Therapeutic uses of biologically active bactericidal/permeability-increasing protein fragments

Abstract

Therapeutic methods using a purified isolated human bactericidal/permeability-increasing protein and biologically-active fragments thereof is provided.

Description

BACKGROUND OF THE INVENTION

The present invention pertains to biologically active, polypeptide fragments of mammalian bactericidal/permeability-increasing proteins and methods for making and using said fragments.

Bactericidal/permeability-increasing protein (BPI) is a 50 to 60 Kd protein, isolated from the granules of mammalian polymorphonuclear leukocytes (PMN) which are blood cells that are essential in the defense against invading microorganisms in mammals. BPI occurs only in cells of the myeloid series of blood cells, is produced at the promyelocytic/myelocytic stage of differentiation and is located in the primary granules in these cells.

BPI is a potent bactericidal agent active against a broad range of gram-negative bacterial species. It exhibits a high degree of specificity in its cytotoxic effect, i.e. 10-40 nM (0.5-2.0 micrograms), producing greater than 90% killing of 10.sup.7 sensitive bacteria whereas 100-fold higher concentrations of BPI are non-toxic for other microorganisms and eukaryotic cells. All available evidence suggests that in the intact PMN and in crude leukocyte fractions, BPI is the principal oxygen-independent agent present which is active against BPI-sensitive bacteria.

BPI isolated from both human and rabbit PMN has been purified to homogeneity. The molecular weight of human BPI is approximately 58,000 Daltons (58 kDa) and that of rabbit BPI is approximately 50 kDa. The amino acid composition of these two proteins is closely similar as is the amino acid sequence of their first 15 NH.sub.2 -terminal amino acid residues. Both proteins are highly basic, having an isoelectric point greater than 9.6.

The biological effects of BPI require attachment of the protein to the surface of the susceptible gram-negative bacteria. Initial binding of BPI to target cells involves electrostatic interactions between the basic protein and the negatively charged sites on the lipopolysaccharides (LPS) on the bacterial outer membrane and leads to an activation of bacterial enzymes that degrade phospholipids and peptidoglycans. The final stage of action is the actual killing of the bacteria by an as yet unknown mechanism. The closely similar amino acid composition and nearly identical bactericidal and membrane-perturbing properties of BPI purified from human and rabbit PMN suggest that this protein has been highly conserved during evolution and is an important member of the anti-bacterial arsenal of the mammalian PMN.

Due to its potent bactericidal action against gram-negative bacteria and lack of cytotoxicity towards other microorganisms and eukaryotic cells, it is envisioned that BPI may be employed as a chemotherapeutic agent and/or as a model for the design of new antibiotic agents. However, due to its large molecular weight (58 kDa for the human holoprotein), both sequencing and determination of the structural organization of BPI have been hampered (hereinafter the entire BPI molecule is referred to as the holoprotein). The possibility has been raised that, as in the case with other cytotoxic proteins, BPI has a structural organization where the different functions, namely binding, envelope-altering and killing reside in different domains within the BPI molecule. Although BPI fragments, obtained by digestion of the holoproteins with the proteolytic enzyme elastase, has been disclosed (Weiss, J. et al., Clin. Res 34: 537A, 1986), the fragments tested remained associated under the non-denaturing conditions employed. No biological activity was ascribed to any isolated fragments. Moreover, antibodies directed against the holoprotein did not recognize these fragments under denaturing conditions when analyzed using the well-known Western blotting procedure.

Therefore, in light of the above, there is a need in the art for biologically active peptide fragments of BPI for use as bactericidal/permeability increasing agents as well as therapeutic agents. Such fragments are also needed to provide sequence information on BPI to direct the design of future generations of antimicrobial agents specific for gram-negative bacteria and to be used as probes into the molecular organization of the holoproteins.

OBJECTS OF THE INVENTION

It is an object of the present invention to provide biologically active peptide fragments of mammalian BPI.

Another object of the present invention is to provide biologically active peptide fragments of mammalian BPI with improved antimicrobial effectiveness.

Yet another object of the present invention is to provide a process for the production of biologically active peptide fragments of mammalian BPI.

Yet another object of the present invention is to provide methods for treating mammals suffering from infections caused by gram-negative bacteria.

A further object of the present invention is to provide a method for increasing the permeability of gram-negative bacteria.

A still further object of the present invention is to increase the effectiveness of gram-negative bactericidal agents.

These and other objects of the present invention will be apparent to those of ordinary skill in the art in light of the present description, accompanying claims and appended drawings.

SUMMARY OF THE INVENTION

The present inventors have unexpectedly discovered biologically active fragments of mammalian BPI substantially shorter in length than the native BPI protein. Although these fragments are substantially smaller than the native molecule, they retain at least substantially all of the bactericidal and permeability-increasing properties of the intact protein.

The biologically active BPI fragments of the present invention can be produced by incubating a sample comprising the BPI holoprotein under BPI cleaving conditions and recovering biologically active fragments of the BPI holoprotein. The preferred BPI cleaving conditions include heating of the BPI holoprotein in an acceptable buffer for a time ranging between about 16 and 24 hours at a temperature between about 20.degree. C. and about 37.degree. C.

In another aspect, the present invention provides a method for treating mammals suffering from infections caused by gram-negative bacteria comprising administering to mammals in need of such treatment a gram-negative bactericidal-effective amount of at least one of the above-mentioned biologically active BPI fragments.

In another aspect, the present invention provides pharmaceutical formulations for treating infections in mammals caused by gram negative bacteria comprising a gram-negative bactericidal-effective amount of at least one of the biologically active BPI fragments or pharmaceutically-acceptable salts thereof.

In yet another aspect, the present invention provides a method for increasing the permeability of gram-negative bacteria comprising incubating the bacteria with a gram-negative-bacterial-permeability-increasing-effective amount of a biologically active fragment of BPI.

In still another aspect, the present invention provides a method for increasing the effectiveness of gram-negative bactericidal agents in mammals in need of such treatments, comprising co-administration of such agents with the biologically active fragments of BPI.

A still further aspect of the present invention is directed to a purified, isolated DNA sequence having the sequence set out in FIG. 5 or its complementary strand and DNA sequences hybridizing under stringent hybridization conditions with said DNA sequences. The DNA sequence encodes the human bactericidal/permeability-increasing protein.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a photograph of a stained SDS-PAGE gel showing the production and purification of the human BPI fragment of a preferred embodiment of the present invention.

FIGS. 2A and B is a graph showing the chromatographic behavior of the human BPI holoprotein (a) and human 25 kDa BPI fragment of the present invention (b) on reverse phase HPLC.

FIGS. 3A-C is a series of graphs comparing the biological activities of the 25 kDa human BPI fragment (SEQ. ID. NO.3) of the present invention and the holoprotein toward E. coli J5. (A) bactericidal activity; (B) effect on bacterial protein synthesis; (C) permeability increasing activity; and (D) phospholipase activation.

FIG. 4 is a graph comparing the bactericidal effect of the 25 kDa human BPI fragment of the present invention and the holoprotein on, E.coli 0111:B4.

FIG. 5 is an index Figure which shows the interrelationship of the sequence shown in the FIG. 5 (A-D).

FIGS. 5(A-D), bottom line, shows the sequence (SEQ. ID. NO.1) of the cDNA encoding human BPI whereas printed above is the corresponding amino acid sequence (SEQ. ID. NO.1). The two potential glycosylation sites are overlined.

FIG. 6 is a photograph of an autoradiogram of a Northern blot analysis of human BPI mRNA.

FIG. 7 is a photograph of an autoradiogram of a Southern blot analysis of human genomic DNA using a BPI cDNA probe.

FIGS. 8A and B are graphs showing (A) the survival of K1-encapsulated and J5 E. coli in whole blood as a function of inoculum size; and (B) TNF production response to isolated endotoxin and whole bacteria containing comparable amounts of LPS.

FIGS. 9A-D is a series of graphs showing (A, B, and C), the dose effect of BPI on survival of increasing numbers of K1-E. coli as a function of time; and (D) the dose dependent inhibition by BPI of TNF-response as a function of bacterial inoculum size.

FIGS. 10A and B are graphs depicting (A) the antibacterial activities of Holo-BPI in whole blood; and (B) the TNF-inhibitory activity in whole blood of Holo-BPI and its N-terminal fragments.

FIGS. 11A and B contains two graphs showing the synergistic bactericidal action of BPI and complement against serum-resistant K1-encapsulated E. coli.

FIG. 12 is a series of graphs showing the inhibition of LPS-induced cytokine production in whole human blood mediated by a recombinant BPI N-terminal fragment.

FIG. 13 is a graph showing the protection of mice against the lethal effects of LPS produced by a recombinant BPI N-terminal fragment.

DETAILED DESCRIPTION OF THE INVENTION

The present inventors have unexpectedly discovered biologically active fragments of BPI isolated from mammalian PMN. NH.sub.2 -terminal amino acid sequence analysis demonstrated that, in the case of human BPI, the fragment represents a portion of the BPI molecule proximal to the NH.sub.2 -terminus, as shown in Example 3 below. The fragment possesses all of the antibacterial and membrane permeability-increasing functions contained in the complete molecule but is substantially smaller (i.e. has a lower molecular weight) than the holoprotein. "Substantially smaller" is defined herein as being up to about half the size of the holoprotein. This is a most surprising finding because, in the case of other cellular toxins and proteins, the entire molecule is necessary for the full manifestation of their biological effects. For example, studies on a wide variety of bacterial and plant cytotoxins, such as diphtheria toxin, cholera toxin and ricin (toxins which do not demonstrate the unique specificity of the BPI holo-protein) have revealed that individual functions, such as binding or catalytic activity, can be expressed by isolated fragments, but that cytotoxicity (comprising both binding to a cell membrane and intracellular toxic activity) requires essentially the entire molecule.

The BPI fragments of the present invention are as potent as the holoprotein against rough E.coli, more potent than the holoprotein against the generally more resistant, smooth E.coli (on a molar basis), and retain the specificity of the holoprotein towards gram-negative bacteria. This is a particularly important finding because smooth gram-negative bacteria (smoothness being due to the presence of longer LPS chains in the bacterial cell membrane) generally are more pathogenic than their corresponding rough counterparts.

The distinctive size, chromatographic behavior (FIGS. 1 and 2 below) amino acid content (Table 1 below) and potency (see Example 4 below) firmly establish that the BPI fragment of the present invention is a molecular entity distinct from the holoprotein.

Non-limiting examples of the BPI fragments of the present invention are approximately 25 kDa for human and rabbit BPI. The human 25 kDa fragment of the preferred embodiment of the present invention was initially isolated after long-term storage (e.g. two months) of the purified holoprotein in a weakly acidic buffer (10 mM ammonium acetate, pH4.6) and can be thus generated. However, it is preferable to produce the BPI fragments of the present invention by incubating the holo-proteins in an acceptable buffer i.e., a buffer having sufficient buffering capacity at concentrations between about 10 and about 150 mM at a pH ranging between about 6.0 and about 8.0, such as Tris/HCl, phosphate, and preferably HEPES/NaOH (Sigma Chemicals, St. Louis, Mo.), or mixtures thereof. The preferred pH is 7.4. The incubations may be performed for a period of time broadly ranging between about 16 and 24 hours and preferably 18 hours, at a temperature ranging between about 20.degree. C. and about 37.degree. C. and preferably 37.degree. C. A particularly preferred condition comprises incubation in 0.1M HEPES/NaOH buffer, pH 7.4 for 18 hours at 37.degree. C. This has led to the conversion of about 50% of the holoprotein into the biologically active fragments of the present invention. Reincubation of the recovered holoprotein, under these conditions again result in formation of the 25 kDa fragment.

The BPI holoproteins, used as starting materials for the production of the biologically active fragments of the present invention, can be obtained from mammalian cells of the myeloid series of blood cells, such as PMN. Although the fragments of the present invention are not limited to a particular mammalian species, it is preferable to employ such fragments isolated from a homologous mammalian species when treating bacterial infections caused by gram-negative bacteria.

In addition, the BPI holoprotein and/or the biologically active fragments of the present invention may be obtained using recombinant DNA techniques employing the sequence information presented below in Example 3 to synthesize DNA probes for the detection of DNA sequences coding for BPI in complementary DNA or genomic libraries using methods well-known in the art. The gene coding for the BPI holoprotein, or a portion of the gene coding for the 25 kDa fragment of the present invention (and possibly smaller biologically active fragments thereof) may be inserted into a suitable expression vector for the production of biologically active polypeptides.

In one embodiment, human BPI holoprotein can be obtained from PMN isolated from normal blood or from blood from patients with chronic myelocytic leukemia, as detailed in Example 1 below. Alternatively, human BPI can be extracted from the human leukemic cell line HL-60 (available as ATCC CCL 240, American Type Culture Collection, Rockville, Md.). The latter have been found to contain approximately 10 micrograms of BPI holoprotein per 10.sup.8 cells. Mature PMN of either normal or leukemic origin contain approximately 60 micrograms per 10.sup.8 cells of the BPI holoprotein and are therefore the preferred starting material.

Once obtained, the mammalian PMN can be fractionated using, for example, the procedures detailed below in Example 1 in order to obtain primary granules (or alternatively by extraction of whole cells with 0.16N sulfuric acid, as described in Elsbach. P. et al., J. Biol. Chem. 254: 11000, 1979, incorporated by reference). Such primary granules isolated from PMN or leukemic cell lines contain the bulk of BPI holoprotein activity. The BPI holoprotein can then be extracted and purified using any technique known in the art which yields a biologically active BPI holoprotein. Although crude extracts obtained from such primary granules can be employed as starting materials for the production of the BPI fragments of the present invention, it is preferable to purify the holoprotein before generating the fragments. Preferred extraction and purification techniques for human and rabbit BPI holoproteins are described in Example 1 below.

The amounts of starting, purified, BPI holoprotein to be employed in practicing the present invention preferably should be at least 200 micrograms of purified holoprotein. Although it is possible to use smaller amounts of material, this may hamper the recovery of the biologically active fragments due to non-specific losses, as is true with many other biologically-active proteins, such as interferons.

Although not wishing to be bound by any theory of operation of the present invention, it is believed that the cleavage of the holoprotein to generate the biologically active fragments of the present invention is due to the presence of serine proteases.

The protein cleaving conditions necessary for the production of the biologically active BPI fragments of the present invention are broadly within the pH, temperature and time optima of such serine proteases, i.e. pH6.0-pH 8.0, 20.degree. C.-37.degree. C., 16-24 hours. Such incubation of the BPI holoprotein will produce cleavage at about 25 kDa from the NH.sub.2 -terminus of the holoproteins.

The biologically active BPI fragments of the present invention can be utilized for the treatment of mammals suffering from diseases caused by gram-negative bacteria such as, bacteremia or sepsis. Due to its exquisite selectivity and lack of cytotoxicity toward cells other than gram-negative bacteria, the BPI fragments of the present invention would be particularly useful as specific therapeutic agents. Currently gram-negative bacterial infections, such as those caused by Escherichia coli, various species of Salmonella, Klebsiella or Pseudomonas are treated with antibiotics, such as penicillin derivatives, aminoglycosides and chloramphenicol. The effectiveness of antibiotics is limited due to the fact that gram-negative bacilli tend to display significant intrinsic resistance to many currently available antibiotics and to readily develop further resistance due to the acquisition of resistance factor plasmids. Under appropriate selective conditions, rapid dissemination of multiple antibiotic resistance among a wide variety of gram-negative pathogens is known to occur.

When employed to treat bacteremia (i.e. the presence of bacteria in the blood stream) or sepsis (bacterial contamination of bodily fluids) caused by gram-negative bacteria, the BPI fragments of the present invention are preferably administered parenterally, and most preferably intravenously in amounts broadly ranging between about 1 microgram and 1000 micrograms and preferably between 10 and about 250 micrograms per treatment. The duration and number of treatments may vary from individual to individual, depending upon the severity of the illness. A typical treatment regime may comprise intravenous administration of about 100 micrograms of the BPI fragments three times a day. To help avoid rapid inactivation of the BPI fragments of the present invention (and indeed the holoproteins) which has been observed in vitro after incubation with serum, the BPI fragments may be coupled with physiologically-acceptable carriers, such as normally occurring serum proteins (e.g. albumin or lysozyme). The BPI fragments of the present invention could also be employed topically to treat mammals suffering from skin infections caused by susceptible gram-negative bacteria which occur in bedridden patients suffering from decubitus ulcers (bed sores) or in burn patients. When employed as a topical antibacterial agent, the BPI fragments may be administered in the same dosages and frequency as described for parenteral administration above.

The BPI fragments of the present invention can be incorporated in pharmaceutical formulations to be used to treat mammals suffering from gram-negative bacterial infections. Pharmaceutical formulations comprising the BPI fragments of the present invention (or physiologically-acceptable salts thereof) as at least one of the active ingredients, would in addition comprise pharmaceutically-acceptable carriers, diluents, fillers, salts and other materials well-known in the art depending upon the dosage form utilized. For example, preferred parenteral dosage forms would comprise a sterile isotonic saline solution, and may comprise between about 1 microgram and 1000 micrograms of the BPI fragments of the present invention covalently coupled to suitable physiologically-acceptable carriers, such as normally occurring serum proteins, for example lysozyme or albumin, to prevent their inactivation. For use in treating mammals with gram-negative bacterial infections in body fluids largely devoid of (lipo) proteins, such as urine, pharmaceutical formulations may comprise the above amounts of BPI fragments of the present invention and sterile, isotonic saline solutions for irrigation of the urinary tract.

In another preferred embodiment, the BPI fragments of the present invention in amounts ranging between 1 microgram and 1000 micrograms per dose, may be mixed with antibiotics and may be formulated in the same type of preparations used in antibiotic creams (such as Silvadene, Marion Laboratories, Kansas City, Mo., Terramycin, Pfipharmecs, New York, N.Y. or Achromycin, Lederle Laboratories, Pearle River, N.Y.) well-known in the art for topical administration.

In another preferred embodiment of the present invention, pharmaceutical formulations for treating mammals suffering from gram-negative bacterial infections may contain the BPI fragments of the present invention in addition to standard amounts (well-known in the art) of antibiotics such as Penicillin-G (available from E.R. Squibb and Sons, Inc., Princeton, N.J.) or cephalosporins (available from Eli Lily & Co., Indianapolis, Ind.). In a particularly preferred embodiment, the BPI fragments of the present invention may be mixed with hydrophobic antibiotics, such as rifampicin (available as RIFAMPIN, CIBA Pharmaceutical Co., Summit, N.J.), and hydrophobic penicillins such as Penicillin-V Benzathine (Lederle Labs, Pearl River, N.Y.). The increased permeability of gram-negative bacteria after BPI treatment is expected to enhance the effectiveness of such antibiotics which cannot easily enter non-permeabilized bacteria.

The BPI fragments of the present invention are expected to be ideally-suited for co-treatment using any antibiotic, immune system cells or factors such as T-cells or interleukin-2, cytotoxic agents or the like, effective against gram-negative bacteria. Because of the increased sensitivity to the fragments of the present invention of the more pathogenic, smooth, gram-negative bacteria, the BPI fragments of the present invention are expected to decrease resistance of such bacteria to such factors. Substantially simultaneous administration of the fragments of the present invention and the antibiotic of choice is preferred.

An example of the above-mentioned embodiment is demonstrated in Example 4 below, wherein actinomycin D (which normally cannot enter and affect gram-negative bacteria due to its hydrophobic properties) significantly inhibited RNA and protein synthesis only in BPI-treated E. coli.

In addition, the present inventors have isolated the gene encoding the human BPI holoprotein and have identified and sequenced BPI cDNA isolated from human promyelocytic leukemia cells (HL-60). The nucleotide sequence of the cDNA and the corresponding amino acid sequence of the holoprotein are set out in FIG. 5 (SEQ. ID. NO.1).

The sequence information contained in FIG. 5 can be employed to synthesize the 25 kDa, biologically active fragment of BPI. In this case, a vector can be generated comprising DNA residues 123 to about 759-780 (SEQ. ID. NO.3) (or amino acid residues 1 to about 210-220 SEQ. ID. NO.2) of FIG. 5 using techniques well-known in the art. In addition, smaller sub-fragments of the cDNA of FIG. 5 can be generated using, for example, limited Ba131nuclease digestion of the entire cDNA, to probe for the minimum sequences necessary for BPI biological activities mentioned above.

Alternatively, the BPI holoprotein can be obtained after synthesis by suitably transfected or transformed eukaryotic (mammalian or yeast) or prokaryotic cells and the biologically-active 25 kDa fragments mentioned above can be obtained using the techniques described in Example 2 below.

The present invention is described further below in specific examples which are intended to illustrate it without limiting its scope.

EXAMPLE 1

Isolation and Purification of Human BPI

Human leukocytes were obtained from heparin-treated (100-200 U.S.P. units/10 ml) peripheral blood collected by venipuncture from healthy donors and patients with chronic myelocytic leukemia.

Populations of human PMN were obtained in two ways. (1) PMN's were isolated by the dextran-sedimentation procedure, followed by centrifugation in an Isopaque-Ficoll gradient (Pharmacia Fine Chemicals, Piscataway, N.J.) as described (Boyum, A. J., J. Clin. Lab. Invest. Suppl. 97: 77-89, 1968, incorporated by reference). The leukocyte-rich plasma from healthy donors was first diluted with isotonic Krebs-ringer phosphate buffer (pH7.4) to a concentration of 10,000 to 20,000 cells/-microliter before layering on the Isopaque-Ficoll mixture. The cells were washed twice in Krebs-ringer phosphate before use.

(2) Alternatively, leukocyte-rich plasma obtained by leukopheresis (using procedures well-known in the art) of 400 ml of venous blood, from a patient with chronic myelocytic leukemia, was sedimented directly at 1000.times.g for five minutes yielding 3.5.times.10.sup.10 leukocytes, essentially all of which were PMN. These cells were washed twice with Krebs-ringer phosphate before homogenization.

For extraction of the human BPI holoprotein, the PMN were first disrupted in one of two ways: 1) Granule-rich fractions, containing the bulk of the BPI activity, were obtained by homogenization at 0.degree. C. of PMN suspended in 0.34M sucrose (2.times.10.sup.8 cells/ml), as described in Weiss, J. et al., J. Biol. Chem. 253: 2664-2672, 1978, incorporated by reference, followed by centrifugation at 400.times.g for 10 and 20,000.times.g for 30 minutes at 4.degree. C. The granule-rich pellet was extracted with approximately 10 volumes of 0.2M sodium acetate (pH 4.0), overnight at 4.degree. C. with continuous stirring. The extract was collected as a supernatant by centrifugation of the extract at 20,000.times.g for 30 minutes.

2) Alternatively, PMN (2-3.times.10.sup.8 cells/ml) were disrupted in distilled water at 0.degree. C. with a Potter-Elvejhem glass homogenizer and a motor-driven teflon pestle (Kontes; subsidiary of Kimble Div. of Owens, Ill.) and extracted at 0.degree. C. for 30 minutes with 0.16N sulfuric acid to solubilize the BPI holoprotein. After centrifugation at 23,000.times.g for 20 minutes at 4.degree. C. to sediment insoluble material, the extract was dialyzed against 200 mM sodium acetate/acetic acid buffer (pH 4.0). The BPI in these extracts was purified by gel filtration chromatography on a molecular sieving column (SEPHADEX G-75, superfine, Pharmacia Fine Chemicals, Piscataway, N.J.) at 4.degree. C. The beads were prepared according to the manufacturer's instructions and equilibrated in the 0.2M sodium acetate (pH 4.0). Using this technique, substantially all of the BPI holoprotein activity was eluted as a single peak (fractions 35-39) corresponding to a discrete protein peak (5-6% of the total protein applied) just after the void volume.

The chromatographic fraction containing the human BPI holoprotein was subjected to further chromatography on an ion exchange resin (SP-SEPHADEX, Pharmacia Fine Chemicals, Piscataway, N.J.). Protein was applied to the column, equilibrated in 0.1N NaCl-0.2M sodium acetate/acetic acid buffer (pH4.6) and eluted with a stepwise gradient of buffered NaCl (0.3, 0.5 and 0.75M). Human BPI holoprotein eluted in the last step.

Purified human BPI holoprotein was then isolated by high performance liquid chromatography (HPLC) on a reverse phase C-4 (Vydac) column (Sota Chromatography, Crompand, N.Y.) using an HPLC system (Model 332, Beckman Instruments, Fullerton, Calif.). The column used a linear gradient of acetonitrile (0-95% volume/volume, J.T. Baker Chemical Co., Philipsburg, N.J.) in 0.1% trifluoroacetic acid (TFA, Pierce Chemical Co., Rockford, Ill.). Human BPI eluted at about 70% acetonitrile and was dialyzed against approximately 50 volumes of 10 mM ammonium acetate/acetic acid buffer (pH4.6). Purified BPI was stored either in 0.2M sodium acetate/acetic acid buffer (pH 4.0) or in 10 mM ammonium acetate/acetic acid buffer (pH4.0) at 4.degree. C.

EXAMPLE 2

Production of Human BPI Fragments

Purified human BPI holoprotein was incubated in 0.1M HEPES-NaOH buffer, pH7.4 for 18 hours, and then analyzed by sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE) in 12% polyacrylamide gels using the buffer system containing 0.375M Tris/HCl and 0.1% SDS of Laemmli, U.K., Nature 227: 680-685 1970 incorporated by reference. The results are shown in FIG. 1. In FIG. 1, lanes A-E were stained using the well-known Coomassie blue technique and lanes F and G were silver stained using a commercial kit (Bio-Rad, Bio-Rad Labs, Richmond, Calif.).

Upon incubation in 10 mM ammonium acetate buffer (pH 4.6) at 4.degree. C. for two months, 10 micrograms of the purified human protein (FIG. 1, lane A) fragmented into two species of approximately 35 and 25 kDa (FIG. 1, lane B). Incubation of purified human BPI holoprotein (10 micrograms) for 24 hours at 37.degree. C. in 0.1M HEPES/NaoH buffer, pH 7.4, enhanced the accumulation of the two species, particularly the 25 kDa species with the concomitant loss of the holoprotein (FIG. 1, lane C). Reverse phase HPLC of this incubated mixture, performed as described above for the holoprotein, yielded two major protein peaks, one co-eluting with native human BPI holoprotein and the other eluting slightly earlier (FIG. 2). Protein from the later peak migrated on SDS-PAGE as a single 60 kDa species and protein from the earlier peak migrated as a single 25 kDa species (FIG. 1, lanes D and E respectively). Fragmentation of the human BPI holoprotein and isolation of the 25 kDa fragment could be repeated with the recovered human holoprotein upon repetition of this procedure, confirming that the 25 kDa fragment was human BPI-derived.

In like manner, rabbit BPI holoprotein, purified as in Example 1 above (500 ng, FIG. 1, lane F) was fragmented after incubation for 18 hours at 37.degree. C. in 0.1M HEPES-NaOH (pH7.4) into a 25 kDa species (FIG. 1, lane G).

EXAMPLE 3

NH.sub.2 -Terminal Amino Acid Composition and Sequence Analysis of BPI Fragments

The human 25 kDa BPI fragment of the present invention was subjected to amino acid analysis, and the results were compared with the amino acid analysis of purified 60 kDa human holoprotein. Amino acid compositions were determined using a Waters Pico-Tag amino acid analyzer (Waters Associates, Milford, Nab.) as described (Bidlingmyer. B. A. et al., J. Chrom. 336: 93-104 1984 incorporated, by reference). Samples were pretreated in vacuo for 24 hours at 110.degree. C. with 5.7N HCl containing 0.05% phenol. The results are shown in Table 1.

TABLE 1______________________________________Amino Acid Composition of the 25 kDa Fragment and of the HumanBPI Holoprotein 25 kDa Fragment Human BPI Holoprotein (% of total)______________________________________Asx 8.7 9.1Glx 8.8 8.9Ser 15.2 8.8Gly 7.1 6.4His 2.9 2.8Arg 3.6 3.7Thr 3.5 4.6Ala 4.1 6.0Pro 5.0 8.1Tyr 2.6 2.7Val 5.8 7.3Met 2.3 2.4Ile 7.3 5.0Leu 7.7 10.3Phe 4.2 6.1Lys 11.4 7.6______________________________________

The values shown above represent the mole fraction (%) of each amino acid and are the mean of three independent determinations. "Asx" stands for asparagine and/or aspartic acid and "Glx" stands for glutamine or glutamic acid.

Amino acid analysis showed that the human 25 kDa fragment was enriched in lysine and serine and contained less non-polar residues when compared with the holoprotein (Table 1).

NH.sub.2 -terminal sequence analysis of the human BPI fragment of the present invention and of the holoprotein were performed using the well-known sequential Edman degradation technique (Edman, P. Eur. J. Biochem. 1: 80-91, 1967, incorporated by reference) using an amino acid sequencer (Beckman, Model 890C, Beckman Instruments Inc., Fullerton, Calif.) for the holoprotein or a gas phase sequencer (Applied Biosystems, Model 470A, Applied Biosystems, Inc., Foster City, Calif.) for the fragment. Phenylthiohydantoin derivatives of amino acids released sequentially by the Edman degradation process were analyzed by reverse-phase HPLC using an 150 mm C-18 column for human BPI (IBM Instruments Inc., Willingford, Conn.) or an ODS column for the fragment of the present invention (Dupont Zorbax ODS column, E.I. Dupont de Nemours, Wilmington, Del.). The results are shown in Table 2 below.

TABLE 2__________________________________________________________________________Holoprotein:Val Asn Pro Gly Val Val Val Arg Ile Ser Gln Lys Gly Leu Asp Tyr1 5 10 15Ala Ser Gln Gln 2025 kD Fragment:Val Asn Pro Gly Val Val Val Arg Ile Ser Gln Lys Gly Leu Asp Tyr1 5 10 15Ala Ser Gln Gln 20__________________________________________________________________________

As can be seen from the data in Table 2, the NH.sub.2 -terminal amino acid sequence of the human 25 kDa fragment (SEQ. ID. NO.5) of the present invention and the holoprotein derived from human PMN were identical in the first 20 amino acid residues, indicating that the fragment was the NH.sub.2 -terminal portion of the human holoprotein.

EXAMPLE 4

Biological Properties of the BPI Fragment of the Present Invention

The antibacterial effects of the 25 kDa human BPI fragment of the present invention were compared with the known activities of the holoprotein. E. coli J5 (obtained from Dr. L. Leive, NIH Bethesda, Md.) which produces short-chain lipo-polysaccharides (LPS) in galactose-free culture medium, were grown overnight and then subcultured at 37.degree. C. in triethanolamine-buffered media as described in Simon, E. G. et al., (Proc. Nat. Acad. Sci. USA 51: 877, 1964, incorporated by reference). 5.times.10.sup.6 E. coli J5 were incubated in a volume of 250 microliters with increasing amounts of either the human holoprotein or the human 25 kDa fragment of the present invention. The effects on bacterial viability were determined either by (1) diluting an aliquot (5.times.10.sup.5 bacteria) of the incubation mixture into 2 ml of nutrient broth (Difco Laboratories, Detroit, Mich.) and measuring bacterial growth (absorbance at 550 nM using a standard spectrophotometer after approximately 4 hours at 37.degree. C.); or (2) plating diluted samples on nutrient agar and counting bacterial colonies after overnight incubation at 37.degree. C. The results are presented in FIG. 3. In FIG. 3, open circles represent BPI holoprotein-treated bacteria and closed circles represent bacteria treated with the human 25 kDa fragment of the present invention.

FIG. 3A shows that the isolated 25 kDa fragment of the present invention killed E. coli J5, a strain of bacteria highly sensitive to the holoprotein, in a dose-dependent manner. A linear regression analysis of the data presented in FIG. 3A further showed that the fragment was about twice as potent as the holoprotein on a mass basis, meaning that it is about equally potent on a molar basis because the fragment is about half the size of the holoprotein (FIG. 3A).

Killing of E. coli by mammalian BPI is initially accompanied by discrete alterations of the outer envelope without causing any apparent damage to the bacterial biosynthetic machinery. FIG. 3B shows that even at almost fully lethal doses, both the human holoprotein and the human 25 kDa fragment of the present invention caused little inhibition of bacterial protein synthesis. In contrast, both the fragment and the holoprotein caused nearly a complete inhibition of E. coli J5 protein synthesis when administered in the presence of 50 micrograms/ml of the antibiotic actinomycin D (Merck, Sharp and Dohme, St. Louis, Mo., FIG. 3C). This effect of actinomycin D reflects increased permeability of the outer membrane of the bacteria permitting the entry of the normally impermeant actinomycin D into the cell where it inhibited RNA and, consequently, protein synthesis. The dose-dependence of the permeability-increasing effect of the fragment of the present invention and the holoprotein was the same as that shown for the bactericidal activity above, and demonstrated that in this respect also the fragment was twice as active as the holoprotein, on a mass basis.

In order to compare the effects of the fragment of the present invention with the holoprotein on bacterial phospholipids, bacteria were prelabeled during growth with (1-.sup.14 C)-oleic acid (New England Nuclear, Boston, Mass.) as described in Elsbach. P. et al., J. Biol Chem. 254: 11000-11009, 1979 incorporated by reference. Incubation mixtures were supplemented with 0.4% bovine serum albumin (W/V) to capture phospholipid breakdown products (.sup.14 C-free fatty acids and .sup.14 C-lysocompounds) permitting their separation from unhydrolyzed bacterial .sup.14 C-phospholipids by filtration through a membrane filter (Millipore HAWP, Millipore Corp. Bedford, Mass.) to measure phospholipid degradation. The results are shown in FIG. 3D.

As shown in FIG. 3D, the dose-dependent activation of bacterial phospholipid degrading enzymes by the holoprotein was also produced by the 25 kDa fragment of the present invention, again requiring only half the mass of protein for a comparable effect.

The action of the BPI holoprotein on E. coli is hindered by the presence in the bacterial outer membrane of lipopolysaccharides with long polysaccharide chains ("smooth strains"). The effectiveness of the 25 kDa fragment of the present invention towards a smooth E. coli strain (0111:B4) was compared with that of the holoprotein. E. coli 0111:B4 is a smooth strain bearing longer polysaccharide chains than E. coli J5. Bacteria (1.times.10.sup.6) were incubated in 125 microliter mixtures with increasing amounts of the BPI holoprotein or the 25 kDa fragment of the present invention. Bacterial viability was measured as above and is expressed as percent of viability of bacteria incubated alone (without any additions). The results are shown in FIG. 4.

As can be seen in FIG. 4, the 25 kDa fragment of the present invention (closed circles) was about five times more potent than the holoprotein (open circles) towards E. coli 0111:B4. The five fold enhancement in activity of the 25 kDa fragment of the present invention with respect to the holoprotein, suggests that the smaller size of the fragment of the present invention is a factor in facilitating access of the fragment to binding sites at the base of the LPS polysaccharide chain.

In order to determine if the human 25 kDa fragment of the present invention retained the same cytotoxic specificity towards gram-negative bacteria as the holoprotein, the activities of the 25 kDa fragment and the holoprotein toward a gram-positive bacterium, Micrococcus lysodeikticus (obtained from Dr. M. Salton, New York University, New York, N.Y.) were compared. The bacteria were grown in brain heart infusion broth (Difco Laboratories, Detroit, Mich.) at 37.degree. C. Bacterial viability was measured as above for E. coli.

Neither the human 25 kDa fragment of the present invention (5-10 micrograms) nor the holoprotein (10-20 micrograms) produced any effect on the viability of Micrococcus lysodeikticus, even at doses twenty times greater than those that are fully lethal towards gram-negative E. coli J5.

The data presented above demonstrate that the spectrum and potency of the antibacterial activities of the human 25 kDa BPI fragment of the present invention are at least equal to and sometimes substantially greater than those of the holoprotein. The data indicate that all of the molecular determinants required for BPI cytotoxicity reside within the portion of the BPI molecule included in the fragment of the present invention.

EXAMPLE 5

Cloning of the cDNA of Human BPI and Identification of the Amino Acid Sequence

Two synthetic oligonucleotides were designed to encode the 33 amino terminal residues of human BPI. The probes BPI-1 (SEQ. ID. NO.6). GTCAATCCTG GTGTTGTGGT CAGGATCTCT CAGAAGGGCC TGGATTATGC CTCCCA and; BPI-2 (SEQ. ID. NO. 7) GCAAGGCACA GCTGCCCTGC AGAAGGAGCT GAAGAGGATC AAGATTCCTG ACTAT; were each designed to encode half of the partially known human BPI sequence as previously disclosed in Ooi, C. E. et al., (J. Biol. Chem. 262: 14891-14894, 1987). The probes were kinase labeled with .sup.32 P using standard techniques well-known in the art and used to independently screen a human genomic liver library as disclosed in Lawn, R. M. et al. (Cell 15: 1157-1174, 1978). Six clones were identified among 500,000 plaques which hybridized independently with each probe. The hybridizing region of one of these clones was sequenced and clearly encoded the amino terminal end of human BPI. This sequence was interrupted by an intron or intervening sequence but nevertheless predicted an additional 22 amino acid residues which preceded the next intron.

Based on the gene sequence, a new DNA probe was then synthesized which corresponded exactly to the encoded 55 amino terminal amino acid residues. This probe was used to screen a small cDNA library prepared from human HL-60 cells (available as ATCC CCL 240, American Type Culture Collection, Rockville, Md.) induced with dimethylsulfoxide, DMSO. In the library of the 300,000 plaques, 4 clones were isolated which hybridized with the exact probe. DNA from the clones was isolated and the hybridizing regions were sequenced by the dideoxy chain termination technique of Smith, A. J. H. (Meth. Enzym. 65: 560-580, 1980). The sequence of the longest clone is presented in FIG. 5.

As shown in FIG. 5, the sequence (SEQ ID NO.1) predicts a 31 amino acid signal peptide, followed by a 456 residue mature protein (SEQ. ID. NO.4). The amino terminal sequence determined by protein sequencing of human BPI matches the encoded cDNA exactly. Furthermore, the deduced amino acid composition of the encoded protein corresponds closely to the amino acid composition determined for purified human BPI as disclosed in Ooi, C. E. et al., supra. The encoded sequence predicts a protein of 50.6 kD; the estimated molecular size of purified human BPI is approximately 58 kD. This difference in the apparent size may reflect the presence of two potential N-linked glycosylation sites at positions 122 and 249 of the protein (indicated by overlines in FIG. 5).

To further demonstrate that this cDNA encoded human BPI, its expression was engineered in mammalian cells. The entire cDNA was subcloned in a mammalian cell expression vector (Wood, W. I. et al., Nature 312: 330-337, 1984), and then transfected into a human kidney cell line. Small amounts of recombinant BPI were transiently produced and characterized by Western Blotting techniques, showing an immunoreactive band with a mobility identical to that of native human BPI (results not shown).

The natural expression of BPI in various human tissues was then analyzed by Northern Blot hybridization. RNA was prepared from various tissues (Chirgwin, J. M. et al., Biochem. 24: 5294-5299, 1979), passed over oligo-dT-cellulose and electrophoresed through a formaldehyde agarose gel (Dobner, P. R. et al., Proc. Nat. Acad. Sci. USA 78: 2230-2234, 1981). The gel was transferred to nitrocellulose as described (Thomas, P. S., Proc. Nat. Acad. Sci. USA 77: 5201-5205, 1980) and hybridized under stringent conditions with BPI cDNA.

As shown in FIG. 6, the BPI cDNA probe hybridized well with mRNA prepared from the spleen of a patient with chronic myelocytic leukemia. The spleen was heavily infiltrated with immature myeloid cells. The size of the hybridizing signal was approximately 2,000 bases in length, suggesting that the cDNA sequence (SEQ. ID. NO.1) presented in FIG. 5 was full length. The BPI probe did not hybridize with mRNA from normal spleen, mature peripheral blood leukocytes, liver, kidney, or brain (FIG. 6). This result is in agreement with previous observations on the location of BPI in various cell types and tissues; the presence of BPI has been previously shown to be restricted to cells of the myeloid series. The BPI cDNA was also used as a probe in Southern hybridizations of human genomic DNA. DNA was isolated from human peripheral blood leukocytes, as described in Blin, N. et al. (Nuc. Acids Res. 3: 2303-2308, 1976), digested with restriction endonucleases Eco RI, BamHI and HindIII, and fractionated on a 1% agarose gel. The DNA was transferred to nitrocellulose (as described in Southern. E. M., J. Molec. Biol. 98: 503-517, 1975) and hybridized with a 5' end fragment of the BPI cDNA probe under stringent conditions (as described in Maniatis et al., Molecular Cloning, a laboratory Manual, pp. 387-389, Cold Spring Harbor Laboratories, N.Y., 1982, incorporated by reference).

As shown in FIG. 7, a single hybridizing band was observed in restriction digests using Eco RI and BamHI when the 5' end of the BPI cDNA was utilized as a probe. This suggested that BPI was encoded by a single gene.

The primary structure of the human BPI protein sequence reveals several features which may be critical for its function. As mentioned above, an amino terminal 25 kD fragment contains all of the bactericidal activity of the holoprotein. A clear charge asymmetry can be observed when the amino terminal 25 kD fragment is compared with the holoprotein. The amino terminal end contains 16 more basic than acidic residues (28 lysine/argine vs. 12 aspartate/glutamate), while the carboxy terminal end is slightly acidic (20 basic vs. 22 acidic residues). The very basic nature of the amino terminal domain may promote an electrostatic interaction of BPI with the negatively charged LPS on the bacterial envelope.

EXAMPLE 6

Co-treatment of Gram-negative Bacteria with the Human BPI Fragment and Penicillins

The human BPI fragment of the present invention will be used to test the effectiveness of compositions containing the fragments and Penicillin-G or a hydrophobic derivative, Penicillin-V. Both smooth (E. coli 0111:B4) and rough (E. coli J5) gram-negative bacteria will be seeded and incubated as in Example 3 above with serial two-fold dilutions containing: the human 25 kDa BPI fragment of the present invention (1 microgram-1000 micrograms) alone, Penicillin-G (3000-300,000 units) alone, Penicillin-V Benzathine (3000-300,000 units) alone and compositions containing the same concentrations of the above as mixtures, e.g. the BPI fragment plus Penicillin-G and the BPI fragment plus Penicillin-V. Bacterial viability will be monitored as above in Example 3.

It is expected that lower amounts of both of the penicillins will be effective in killing both smooth and rough E. coli strains in the presence of the human 25 kDa BPI fragments showing the efficacy of this embodiment of the present invention.

EXAMPLE 7

The Bactericidal/Permeability Increasing protein (BPI), a product of PMN of man and animals that is stored in the azurophilic granules, has been shown to be cytotoxic for Gram-negative bacteria only. This remarkable target-cell specifity of BPI is attributable to its strong attraction to the LPS in the outer membrane of the gram-negative bacterial envelope. This feature of BPI has led to the recognition that BPI is a member of a family of LPS-binding proteins and is capable, when added extracellularly, of inhibiting the effects of purified LPS in several in vitro settings as well as in animal experiments. It has been suggested that these conditions, directed at cell-free LPS, represents BPI's main function, outweighing its importance as an antibacterial agent (J. N. I. H. Res. 3: 61-65, 1991). However, the most common presentation of LPS to the host is as an envelope component of invading bacteria. Therefore the ability of added BPI and its bioactive fragments to attach to LPS in the bacterial envelope and cause bacterial damage may be an important determinant of its protective role in vivo.

Data presented below shows that the addition of nM concentrations of BPI or of the approximately 25 kDa N-terminal bioactive portion of the molecule (disclosed above) to whole blood, inoculated with live E. coli, results in: 1) killing of E. coli that survive the cellular and extracellular antibacterial systems normally present in whole blood, and in parallel, 2) inhibition of the release of TNF, prompted by the bacteria.

Materials and Methods

In the experiments described below, the following materials and methods were used.

FIG. 8. Incubation of E. coli in whole blood: Effect on survival and accumulation of TNF. Human blood was collected from healthy volunteers into Vacutainer tubes containing buffered sodium citrate as an anticoagulant. A clinical isolate of E. coli, producing a K1-type capsule, and a rough mutant of E. coli (J5) were grown to mid-log phase in trypticase soy broth and, after harvesting, the bacteria were added to blood at the indicated concentrations. Suspensions of these E. coli were estimated to contain approximately 1 ng of LPS/10.sup.5 bacteria. For comparison increasing concentrations of purified LPS from Salmonella minnesota Re595 and E. coli J5 (each obtained from List Biological Laboratories, Inc., Campbell, Calif.) were added to parallel samples of blood as indicated. Samples were incubated at 37.degree. C.: after 1 h and 5 h incubation, aliquots of the bacterial samples were taken and mixed with molten nutrient agar. After solidification of the nutrient agar, the samples were incubated at 37.degree. C. for 18-24 h to permit growth of individual viable bacteria as individual colonies. The number of viable E. coli recovered following incubation in blood is expressed as the percent of the number of viable E. coli (i.e. colony-forming units; CFU) initially added to the blood. The results shown in FIG. 8A represent the mean+/-SEM of at least 3 independent experiments. At the end of the incubation of the blood samples (5 h), the extracellular medium was collected by centrifugation at 500 g. TNF in the recovered medium was measured by ELISA using the Biokine TNF test kit (T Cell Sciences, Cambridge, Mass.). The results shown in FIG. 8B represent the mean+/-SEM of at least 3 independent experiments.

FIG. 9. BPI potently inhibits both survival of encapsulated E. coli and bacterial induction of TNF in whole blood. Increasing numbers of K1-encapsulated E. coli were added as indicated to citrated blood that was either unsupplemented or supplemented with purified native (holo-) human BPI (either 4 or 40 nM final concentration of BPI in blood). Bacterial viability (top left and right panels and the lower left panel) and accumulation of extracellular TNF (lower right panel) following incubation of E. coli in blood in the presence or absence of BPI was measured as described above in FIG. 8. The results shown represent the mean+/-SEM of at least 4 independent experiments.

FIG. 10. Synergistic bactericidal action of BPI and Complement against serum-resistant K1-encapsulated E. coli. E. coli (2.times.10.sup.6 /ml) were incubated in the absence (left panel) and presence (right panel) of native (holo-)BPI (2 .mu.g/ml) in buffered (20 mM sodium phosphate pH 7.4) nutrient broth supplemented with physiological (0.9%) saline or saline containing purified albumin (12.5 mg/ml) or 25% (normal or C7 depicted) serum (v/v) where indicated. After incubation at 37.degree. C. for the indicated times, aliquots were taken to measure the number of viable bacteria (CFU) in unsupplemented nutrient (NT) agar (broken lines) or in NT agar supplemented with albumin (1 mg/ml; solid lines). In the absence of BPI, there was no difference in the number of CFU apparent in NT agar+/-albumin. The CFU in a given sample are expressed as the percent of the CFU of the added bacteria at time zero. The data shown represent the mean+/-SEM of at least 3 independent experiments.

To provide a measure of the interaction of BPI and the N-terminal fragment(s) with bacteria added to whole blood, a serum-resistant (encapsulated) E. coli strain was selected that survives the cellular and extracellular antibacterial systems in normal human blood so that a decrease in bacterial survival reflects the effect of added BPI/fragments. In addition the effect was examined of the added purified proteins on the release of TNF triggered by the E. coli.

FIG. 8A shows the percentage of surviving K1-encapsulated E. coli as a function of the number of organisms added to the blood. With increasing inoculum more bacteria survive. Addition of 10.sup.6 bacteria/ml of blood was followed by substantial growth during a 5 hour incubation. In contrast, E. coli J5, a "rough" strain was killed promptly. E. coli strains with long-chain LPS, including several clinical isolates also did not survive (results not shown). FIG. 8B shows the TNF released in response to increasing numbers of either E. coli K1, or E. coli J5. Both bacterial strains, whether killed or surviving, trigger a progressive increase in TNF release with increasing inoculum. This response is comparable to that seen with amounts of isolated LPS from Salmonella RE 595 or E. coli J5 that match approximately the LPS content of the whole bacteria. These findings set the stage for the assessment of the effects of added BPI/fragments.

BPI either at a final concentration of 4 or 40 nM inhibited growth of E. coli K1, surviving in the blood (FIG. 9 A,B,C). This effect of BPI was dose dependent and evident over a broad range of bacterial concentrations. In parallel with the bactericidal action of BPI in whole blood, BPI also inhibited in dose-dependent fashion the release of TNF (FIG. 9D). At all levels of bacterial inoculum the lower BPI dose inhibited TNF release approximately 10-fold and the high dose approximately 100-fold.

The inhibition of bacterial growth upon addition of BPI was maintained during the entire incubation period of 5 hours. Mannion et al. have recently shown that the addition of 0.1% albumin to the incubation medium blocks the late (bactericidal) effects of BPI. In this setting initially non-growing E. coli grow out after 1-2 hours (Mannion et al. J. Clin. Invest. 85: 853-860, 1990). Thus, the sustained growth inhibition for 5 hours suggests that in whole blood BPI actually caused bacterial killing and that in whole blood albumin had no protective effect. The study by Mannion showed also that pre-exposure of E. coli to non-lethal normal human serum concentrations accelerates the bactericidal action of BPI against non-encapsulated E. coli. These observations prompted comparison of the antibacterial action of BPI toward E. coli K1 under 4 incubation conditions: 1) the typical incubation medium (see methods); 2) this medium plus albumin; 3) plus non-bactericidal concentrations of normal serum containing the same albumin concentration,; 4) plus C7-depleted serum. In the absence of BPI the bacteria grow both in the presence or absence of albumin, but do not multiply in either normal or C7-depleted serum (FIG. 10A). BPI added to all four incubation media inhibited subsequent colony formation in normal nutrient agar by >98% (FIG. 10B). However, plating of the bacteria in nutrient agar, supplemented with albumin, revealed that 30% of the E. coli previously incubated in unsubstituted medium were still viable. When albumin was added to the incubation medium no loss of colony forming units occurred, showing that albumin allows the bacteriostatic effect of BPI but blocked the late irreversible growth inhibitory effects of BPI. These observations on K1-encapsulated E. coli confirm those of Mannion et al. (supra) on non-encapsulated strains. In contrast, in the presence of normal serum bacterial killing was actually substantially amplified. This enhancement of bacterial killing by normal serum plus BPI was abolished by removal of C7, implicating the late components of complement in this potentiation of antibacterial action. These findings demonstrate that the protection of E. coli against the bactericidal action of BPI by albumin is not evidenced in normal serum and that late components of complement, at non-lethal concentrations, act synergistically with BPI.

A 25 kDa N-terminal fragment of BPI, generated during limited proteolysis as described above, exhibited all the known biological activities of the holo-protein as disclosed above. FIG. 11 shows that the bactericidal and TNF-inhibitory potencies in whole blood of this proteolytically prepared fragment and of a recombinant N-terminal fragment equal those of holo-BPI.

Discussion

BPI is a major constituent of the primary granule of human and rabbit PMN and is the most potent antibacterial agent yet identified in the antimicrobial arsenal of this phagocyte, directed specifically at a broad range of Gram-negative bacterial species. It has been demonstrated before that the remarkable target cell specificity of BPI reflects the strong attraction of this protein for the lipopolysaccharides (LPS) that are the dominant surface molecules of the outer membrane of the Gram-negative bacterial envelope. It is to this interaction the prompt growth inhibitory effects and surface alterations that isolated BPI exhibits upon binding to Escherichia coli and other Gram-negative bacteria has been attributed. The fate of bacteria ingested by PMN in vitro, both under aerobic and anaerobic conditions, closely mimicks that of bacteria exposed to purified BPI, lending credence to the conclusion that BPI also is primarily responsible for growth arrest within the phagocyte.

In light of the strong evidence implicating the essential role, in the selective action of BPI on Gram-negative bacteria, of the recognition by BPI of the LPS in the bacterial envelope, it is not surprising that recent studies have revealed that BPI is one member of a family of several LPS-binding proteins. One of these, LPS-binding protein or LBP, has been shown to mediate and amplify host-responses against LPS. In contrast BPI has been shown to mute such responses by inhibiting the actions of isolated LPS in vitro as well as in whole animal experiments, confirming that BPI and bioactive fragments of BPI may be used as therapeutic agents directed against the clinical consequences of endotoxemia.

Because the systemic entry of LPS into the host is usually secondary to invasion by Gram-negative organisms the following questions were addressed: can BPI and its bioactive fragments perform their antibacterial functions in the complex environment of whole blood and prevent in this setting the effects of the bacteria on cellular responses typical of gram-negative bacteremia?

BPI and its bioactive fragments, not only inhibit the accumulation of TNF in whole blood in response to the introduction of live E. coli, but also increase killing of E. coli in blood. These effects are evident at the same nM concentrations that are effective in simpler laboratory media, indicating that in the far more complex environment of whole blood neither cellular nor extracellular elements prevent BPI and its N-terminal fragments from finding their natural targets.

The ability of E. coli to trigger a TNF response in blood ex vivo does not require live organisms. Presentation to blood of equal numbers of K1-encapsulated E. coli, of which many survive, and of promptly killed E. coli J5 trigger comparable TNF responses. Thus, the detection in blood cultures from septic patients of viable organisms is not an accurate index of the bacterial challenge to host responses. In the uncompromised host with gram-negative bacteremia, most species of gram-negative bacteria are effectively killed by the intrinsic antimicrobial systems, but without protection against the actions of cytokines released in response to circulating dead bacteria or their products. However, sepsis is particularly prevalent among patients with impaired antibacterial defenses in whom the bacteremia includes viable and proliferating organisms. It is this setting that was mimicked, by selecting the serum-resistant encapsulated E. coli in order to explore the ability of BPI and the N-terminal fragment to promote the killing in blood of surviving bacteria. While the apparent combined effects of added BPI and late components of complement on the bacteria suggest an extracellular bactericidal action, contributory intracellular events, including phagocytes may obviously occur.

The results of this ex vivo study, in combination with whole animal experiments described below in Example 7, showing protection against administered LPS by recombinant holo-BPI, as well as by the recombinant N-terminal fragment support the notion that BPI and the bioactive N-terminal portion of the molecule are important additions to a group of potential therapeutic proteins and agents that serve in the treatment of gram-negative bacteremia and endotoxemia. BPI stands out among these agents in two ways: 1) as a natural component of the antimicrobial systems of the host, and 2) as the only agent so far identified with both bactericidal and endotoxin-neutralizing activities.

EXAMPLE 8

As shown in FIG. 12, recombinant human BPI inhibited the LPS-induced production of TNF, IL-6 and IL-8.

In these experiments, whole blood, obtained from two healthy donors, was collected into heparinized tubes. BPI was added directly to 225 .mu.l of whole blood followed by the addition of 25 .mu.l of LPS. The tubes were gently vortexed and incubated for 4 hours at 37.degree. C. Thereafter, 750 .mu.l of RPMI media was added and the tubes centrifuged to obtain the plasma (i.e. the supernatant). The plasma was stored overnight at 4.degree. C. before assay. The assays for TNF and IL-6 were performed using commercial assay kits according to the manufacturer's instructions (T-Cell Sciences).

The efficacy of a recombinantly produced human BPI 25 kDa N-terminal fragment in Actinomycin-D sensitized CD-1 mice challenged with E. coli 0111: B4 lipopolysaccharide was examined. In the experiment described below, LPS, obtained from E. coli 0111: B4, was inoculated intravenously into the tail vein of groups of CD-1 male mice (25-30 grams weight, 20 mice per group) at a dose of 1 .mu.g/Kg. The mice had been treated with Actinomycin-D at a dose of 800 .mu.g/Kg weight introduced intravenously in the tail vein. Immediately following the LPS and Actinomycin D administration, a recombinant human BPI 25 kDa fragment was administered intravenously into the tail vein at concentrations of 2.5 and 3.9 mg/Kg. The mice were monitored twice daily and thus recorded for seven days following the initiation of the study. The results are shown in FIG. 13.

As shown in FIG. 13, the recombinant human BPI 25 kDa N-terminal fragment was able to substantially increase the survival of mice at both concentrations tested. At seven days following the LPS administration, only two mice survived in the control group whereas 16 mice inoculated at the higher concentration of BPI (3.9 mg/Kg) or 11 mice at the lower concentration of BPI (2.5 mg/Kg) survived seven days after LPS inoculation. These results show that the recombinantly produced human BPI N-terminal fragment was able to substantially protect mice against the lethal effects of LPS.

__________________________________________________________________________# SEQUENCE LISTING- (1) GENERAL INFORMATION:- (iii) NUMBER OF SEQUENCES: 7- (2) INFORMATION FOR SEQ ID NO:1:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1814 (B) TYPE: nucleic a - #cid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (vi) ORIGINAL SOURCE: Available as AT - #CC CCL 240,#Type Culture Collection, Rockville, MD, USA (A) ORGANISM: Human (B) STRAIN: (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (E) HAPLOTYPE: (F) TISSUE TYPE: Bl - #ood (G) CELL TYPE: Prom - #yelocytic leukemia cells (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: (B) LOCATION: (C) IDENTIFICATION METHOD:# This SequenceTHER INFORMATION:#to Figure 5 in theesponds application, - # as filed. Note that N at#1814 corresponds to a poly A tail.- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) ISSUE: (F) PAGES: (G) DATE: (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-1814- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #1:- CAGGCCTTGA GGTTTTGGCA GCTCTGGAGG ATG AGA GAG AAC AT - #G GCC AGG GGC 54Met Arg 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 1- 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 CCT 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#95 1 - #00 1 - #05- 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 AGG 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 Arp 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 AAA TGA1494Pro His Gln Asn Phe Leu Leu Phe Gly Ala As - #p Val Val Tyr Lys# 455- AGGCACCAGG GGTGCCGGGG GCTGTCAGCC GCACCTGTTC CTGATGGGCT GT - #GGGGCACC1554- GGCTGCCTTT CCCCAGGGAA TCCTCTCCAG ATCTTAACCA AGAGCCCCTT GC - #AAACTTCT1614- TCGACTCAGA TTCAGAAATG ATCTAAACAC GAGGAAACAT TATTCATTGG AA - #AAGTGCAT1674- GGTGTGTATT TTAGGGATTA TGAGCTTCTT TCAAGGGCTA AGGCTGCAGA GA - #TATTTCTT1734- CCAGGAATCG TGTTTCAATT GTAACCAAGA AATTTCCATT TGTGCTTCAT GA - #AAAAAAAC1794# 181 - #4- (2) INFORMATION FOR SEQ ID NO:2:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 221 (B) TYPE: amino aci - #d (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: Protein- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (vi) ORIGINAL SOURCE: Available as AT - #CC CCL 240,#Type Culture Collection, Rockville, MD, USA (A) ORGANISM: Human (B) STRAIN: (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (E) HAPLOTYPE: (F) TISSUE TYPE: Bl - #ood (G) CELL TYPE: Prom - #yelocytic leukemia cells (H) CELL LINE: (I) ORGANELLE:- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) ISSUE: (F) PAGES: (G) DATE: (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-221- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #2:- Val Asn Pro Gly Val Val Val Arg Ile Ser Gl - #n Lys Gly Leu Asp Tyr# 15- Ala Ser Gln Gln Gly Thr Ala Ala Leu Gln Ly - #s Glu Leu Lys Arg Ile# 30- Lys Ile Pro Asp Tyr Ser Asp Ser Phe Lys Il - #e Lys His Leu Gly Lys# 45- Gly His Tyr Ser Phe Tyr Ser Met Asp Ile Ar - #g Glu Phe Gln Leu Pro# 60- Ser Ser Gln Ile Ser Met Val Pro Asn Val Gl - #y Leu Lys Phe Ser Ile#80- Ser Asn Ala Asn Ile Lys Ile Ser Gly Lys Tr - #p Lys Ala Gln Lys Arg# 95- Phe Leu Lys Met Ser Gly Asn Phe Asp Leu Se - #r Ile Glu Gly Met Ser# 110- Ile Ser Ala Asp Leu Lys Leu Gly Ser Asn Pr - #o Thr Ser Gly Lys Pro# 125- Thr Ile Thr Cys Ser Ser Cys Ser Ser His Il - #e Asn Ser Val His Val# 140- His Ile Ser Lys Ser Lys Val Gly Trp Leu Il - #e Gln Leu Phe His Lys145 1 - #50 1 - #55 1 -#60- Lys Ile Glu Ser Ala Leu Arg Asn Lys Met As - #n Ser Gln Val Cys Glu# 175- Lys Val Thr Asn Ser Val Ser Ser Lys Leu Gl - #n Pro Tyr Phe Gln Thr# 190- Leu Pro Val Met Thr Lys Ile Asp Ser Val Al - #a Gly Ile Asn Tyr Gly# 205- Leu Val Ala Pro Pro Ala Thr Thr Ala Glu Th - #r Leu Asp# 220- (2) INFORMATION FOR SEQ ID NO:3:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 658 (B) TYPE: nucleic a - #cid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: cDNA to mRNA- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (vi) ORIGINAL SOURCE: Available as AT - #CC CCL 240,#Type Culture Collection, Rockville, MD, USA (A) ORGANISM: Human (B) STRAIN: (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (E) HAPLOTYPE: (F) TISSUE TYPE: Bl - #ood (G) CELL TYPE: Prom - #yelocytic leukemia cells (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: (B) LOCATION: (C) IDENTIFICATION METHOD:# This sequenceTHER INFORMATION:#to nucleotide nos. 123 to 780 in Figure - # 5 in the application, as filed.- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) ISSUE: (F) PAGES: (G) DATE: (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-658- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #3:#CAG AAG GGC CTG GAC 46 AGG ATC TCC- TAC GCC AGC CAG CAG GGG ACG GCC GCT CTG CA - #G AAG GAG CTG AAG AGG 94- ATC AAG ATT CCT GAC TAC TCA GAC AGC TTT AA - #G ATC AAG CAT CCT GGG 142- AAG GGG CAT TAT AGC TTC TAC AGC ATG GAC AT - #C CGT GAA TTC CAG CTT 190- CCC AGT TCC CAG ATA AGC ATG GTG CCC AAT GT - #G GGC CTT AAG TTC TCC 238- ATC AGC AAC GCC AAT ATC AAG ATC AGC GGG AA - #A TGG AAG GCA CAA AAG 286- AGA TTC TTA AAA ATG AGC GGC AAT TTT GAC CT - #G AGC ATA GAA GGC ATG 334- TCC ATT TCG GCT GAT CTG AAG CTG GGC AGT AA - #C CCC ACG TCA GGC AAG 382- CCC ACC ATC ACC TGC TCC AGC TGC AGC AGG CA - #C ATC AAC AGT GTC CAC 430- GTG CAC ATC TCA AAG AGC AAA GTC GGG TGG CT - #G ATC CAA CTC TTC CAC 478- AAA AAA ATT GAG TCT GCG CTT CGA AAC AAG AT - #G AAC AGC CAG GTC TGC 526- GAG AAA GTG ACC AAT TCT GTA TCC TCC AAG CT - #G CAA CCT TAT TTC CAG 574- ACT CTG CCA GTA ATG ACC AAA ATA GAT TCT GT - #G GCT GGA ATC AAC TAT 622# 658GTG GCA CCT CCA GCA ACC ACG GCT GA - #G ACC- (2) INFORMATION FOR SEQ ID NO:4:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 487 (B) TYPE: amino aci - #d (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: Protein- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (vi) ORIGINAL SOURCE: Available as AT - #CC CCL 240,#Type Culture Collection, Rockville, MD, USA (A) ORGANISM: Human (B) STRAIN: (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (E) HAPLOTYPE: (F) TISSUE TYPE: Bl - #ood (G) CELL TYPE: Prom - #yelocytic leukemia cells (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: (B) LOCATION: (C) IDENTIFICATION METHOD:# This amino acidER INFORMATION:#can be found in Figure 5 in the application, - # as filed.- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) ISSUE: (F) PAGES: (G) DATE: (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-487- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #4:- 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- (2) INFORMATION FOR SEQ ID NO:5:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 20 (B) TYPE: amino aci - #d (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: Protein- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (vi) ORIGINAL SOURCE: (A) ORGANISM: Human (B) STRAIN: (C) INDIVIDUAL ISOLATE: (D) DEVELOPMENTAL STAGE: (E) HAPLOTYPE: (F) TISSUE TYPE: Pe - #ripheral Blood (G) CELL TYPE: Poly - #morphonuclear leucocytes (H) CELL LINE: (I) ORGANELLE:- (ix) FEATURE: (A) NAME/KEY: (B) LOCATION: (C) IDENTIFICATION METHOD:# This sequence can beFORMATION:#the application, as filed, on#line 13. page 19,- (x) PUBLICATION INFORMATION: (A) AUTHORS: (B) TITLE: (C) JOURNAL: (D) VOLUME: (E) ISSUE: (F) PAGES: (G) DATE: (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-20- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #5:- Val Asn Pro Gly Val Val Val Arg Ile Ser Gl - #n Lys Gly Leu Asp Tyr# 15- Ala Ser Gln Gln 20- (2) INFORMATION FOR SEQ ID NO:6:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 56 (B) TYPE: nucleic a - #cid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: Other nucleic aci - #d- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (ix) FEATURE: (A) NAME/KEY: (B) LOCATION: (C) IDENTIFICATION METHOD:# This sequence can beFORMATION:#the application, as filed, on#line 6. page 23,- (x) PUBLICATION INFORMATION: (A) AUTHORS: Ooi, C - #. E. et al. (B) TITLE: (C) JOURNAL: J. Bio - #l. Chem. (D) VOLUME: 262 (E) ISSUE: (F) PAGES: 14891-14894 (G) DATE: 1987 (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-56- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #6:- GTCAATCCTG GTGTTGTGGT CAGGATCTCT CAGAAGGGCC TGGATTATGC CT - #CCCA 56- (2) INFORMATION FOR SEQ ID NO:7:- (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 55 (B) TYPE: nucleic a - #cid (C) STRANDEDNESS: single (D) TOPOLOGY: linear- (ii) MOLECULE TYPE: Other nucleic aci - #d- (iii) HYPOTHETICAL: No- (iv) ANTI-SENSE: No- (ix) FEATURE: (A) NAME/KEY: (B) LOCATION: (C) IDENTIFICATION METHOD:# This sequence can beFORMATION:#the application, as filed, on#line 7. page 23,- (x) PUBLICATION INFORMATION: (A) AUTHORS: Ooi, C - #.E. et al. (B) TITLE: (C) JOURNAL: J. Bio - #l. Chem. (D) VOLUME: 262 (E) ISSUE: (F) PAGES: 14891-14894 (G) DATE: 1987 (H) DOCUMENT NUMBER: (I) FILING DATE: (J) PUBLICATION DATE: (K) RELEVANT RESIDUES I - #N SEQ ID NO: 1-55- (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #7:- GCAAGGCACA GCTGCCCTGC AGAAGGAGCT GAAGAGGATC AAGATTCCTG AC - #TAT 55__________________________________________________________________________

Claims

1. A method for treating gram-negative bacterial infections in mammals comprising administering to gram-negative bacterialy infected mammals an effective amount of a purified, isolated polypeptide having bactericidal/permeability-increasing protein activity, said polypeptide comprising an NH.sub.2 -terminal fragment of human bactericidal/permeability-increasing protein which is up to about half the size of said protein.

2. A method for treating gram-negative bacteremia in mammals comprising administering to gram-negative bacteremic mammals an effective amount of a purified, isolated polypeptide having bactericidal/permeability-increasing protein activity, said polypeptide comprising an NH.sub.2 -terminal fragment of human bactericidal/permeability-increasing protein which is up to about half the size of said protein.

3. A method for treating gram-negative sepsis in mammals comprising administering to gram-negative septic mammals an effective amount of a purified, isolated polypeptide having bactericidal/permeability-increasing protein activity, said polypeptide comprising an NH.sub.2 -terminal fragment of human bactericidal/permeability-increasing protein which is up to about half the size of said protein.

4. The method according to claims 1, 2 or 3 wherein said effective amount comprises between about 1 microgram and about 1000 micrograms of said polypeptide.

5. The method according to claims 1, 2 or 3 comprising administering said polypeptide parenterally.

6. The method according to claims 1, 2 or 3 comprising administering said polypeptide intravenously.

7. The method according to claims 1, 2 or 3 wherein said polypeptide has an apparent molecular weight of about 25,000 Daltons as determined by SDS-PAGE.

8. The method according to claims 1, 2 or 3 wherein said polypeptide has an amino terminal amino acid sequence V-N-P-G-V-V-V-R-I-S-Q-K-G-L-D-Y-A-S-Q-Q.

9. The method according to claim 8 wherein said polypeptide has an amino acid sequence of from about amino acid residue 1 to about amino acid residue 220 as set out in FIG. 5.

10. In a method for treating gram-negative bacterial infections in mammals by administering to gram-negative bacterially infected mammals a gram-negative bacterial antibiotic, the improvement comprising:

administering with said antibiotic an effective amount of a purified, isolated polypeptide having bactericidal/permeability-increasing protein activity, said polypeptide comprising an NH.sub.2 -terminal fragment of human bactericidal/permeability-increasing protein which is up to about half the size of said protein.

11. The improvement of claim 7 wherein the antibiotic administered is selected form the group consisting of a penicillin, a cephalosporin, rifampicin or Actinomycin D.