AU746888B2 - Anti-selectin antibodies for prevention of multiple organ failure and acute organ damage - Google Patents

Description

AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANTS: SCP\ IoDenecCOJS CmbOAA Protein Design Labs, Inc. AND Rochc Diagnostics GmbH 0*

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.455 4 ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.

INVENTION TITLE: Anti-selectin antibodies for prevention of multiple organ failure and acute organ damage The following statement is a full description of this invention, including the best method of performing it known to us: Q:\OPER\MJC\67735.96.DV 20/3/0 p:NOPER MJ067735-9 6 .1 20/3/00 -1A- ANTI-SELECTIN ANTIBODIES FOR PREVENTION OF MULTIPLE

ORGAN

FAILURE AFTER POLYTRAUMA AND FOR PREVENTION OF ACUTE ORGAN DAMAGE AFTER EXTRACORPOREAL BLOOD CIRCULATION This application is a divisional of Australian Application No. 67735/96, the entire contents of which are incorporated herein by reference.

FIELD OF THE INVENTION This invention relates to the use of anti-selectin antibodies for the prevention of multiple organ failure associated with polytrauma and for the prevention of acute organ damage associated with extracorporeal blood circulation. Especially preferred are antibodies to Eselectin, L-selectin, and/or P-selectin.

BACKGROUND OF THE INVENTION A polytrauma is understood as an injury of a number of tissues (bones or soft tissues). In a polytraumatic event, mediator systems cytokines, arachidonic acid products, oxygen radicals, proteases) as well as leukocytes and other cells are activated. This can lead to secondary organ damage destruction of tissue structures by Sliberated proteases). This secondary organ damage can occur in the whole body independently of the site of the primary trauma.

A polytrauma may also be associated with hemorrhagic shock. Hemorrhagic shock is understood as a shock which is characterized by a rapid and substantial loss of blood toward the inside or outside. At present, hemorrhagic shock can be treated successfully by intensive medical therapy, especially by volume substitution and blood transfusion. The combination of hemorrhagic shock and 2 trauma is referred to as hemorrhagic-traumatic shock. In contrast to pure hemorrhagic shock, there is, at present, no specific therapy for traumatic or hemorrhagic-traumatic shock and no prophylaxis at all for later organ failure following polytrauma.

Multiple organ failure (MOF) is a severe problem which often occurs after polytraumas. The more organs affected, the higher the mortality. Organs and systems which can fail include the heart, lung, kidney, liver, stomach, 10 intestinal system and central nervous system. Although in recent years it has been possible to reduce the very high mortality of trauma patients to about 20 by improvements in rescue service and emergency medicine, so far there is no specific therapy for organ failure.

Marzi et al., J. Trauma 35: 110-119 (1993) discloses that superoxide dimutase can be given 24 hours after trauma. However, the results are not unequivocal and merely show a trend towards a partial improvement. A substantial reduction, in mortality and MOF was, however, not observed. Mileski, W.J. et al., Surgery 108: 206-212 (1990) discloses that the binding of neutrophils or their aggregation contributes substantially to the development of hemorrhagic shock after organ damage. In this case, experimental animals were given anti-CD18 antibodies immediately after a 90 minute phase of hemorrhagic shock.

Therapeutic methods for treatment of multiple organ failure after polytrauma is not described by Mileski. Vedder N.B.

et al., Surgery 106: 509-516 (1989) also propose the use of anti-CD18 antibodies to treat hemorrhagic shock.

Selectins, such as L, E, and P-selectin, have been found to be associated with tissue damage during the course of ischemia and reperfusion. Neutrophils play an important role in this connection. It is assumed that selectin is required for the recruitment of neutrophils. Apparently L-selectin is necessary for the complete development of damage in skeletal muscle as well as in the lung (Seekamp 10 A. et al., Am. J. Pathol. 11: 592-598 (1994). Mulligan, M.S. et al., J. Immunol. 151: 832-840 (1994) describe a similar phenomenon.

The production of humanized anti-L-selectin antibodies is described in WO 94/12215, incorporated herein by reference. The use of such antibodies in the treatment of inflammatory diseases and in particular of myocardial infarction is proposed. A dose of 1 50 mg is proposed to prevent acute lung failure. However, the reference does Snot describe a method for preventing MOF after polytrauma.

Thus, there is a need for effective treatment of preventing and/or treating multiple organ failure after polytrauma.

Acute organ damage can also be caused during cardiovascular surgery, such as an aorto-coronary vein bypass operation or a cardiac valve operation, where the blood of the patient circulates extracorporeally through a 4 heart-lung machine. The extent of the damage depends upon the period during which the machine is in operation. This can lead, to failure of the lungs, which can necessitate artificial respiration of the patient well after the operation (Birnbaum, D. et al., Z. Kardiol. 79, Suppl. 4: 87 93 (1990)). Other organs, such as the heart, kidneys, liver or systems such as the blood and coagulation system may also be damaged and fail.

It is known from Mulligan, M.S. et al., J. Immunol.

10 151: 832-840 (1994) that molecules which promote adhesion '.such as L, E, and P-selectins are involved in acute inflammatory processes. These molecules mediate the adhesive interaction of leukocytes with endothelial cells.

In this connection L-selectin seems to play an important role in the initial phase (rolling) of acute intrapulmonary inflammatory reactions. Mulligan states further that anti-L-selectin antibodies are suitable for shortening the duration of the lung damage that can be triggered by L-selectin.

However, up to now no preventive therapy is known which can be used to prevent acute organ damage that is caused by extracorporeal circulation of the blood. Thus, there is a need for effective treatment of preventing acute organ damage caused by extracorporeal circulation of the blood.

P:\OPER\MJC\67735-96.SPE 14/3/00

SUMMARY

In a first aspect the present invention provides a method for prevention of multiple organ failure in a patient who has suffered a severe polytraumatic event, comprising the step of administering a therapeutically effective amount of a dose of humanised anti-selectin antibody in a pharmaceutically acceptable carrier to said patient during the first 8 hours after the polytraumatic event, wherein the maximum concentration of the antibody to be administered per single dose is 10mg/kg of body weight of the patient; the doses of the anti-selectin antibody and a pharmaceutically acceptable :carrier are administered up to 10 days after the severe polytraumatic event; and the concentration and time of administration of each dose is determined by the 15 concentration of the anti-selectin antibody in the serum or plasma of the patient at intervals of 6-24 hours after administration of the previous dose, wherein when the concentration of said anti-selectin antibody is less than 10 pg/ml of said 20 patient's serum or plasma, then a dose at least as high as the previous dose, up to a maximum dose of 10 mg/kg, is administered, or when the concentration of said anti-selectin antibody is between 10 pg/ml and /zg/ml of said patient's serum or plasma, then a dose which is half that of the previous dose, up to a maximum per dose of 5 mg/kg, is administered, or when the concentration of said anti-selectin antibody is greater than 50 pg/ml of said patient's serum or plasma, then a dose of anti-L-selectin antibody is not administered.

P:\OPER\MJC\67735-96.SPE 14/3/00 In a second aspect the present invention provides use of a humanised anti-selectin antibody in the preparation of a pharmaceutical agent for the prevention of multiple organ failure in a patient who has suffered a severe polytraumatic event, wherein the agent is administered during the first 8 hours after the severe polytraumatic event.

The invention advantageously provides a method and a therapeutic composition which can be used to effectively prevent multiple organ failure after severe polytrauma in humans, thereby considerably reducing the mortality rate of severe polytrauma patients. The invention concerns the use of anti-selectin antibodies therapeutically and for the production of pharmaceutical compositions useful in the prevention of multiple organ failure and death after 10 severe polytrauma.

BRIEF DESCRIPTION OF THE FIGURES Fig. 1 shows the lung wet weight of experimental animals with respect to the 15 observation time.

Fig. 2 shows the cardiovascular parameter CO (cardiac output) with respect to time for the various experimental animals.

Fig. 3 shows the cardiovascular parameter MAP (mean arterial blood pressure) with respect to time for the experimental animals.

Fig. 4 shows the BE value (arterial base excess) with respect to time for the experimental animals.

Fig. 5 shows the number of white blood cells with respect to time for the various experimental animals.

DETAILED DESCRIPTION OF THE INVENTION The invention concerns the use of at least one anti-selectin antibody for the production of a pharmaceutical composition to prevent acute organ damage after extracorporeal circulation of a patient's blood 10 through a heart-lung machine, wherein 1 to 30 minutes before ending the extracorporeal circulation the anti-selectin antibody is added extracorporeally into the tube system of the heart-lung machine at a dose of 1.0 mg/kg of body weight of the patient and preferably 2 4 mg/kg.

Surprisingly, acute organ damage after extracorporeal circulation of a patient's blood can be prevented to a large extent by this preventive extracorporeal administration. In a preferred embodiment a total of 1 3 further doses of 1 4 mg/kg anti-selectin antibody, such as an anti-L-selectin antibody, are administered to the patient within 1 3 days. Polyclonal or monoclonal, murine, human, chimeric or humanized antibodies/immunoglobulins and their binding fragments can be used as the anti-selectin antibodies. In one aspect of the invention, the therapeutic compositions are not administered into the body of the patient, but 7 extracorporeally, directly into the tube system of a heart-lung machine.

"Anti-selectin antibodies", as used herein, refers to any antibody which binds to a selectin. Especially preferred are antibodies which bind specifically to one of L-selectin, E-selectin, or P-selectin, as well as combinations of these. Also preferred are antibodies which react with more than one selectin, such as antibodies which react with both L- and E-selectin. L-selectin is a known 10 glycoprotein that is constitutively expressed by all leukocytes. Both L-selectin and its murine homologues, GP90 and Mell4, are involved in the normal recirculation of lymphocytes each mediates the interaction between circulating lymphocytes and vascular ligands (often 15 referred to as "addressins") on the high endothelial venules (HEVs) of lymphoid organs Lasky, et al., Cell 69: 927-938 (1992); E.L. Berg, et al., J. Cell. Biol. 114: 343-349 (1991)). In addition to its role as a lymphocyte homing receptor, L-selectin is also involved in the 20 adhesion of circulating leukocytes to non-lymphoid tissues, such as endothelium, during inflammation. L-selectin is shed from the leukocyte surface following leukocyte activation Kishimoto, et al., Science 245: 1238-1241 (1989)), and this may be an important process in retaining activated leukocytes at sites of inflammation. L-selectin has an amino-terminal carbohydrate-recognition domain (CRD) that has considerable homology with C-type lectins (K.

Trickhamer, J. Biol. Chem. 263 9557-9560 (1988)), followed by a single epidermal-growth-factor-like domain, 8 complement-regulatory domains, a single transmembrane polypeptide and a carboxy-terminal cytoplasmatic domain.

L-selectin interacts with its cognate ligand through the amino-terminal CRD in a calcium dependent manner.

In accordance with the invention, anti-selectin antibodies are preferred which modulate, and more preferably inhibit, the interaction between the CRD domain and the corresponding carbohydrate receptors on the surface of cells. Such carbohydrate receptors are described by 10 R.B. Parekh, Tibtech 12: 339-345 (1994), incorporated by reference. These carbohydrate receptors may be phosphorylated or sulfated sugars.

In a further embodiment of the invention, anti-Pand/or anti-E-selectin antibodies are used instead of, or in addition to, anti-L-selectin antibodies. Such antibodies can be produced using P- or E-selectin (described in R.B. Parekh and T.F. Tedder, FASEB Journal 9: 866-873 (1995), incorporated by reference). In an :especially preferred embodiment of the invention, anti-Pand/or anti-E-selectin antibodies are used which show considerable cross-reactivity with L-selectin antibodies, especially cross-reactivity with antibody HuDreg-55 or HuDreg-200.

As used herein, the term "humanized immunoglobulin" refers to an immunoglobulin comprising a human framework, at least one complementarity determining region (CDR) from a non-human antibody, and in which any constant region present is substantially identical to a human immunoglobulin constant region, at least about preferably at least 95% identical. Hence, all parts of a humanized immunoglobulin, except possibly the CDRs, are substantially identical to corresponding parts of one or more native human immunoglobulin sequences. For example, a humanized immunoglobulin would not encompass a chimeric mouse variable region/human constant region antibody. See, European Patent Application EP A 10 451216, incorporated by reference The invention also concerns the use of such anti- S"selectin antibodies to reduce MOF and mortality after polytrauma. It has surprisingly turned out that it is possible to prevent multiple organ failure when 15 anti-selectin antibodies, especially anti-L-selectin antibodies, are administered very soon after the polytrauma. This is also surprising because there are no acute symptoms at this early stage and there would therefore have been no reason to administer such a dose as 20 a preventive measure.

It also has surprisingly turned out that anti-selectin antibodies in doses of 1.0 10 mg/kg, preferably of 2 4 mg/kg, administered one to five times, preferably once or twice after the polytraumatic event can advantageously be used, where the first application is given as early as possible, preferably 0.5 8 hours, and especially preferably, 0.5 4 hours after the polytraumatic event.

The intervals between the individual applications are between about 6 and about 72 hours, preferably between 6 and 36 hours.

In a preferred embodiment the dose and time of the second and subsequent preventive applications is selected depending on the concentration of the anti-selectin antibodies in the blood and preferably in plasma or serum, which is an early determinable parameter. In this connection it is preferable that the plasma concentration of the anti-selectin antibody is maintained at 10 100 o 10 4g/ml over a time period of 7 10 days after the polytraumatic event. This concentration is equivalent to about a 10 100 fold excess over the concentration of soluble selectin in plasma. The dose and time for the second and subsequent applications are determined by determining the concentration of the anti-selectin antibody in blood, serum or plasma at intervals of 6 24 hours and immediately administering a dose which essentially corresponds to the dose of the first application when the plasma concentration falls below 10 Ag/ml antibody. When :20 the antibody concentration is between 10 and 50g/ml, the antibody is administered at about half the concentration of the first application, and at an antibody concentration between 50 and 100 no further antibody is administered. In this case only the antibody concentration is monitored further.

The anti-selectin antibody concentration in blood, serum or plasma is determined by the usual methods, preferably by an immunological method of determination.

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11 Such methods are known to a person skilled in the art. For example the determination can be carried out by means of an ELISA test in which a labelled selectin specific antibody, preferably the antibody which is also used therapeutically, competes for a specific selectin. In a subsequent step the amount of labelled antibody which has bound to the antigen is then determined and the concentration of the anti-selectin antibody in the sample is determined from this.

10 The therapeutic compositions of the invention are usually administered parenterally such as intravenously, intraarterially, intraperitoneally, subcutaneously or intramuscularly. Intravenous administration is preferred. The active components of the composition can be 15 used in a liquid or solid form, preferably in a lyophilized form and be used together with a suitable diluent or carrier such as water or aqueous solutions of sodium chloride, dextrose, buffers and so forth. Other suitable pharmaceutical auxiliary substances can also be added.

Antibodies to selectin are known from the state of the art and are described for example in EP-A 0 386 906, WO 93/00111 and WO 94/12215 and by Kishimoto, T.K. et al., in Blood 78: 805-811 (1991) and Proc. Natl. Acad. Sci. USA 87: 2241-2248 (1990), all of which are incorporated by reference. L-selectin is also denoted LECAM-1, Mel 14 or Lam-1 in the literature. The cloning and sequence of Lam-1 have been described in WO 93/02698. Antibodies which bind specifically to selectin are suitable. Humanized antibodies, especially HuDreg 200 which is described in WO 94/12215 and is expressly incorporated herein by reference, are suitable. Other antibodies which bind to selectin, such as HuDreg 55, (sequence: SEQ ID NO: 1 are also particularly preferred.

""10 10 o go go *2 oo o 15 o oo .1 20 o oe "Antibody" as used herein is understood as a protein that is composed of one or several polypeptide chains which are essentially encoded by antibody genes. The antibody genes code for the antigen-specific variable regions and may also code for the genes for the constant regions.

Antibodies within the sense of the invention are also understood as various derivatives and fragments of antibodies such as Fv, Fab and F(ab) 2 and individual antibody chains (Houston et al., PNAS USA 85 5879-5883 (1988), Bird et al., Science 242: 423-426 (1988), Hood et al., Immunology, Benjamin 2nd edition (1984), Hunkapiller and Hood, Nature 323 15-16 (1986)). Monoclonal antibodies and fragments thereof are preferably used and particularly preferably chimeric or humanized antibodies preferably of the IgG1 or IgG4 subtype.

The antibodies preferably contain at least two light polypeptide chains and two heavy polypeptide chains. Each of these chains contains a variable region (usually the N-terminal part of the polypeptide chain) which in turn contains a domain which binds the antigen. Heavy and light chains additionally contain a constant region of the polypeptide (usually the C-terminal part) which mediates the binding of the antibody to leukocytes (neutrophils, 13 lymphocytes etc.). Usually the light and heavy chains are complete antibody chains which are composed of the variable region and the complete constant region. In this connection, the variable regions and the constant regions can be derived from different antibodies, for example different isotypes. For example a polypeptide which contains the variable region of a heavy chain of an anti-selectin antibody of the y-1 isotype may be linked to the constant region of the heavy chain of an antibody from 10 another class (or subclass).

Anti-selectin antibodies are also suitable in which one or several amino acids are substituted. In this case, amino acids are preferably substituted by other amino acids with similar characteristic features the acidic amino 15 acid Asp by the acidic amino acid Glu). The structural characteristics of the original sequence are not changed by such substitutions. Examples of such polypeptide structures are described in Proteins, Structures and S. Molecular Principles, Creighton (editor), W.H. Freeman and 20 Company, New York (1984); Introduction to Protein Structure, C. Brandon and J. Tooze, Garland Publishing, New York (1981); Thornton et al., Nature 354 105 (1991). In general, antibodies which are suitable as anti-selectin antibodies are those which bind to one or more of L-selectin, E-selectin, and P-selectin and/or inhibit the rolling of leukocytes neutrophils).

In addition to the humanized immunoglobulins specifically described herein, other "substantially homologous" modified immunoglobulins can be readily designed and manufactured utilizing various recombinant DNA techniques well known to those skilled in the art. Human antibodies, including, for example, the Eu or GAL antibodies, as well as other human antibodies known in the art, can be used as a source of framework sequence. These framework sequences should exhibit a high degree of sequence identity with the mouse Dreg 55 or mouse Dreg 200 variable region domains from which the CDRs were derived.

The heavy and light chain variable framework regions can be derived from the same or different human antibody sequences. Indeed, the heavy and light chain framework regions can each be derived from more than one human antibody. The human antibody sequences can be the sequences of naturally occurring human antibodies or can be consensus sequences of several human antibodies. See Carter et al., WO 92/22653 (1992), incorporated by reference.

"Antibodies which are capable of binding in an 20 equivalent manner" are understood as those antibodies which bind to the same or an overlapping epitope of a selectin.

Epitope overlap can be determined by methods known in the art, for example with the aid of a competitive test system.

A competitive binding assay may be carried out for this and the extent to which the antibody competes with, e.g., HuDreg 55 for binding to an immobilized L-selectin antigen is determined. For this, L-selectin immobilized in a suitable manner (preferably L-selectin on leukocytes) is incubated with HuDreg 55 in a labelled form and an excess r of the antibody to be tested. The extent of the binding of the antibody to be tested to L-selectin is determined in comparison to HuDreg 55 by determining the bound label of the anti-leucocyte-bound label. If the labelled HuDreg is displaced by at least 50 by the antibody to be tested an epitope overlap is present. Antibodies that bind in an equivalent manner as HuDreg 55 are preferred for use in the invention.

"Antibodies which are capable of binding in an 10 equivalent manner" can also be identified by screening for the capacity to block neutrophil-endothelial cell interaction. A simple visual assay for detecting such interaction has been described by Kishimoto et al. (Blood, 78:805 (1991)). Briefly, monolayers of human umbilical 15 vein cells are stimulated with interleukin-l. Neutrophils, with or without pretreatment with the antibody under test, are added to the monolayer under defined conditions, and the number of adhering neutrophils is determined microscopically. In one method, the neutrophils are 20 obtained from human leukocyte adhesion deficient patients.

See Anderson et al., Ann. Rev. Med. 38:175 (1987). The neutrophils from such patients lack integrin receptors, whose binding to neutrophils might obscure the effects of blocking L-selectin binding.

The antibodies can be used as complete monoclonal antibodies, fragments thereof (Fv, (Fv) 2 Fab', F(ab') 2 chimeric, humanized or human antibodies. Short antibody fragments which only contain the CDR regions or parts thereof which bind specifically to L-selectin can also be used.

The production of antibodies and in particular of monoclonal antibodies and fragments thereof is familiar to a person skilled in the art and described for example in E.

Harlow and D. Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Press (1988), Bessler et al., Immunobiol.

170: 239-244 (1985), Jung et al., "Angewandte Chemie" 97: 883 (1985), Cianfiglia et al., Hybridoma Vol. 2: 451-457 (1993).

.9 9 9 Anti-selectin antibodies that can be used according to the invention can also be produced by recombinant means.

Such processes are described in Sambrook et al., Molecular 9 Cloning: A Laboratory Manual, 2nd edition Cold Spring Harbor, New York, Berger and Kimmel, Methods in Enzymology, Vol. 152, Guide to Molecular Cloning Techniques (1987), Academic Press Inc., San Diego CA, which are incorporated by reference. Such recombinant antibodies can be produced either in eukaryotic or prokaryotic cells by processes known to the art. Mammalian cells, especially lymphocytic cell lines, are preferably used as host cells.

Chimeric, humanized or human antibodies are preferably produced by recombinant methodalogue. Regions can be selected for the non-antigen binding regions of the antibodies which are for example described in E.A. Kabat et al., Sequences of Proteins of Immunological Interest (1987), National Institute of Health, Bethesda MD. The production of recombinant anti-L-selectin antibodies of 1 17 humanized and human antibodies is described in WO 94/12215, which is hereby incorporated by reference. A particularly preferred, humanized anti-L-selectin antibody is HuDreg which may be constructed in the same manner as HuDreg 200 described therein, and comprises two light chains having the sequence SEQ ID NO: 2 and two heavy chains having the sequence SEQ ID NO: 4.

Preferred humanized immunoglobulins are those which bind to selectin with a binding affinity of at least 1 x 10 7 10 M- 1 in standard binding conditions phosphate-buffered saline with 2 percent fetal bovine serum at 25°C). Examples of such humanized immunoglobulins are HuDreg 55 and HuDreg S" 200. More preferred are humanized antibodies, which preferably bind, in standard binding conditions, to human 15 selectin with an affinity of at least 1 x 101 and more preferably, with an affinity of at least 1 x 10 9

M-

1 and S* advantageously with an affinity of at least 1 x 1010 M 1 or i more. Usually, the binding affinity of a humanized immunoglobulin is within a factor of 3-10 of the mouse 20 immunoglobulin from which it was derived. For example, the affinity of the mouse Dreg 200 antibody is about 10 8 M and that of mouse Dreg 55 is about 109 M-.

The following examples, sequence protocols, publications and figures further elucidate the invention.

The described processes are to be understood as examples of illustration, not of limitation, which also after modifications, describe the subject matter of the invention.

EXAMPLE 1 Use Of Anti-L-Selectin Antibody To Reduce Post-Trauma Organ Failure The protective action of a humanized antibody against L-selectin (anti-L-selectin) in reducing post-traumatic organ failure such as that which typically occurs after injury in patients with severe polytrauma is demonstrated.

Humanized anti-L-selectin antibody (HuDreg 55) is used as t* the antibody. It also reacts with baboon L-selectin. This .o mouse form of this antibody is described by Kishimoto PNAS, USA 87 (1990) 2244-2248. The humanized sequence is shown in SEQ ID NO: 1 4.

The HuDreg 55 and HuDreg 200 antibodies react with L-selectin on human leukocytes; however, only HuDreg reacts with L-selectin of baboon leukocytes. Therefore HuDreg 55 was used. Since HuDreg 55 and HuDreg 200 bind in the same concentration range to human leukocytes in FACS analysis), the effects of HuDreg 55 on baboons is presumptively equivalent to the effect of HuDreg 200.

As a model, severe tissue damage with associated hypovolemia loss of liquid and blood towards the inside I- 19 and/or outside) was induced in baboons. The pure blood loss with subsequent shock (hemorrhagic shock) is less relevant for the lung damage (Pretorius et al., J. Trauma 1987; 27: 1344 1353; Schlag et al., page 384-402, in Schlag, Redl: Pathophysiology of Shock, Sepsis, and Organ Failure, Springer Verlag, Berlin, 1993). This is in agreement with clinical experience which shows that lung complications only occur very rarely in pure hemorrhagic shock (Schlag et al., 1993 see above).

S

S

S

S

S. In order to determine the frequency and severity of post-traumatic lung failure it was necessary to observe the animals (named: SELEC 971, SELEC 979 (treated); and Co 968, Co 969, Co 970 (control)) over several days; however, for ethical reasons, it was not possible to induce bone fractures in conscious animals and leave them untreated for several days so that in this subchronic model the tissue trauma is simulated. The activation of the complement system appears to be the earliest trigger for the activation of cellular systems and plays a key role in the rapid occurrence of a non-bacterial inflammatory reaction of the body (Schlag et al., 1993, supra). Therefore, in the model, complement was activated by cobra venom factor.

The mortality for multiple organ failure after severe polytrauma is given as 15 30 in the relevant literature. In the present animal model the severity of the polytrauma was increased to the extent that the mortality is at least twice as high and occured earlier than in humans. Therefore the observation period was limited to three days.

*o Adult baboons with a body weight (BW) between 18 and o* 22 kg were admitted to the study after three months 10 quarantine. The fasted animals were sedated with ketamine (6-8 mg/kg), subsequently intubated and attached to a CPAP respirator (continuous positive airway pressure) (inspiratory O2 concentration of 25 The anesthesia was maintained with 1-3 mg/kg/h pentobarbital. The animals breath spontaneously. A Swan Ganz catheter was pushed forward into the pulmonary artery via the right femoral vein. A catheter for withdrawing blood and measuring blood pressure was tied into the right arm artery. A large lumen catheter is introduced into the femoral artery for the temporary collection of blood. A catheter for infusions, medication and blood collection was introduced into the left arm vein. The bladder was catheterized for the 21 measurement of urine production. The Swan Ganz catheter and the arterial catheter were left for three days. For fluid balance the animals received 5 ml/kg/h Ringer solution (electrolyte solution for parenteral liquid substitution) during the anaesthetic phase. The blood temperature of the animals was kept at a 37*C with the aid of an infrared lamp. Blood gas analyses were carried out (PO2, pCO 2 pH, BE, HCO 3 and hemodynamic parameters were determined (MAP, RAP, PAP, CO, HR). Lung function was 10 determined by means of the respiratory rate (RR) and end expiratory CO 2 Blood samples were collected repeatedly in order to measure the number of white blood cells (WBCs).

Cobra venom factor was administered at a dose of 10 U/kg per i.v. at the beginning of the retransfusion and 15 administered again at a dose of 5 U/kg 1 hour after beginning the retransfusion of the blood. The blood withdrawal for triggering the hypovolemia was regulated such that the MAP (mean arterial pressure) came to lie between 40 and 50 mm Hg and the CO (cardiac output) is reduced by 50 to 70%. Approximately 50 ml/kg blood were usually withdrawn for this and stored until retransfusion.

The deficient circulation was maintained for two to three hours and was controlled in such a way that the base excess I- 22 was no more than -5 to -7 mEq. At the end of this shock phase retransfusion of the previously collected blood was begun. This phase lasted 4 hours.

The retransfusion was complemented by an additional administration of Ringer solution. Humanized antibody HuDreg 55 or the corresponding volume of saline solution as a placebo was administered intravenously 15 minutes after j the start of retransfusion. Anti-L-selectin antibody was administered at a dose of 2 mg/kg. At the end of 10 retransfusion the animals were awakened from anaesthesia and were returned to their cages for observation. At times 24 h, 48 h and 72 h a low level of anesthesia was again induced and the measuring parameters were registered and blood was withdrawn. If the animals had not died before the end of the three day observation period, they were then sacrificed and autopsied. The main terminal points of the study were mortality, survival period and organ damage, for example, to the lung.

In the first experiment, three control animals were treated with placebo solution and two with the HuDreg humanized antibody. Of the three control animals, two died before the end of the three day observation period at 38 h and 41 h whereas both anti-L-selectin treated animals survived. The lung wet weight, as an expression of organ damage, was almost normal in the antibody treated animals (normal values 7-8 g/kg BW) whereas it had increased considerably in all three placebo-treated control animals (Fig. This is due to infiltration of fluid after the permeability disorder. The cardiovascular parameters CO 2 and MAP (Fig. 2 and 3) are better at 24 hours in the surviving animals than in the control animals. The dying control animals also have a negative arterial base excess (BE) indicating a disturbed acid-base balance (Fig. 4).

The leucocytosis (increase in white blood cells) observed in the control animals is absent in the antibody animals 15 (Fig. EXAMPLE 2 Use Of Anti-L-Selectin Antibody To Reduce Post-Traumatic Mortality The experiments reported in Example 1, supra, were continued and expanded to include 28 baboons which were randomly assigned to one of two experimental groups conducted as described in Example 1. The baboons received either 2 mg/kg i.v. of anti-L-Selectin antibody or the appropriate placebo volume-dose as control 15 minutes after initiation of reperfusion after the ischemia period. The main endpoints for statistical analysis of the study were mortality at the end of the 3-day observation period and survival time. Fisher's exact test was used for mortality analysis and the log-rank-test was used for survival time analysis. One-sided p-values (reduction of mortality or prolongation of survival time by active treatment) are reported. The null hypothesis was rejected only when the 10 probability of the calculated statistic was p<0.05.

Anti-L-selectin antibody reduced (p<0.05) mortality from 10 out of 14 baboons in the control group to 3 out of 14 baboons in the active treatment group at a level of statistical significance. In addition, survival time in the anti-L-Selectin group was prolonged to 64.4 h, whereas animals in the control group died earlier (p<0.05), on an average at 42.1 h. This difference was statistically significant.

The table summarizes the results: Mortality Survival time (h) Anti-L-Selectin 3/14* 64.4±4.7* Antibody Placebo-control 10/14 42.4±5.7 Mean standard error of mean; n 14 per group; p 0.05 by Fisher's exact test; p<0.05 by log-rank-test.

Observation period was 72 h.

0 These data show that early treatment of baboons suffering from ischemia-reperfusion injuries due to hemorrhgaic-traumatic shock with administration of anti-L- Selectin significantly prolongs survival time and reduces mortality as compared to placebo-control.

1 a 5 EXAMPLE 3- Use of Anti-L-Selectin Antibody To Reduce Organ Damage After Extracorporeal Blood Circulation The protective action of a humanized antibody against L-selectin, preferably HuDreg 55, in reducing organ damage after extracorporeal blood circulation such as that which typically occurs after long operating periods of the heart-lung machine in cardiac surgery was studied.

As a model, severe lung damage was caused in baboons by letting the heart-lung machine, which takes over the function of the lungs and heart after the heart is stopped, run for several hours. After the machine was turned off, the pumping action of the heart was resumed, and endogenous circulation and respiration restarted, massive infiltration of activated leukocytes into the pulmonary circulation caused severe damage to the lungs. The leukocytes present a in the pulmonary circulation locally release toxic 10 mediators at a high concentration which led to damage of the vascular endothelium with subsequent increase in permeability. In this process fluid crossed over from the vascular space into the alveoli (smallest pulmonary alveoli) which led to an accumulation of fluid in the lung.

15 This impeded gas exchange in the lung and artificial respiration becomes necessary. The oxygen demand increased as the impairment in gas exchange increases in severity and this was further aggravated by a fibroproliferative transformation of the alveolo-endothelial barrier. Thus, in particularly severe cases, the concentration of inhaled oxygen in the respiratory air which is usually about 20 has to be increased to about 100 Nevertheless, in such cases, the supply of pure oxygen is insufficient to maintain the arterial oxygen concentration or oxygen partial pressure in the blood (pa02) at an adequate level.

The fibroproliferative transformation process and pulmonary edema result in an increase in the pressures in the arteria pulmonalis which is connected to the lung and this leads to a strain on the right heart. If these reactions build up further this finally leads to death by heart-lung failure.

Adult baboons with a body weight (BW) between 18 and 10 22 kg are admitted to the study after three months quarantine. The fasted animals were sedated with ketamine (6-8 mg/kg), intubated, and attached to a CPAP respirator (inspiratory 02 concentration of 25 The anesthesia was maintained with 1-3 mg/kg/h pentobarbital. The animals breathed spontaneously. A Swan Ganz catheter was pushed forward into the pulmonary artery via the right femoral vein. A catheter for withdrawing blood and measuring blood pressure was tied into a right arm artery. A catheter for infusions, medication and blood collection was introduced into a left arm vein. The bladder is catheterized to measure the production of urine. For fluid balance the 28 animals receive 5 ml/kg/h Ringer solution. The temperature of the animals is maintained at 37C with the aid of an infrared lamp. Blood gas analyses are carried out (p 0 2, pCO 2 pH, BE, HC03-) and hemodynamic parameters are determined (MAP, RAP, PAP, CO, HR). The lung function is determined by means of the respiratory rate (RR) and end expiratory CO 2 Blood samples are collected repeatedly in order to measure the number of white blood cells (WBC).

At the start of the experiment the thorax was opened 10 (thoracotomy) and the vena cava and the aorta was prepared.

Afterwards, first the vena cava and then the aorta were cannulated so that blood from the vena cava flowed into the heart-lung machine and later back into the aorta. A peristaltic pump assumes the pumping function of the heart in the heart-lung machine and ensures maintenance of the pressure gradient required for circulation. Exchange of oxygen and binding of carbon dioxide is achieved by membrane oxygenation. The blood was heparinized so that the tubes and blood vessels do not get blocked. The blood flows back to the aorta via the tube system and is distributed in the body via the normal vascular system.

29 The heart-lung machine takes over the function of the heart and lung. The heart is stopped while the machine is in operation so that the operating surgeon can for example work on the cardiac valves (insert prostheses).

Fifteen minutes before the end of the four hour extra-corporeal circulation, a dose of 2 mg/kg HuDreg 55 or the same volume dose of placebo was administered directly

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into the tube system of the heart-lung machine. The animal was observed for a further four hours after ending the 5* extracorporeal circulation. Measurements are carried out repeatedly before, during and after the extra-corporeal circulation. In particular arterial blood gases and parameters for acid-base balance are recorded, cardiovascular parameters such as the mean arterial blood S 15 pressure, right atrial pressure, pulmonary artery pressure, cardiac output and heart rate are determined, the lung function is measured end expiratory C02) and blood samples are withdrawn for hematological, clinical-chemical kidney and liver function) and biochemical analyses.

In addition, urine production (kidney function) is measured. Further, parameters for permeability disorders in the lung were determined. At the end of the experiment, the animals were sacrificed and necropsy and histological examinations were carried out in order to determine the degree of damage to the various organs and systems such as heart, lung, liver, kidney, intestine, CNS, blood etc. It is expected that the animals treated with HuDreg 55 sustain less organ damage than those treated with placebo.

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APPLICANTS:

NAME: Martin, Ulrich, et al.

(ii) TITLE OF INVENTION: Anti-L-selectin antibodies for prevention of multiple organ failure after polytrauma and for prevention of acute organ damage after extracorporeal blood circulation.

(iii) NUMBER OF SEQUENCES: 4 (iv) CORRESPONDENCE ADDRESS: Felfe Lynch Attn: Norman D. Hanson 805 Third Avenue New York New York

U.S.A.

10022 COMPUTER READABLE FORM: MEDIUM TYPE: 3.5" Computer Disk COMPUTER: IBM PC compatible OPERATING SYSTEM: PC-DOS/MS-DOS SOFTWARE: ASCII

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eq 0 0 0 0 Goo*o *0 0 00oo *oo* o S S 9 b S 0 0 .00 0 *650 0 S 5 0500 0 *0@S *0 S (vi) CURRENT APPLICATION DATA: APPLICATION NUMBER: 20-Dec-95 CLASSIFICATION: 530 To be assigned (vii) PRIOR APPLICATION DATA: APPLICATION NUMBER: EP 95 FILING DATE: 17-Aug-1995 APPLICATION NUMBER: EP 95 FILING DATE: 19-Sep-1995 APPLICATION NUMBER: US 08 FILING DATE: 27-Dec-1995 112 895.8 114 969.9 578 953 (viii) ATTORNEY/AGENT INFORMATION NAME: Hanson, Norman D.

REGISTRATION NUMBER: 30,946 REFERENCE/DOCKET NUMBER: BOER (ix) TELECOMMUNICATION INFORMATION TELEPHONE: (212) 688-9200 TELEFAX: (212) 838-3884 1059-PFF/NDH INFORMATION FOR SEQ ID NO: 1: SEQUENCE CHARACTERISTICS: LENGTH: 654 base pairs TYPE: nucleic acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: CDS LOCATION: 1,.654 (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1:

GAC

Asp

I

ATT CAG ATG Ile Gin Met

ACC

Thr

S

CAR TCT CCG AGC Gin Ser Pro Ser

TCT

Ser 10 TTG TCT GCG TCT Leu Ser Ala Ser GTA GGG Val Gly is CAT AGG CTC Asp Arg Val GGT GAT AGT Gly Asp Ser

ACT

Thr ATC ACC TCC AAG Ile Thr Cys Lys

CC

Ala 25 AGC CAR AGT GTT CAT TAT GAT Scr Gin Ser Val Asp Tyr Asp TAT ATO ARC TG Tyr Met Asn Trp,

TAC

40 CAR CAC AAA CCA Gin Gin Lys Pro

GGA

Cly ARC CCA CCC 144 Lys Ala Pro ARC CTT Lys Leu CTC ATC TAT GCT Leu Ile Tyr Ala

GCA.

Ala 55 TCC ARC CTA CAR TCT GGT ATC CCA TCC 192 Ser Asn Leu Giu Ser Gly Ile Pro Ser

AGG

Arg 65 TTT AGT CCC ACT Phe 5cr Cly Ser

GG

Cly 70 TCT CGG ACA CAC 5cr Gly Thr Asp

TTC

Phe 75 ACC CTC ACC ATC Thr Leu Thr Ile TCT 240 so TCT CTG CAG CCG Leu Gin Pro

GAG

Clu GAT TTC CCA ACC Asp Phe Ala Thr

TAT

Tyr 90 TAC TGT CAG Tyr Cys Gin CAR ACT ART 288 Gin Ser Asn CAR GAT CCG Ciu Asp Pro

TCC

Trp 100 ACC TTC GGT CAR Thr Phe Cly Gin

GGC

Giy 105 ACC ARG, GTG GAR ATC AAA CGA 336 Thr Lys Val Ciu Ile Lys Arg 110 ACT GTG GCT CCA CCA TCT GTC Thr Val Ala Ala Pro Ser Vai 115

TTC

Phe 120 ATC TTC CCC CCA Ile Phe Pro Pro

TCT

Ser 125 CAT GAG CAC 384 Asp Giu Gin TTG AAA Leu Lys 130 TCT GCA ACT CC Ser Gly Thr Ala

TCT

Ser 135 GTT GTC TGC Val Val Cys CTG CTC Leu Leu 140 ART ARC TTC TAT 432 Asn Asn Phe Tyr 33 CCC AGA GAG GCC AAA GTA CAG TGG AAG GTG GAT AAC GCC CTC CAA TCG 480 Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gin Ser 145 iSO 155 160 GGT AAC TCC CAG GAG AGT GTC ACA GAG CAG GAC AGC AAG GAC AGC ACC 528 Gly Asn Ser Gin Glu Ser Val Thr Giu Gin Asp Ser Lys Asp Ser Thr 165 170 175 TAC AGC CTC AGC AGC ACC CTG ACG CTG AGC AAA GCA GAC TAC GAG AAA 576 Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys 180 185 190 CAC AAA GTC TAC GCC TGC GAA GTC ACC CAT CAG GGC CTG AGC TCG CCC 624 His Lys Val Tyr Ala Cys Giu Val Thr His Gin Gly Leu Ser Ser Pro 195 200 205 GTC ACA AAG AGC TTC AAC AGG OGA GAG TGT 654 Val Thr Lys Ser Phe Asn Arg Gly Giu Cys 210 215 INFORMATION FOR SEQ ID NO: 2: Wi SEQUENCE CHARACTERISTICS: LENGTH: 218 TYPE: amino acid STRANDEDNESS: single TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2: Asp Ile Gin Met Thr Gin Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 1s Asp Arg Val Thr Ile Thr Cys Lys Ala Ser Gin Ser Val Asp Tyr Asp 25 Gly Asp Ser Tyr Met Asn Trp Tyr Gin Gin Lys Pro Gly Lys Ala Pro 40 Lys Leu Leu Ile Tyr Ala Ala Ser Asn Leu Glu Ser Gly Ile Pro Ser 55 Arg Phe Ser Gly Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser 70 7S Ser Leu Gin Pro Glu Asp Phe Ala Thr Tyr Tyr Cys Gin Gin Ser Asn 90 Giu Asp Pro Trp, Thr Phe Gly Gin Gly Thr Lys Val Glu Ile Lys Arg 100 105 34 Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln 115 120 125 Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr 130 135 140 Pro Arg Glu Ala Lys Val Gin Trp Lys Val Asp Asn Ala Leu Gin Ser 145 150 155 160 Gly Asn Ser Gin Glu Ser Val Thr Glu Gin Asp Ser Lys Asp Ser Thr 165 170 175 Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys 180 185 190 His Lys Val Tyr Ala Cys Glu Val Thr His Gin Gly Leu Ser Ser Pro 195 200 205 Val Thr Lys Ser Phe Asn Arg Gly Glu Cys 210 215 INFORMATION FOR SEQ ID NO: 3: SEQUENCE CHARACTERISTICS: LENGTH: 1329 base pairs TYPE: nucleic acid STRANDEDNESS: double S(D) TOPOLOGY: linear (ii) MOLECULE TYPE: cDNA (ix) FEATURE: NAME/KEY: CDS LOCATION:1,,1329 (ix) FEATURE: NAME/KEY: mat_peptide LOCATION:1 (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 3: GAA GTG CAA CTG GTG GAG TCT GGG GGA GGC TTA GTG CAG CCT GGA GGA 48 Glu Val Gin Leu Val Glu Ser Gly Gly Gly Leu Val Gin Pro Gly Gly 1 5 10 AGC TTG AGA CTC TCC TGT GCA GCC TCT GGA TTC ACT TTC AGT ACC TAT 96 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Thr Phe Ser Thr Tyr 25 GCC ATG TCT TGG GTT CGC CAG GCT CCA GGG AAG GGA CTC GAG TGG GTC 144 Ala Met Ser Trp Val Arg Gin Ala Pro Gly Lys Gly Leu Glu Trp Val 40 CCA TCC ATT ACT ACT GGT GGT AGC ACC Ala Ser Ile Ser Thr Gly Giy Ser Thr 55 TAC TAT CCA GAC ACT GTG AAC 192 Tyr Tyr Pro Asp Ser Val Lys GGC CGA TTC ACC ATC TCC ACA Gly Arg Phe Thr Ile Ser Arg 70 GAT AAT GCC AAC AAC Asp Asn Ala Lys Asn 75 ACC CTG TAC Thr Leu Tyr CTG 240 Leu CAA-ATG AAT TCT CTG AGG GCT GAG GAC Arg Ala Glu Asp Gin Met Asn AGA GAC TAT Arg Asp Tyr ACA GTC TCC Thr Val Ser 115 Ser Leu

ACG

Thr 90 CCC GTG TAT Ala Val Tyr COG TAT TTT GAC Gly Tyr Phe Asp

TAC

105 TGG GGC CAA CGC Trp Cly Gin Gly TAC TGT GCA 288 Tyr Cys Ala ACC CTG CTC 336 Thr Leu Val 110 CCC CTG GCG 384 Pro Leu Ala b a TCA GCT TCC ACC Ser Ala Ser Thr

AAG

Lys 120 CCC CCA TCC CTC Giy Pro Ser Vai

TTC

Phe 125 CCC TGC Pro Cys 130 TCC AGG AGC ACC TCC GAG AGC ACA CC Ser Arg Ser Thr Ser Clii Ser Thr Ala 135

CC

Ala 140 CTG GGC TGC CTG 432 Leu Gly Cys Leu

CTC

Val 145 AAG GAC TAC TTC Lys Asp Tyr Phe

CCC

Pro 150 GAA CCG GTG ACG Ciii Pro Val Thr

GTC

Val 155 TCG TGG AAC TCA Ser Trp Asn Ser CCC 480 Gly 160 GCC CTG ACC AGC Ala Leu Thr Ser

GCC

Gly 165 GTC CAC ACC TTC Val His Thr Phe

CCG

Pro 170 GCT GTC CTA Ala Val Leu GGA CTC TAC Cly Leu Tyr CC;C ACC. AAC Gly Thr Lys 195

TCC

Ser 180 CTC ACC AGC GTG Leu Ser Ser Val

GTG

Val 185 ACC GTC CCC TCC Thr Val Pro Ser CAG TCC TCA 528 Gin Ser Ser 175 AGC AGC TTC 576 Ser 5cr Leu 190 AGC AAC ACC 624 Ser Asn Thr ACC TAC ACC TC Thr Tyr Thr Cys

AAC

Asn 200 GTA CAT CAC AAC Val Asp His Lys AAC GTG Lys Val 210 GAC AAC AGA GTT Asp Lys Arg Val

GAG

Clu 215 TCC AAA TAT COT Ser Lys Tyr Gly

CCC

Pro 220 CCA TCC CCA TCA 672 Pro Cys Pro

TGC

Cys 225 CCA CCA CCT GAG Pro Ala Pro Glu

TTC

Phe 230 CTG CCC CGA CCA Leu Gly Cly Pro

TCA

Ser 235 GTC TTC CTG TTC Val Phe Leu Phe CCC 720 Pro 240 CCA AAA CCC AAG Pro Lys Pro Lys

GAC

Asp 245 ACT CTC ATG ATC Thr Lcu Met Ile

TCC

Ser 250 CCC ACC CCT GAG Arg Thr Pro Clu GTC ACG 768 Val Thr 255 TGC GTG GTG Cys Val Val TGG TAC GTG Trp Tyr Val 275 GTG GAC GTG AGC CAG GAA GAC CCC GAG GTC CAG TTC Val Asp Val Ser Gin Giu 265 Asp Pro Giu Val Gin 270 Phe AAC 816 Asn GAT GGC OTG GAG Asp Gly Val Glu

GTG

Val 280 CAT AAT GCC AAG His Asn Ala Lys

ACA

Thr 285 AAG CCG CGG 864 Lys Pro Arg GAG GAG Giu Olu 290 CAG TTC AAC AGC Gin Phe Asn Ser

ACG

Thr 295 TAC COT GTG GTC Tyr Arg Val Val

AGC

Ser 300 GTC CTC ACC GTC 912 Vai Leu Thr Val

CTG

Leu 305 CAC CAG GAC TG His Gin Asp Trp AAC GGC AAG GAG Asn Gly Lys Giu

TAC

Tyr 315 AAG TGC AAG GTC Lys Cys Lys Val TCC 960 Ser 320 AAC AAA GGC CTC Asn Lys Gly Leu

CCG

Pro 325 TCC TCC ATC GAG Ser Ser Ile Giu

AAA

Lys 330 ACC ATC TCC Thr Ile Ser GGG CAG CCC Gly Gin Pro GAG ATG ACC Giu Met Thr 355

CGA

Arg 340 GAG CCA GAG GTG Giu Pro Gin Val

TAC

Tyr 345 ACC CTG CCC CCA Thr Leu Pro Pro AAA GCC AAA 1008 Lys Ala Lys 335 TCC CAG GAG 1056 Ser Gin Giu 350 AAA GGC TTC 1104 Lys Gly Phe AAG AAC GAG GTC Lys Asn Gin Val

AGC

Ser 360 CTG ACC TGC CTG Leu Thz Cys Leu

GTC

Val 365 TAC CCC Tyr Pro 370 AOC GAC ATC 0CC Ser Asp Ile Ala

GTG

Val 375 GAG TGG GAG AGC Giu Trp Glu Ser

AAT

Asn 380 000 GAG CCG GAG 1152 Gly Gin Pro Giu

AAC

Asn 385 AAC TAC AAG ACC ACG CCT CCC GTG CTG Asn Tyr Lys Thr Thr Pro Pro Val Leu 390

GAC

Asp 395 TCC GAC GGC TCC Ser Asp Gly Ser TTC 1200 Phe 400 TTe CTC TAC AGC Phe Leu Tyr Ser

AGO

Arg 405 CTA ACC GTG GAC Leu Thr Val Asp

AAG

Lys 410 AGC AGO TG Ser Arg Trp GAG GAG 000 1248 Gin Giu Gly 415 AAC CAC TAC 1296 Asn His Tyr 430 AAT GTC TTC Asn Val Phe ACA GAG AAG Thr Gin Lys 435

TCA

Ser 420 TGC TCC GTG ATG Cys Ser Val Met

CAT

His 425 GAG OCT CTG CAC 0Th Ala Leu His AOC CTC TCC CTG Ser Leu Ser Leu

TCT

Ser 440 CTG, GOT AAA Leu Gly Lys 1329 INFORMATION FOR SEQ ID NO: 4: SEQUENCE CHARACTERISTICS: LENGTH: 443 TYPE: amino acid STRANDEDNESS: double TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 4: Glu Val Gin Leu Val Glu Ser Gly Gly Gly Leu Val Gin Pro Gly Gly a a 1 Ser Ala Ala Gly Gin Arg Thr Pro Val 145 Ala Gly Gly Leu Met Ser Arg Met Asp Val Cys 130 Lys Leu Leu Thr Arg Ser 35 Ile Phe Asn Tyr Ser 115 Ser Asp Thr Tyr Lys 195 Leu Trp Ser Thr Ser Asp 100 Ser Arg Tyr Ser Ser 180 Thr 5 Ser Val Thr Ile Leu 85 Gly Ala Ser Phe Gly 165 Leu Tyr Cys Arg Gly Ser 70 Arg Tyr Ser Thr Pro 150 Val Ser Thr Ala Gin Gly 55 Arg Ala Phe Thr Ser 135 G~u His Ser Cys Ala Ala Ser Asp Glu Asp Lys 120 Glu Pro Thr Val Asn 200 Ser 25 Pro Thr Asn Asp Tyr 105 Gly Ser Val Phe Val 185 Val 10 Gly Gly Tyr Ala Thr 90 Trp Pro Thr Thr Pro 170 Thr Asp Phe Lys Tyr Lys 75 Ala Gly Ser Ala Val 155 Al a Val His Thr Gly Pro Asn Val Gln Val Ala 140 5cr Val Pro Lys Ser Glu 5cr Leu Tyr Thr 110 Pro Gly Asn Gin Ser 190 5cr Thr Trp Val Tyr Cys Leu Leu Cys Ser 5cr 175 Ser Asn Tyr Val Lys Leu so Ala Val Ala Leu Gly 160 Leu Thr Lys Val Asp Lys Arg Val Glu 5cr Lys Tyr Giy Pro Pro Cys Pro Ser 210 215 38 Cys Pro Ala Pro Glu Phe Leu Gly Gly Pro Ser Val Phe Leu Phe Pro 225 230 235 240 Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr 245 250 255 Cys Val Val Val Asp Val Ser Gin Glu Asp Pro Glu Val Gin Phe Asn 260 265 270 Trp Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg 275 280 285 Glu Glu Gin Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val 290 295 300 Leu His Gin Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser 305 310 315 320 Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile Ser Lys Ala Lys 325 330 335 Gly Gin Pro Arg Glu Pro Gin Val Tyr Thr Leu Pro Pro Ser Gin Glu 340 345 350 Glu Met Thr Lys Asn Gin Val Ser Leu Thr Cys Leu Val Lys Gly Phe 355 360 365 Tyr Pro S e r Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gin Pro Glu 370 375 380 Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe 385 390 395 400 Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg Trp Gin Glu Gly 405 410 415 o S Asn Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr S.o 420 425 430 Thr Gin Lys Ser Leu Ser Leu Ser Leu Gly Lys 435 440 Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the common R/general knowledge in Australia.

-0 i~ L

Claims (4)

1. A method for prevention of multiple organ failure in a patient who has suffered a severe polytraumatic event, comprising the step of administering a therapeutically effective amount of a dose of humanised anti-selectin antibody in a pharmaceutically acceptable carrier to said patient during the first 8 hours after the polytraumatic event, wherein the maximum concentration of the antibody to be administered per single dose 10 is 10mg/kg of body weight of the patient; o the doses of the anti-selectin antibody and a pharmaceutically acceptable carrier are administered up to 10 days after the severe polytraumatic event; and the concentration and time of administration of each dose is determined by the concentration of the anti-selectin antibody in the serum or plasma of the patient at intervals of 6-24 hours after administration of the previous dose, wherein when the concentration of said anti-selectin antibody is less than 10 pg/ml of said patient's serum or plasma, then a dose at least as high as the previous dose, up to a maximum dose of 10 mg/kg, is administered, or when the concentration of said anti-selectin antibody is between 10 pg/ml and pg/ml of said patient's serum or plasma, then a dose which is half that of the previous dose, up to a maximum per dose of 5 mg/kg, is administered, or when the concentration of said anti-selectin antibody is greater than 50 pg/ml of said patient's serum or plasma, then a dose of anti-L-selectin antibody is not administered. P:AOPER\MKR\SPECI22396-00-039 doc-08/020

2. The method of claim 1, wherein the humanized antibody is anti-L-selectin antibody HuDreg 55 or HuDreg 200.

3. Use of a humanised anti-selectin antibody in the preparation of a pharmaceutical agent for the prevention of multiple organ failure in a patient who has suffered a severe polytraumatic event, wherein the agent is administered during the first 8 hours after the severe polytraumatic event.

4. The method of claim 1, substantially as hereinbefore described with reference to the examples. DATED this 8th day of February, 2002 Protein Design Labs, Inc and Scil Biomedicals GmbH by DAVIES COLLISON CAVE Patent Attorneys for the applicants