO 97/04008 (PCT/US96/03845), all of which are incorporated herein by reference. BPI protein products are further known to exhibit anti-protozoan activity, as described in U.S. Pat. No. 5,646,114 and corresponding International Publication No. WO 96/01647 (PCT/US95/08624), all of which are incorporated herein by reference. BPI protein products are known to exhibit anti-chlamydial activity, as described in U.S. Pat. No. 5,888,973 and corresponding International Publication No. WO 98/06415 (PCT/US97/13810), all of which are incorporated herein by reference. Finally, BPI protein products are known to exhibit anti-mycobacterial activity, as described in co-owned, co-pending U.S. application Ser. No. 08/626,646 filed Apr. 1, 1996, which is in turn a continuation of U.S. application Ser. No. 08/285,803 filed Aug. 14, 1994, which is in turn a continuation-in-part of U.S. application Ser. No. 08/031,145 filed Mar. 12, 1993 and corresponding International Publication No. WO94/20129 (PCT/US94/02463), all of which are incorporated herein by reference.

The effects of BPI protein products in humans with endotoxin in circulation, including effects on TNF, IL-6 and endotoxin are described in U.S. Pat. Nos. 5,643,875 and 5,753,620 and corresponding International Publication No. WO 95/19784 (PCT/US95/01151), all of which are incorporated herein by reference.

BPI protein products are also known to be useful for treatment of specific disease conditions, such as meningococcemia in humans (as described in co-owned, co-pending U.S. application Ser. No. 08/644,287 filed May 10, 1996, a continuation of which issued as U.S. Pat. No. 5,888,977 and corresponding International Publication No. WO 97/42966 (PCT/US97/08016), which are incorporated herein by reference), hemorrhagic trauma in humans, (as described in co-owned, co-pending U.S. application Ser. No. 08/862,785, a continuation-in-part of U.S. Ser. No. 08/652,292 filed May 23, 1996, now U.S. Pat. No. 5,756,464, and corresponding International Publication No. WO 97/44056 (PCT/US97/08941), all of which are incorporated herein by reference), burn injury (as described in U.S. Pat. No. 5,494,896 and corresponding International Publication No. WO 96/30037 (PCT/US96/02349), both of which are incorporated herein by reference), ischemia/reperfusion injury (as described in U.S. Pat. No. 5,578,568, incorporated herein by reference), and liver resection (as described in co-owned, co-pending U.S. application Ser. No. 08/582,230 filed Mar. 16, 1998 which is a continued prosecution application of the same serial no. filed Jan. 3, 1996, which is in turn a continuation of U.S. application Ser. No. 08/318,357 filed Oct. 5, 1994, which is in turn a continuation-in-part of U.S. application Ser. No. 08/132,510 filed Oct. 5, 1993, and corresponding International Publication No. WO 95/10297 (PCT/US94/11404), all of which are incorporated herein by reference).

BPI protein products are also known to neutralize the anti-coagulant activity of exogenous heparin, as described in U.S. Pat. No. 5,348,942, incorporated herein by reference, as well as to be useful for treating chronic inflammatory diseases such as rheumatoid and reactive arthritis, as described in U.S. Pat. No. 5,639,727, incorporated herein by reference, and for inhibiting angiogenesis and for treating angiogenesis-associated disorders including malignant tumors, ocular retinopathy and endometriosis, as described in co-owned, co-pending U.S. application Ser. Nos. 08/435,855, 08/466,624 and 08/466,826, and corresponding International Publication No. WO 94/20128 (PCT/US94/02401), all of which are incorporated herein by reference.

BPI protein products are also known for use in antithrombotic methods, as described in U.S. Pat. No. 5,741,779 and corresponding International Publication No. WO97/42967 (PCT/US97/08017), which are incorporated herein by reference.

U.S. Pat. Nos. 5,420,019 and 5,674,834 and corresponding International Publication No. WO94/18323 (PCT/US94/01235), all of which are incorporated herein by reference, discloses that the replacement of the cysteine residue at amino acid position 132 or 135 with another amino acid renders the resulting BPI polypeptide resistant to dimerization and cysteine adduct formation. It also discloses that terminating the N-terminal BPI fragment at BPI amino acid position 193 resulted in an expression product with reduced carboxy-terminal heterogeneity.

Of interest is the report in Capodici and Weiss, J. Immunol., 156: 4789-4796 (1996) that the in vitro transcription/translation products of DNA encoding amino acid residues 1 through 193 (BPI.sub.1-193) and residues 13 through 193 (BPI.sub.13-193) of mature BPI showed similar LPS-dependent binding to immobilized LPS.

There continues to be a need in the art for improved biologically active BPI protein product preparations, particularly those with enhanced stability, homogeneity and/or in vivo biological activity.

SUMMARY OF THE INVENTION

The present invention provides novel biologically active BPI deletion analogs and preparations thereof characterized by enhanced stability and homogeneity, including for example, resistance to dimerization and cysteine adduct formation and reduced amino-terminal and carboxy-terminal heterogeneity of the recombinant product, as well as by enhanced in vivo biological activity, properties which render it highly suitable for therapeutic and diagnostic uses. Novel BPI deletion analogs are the expression product of DNA encoding amino acid residues 10 through 193 of mature human BPI (SEQ ID NO: 2), in which the cysteine at position 132 has been replaced with a different amino acid, preferably a non-polar amino acid such as serine or alanine. In a preferred embodiment, designated "rBPI(10-193)C132A" or "rBPI(10-193)ala.sup.132," the cysteine at position 132 is replaced with an alanine.

The invention further provides novel purified and isolated polynucleotide sequences (e.g., DNA or RNA) encoding these BPI protein products; materials and methods for their recombinant production, including vectors and host cells comprising the DNA; improved stable pharmaceutical compositions comprising these BPI protein products; and improved treatment methods using these compositions, either alone or concurrently administered with other therapeutic agents. Also contemplated is the use of the BPI deletion analogs of the invention in manufacture of a medicament for treating a subject that would benefit from administration of BPI protein product.

Numerous additional aspects and advantages of the invention will become apparent to those skilled in the art upon considering the following detailed description of the invention, which describes the presently preferred embodiments thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the elevation in blood pressure, measured as area under the curve (AUC) occurring after administration of either rBPI(10-193)C132A or rBPI.sub.21.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides novel BPI deletion analogs consisting of amino acid residues 10 through 193 of mature human BPI (set forth in SEQ ID NO: 2) wherein the cysteine residue at BPI amino acid position 132 is replaced by another amino acid, preferably a non-polar amino acid such as serine or alanine. A preferred embodiment, in which the cysteine at position 132 is replaced with an alanine, has been designated rBPI(10-193)C132A or rBPI(10-193)ala.sup.132.

The BPI protein product rBPI.sub.21 is the expression product of DNA encoding amino acid residues 1 to 193 of mature human BPI wherein the cysteine at residue number 132 is substituted with alanine, described in U.S. Pat. No. 5,420,019. Changes in the fermentation processes used to produce rBPI.sub.21 by recombinant methods that achieved higher cell densities and higher rBPI.sub.21 titers also resulted in an apparent increase in amino-terminal heterogeneity of the purified product. In some fermentation runs, up to about 20% of the purified product was observed to be a species with amino acids 10-193 of BPI, rather than the encoded 1-193 amino acids. SDS-PAGE gels of 500-liter fermentor samples over the course of a fermentation run showed that this 10-193 species appeared in the last 2-3 days of the run, with the greatest amount appearing on the day of harvest. Further investigation revealed that incubation of rBPI.sub.21 with a CHO-K1 cell homogenate yielded a digested product, suggesting that protease activity associated with the cells was involved. To simulate protease activity in a controlled manner, rBPI.sub.21 was incubated with aminopeptidase M and elastase. The rBPI.sub.21 was resistant to aminopeptidase M digestion, but elastase rapidly converted the rBPI.sub.21 into 40% BPI(8-193) and 60% BPI(10-193).

As described herein, stable homogeneous preparations of rBPI(10-193)C132A were produced proteolytically and by recombinant methods. The protein was purified and was tested for biological activity. Experiments were performed to compare rBPI(10-193)C132A to rBPI.sub.21 in several in vitro biological assays, two different animal efficacy models and in pharmacokinetic and toxicology studies. As described in Examples 5-7, rBPI(10-193)C132A and rBPI.sub.21 had similar in vitro activities when compared in radial diffusion and broth microdilution bactericidal assays with Escherichia coli J5, a radial diffusion assay with an L-form of Staphylococcus aureus, a competition binding assay with E. coli J5 LPS, and in LPS neutralization assays with RAW and THP1 cells. As described in Example 8, purified rBPI(10-193)C132A and rBPI.sub.21 had similar toxicity profiles in a GLP toxicology study in rats at doses up to 120 mg/kg/day for three days and similar pharmacokinetics in rats at a dose of 2 mg/kg. Experiments described in Example 8 also showed that in a mouse endotoxin challenge model, rBPI(10-193)C132A appeared to be at least two-fold more potent than rBPI.sub.21 in two studies whereas in a mouse model of lethal bacteremia, rBPI(10-193)C132A and rBPI.sub.21 were similarly potent. In additional in vivo experiments in conscious rats, doses of 40 and 50 mg/kg of infused rBPI.sub.21 caused significant transient decreases in blood pressure relative to the vehicle control, while the same doses of rBPI(10-193)C132A did not result in a statistically significant transient decrease in blood pressure relative to control. Thus, infusion of rBPI(10-193)C132A appears to provide a reduction in an adverse effect in blood pressure compared with infusion of rBPI.sub.21.

The invention further contemplates fusion of rBPI(10-193)C132A with at least a portion of at least one other polypeptide. Examples of such hybrid fusion proteins are described in U.S. Pat. No. 5,643,570 and corresponding International Publication No. WO 93/23434 (PCT/US93/04754), which are all incorporated herein by reference and include hybrid fusion proteins comprising, at the amino-terminal end, a BPI protein or a biologically active fragment thereof and, at the carboxy-terminal end, at least one constant domain of an immunoglobulin heavy chain or allelic variant thereof.

The invention additionally contemplates purified and isolated polynucleotide sequences (e.g., DNA or RNA) encoding the novel BPI deletion analogs or fusion proteins of the present invention; expression vectors containing such polynucleotides, preferably operatively linked to an endogenous or heterologous expression control sequence; prokaryotic or eukaryotic host cells stably transfected or transformed with a DNA or vector of the present invention; and methods for the recombinant production of the novel deletion analog BPI protein products of the present invention, e.g., methods in which a host cell is grown in a suitable nutrient medium and the deletion analog BPI protein product is isolated from the cell or the medium. Such polynucleotide sequences or vectors may optionally encode the 27-amino acid BPI leader sequence and the mouse light chain polyadenylation signal.

The recombinantly produced novel BPI deletion analog of the present invention may be produced according to the methods described in U.S. Pat. No. 5,439,807 and corresponding International Publication No. WO 93/23540 (PCT/US93/04752), which are all incorporated herein by reference. U.S. Pat. No. 5,439,807 discloses methods for the purification of recombinant BPI protein products expressed in and secreted from genetically transfected mammalian host cells in culture, and discloses how one may produce large quantities of recombinant BPI products suitable for incorporation into stable, homogeneous pharmaceutical preparations.

The present invention further provides improved stable pharmaceutical compositions comprising the novel BPI deletion analogs and improved treatment methods using these compositions, either alone or concurrently administered with other therapeutic agents. It is contemplated that such compositions may be utilized in any of the therapeutic uses known for BPI protein products, including those discussed supra.

The administration of BPI protein products in general, including BPI deletion analogs, is preferably accomplished with a pharmaceutical composition comprising a BPI protein product and a pharmaceutically acceptable diluent, adjuvant, or carrier. The BPI protein product may be administered without or in conjunction with known surfactants, other chemotherapeutic agents or additional known anti-chlamydial agents. A stable pharmaceutical composition containing BPI protein products (e.g., rBPI.sub.23) comprises the BPI protein product at a concentration of 1 mg/ml in citrate buffered saline (5 or 20 mM citrate, 150 mM NaCl, pH 5.0) comprising 0.1% by weight of poloxamer 188 (Pluronic F-68, BASF, Parsippany, N.J.) and 0.002 % by weight of polysorbate 80 (Tween 80, ICI Americas Inc., Wilmington, Del. or JT Baker, Phillipsburg, N.J.). Another stable pharmaceutical composition containing BPI protein products (e.g., rBPI.sub.21) comprises the BPI protein product at a concentration of 2 mg/ml in 5 mM citrate, 150 mM NaCl, 0.2% poloxamer 188 and 0.002% polysorbate 80. Such preferred combinations are described in U.S. Pat. Nos. 5,488,034 and 5,696,090 and corresponding International Publication No. WO 94/17819 (PCT/US94/01239), the disclosures of all of which are incorporated herein by reference. As described in U.S. application Ser. No. 08/586,133 filed Jan. 12, 1996, which is in turn a continuation-in-part of U.S. application Ser. No. 08/530,599 filed Sep. 19, 1995, which is in turn a continuation-in-part of U.S. application Ser. No. 08/372,104 filed Jan. 13, 1995, and corresponding International Publication No. WO96/21436 (PCT/US96/01095), all of which are incorporated herein by reference, other poloxamer formulations of BPI protein products with enhanced activity may be utilized.

Therapeutic compositions comprising BPI protein product may be administered systemically or topically. Systemic routes of administration include oral and parenteral routes, including intravenous, intramuscular or subcutaneous injection (including into a depot for long-term release), intraocular and retrobulbar, intrathecal, intraperitoneal (e.g. by intraperitoneal lavage), intrapulmonary (using powdered drug, or an aerosolized or nebulized drug solution), or transdermal. Improved aerosolized formulations are described in co-owned, co-pending U.S. application Ser. No. 08/962,217 filed Oct. 31, 1997 and corresponding International Publication No. WO 98/19694 (PCT/US97/19850), which are both incorporated herein by reference.

When given parenterally, BPI protein product compositions are generally injected in doses ranging from 1 .mu.g/kg to 100 mg/kg per day, preferably at doses ranging from 0.1 mg/kg to 20 mg/kg per day, more preferably at doses ranging from 1 to 20 mg/kg/day and most preferably at doses ranging from 2 to 10 mg/kg/day. The treatment may continue by continuous infusion or intermittent injection or infusion, at the same, reduced or increased dose per day for, e.g., 1 to 3 days, and additionally as determined by the treating physician. When administered intravenously, BPI protein products are preferably administered by an initial brief infusion followed by a continuous infusion. The preferred intravenous regimen is a 1 to 20 mg/kg brief intravenous infusion of BPI protein product followed by a continuous intravenous infusion at a dose of 1 to 20 mg/kg/day, continuing for up to one week. A particularly preferred intravenous dosing regimen is a 1 to 4 mg/kg initial brief intravenous infusion followed by a continuous intravenous infusion at a dose of 1 to 4 mg/kg/day, continuing for up to 72 hours.

Topical routes include administration in the form of salves, creams, jellies, ophthalmic drops or ointments (as described in co-owned, co-pending U.S. application Ser. No. 08/557,289 filed Nov. 14, 1995 and U.S. Pat. No. 5,686,414 and corresponding International Publication Nos. WO 97/17990 (PCT/US96/18632) and WO 97/17989 (PCT/US96/18416), all of which are incorporated herein by reference), ear drops, suppositories, irrigation fluids (for, e.g., irrigation of wounds) or medicated shampoos. For example, for topical administration in drop form, about 10 to 200 .mu.L of a BPI protein product composition may be applied one or more times per day as determined by the treating physician.

Those skilled in the art can readily optimize effective dosages and administration regimens for therapeutic compositions comprising BPI protein product, as determined by good medical practice and the clinical condition of the individual patient.

Other aspects and advantages of the present invention will be understood upon consideration of the following illustrative examples. Example 1 addresses the construction of an expression vector, pING1742, encoding rBPI(10-193)C132A. Example 2 addresses transformation of CHO cells with pING1742 and selection of the highest producing clones secreting rBPI(10-193)C132A. Example 3 addresses the production and purification of rBPI(10-193)C132A in 2-L and 500-L fermenters. Example 4 addresses the biochemical characterization of rBPI(10-193)C132A and rBPI.sub.21. Examples 5, 6 and 7 respectively address the in vitro LPS-binding activity, bactericidal activity, and LPS neutralization activity of rBPI(10-193)C132A as compared to rBPI.sub.21. Example 8 addresses the in vivo activity of rBPI(10-193)C132A.

EXAMPLE 1

Construction of Expression Vector pING1742

The rBPI(10-193)C132A expression vector, pING1742, was constructed as follows. The expression vector pING4155 was first constructed by ligating a BamHI-BsaI fragment containing the neo gene from pING3174 with a BsaI-XhoI fragment containing the CMV promoter and rBPI.sub.21 gene from pING4144 and an XhoI-BamHI fragment containing the mouse (kappa) light chain 3' untranslated region from pING4537 (pING3174, pING4144 and pING4537 are described in U.S. Pat. No. 5,420,019, incorporated by reference). The resulting pING4155 vector contains the gene encoding rBPI.sub.21 fused to the human IgG enhancer, the human CMV promoter and the mouse (kappa) light chain 3' untranslated region. It also contains the neo gene encoding neomycin phosphotransferase, for selection of transfectants resistant to the antibiotic Geneticin.RTM. (G418).

The vector pING1732 was produced by deleting the 0.7 kbp HindIII--HindIII fragment of pING4155 containing the human Ig enhancer. Then, the 27 nucleotides encoding amino acids 1 through 9 of the mature portion of rBPI.sub.21 were deleted from pING1732 by overlap PCR mutagenesis using the following primers:

__________________________________________________________________________Primer 1: 5'-CTGCTCTAAAAGCTGCTGCAG-3' [SEQ ID NO:3]Primer 2: 5'-CCAGGCCCTTCTGGGAGGCCGCTGTCACGGCGG-3' [SEQ ID NO:4]Primer 3: 5'-GCCGTGACAGCGGCCTCCCAGAAGGGCCTGGAC-3' [SEQ ID NO:5]Primer 4: 5'-CTGGGAACTGGGAAGCTG-3' [SEQ ID NO:6]__________________________________________________________________________ Overlapping complementary primers 2 and 3 incorporated the 27 bp deletion of nucleotides encoding amino acids 1 through 9, while primers 1 and 4 encoded nucleotides immediately upstream and downstream, respectively, of unique SalI and EcoRI sites in pING1732. First, fragments were obtained by PCR amplification using the combination of oligonucleotide primers 1 and 3, and primers 2 and 4. After these individual fragments were obtained, they were annealed, extended and re-amplified using primers 1 and 4. This amplified fragment was then digested with SalI and EcoRI and cloned into SalI-EcoRI-digested pING1732 to generate the plasmid pING1742.

To confirm that no mutations had occurred during PCR, the SalI-EcoRI region from pING1742 was sequenced. No changes were observed in the mature coding region for BPI. However, a two base-pair change (ACC.fwdarw.GCT) was found in DNA encoding the signal sequence, which resulted in the conversion of a Thr to an Ala at amino acid position -6 relative to the start of the mature protein sequence.

EXAMPLE 2

Transformation of CHO Cells with pING1742

CHO-K1 cells (American Type Culture Collection (ATCC) Accession No. CCL61) were adapted to growth in serum-free EX-Cell 301 medium as follows. CHO-K1 cells grown in Ham's F12 medium were trypsinized, centrifuged and resuspended in Ex-Cell 301 medium. Cells were grown in a 125-ml flask at 100 rpm and passaged every two to three days in either a 125-ml or 250-ml flask.

These Ex-Cell 301-adapted CHO cells were transfected by electroporation with pING1742. Prior to transfection, pING1742 was digested with NotI, which linearizes the plasmid. Following a 48-hour recovery, cells were plated at approximately 104 cells/well into 96-well plates containing Ex-Cell 301 medium supplemented with 0.6 mg/mL G418 (Life Technologies, Gaithersburg, Md.). At approximately 2 weeks, supernatants from approximately 250 wells containing single colonies were screened by ELISA for the presence of BPI-reactive protein using an anti-BPI monoclonal antibody.

Fifteen clones having the highest expression levels were transferred to 24-well plates containing Ex-Cell 301 medium. To screen for productivity, the cells were grown in 24-well plates containing Ex-Cell medium supplemented with 2% FBS and 40 .mu.L sterile S-Sepharose beads for 10 days, after which the beads were removed, washed with low salt buffer (0.1 M NaCl in 10 mM Na acetate, pH 4.0) and the BPI eluted with 1.5 M NaCl in the same buffer. The levels of secreted rBPI(10-193)C132A were determined by ELISA. Western blot analysis of eluates run on a 12% non-reducing SDS gel revealed a prominent band which migrated slightly faster than rBPI.sub.21.

The top eight producers were transferred to sterile 125 mL Erlenmeyer flasks and grown in Ex-Cell medium. These cells were evaluated again for productivity by growing them in flasks containing Ex-Cell 301 medium supplemented with 2% FBS and 1% (V/V) sterile S-sepharose beads. The rBPI(10-193)C132A was eluted from the S-Sepharose beads that had been incorporated in the culture medium and the levels of rBPI(10-193)C132A determined by HPLC. Clone 139, which was among the highest producers, was chosen for further growth and product production.

EXAMPLE 3

Production and Purification of rBPI(10-193)C132A

Large quantities of rBPI(10-193)C132A were produced for characterization by growing Clone 139 cells in 2-liter research fermenters (Biolafitte, St. Germain en Laye, France) and then in a 500 liter ABEC fermenter (ABEC, Allentown, Pa.). Protein product obtained from the 2-liter fermenters was used for the in vitro studies described below, while product obtained from the 500 liter fermenter was used for animal toxicology and efficacy studies.

A. Growth in Two-Liter Fermenters

Clone 139 cells were passaged in spinner flasks of increasing volumes containing Ex-Cell medium supplemented with 1% FBS until sufficient volume and cell density was achieved to inoculate the 2 liter bioreactors at approximately 2.times.10.sup.5 cells/mL. Cells were grown in three 2-liter fermenters in Ex-Cell medium supplemented with 1% FBS, at 37.degree. C., pH 7.2, 150 rpm with dissolved oxygen maintained at 5-10%. Large sterile SP-Sepharose beads (Pharmacia and Upjohn, Piscataway, N.J.) were added at 1.5% (V/V). The initial glucose level was approximately 3.5 g/L and glucose was pulsed daily to 3 g/L during the course of the run. The fermentation was terminated at 238 hours, at which time the cell viabilities were from 63%, 80% and 84%.

Following fermentation, the beads from each fermenter were harvested, allowed to settle, and washed several times with 10 mM Na phosphate(0.15M NaCl, pH 7.0, to remove cellular components and weakly bound impurities from the beads. The washed beads were packed into a column, washed with 10 mM Na phosphate, 0.25 M NaCl, pH 7.0, and eluted with the same buffer containing 0.8 M NaCl, 5 mM glycine. The eluate was then diluted with three volumes of sterile water for injection (WFI), loaded onto a CM-spherodex column (Sepracor, Marlborough, Mass.) and washed with 10 mM Na phosphate, 0.25 M NaCl, pH 7.0, followed by 20 mM Na acetate, 0.2 M NaCl, pH 4.0, followed by 20 mM Na acetate, 0.3 M NaCl, pH 4.0, and sample was eluted at 1.0 M NaCl in the same buffer. Following concentration on a Centricon membrane with a 10,000 MW cutoff (Amicon, Beverly, Mass.), the eluate from the CM column was loaded onto a Sephacryl S-100 column (Pharmacia and Upjohn) equilibrated with 5 mM Na citrate, 0.15 M NaCl, pH 5.0. Fractions containing rBPI(10-193)C132A identified by absorbance at 280 nm were pooled, concentrated on an Amicon filter to 1.9 mg/mL and formulated with 0.002% polysorbate 80 (JT Baker, Phillipsburg, N.J.), 0.2% poloxamer 188 (Pluronic F-68, BASF, Parsippany, N.J.). The final preparation was filter sterilized using a 0.2 .mu.m filter.

B. Growth in 500-Liter Fermenter

Clone 139 cells were passaged in fetuin-free Ex-Cell medium with 1% FBS in a series of spinner flasks of increasing volumes to provide inoculum for the 35L Bellco spinner flask (Bellco Glass, Vineland, N.J.), which in turn provided the inoculum for the 500 liter ABEC fermenter. Cells were grown in complete Ex-Cell medium without fetuin but supplemented with 1% FBS, additional glucose (to 10 g/L) and glutamine (to 10 mM). The fermenter was operated in a fed-batch mode with one 0.5% Primatone RL supplement pulse and one glucose/glutamine pulse added during the run. Five to six liters of large SP-Sepharose beads were added 24 hours after the 500 liter fermenter was inoculated. The pH was controlled manually with 10% sodium bicarbonate to pH 7.0, oxygen was controlled at 5% and temperature at 37.degree. C. Agitation was maintained at 25 rpm with two three-blade paddle impellers. The fermentation run was terminated at 184 hours, at which time the cell viability was 90%.

As described above for the 2-liter fermentation, the beads were allowed to settle following fermentation and then washed several times with low salt (0.1M) phosphate buffer. The steps for this purification were similar to those described above for the 2-liter samples except that a pH 3.0 viral inactivation step was included after elution from the S-Sepharose beads and a second CM-spherodex column was included as a concentration step. For the second CM column, the eluate was diluted with three volumes of WFI, the pH adjusted to 5.0, the column was equilibrated and washed with 20 mM Na acetate, 0.3 M NaCl, pH 5.0 and the sample was eluted at 1.0 M NaCl in the same buffer. The rBPI(10-193)C132A was eluted from the Sephacryl S-100 column in 5 mM Na citrate, 0.15 M NaCl, pH 5.0, adjusted to 2 mg/mL, and filtered through a 0.2 .mu.m filter. The rBPI(10-193)C132A was then formulated with 0.002% polysorbate 80, 0.2% poloxamer 188, sterile filtered, and filled into 10 mL Type I glass serum vials.

EXAMPLE 4

Biochemical Characterization of rBPI(10-193)C132A

A. Protein from the 2-Liter Fermentations

The purified rBPI(10-193)C132A product from Example 3 was observed to be a single band that migrated slightly faster on SDS polyacrylamide gel elecrphoresis (SDS-PAGE than the rBPI.sub.21 band, consistent with the deletion of nine N-terminal amino acids from rBPI.sub.21. Sequence analysis demonstrated that the rBPI(10-193)C132A contained the predicted N-terminal sequence of SQKGLDYASQQGTAALQKEL (SEQ ID NO: 7). On mass spectroscopy analysis (ESI-MS) two components were observed, one with a mass of 20,470 daltons, which was consistent with the predicted mass of 20,472 daltons for rBPI(10-193)C132A, and a second with a mass of 20,255 daltons, consistent with the predicted mass of 20,258 daltons for rBPI(10-191). The ion-exchange HPLC profiles (Hewlett-Packard, Model 1050, Palo Alto, Calif.) of rBPI(10-193)C132A and rBPI.sub.21 both exhibited single peaks with similar retention times.

B. Protein from the 500-Liter Fermentation

On SDS-PAGE, the rBPI(10-193)C132A was a single band that migrated slightly faster than the rBPI.sub.21 band. On mass spectroscopy, there was a major component with a mass of 20,471 daltons, which is consistent with the predicted mass of 20,474 Da for rBPI(10-193)C132A), and two minor components with a mass of 20,668 daltons, which is consistent with addition of N-Acetylhexosamine (predicted mass 20,677 daltons) and a mass of 20,843 daltons, which is consistent with addition of N-Acetylhexosamine plus hexose (predicted mass 20,839 daltons). A similar component with added N-Acetylhexosamine is routinely observed during production of rBPI.sub.21.

On reverse phase HPLC (Shimadzu, Kyoto, Japan) both the rBPI(10-193)C132A and rBPI.sub.21 eluted as one major peak and one minor peak. However, the rBPI(10-193)C132A peaks eluted slightly earlier than the corresponding rBPI.sub.21 peaks in the control. The minor peak in the rBPI(10-193)C132A profile most likely represents the glycosylated forms identified in the mass spectrum. The ion-exchange HPLC profiles of rBPI(10-193)C132A and rBPI.sub.21 both exhibited single peaks with similar retention times.

Tryptic mapping analysis was performed according to conventional methods. Acetone precipitated rBPI.sub.21 or rBPI(10-193)C132A was first treated with dithiothreitol (DTT) followed by iodoaceamide and then with trypsin. The trypsin-treated product was analyzed by HPLC (Beckman Model 126) with a C18 column (Beckman Ultrasphere). In rBPI.sub.21, there are two N-terminal tryptic fragments (T1 and Ala-Ti) which result from imprecise cleavage of the leader sequence. As predicted, the tryptic map of the rBPI(10-193)C132A was similar to rBPI.sub.21 except that the N-terminal fragments were missing.

EXAMPLE 5

In Vitro LPS-Binding Activity of rBPI(10-193)C132A

The ability of purified rBPI(10-193)C132A produced according to Example 3A and rBPI.sub.21 to compete with labeled rBPI.sub.21 for binding to LPS was evaluated in a competition binding assay. Briefly, a fixed concentration (0.5 nM) of .sup.125 I-labeled rBPI.sub.21 was mixed with unlabeled rBPI.sub.21 or rBPI(10-193)C132A at dilutions ranging from 5 .mu.M to 0.01 nM in DMEM containing HEPES buffer and bovine serum albumin (BSA) [U.S. Biochemicals, Cleveland, Ohio] and 100 .mu.L of the mixture was added to Immulon-II plate wells pre-coated with 2.5 .mu.g/mL E. coli J5 LPS (Calbiochem, San Diego, Calif.). The plates were incubated at 4.degree. C. for 5 hours and washed 3 times with the DMEM medium. 75 .mu.L of 0.1 N NaOH was added and the bound .sup.125 I-rBPI.sub.21 was removed and counted. The results demonstrated that both proteins competed similarly with radiolabeled rBPI.sub.21.

EXAMPLE 6

In Vitro Bactericidal Activity of rBPI(10-193)C132A

All of the assays in this example were conducted with rBPI(10-193)C132A produced in the 2-liter fermenters according to Example 3A.

A. Effect on E. coli in a Radial Diffusion Assay

This radial diffusion assay compared the bactericidal effect of purified rBPI(10-193)C132A and rBPI.sub.1 on E. coli J5, which is a UDP-galactose-4-epimerase "rough" mutant of the smooth strain E. coli 011B4, and is relatively sensitive to rBPI.sub.21. E. coil J5 cells (Mannion et al., J. Clin. Invest., 85: 853-860 (1990); List Biological Laboratories, Campbell, Calif.) were grown to exponential phase, centrifuged and washed twice in 10 mM Na phosphate, pH 7.4, and added at a final concentration of approximately 1.times.10.sup.6 CFU/ml to molten agarose supplemented with 3% Trypticase Soy Broth (TSB, DIFCO Laboratories, Detroit, Mich.), 10 mM Na phosphate. Wells of 3 mm diameter were prepared in the hardened agarose and 5 .mu.L of serially diluted rBPI.sub.21 or rBPI(10-193)C132A was added to the wells. The plates were incubated at 37.degree. C. for 3 hours to allow diffusion to occur, and then a molten agarose overlay containing 6% TSB was added. The plates were incubated overnight at 37.degree. C. and the net area of inhibition was plotted vs. concentration. The results demonstrated that rBPI(10-193)C132A and rBPI.sub.21 behaved in a similar manner in this assay.

B. Effect on S. Aureus L-Form in a Radial Diffusion Assay

This radial diffusion assay compared the bactericidal effect of purified rBPI(10-193)C132A and rBPI.sub.21 on the gram-positive bacteria S. aureus grown as L-forms without their cell walls. As described in U.S. Pat. No. 5,578,572, incorporated herein by reference, S. aureus L-form cells were grown to log phase in heart infusion (HI) broth supplemented with 3.5% NaCl, 10 mM CaCl.sub.2 and 1000 U/mL penicillin G. The cells were diluted to approximately either 5.times.10.sup.4 or 5.times.10.sup.5 cells/mL in molten 0.8% agarose containing the NaCl-supplemented HI medium, and 8 ml of the cell-agarose suspension was poured into 10 cm plates. Wells of 3 mm diameter were prepared, and 5 .mu.L of serially diluted rBPI.sub.21 or rBPI(10-193)C132A was added to the wells. The plates were incubated at 37.degree. C. for 24 hours and the net area of inhibition was plotted vs. concentration. The results demonstrated that both rBPI.sub.21 and rBPI(10-193)C132A inhibited growth of the S. aureus L-forms, at cell densities of about 5.times.10.sup.4 and 5.times.10.sup.5, in a similar fashion in this assay.

C. Effect on E. coli J5 in a Broth Microdilution Assay

This broth microdilution assay compared the bactericidal effect of purified rBPI(10-193)C132A and rBPI.sub.21 on E. coli J5. E. coli J5 cells were grown overnight in tryptone yeast extract (TYE) broth and then to logarithmic phase in TEA medium as previously described in Horwitz et al., Infect. Immun., 63: 522-527 (1995). The cells were inoculated at approximately 1.times.10.sup.4 and 1.times.10.sup.5 cells/mL in heart infusion (HI) broth, and 95 .mu.L was added to 96 well plates. Five .mu.L of various dilutions of rBPI(10-193)C132A or rBPI.sub.21, prepared in formulation buffer, was added to each well and the plates were incubated at 37.degree. C. for 24 hours. The results demonstrated that rBPI(10-193)C132A and rBPI.sub.21 have similar activities in these assays.

EXAMPLE 7

In Vitro LPS Neutralization Activity of rBPI(10-193)C132A

The assay in section A of this example was conducted with rBPI(10-193)C132A produced in the 2-liter fermenters according to Example 3A, while the assay in section B of this example was conducted with rBPI(10-193)C132A produced in the 500-liter fermenter according to Example 3B.

A. Activity in a RAW Cell Proliferation Assay

The RAW cell proliferation assay was used to compare the in vitro LPS neutralization activity of rBPI.sub.21 and rBPI(10-193)C132A. In this assay, the LPS inhibits the proliferation of RAW cells, and rBPI.sub.21 neutralizes this effect of LPS.

Mouse RAW 264.7 cells (ATCC Accession No. T1B71), maintained in RPMI 1640 medium (GIBCO), supplemented with 10 mM HEPES buffer (pH 7.4), 2 mM L-glutamine, penicillin (100 U/mL), streptomycin (100 .mu.g/mL), 0.075% sodium bicarbonate, 0.15M 2-mercaptoethanol and 10% fetal bovine serum (Hyclone, Inc., Logan, Utah), were first induced by incubation in the presence of 50 U/mL recombinant mouse y-interferon (Genzyme, Cambridge, Mass.) for 24 hours prior to assay. Induced cells were then mechanically collected and centrifuged at 500.times.g at 4.degree. C. and then resuspended in 50 mL RPMI 1640 medium (without supplements), re-centrifuged and again resuspended in RPMI 1640 medium (without supplements). The cells were counted, their concentration adjusted to 2.times.10.sup.5 cells/mL and 100 .mu.L aliquots were added to each well of a 96-well plate.

The cells were then incubated for about 15 hours with E. coli O113 LPS (Control Standard, Assoc. of Cape Code, Woods Hole, Mass.), which was added in 100 .mu.L/well aliquots at a concentration of 1 ng/mL in serum-free RPMI 1640 medium (this concentration being the result of titration experiments in which LPS concentration was varied between 50 pg/mL and 100 ng/mL). This incubation was performed in the absence or presence of rBPI.sub.21 or rBPI(10-193)C132A in varying concentrations between 25 ng/mL and 50 .mu.g/mL. Recombinant human rBPI.sub.21, also designated rBPI.sub.21 .DELTA.cys, which is rBPI 1-193 with alanine substituted at position 132 for cysteine [see co-owned U.S. Pat. No. 5,420,019], was used as a positive control at a concentration of 1 .mu.g/mL. Cell proliferation was quantitatively measured by the addition of 1 .mu.Ci/well [.sup.3 H]-thymidine 5 hours after the time of initiation of the assay. After the 15-hour incubation, labeled cells were harvested onto glass fiber filters with a cell harvester (Inotech Biosystems, INB-384, Sample Processing and Filter Counting System, Lansing, Mich.). The LPS-mediated inhibition of RAW 264.7 cell proliferation is dependent on the presence of LBP, as added to the reaction mixture either as a component of serum or as recombinant LBP (at a concentration of 1 .mu.g/mL.

In these experiments, both rBPI.sub.21 and rBPI(10-193)C132A similarly inhibited the LPS-mediated inhibition of RAW cell proliferation.

B. Activity in a TNF Inhibition Assay

A tumor necrosis factor (TNF) inhibition assay was used to compare the in vitro LPS neutralization activity of rBPI.sub.21 and the rBPI(10-193)C132A. In this assay, the IPS, in combination with purified LBP (or serum containing LBP) stimulates synthesis of TNF by THP-1 cells (a human monocyte cell line), and rBPI.sub.21 neutralizes this effect of LPS.

THP.1 cells (ATCC Accession No. TIB-202) were maintained in RPMI (GibcoBRL, Gaithersburg, Md.) with 10% FBS and were cultured in RPMI with 10% FBS plus 50 ng/ml 1,25 dihydroxy vitamin D (BIOMOL Research Laboratories Inc. Plymouth Meeting, Pa.) for three days prior to treatment with LPS to induce CD14 expression. Before inducing with LPS, cells were washed three times with RPMI and suspended in either RPMI with 10% FBS or in serum free medium [RPMI supplemented with 1% HB101 (Irvine Scientific, Santa Ana, Calif.)]. Expression of TNF was induced with 1 ng/ml E. coli 0128 LPS (Sigma, St. Louis, Mo.) in 96 well plates with approximately 5.times.10.sup.4 cells per well. Plates were incubated for three hours at 37.degree. C., 5% CO.sub.2, then an aliquot of the supernatant liquid was removed and assayed for TNF by the WEHI 164 toxicity assay, using CellTiter 96.TM. AQ (Promega Corp., Madison, Wis.) to monitor cell viability. Recombinant human TNF.alpha. (Genzyme Diagnostics, Cambridge, Mass.) was used as a positive standard. Both rBPI.sub.21 and rBPI(10-193)C132A similarly inhibited LPS-induced stimulation of TNF synthesis.

EXAMPLE 8

In Vivo Biological Activity of rBPI(10-193)C132A

The in Vivo assays described below were performed using the purified rBPI(10-193)C132A produced in the 500-liter fermenter according to Example 3B.

A. Toxicity Study in Rats

Toxicity profiles of rBPI.sub.21 and rBPI(10-193)C132A were compared in rats. In this study, groups of six male and six female Sprague-Dawley rats received either vehicle control (formulation buffer), low (50 mg/kg/day) or high (120 mg/kg/day) doses of either rBPI.sub.21 or rBPI(10-193)C132A. Doses were administered by continuous intravenous infusion via an indwelling femoral catheter for three consecutive days at an infusion rate of 4.2 mL/kg/hour (100 ml/kg/day). Clinical observations were recorded at least twice daily and body weights were recorded daily. Blood and urine samples were collected near termination for hematology, clinical chemistry and urinalysis assessments. At termination, organs were weighed and tissues collected by histopathological examination. There were no deaths or significant test article-related effects. The data indicated similar toxicity profiles for rBPI.sub.21 and the rBPI(10-193)C132A when given by continuous infusion.

B. Pharmacokinetics

The pharmacokinetics of rBPI.sub.21 and rBPI(10-193)C132A at 2 mg/kg were investigated in rats. The plasma clearances of rBPI.sub.21 and rBPI(10-193)C132A were well described by a tri-exponential pharmacokinetic disposition function. No statistical differences in the pharmacokinetic parameters among the rBPI products were determined (non parametric Wicoxon rank test, p<0.05). Most of the administered drug (>96%) was cleared with an alpha phase half-life of 0.2-0.4 minutes and a beta half-life of 3.9-4.3 minutes, while the remainder was cleared during the gamma phase with a half-life of 27-33 minutes. The volume of distribution of the central compartment (Vc) was 41-45 ml/kg, and the clearance rate (CL) was 24-30 mL/min/kg. The steady state volume of distribution was 152-184 ml/kg.

C. Efficacy In Mouse Endotoxin Challenge

Two separate studies were conducted to examine relative potencies of rBPI.sub.21 and rBPI(10-193)C132A in a mouse model of lethal endotoxemia generally according to Ammons et al., in "Novel Therapeutic Strategies in the Treatment of Sepsis," Morrison and Ryan, eds., Marcel Dekker, New York (1996), pages 55-69. In both studies, there were 14 mice in each treatment and control group. In the first study, CD1 mice were challenged intravenously with 25 mg/kg of lipopolysaccharide (LPS) from E. coli O111:B4. Immediately after the challenge, the mice were treated intravenously with rBPI.sub.21 or rBPI(10-193)C132A at doses of 15, 20, 25 and 30 mg/kg, or with the control vehicle (formulation buffer only). Mortality was recorded twice daily for seven days.

The results from the first study, shown in Table 1 below, indicate that treatment with both rBPI(10-193)C132A and rBPI.sub.21 significantly increased survival compared to the vehicle controls. In addition, rBPI(10-193)C132A was at least two-fold more potent than rBPI.sub.21 with a similar survival benefit seen with a two-fold lower dose of rBPI(10-193)C132A compared to rBPI.sub.21.

TABLE 1______________________________________ No. of Survivors out of 15 rBPI(10-Dose (mg/kg) Control rBPI.sub.21 193)C132A______________________________________0(Vehicle) 0 NA.sup.1 NA15 0 15**.##20 4 15**,#25 11** 15**30 13** 13**______________________________________ .sup.1 NA, Not Applicable **,p < 0.01 vs. control #,p < 0.05 vs. rBPI.sub.21 ##,p < 0.01 vs. control

In the second study, a wider range of rBPI(10-193)C132A doses (5, 10, 15, 20, 25, 30 mg/kg) was studied. The results, shown in Table 2 below, confirm that while both rBPI.sub.21 and rBPI(10-193)C132A offered a significant survival benefit over the control, as in the first study, rBPI(10-193)C132A was at least two-fold more potent, achieving similar efficacy as rBPI.sub.21 with a 2-fold lower dose.

TABLE 2______________________________________ No. of Survivors out of 15 rBPI(10-Dose (mg/kg) Control rBPI.sub.21 193)C132A______________________________________0(Vehicle) 2 NA.sup.1 NA5 ND.sup.1 310 ND 10*15 ND 14**20 7 14**,#25 13** 15**30 14** 15*______________________________________ .sup.1 NA, Not Applicable; ND, Not Done **, p < 0.05 vs. control **, p < 0.01 vs. control #, p < 0.05 vs. rBPI.sub.21 D. Efficacy in Murine Model of Lethal Bacteremia

Two separate studies were conducted to examine the relative potencies or rBPI.sub.21 and rBPI(10-193)C132A in a mouse model of lethal bacteremia. In both studies, there were 20 mice per treatment group. In the first study, CD1 mice were challenged with 6.8.times.10.sup.7 colony forming units (CFU) of E. coli 07:K1 administered intravenously. Immediately after the challenge, the mice were treated intravenously with rBPI.sub.21 or rBPI(10-193)C132A at doses of 10, 20 and 30 mg/kg, or with control vehicle (formulation buffer only). Mortality was recorded twice daily for seven days.

The results from the first study, shown in Table 3 below, demonstrate a significant increase in survival for the groups treated with 10 and 30 mg/kg of rBPI.sub.21 (p<0.05 vs. control). While a similar significant increase in survival was not observed with the rBPI(10-193)C132A vs. control, there was not a significant difference in survival advantage between the rBPI.sub.21 and rBPI(10-193)C132A treated groups in this study.

TABLE 3______________________________________ No. of Survivors out of 20 rBPI(10-Dose (mg/kg) Control rBPI.sub.21 193)C132A______________________________________0(Vehicle) 6 NA10 14* 1220 12 1030 14* 10______________________________________ *,p < 0.05 vs. control

To more fully characterize the effects of rBPI.sub.21 and rBPI(10-193)C132A in this model, a second study was conducted in which a wider range of doses was studied. In this study, CD1 mice were challenged with 2.57.times.10.sup.8 colony forming units (CFU) of E. coli 07:K1 administered intravenously. Immediately after the challenge, the mice were treated intravenously with 1.0, 3.0, 10 and 30 mg/kg rBPI.sub.21 and 0.3, 1.0, 3.0, 10 and 30 mg/kg rBPI(10-193)C132A. The results, shown in Table 4 below, indicate that both proteins provided protection, and that there was no significant difference in the protective effects of the two variants at any dose.

TABLE 4______________________________________ No. of Survivors out of 20 rBPI(10-Dose (mg/kg) Control rBPI.sub.21 193)C132A______________________________________0(Vehicle) 60.3 ND.sup.1 61.0 4 63.0 9 10*10 13** 830 11* 14**______________________________________ .sup.1 ND, Not Done *, p < 0.05 vs. control **, p < 0.01 vs. control E. Cardiovascular Effects in Conscious Rats

A series of experiments were conducted to determine the relative effects of rBPI.sub.21 and rBPI(10-193)C132A on blood pressure in rats. Each rat was anesthetized with a mixture of ketamine (Fort Dodge Labs, Fort Dodge, Iowa) and Rompum (Bayer Corp., Shawnee Mission, Kans.). A catheter was then placed in the right carotid artery and connected to a pressure transducer to record blood pressure. A second catheter was placed in the right jugular vein to inject rBPI or vehicle. The rats were then allowed to recover before the experiments began. Experiments were initiated when the rats were alert, mobile and when blood pressure was stable within the normal range. rBPI.sub.21, rBPI(10-193)C132A or control vehicle (formulation buffer) were then injected as a bolus over 15 seconds and mean arterial blood pressure (mm Hg) was recorded over the next 60 minutes.

In preliminary experiments, it was determined that doses of 20 and 30 mg/kg of rBPI.sub.21 had no significant effect on blood pressure relative to the vehicle but that a dose of 40 mg/kg resulted in a significant decrease in blood pressure that was evident within 5 minutes. This hypotensive response was greatest 15 minutes after the injection when blood pressure had decreased by 48.+-.12 mm Hg (mean .+-.SE; p>0.05). After 60 minutes, the blood pressure of the rBPI.sub.21 -treated animals recovered and was not significantly different from that of the vehicle-treated animals.

To compare effects of rBPI.sub.21 and rBPI(10-193)C132A, groups of 5 rats were given 40 mg/kg of each drug substance or vehicle control, and blood pressure responses were analyzed as area under the curve (AUC). FIG. 1 shows that, as previously observed, rBPI.sub.21 caused a significant drop in blood pressure indicated by the elevated AUC relative to the vehicle control. By comparison, rBPI(10-193)C132A had no significant effect on blood pressure compared with the vehicle control. A dose of 50 mg/kg rBPI.sub.21 (N=4 rats) had an even greater hypotensive effect than that of the 40 mg/kg dose as indicated by a further increase in the AUC in FIG. 1. At this higher dose, some reduction in blood pressure also occurred in rats administered rBPI(10-193)C132A (N=3), but this effect was not significant compared to the vehicle control.

Numerous modifications and variations of the above-described invention are expected to occur to those of skill in the art. Accordingly, only such limitations as appear in the appended claims should be placed thereon.

__________________________________________________________________________# SEQUENCE LISTING- <160> NUMBER OF SEQ ID NOS: 7- <210> SEQ ID NO 1<211> LENGTH: 1813<212> TYPE: DNA<213> ORGANISM: Homo sapiens<220> FEATURE:<221> NAME/KEY: CDS<222> LOCATION: (31)..(1491)<220> FEATURE:<221> NAME/KEY: mat.sub.-- peptide<222> LOCATION: (124)..(1491)<220> FEATURE:<223> OTHER INFORMATION: rBPI- <400> SEQUENCE: 1- caggccttga ggttttggca gctctggagg atg aga gag aac at - #g gcc agg ggc 54#Glu Asn Met Ala Arg Gly25- cct tgc aac gcg ccg aga tgg gtg tcc ctg at - #g gtg ctc gtc gcc ata 102Pro Cys Asn Ala Pro Arg Trp Val Ser Leu Me - #t Val Leu Val Ala Ile10- ggc acc gcc gtg aca gcg gcc gtc aac cct gg - #c gtc gtg gtc agg atc 150Gly Thr Ala Val Thr Ala Ala Val Asn Pro Gl - #y Val Val Val Arg Ile# 5- tcc cag aag ggc ctg gac tac gcc agc cag ca - #g ggg acg gcc gct ctg 198Ser Gln Lys Gly Leu Asp Tyr Ala Ser Gln Gl - #n Gly Thr Ala Ala Leu# 25- cag aag gag ctg aag agg atc aag att cct ga - #c tac tca gac agc ttt 246Gln Lys Glu Leu Lys Arg Ile Lys Ile Pro As - #p Tyr Ser Asp Ser Phe# 40- aag atc aag cat ctt ggg aag ggg cat tat ag - #c ttc tac agc atg gac 294Lys Ile Lys His Leu Gly Lys Gly His Tyr Se - #r Phe Tyr Ser Met Asp# 55- atc cgt gaa ttc cag ctt ccc agt tcc cag at - #a agc atg gtg ccc aat 342Ile Arg Glu Phe Gln Leu Pro Ser Ser Gln Il - #e Ser Met Val Pro Asn# 70- gtg ggc ctt aag ttc tcc atc agc aac gcc aa - #t atc aag atc agc ggg 390Val Gly Leu Lys Phe Ser Ile Ser Asn Ala As - #n Ile Lys Ile Ser Gly# 85- aaa tgg aag gca caa aag aga ttc tta aaa at - #g agc ggc aat ttt gac 438Lys Trp Lys Ala Gln Lys Arg Phe Leu Lys Me - #t Ser Gly Asn Phe Asp#105- ctg agc ata gaa ggc atg tcc att tcg gct ga - #t ctg aag ctg ggc agt 486Leu Ser Ile Glu Gly Met Ser Ile Ser Ala As - #p Leu Lys Leu Gly Ser# 120- aac ccc acg tca ggc aag ccc acc atc acc tg - #c tcc agc tgc agc agc 534Asn Pro Thr Ser Gly Lys Pro Thr Ile Thr Cy - #s Ser Ser Cys Ser Ser# 135- cac atc aac agt gtc cac gtg cac atc tca aa - #g agc aaa gtc ggg tgg 582His Ile Asn Ser Val His Val His Ile Ser Ly - #s Ser Lys Val Gly Trp# 150- ctg atc caa ctc ttc cac aaa aaa att gag tc - #t gcg ctt cga aac aag 630Leu Ile Gln Leu Phe His Lys Lys Ile Glu Se - #r Ala Leu Arg Asn Lys# 165- atg aac agc cag gtc tgc gag aaa gtg acc aa - #t tct gta tcc tcc aag 678Met Asn Ser Gln Val Cys Glu Lys Val Thr As - #n Ser Val Ser Ser Lys170 1 - #75 1 - #80 1 -#85- ctg caa cct tat ttc cag act ctg cca gta at - #g acc aaa ata gat tct 726Leu Gln Pro Tyr Phe Gln Thr Leu Pro Val Me - #t Thr Lys Ile Asp Ser# 200- gtg gct gga atc aac tat ggt ctg gtg gca cc - #t cca gca acc acg gct 774Val Ala Gly Ile Asn Tyr Gly Leu Val Ala Pr - #o Pro Ala Thr Thr Ala# 215- gag acc ctg gat gta cag atg aag ggg gag tt - #t tac agt gag aac cac 822Glu Thr Leu Asp Val Gln Met Lys Gly Glu Ph - #e Tyr Ser Glu Asn His# 230- cac aat cca cct ccc ttt gct cca cca gtg at - #g gag ttt ccc gct gcc 870His Asn Pro Pro Pro Phe Ala Pro Pro Val Me - #t Glu Phe Pro Ala Ala# 245- cat gac cgc atg gta tac ctg ggc ctc tca ga - #c tac ttc ttc aac aca 918His Asp Arg Met Val Tyr Leu Gly Leu Ser As - #p Tyr Phe Phe Asn Thr250 2 - #55 2 - #60 2 -#65- gcc ggg ctt gta tac caa gag gct ggg gtc tt - #g aag atg acc ctt aga 966Ala Gly Leu Val Tyr Gln Glu Ala Gly Val Le - #u Lys Met Thr Leu Arg# 280- gat gac atg att cca aag gag tcc aaa ttt cg - #a ctg aca acc aag ttc1014Asp Asp Met Ile Pro Lys Glu Ser Lys Phe Ar - #g Leu Thr Thr Lys Phe# 295- ttt gga acc ttc cta cct gag gtg gcc aag aa - #g ttt ccc aac atg aag1062Phe Gly Thr Phe Leu Pro Glu Val Ala Lys Ly - #s Phe Pro Asn Met Lys# 310- ata cag atc cat gtc tca gcc tcc acc ccg cc - #a cac ctg tct gtg cag1110Ile Gln Ile His Val Ser Ala Ser Thr Pro Pr - #o His Leu Ser Val Gln# 325- ccc acc ggc ctt acc ttc tac cct gcc gtg ga - #t gtc cag gcc ttt gcc1158Pro Thr Gly Leu Thr Phe Tyr Pro Ala Val As - #p Val Gln Ala Phe Ala330 3 - #35 3 - #40 3 -#45- gtc ctc ccc aac tcc tcc ctg gct tcc ctc tt - #c ctg att ggc atg cac1206Val Leu Pro Asn Ser Ser Leu Ala Ser Leu Ph - #e Leu Ile Gly Met His# 360- aca act ggt tcc atg gag gtc agc gcc gag tc - #c aac agg ctt gtt gga1254Thr Thr Gly Ser Met Glu Val Ser Ala Glu Se - #r Asn Arg Leu Val Gly# 375- gag ctc aag ctg gat agg ctg ctc ctg gaa ct - #g aag cac tca aat att1302Glu Leu Lys Leu Asp Arg Leu Leu Leu Glu Le - #u Lys His Ser Asn Ile# 390- ggc ccc ttc ccg gtt gaa ttg ctg cag gat at - #c atg aac tac att gta1350Gly Pro Phe Pro Val Glu Leu Leu Gln Asp Il - #e Met Asn Tyr Ile Val# 405- ccc att ctt gtg ctg ccc agg gtt aac gag aa - #a cta cag aaa ggc ttc1398Pro Ile Leu Val Leu Pro Arg Val Asn Glu Ly - #s Leu Gln Lys Gly Phe410 4 - #15 4 - #20 4 -#25- cct ctc ccg acg ccg gcc aga gtc cag ctc ta - #c aac gta gtg ctt cag1446Pro Leu Pro Thr Pro Ala Arg Val Gln Leu Ty - #r Asn Val Val Leu Gln# 440- cct cac cag aac ttc ctg ctg ttc ggt gca ga - #c gtt gtc tat aaa1491Pro His Gln Asn Phe Leu Leu Phe Gly Ala As - #p Val Val Tyr Lys# 455- tgaaggcacc aggggtgccg ggggctgtca gccgcacctg ttcctgatgg gc - #tgtggggc1551- accggctgcc tttccccagg gaatcctctc cagatcttaa ccaagagccc ct - #tgcaaact1611- tcttcgactc agattcagaa atgatctaaa cacgaggaaa cattattcat tg - #gaaaagtg1671- catggtgtgt attttaggga ttatgagctt ctttcaaggg ctaaggctgc ag - #agatattt1731- cctccaggaa tcgtgtttca attgtaacca agaaatttcc atttgtgctt ca - #tgaaaaaa1791# 1813atg tg- <210> SEQ ID NO 2<211> LENGTH: 487<212> TYPE: PRT<213> ORGANISM: Homo sapiens- <400> SEQUENCE: 2- Met Arg Glu Asn Met Ala Arg Gly Pro Cys As - #n Ala Pro Arg Trp Val20- Ser Leu Met Val Leu Val Ala Ile Gly Thr Al - #a Val Thr Ala Ala Val#1- Asn Pro Gly Val Val Val Arg Ile Ser Gln Ly - #s Gly Leu Asp Tyr Ala# 15- Ser Gln Gln Gly Thr Ala Ala Leu Gln Lys Gl - #u Leu Lys Arg Ile Lys# 30- Ile Pro Asp Tyr Ser Asp Ser Phe Lys Ile Ly - #s His Leu Gly Lys Gly# 45- His Tyr Ser Phe Tyr Ser Met Asp Ile Arg Gl - #u Phe Gln Leu Pro Ser# 65- Ser Gln Ile Ser Met Val Pro Asn Val Gly Le - #u Lys Phe Ser Ile Ser# 80- Asn Ala Asn Ile Lys Ile Ser Gly Lys Trp Ly - #s Ala Gln Lys Arg Phe# 95- Leu Lys Met Ser Gly Asn Phe Asp Leu Ser Il - #e Glu Gly Met Ser Ile# 110- Ser Ala Asp Leu Lys Leu Gly Ser Asn Pro Th - #r Ser Gly Lys Pro Thr# 125- Ile Thr Cys Ser Ser Cys Ser Ser His Ile As - #n Ser Val His Val His130 1 - #35 1 - #40 1 -#45- Ile Ser Lys Ser Lys Val Gly Trp Leu Ile Gl - #n Leu Phe His Lys Lys# 160- Ile Glu Ser Ala Leu Arg Asn Lys Met Asn Se - #r Gln Val Cys Glu Lys# 175- Val Thr Asn Ser Val Ser Ser Lys Leu Gln Pr - #o Tyr Phe Gln Thr Leu# 190- Pro Val Met Thr Lys Ile Asp Ser Val Ala Gl - #y Ile Asn Tyr Gly Leu# 205- Val Ala Pro Pro Ala Thr Thr Ala Glu Thr Le - #u Asp Val Gln Met Lys210 2 - #15 2 - #20 2 -#25- Gly Glu Phe Tyr Ser Glu Asn His His Asn Pr - #o Pro Pro Phe Ala Pro# 240- Pro Val Met Glu Phe Pro Ala Ala His Asp Ar - #g Met Val Tyr Leu Gly# 255- Leu Ser Asp Tyr Phe Phe Asn Thr Ala Gly Le - #u Val Tyr Gln Glu Ala# 270- Gly Val Leu Lys Met Thr Leu Arg Asp Asp Me - #t Ile Pro Lys Glu Ser# 285- Lys Phe Arg Leu Thr Thr Lys Phe Phe Gly Th - #r Phe Leu Pro Glu Val290 2 - #95 3 - #00 3 -#05- Ala Lys Lys Phe Pro Asn Met Lys Ile Gln Il - #e His Val Ser Ala Ser# 320- Thr Pro Pro His Leu Ser Val Gln Pro Thr Gl - #y Leu Thr Phe Tyr Pro# 335- Ala Val Asp Val Gln Ala Phe Ala Val Leu Pr - #o Asn Ser Ser Leu Ala# 350- Ser Leu Phe Leu Ile Gly Met His Thr Thr Gl - #y Ser Met Glu Val Ser# 365- Ala Glu Ser Asn Arg Leu Val Gly Glu Leu Ly - #s Leu Asp Arg Leu Leu370 3 - #75 3 - #80 3 -#85- Leu Glu Leu Lys His Ser Asn Ile Gly Pro Ph - #e Pro Val Glu Leu Leu# 400- Gln Asp Ile Met Asn Tyr Ile Val Pro Ile Le - #u Val Leu Pro Arg Val# 415- Asn Glu Lys Leu Gln Lys Gly Phe Pro Leu Pr - #o Thr Pro Ala Arg Val# 430- Gln Leu Tyr Asn Val Val Leu Gln Pro His Gl - #n Asn Phe Leu Leu Phe# 445- Gly Ala Asp Val Val Tyr Lys450 4 - #55- <210> SEQ ID NO 3<211> LENGTH: 21<212> TYPE: DNA<213> ORGANISM: Artificial Sequence<220> FEATURE:#Sequence: primerMATION: Description of Artificial- <400> SEQUENCE: 3#21 tgca g- <210> SEQ ID NO 4<211> LENGTH: 33<212> TYPE: DNA<213> ORGANISM: Artificial Sequence<220> FEATURE:#Sequence: primerMATION: Description of Artificial- <400> SEQUENCE: 4# 33 ggcc gctgtcacgg cgg- <210> SEQ ID NO 5<211> LENGTH: 33<212> TYPE: DNA<213> ORGANISM: Artificial Sequence<220> FEATURE:#Sequence: primerMATION: Description of Artificial- <400> SEQUENCE: 5# 33 ccca gaagggcctg gac- <210> SEQ ID NO 6<211> LENGTH: 18<212> TYPE: DNA<213> ORGANISM: Artificial Sequence<220> FEATURE:#Sequence: primerMATION: Description of Artificial- <400> SEQUENCE: 6# 18 tg- <210> SEQ ID NO 7<211> LENGTH: 20<212> TYPE: PRT<213> ORGANISM: Artificial Sequence<220> FEATURE:#Sequence: N-terminalON: Description of Artificial sequence- <400> SEQUENCE: 7- Ser Gln Lys Gly Leu Asp Tyr Ala Ser Gln Gl - #n Gly Thr Ala Ala Leu# 15- Gln Lys Glu Leu 20__________________________________________________________________________

Claims

1. A bactericidal/permeability-increasing protein (BPI) deletion analog consisting of amino acid residues 10 through 193 of mature human BPI (SEQ ID NO:2), wherein a cysteine residue at position 132 is replaced by a different amino acid and wherein the amino acid at position number 185 is selected from the group consisting of lysine and glutamic acid.

2. The BPI deletion analog of claim 1 wherein the amino acid replacing said cysteine residue is a non-polar amino acid selected from the group consisting of alanine and serine.

3. The BPI deletion analog of claim 1 wherein the cysteine residue at position 132 is replaced by alanine.

4. The polypeptide product of a method comprising

(a) growing a host cell stably transformed or transfected with DNA encoding the BPI deletion analog of claim 1 or 3 in a suitable culture medium, and

(b) isolating said BPI deletion analog from said host cell or said culture medium.

5. A composition comprising the BPI deletion analog of claim 1 and a pharmaceutically-acceptable diluent, adjuvant, or carrier.

6. A composition comprising the BPI deletion analog of claim 3 and a pharmaceutically-acceptable diluent, adjuvant, or carrier.

7. A composition comprising the BPI deletion analog of claim 4 and a pharmaceutically-acceptable diluent, adjuvant, or carrier.