AU728984B2 - Syngeristic interplay of lymphokines and dsRNAs - Google Patents

Description

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT Name of Applicant: Actual Inventor: Address for Service: Invention Title: HEM RESEARCH, INC.

WILLIAM A CARTER CULLEN CO., Patent Trade Mark Attorneys, 240 Queen Street, Brisbane, Qld. 4000, Australia.

S.

S.

SYNERGISTIC INTERPLAY LYMPHOKINES AND dsRNAs The following statement is a full description of this invention, including the best method of performing it known to us: Present use of lymphokines (interleukin-1, 2 and 3, interferon, tumor necrosis factor, etc.) is handicapped severely because of narrow therapeutic range and severe toxicity usually observed at the S 5 high doses necessary to effect responses in human S. cancers or viral diseases. The present invention describes unexpected synergistic interplay between lymphokines and dsRNAs which dramatically reduce the necessary dosages of lymphokines, especially IL-2,and simultaneously widen their therapeutic range.

Specific combinations of dsRNA plus IL-2 in cancer, viral and inflammatory disease treatments significantly increase survival in human melanoma-bearing animals in part because of 15 augmentation by dsRNA of lymphokine activated killer cells (LAK) which are first formed in response to IL-2 exposure. The invention has wide applicability to non-toxic, efficacious control of both human cancer and various human viral infections.

BACKGROUND OF THE INVENTION Present Therapy with Interleukin-2 (IL-2) as the Prototype Lymphokine. Lymphokines are now routinely manufactured by recombinant DNA technology. rIL-2 refers to recombinant lymphokine activated killer cells. The latter cells are generated in vitro by exposing human blood cells (obtained by leukapheresis) to rIL-2. The cells are then customarily reinfused into the patient where it is at least hoped that the LAK cells, with continued IL-2 stimulation, will kill or control the patient's tumor. The presently available regime is described in Figure 1. The arrows inside the 5 brackets indicate IL-2 doses which usually cannot be given due to overwhelming toxicities. Toxicities reported in a clinical trial and measures used to counteract these toxic reactions are given in Tables 1 and 2. Due to the massive side-effects, therapeutic effects are only seen in 10-20% of patients treated with lymphokines (see Rosenberg et al New England Journal of Medicine, volume 313, p.

1485, 1985). The most responsive tumors seem to be kidney and melanoma when lymphokines are given by 15 themselves, but my invention has wide applicability to other cancers, viral disorders in general and various inflammatory states. There is no evidence that their efficacy can be increased by combining them with routinely-used chemotherapeutic agents.

Toxicities of Lymphokines are Dose-Related.

Figure 2 summarizes available clinical data which shows that at IL-2 doses greater than 10 units per kilogram body weight, devastating toxicities can be seen in man. However, such doses have been generally deemed necessary in order to effect tumor regressions. Unfortunately, often the patient will die from the IL-2 toxicity before the tumor will become measurably smaller as lymphokine therapy is currently practiced.

BRIEF DESCRIPTION OF THE DRAWINGS FIGURE 1 is a representation of current tumor therapy with recombinant Interleukin-2 (rIL-2) and 5 lymphokine activated killer (LAK) cells and is adapted from the NIH therapeutic protocol of LAK/IL-2 therapy reported by Rosenberg, S.A. et al in New England Journal of Medicine 313:1485 (September 12, 1985); FIGURE 2 is a bar graph summarizing available clinical data comparing various IL-2 doses with toxicity and dose limiting toxicity; FIGURES 3A and 3B are bar graphs comparing the cytotoxicity at different doses of IL-2 with a constant dose (50:1 and 25:1, respectively) of dsRNA; FIGURES 4 and 4B are bar graphs showing the increased human LAK cell activity of combination rIL-2 and dsRNA therapy; FIGURE 5 is a bar graph reporting the number melanoma lung metastases for four different groups including the combination of dsRNA and rIL-2; FIGURE 6 is a graph comparing the survival in malignant melanoma xenograft bearing athymic mice for the indicated number of days for four different and groups; and FIGURE 7 is a bar graph similar to Figure 1, illustrating toxicities associated with increasing bolus doses of IL-2 in man and comparing current IL-2 dosage ranges with combined IL-2 and dsRNA projected doses.

SUMMARY OF THE INVENTION A synergistic combination of dsRNA, as the non-toxic member, and a lymphokine, as a toxic member, dramatically reduces the necessary doses of lymphokines, especially IL-2 to a moderate to no toxicity dose, and simultaneously widens their therapeutic range. The synergist combination, particularly of interferon or various interleukins 15 such as IL-2 as the lymphokine component, is effective to control human cancer, especially cancer of the lung and kidney and malignant melanoma or S* other disorders, according to the therapeutic methods described. The combination is also effective for treating various human viral infections. Therapeutic compositions are also described.

The methods and compositions of this invention present a dsRNA and an interleukin administered simultaneously or sequentially, which concentrations result in enhanced levels of both NK and LAK cells in the organism without increased toxicity, that is in excess of the toxicity, if any, of the individual component administered individually, resulting in an enhanced antitumor, antiviral or immunomodulatory response. Concurrently with this dsRNA/lymphokine therapy, my invention also includes the administration of a substance which inhibits cyclooxygenase activator. As an example, the invention includes concurrent administration of indomethacin, a prostaglandin inhibitor, thereby abrogating prostaglandin release and the resultant NK cell down regulation response.

In this manner, the natural inhibitors of desirable NK cells are removed, and the NK cell population increased accordingly. This invention includes the novel combinations therapeutic treatments and pharmaceutical compositions, where appropriate of dsRNA, lymphokine and a substance which inhibits cyclooxygenase activator.

Quantities of the members of the combination vary in accordance with clinical observation and results of therapy. Usual amounts of the dsRNA component provide a peak blood concentration of from 0.1 to 1000 micrograms dsRNA per milliliter in the systemic blood circulation immediately following administration measured at a point distal from the site of infusion. When interferon, preferably interferon (alpha), is the lymphokine, an amount of from 0.01 to 100,000 IRU per milliliter of the patient's body fluid is provided. When IL-2, preferably rIL-2, is the lymphokine, the amount 2 administered lies within a range of about 10 IL-2 units per kg of the patient's body weight up to a value approaching unacceptable levels of toxicity, which may be as high as 106 units. Most effective, toxic-reaction manageable values are in the range 3 4 of from about 10 to about 10 IL-2 units per kg body weight.

In vitro and in vivo experiments confirm that dsRNAs (and mismatched dsRNAs in particular) confer a synergistic pharmacologic action with interleukins in general (IL-2 in particular) which results in an enhanced biologic response (antitumor, antivirus, immune modulator) with greatly reduced toxicity. Typically, experiments with mismatched dsRNA demonstrate that the dosage of IL-2 required, as for an antitumor response, can be reduced at least 30 to 100 fold. The synergistic pharmacologic effect is conferred at (but not limited to) both the levels of NK (natural killer)-sensitive and also NK-resistant tumor or viral infected cells. NK-resistant tumor or viral-infected cells are also referred to as LAk.

(lymphokine activated killer) cells. I demonstrated this activity unequivocally by the use of monoclonal antibody markers in which I observed dramatic increases concurrently in both NK cells (using asialo-Gml monoclonal antibody) and LAK cells (using Thy 1.2 monoclonal antibody). Such antibodies are readily available monoclonal antibody reagents to those familiar with this art. I also observed that the concurrent use of compounds which reduce the biologic level of various NK cell natural antagonists (such as prostaglandins) would further amplify this synergy in an essentially non-toxic, or minimally toxic, manner. As an example, the use of indomethacin (25 mg per day for a 60 kilogram individual) dramatically increased the pharmacologic synergy in part by reducing endogenous prostaglandin concentration.

DETAILED DESCRIPTION OF THE INVENTION I have determined that dsRNAs act as biochemical i. catalysts to increase the specific killing of tumor 5 cells by IL-2 generated LAK cells in a non-toxic manner. This is demonstrated by the following cell I0** culture experiments. The human renal cancer cell line designated 7860 was grown in standard petri dishes and exposed to various potential killer 10 cells. The peripheral blood cells obtained from normal individuals were designated "effector cells" (killer cells) and the renal cancer cells designated "target cells". The killing (termed cytotoxicity) was measured in various ways including use of supravital stains or radioisotopes: in general, dead tumor cells release previously engulfed radioactive metabolic precursors and can no longer take up extracellular nutrients, etc. Figure 3 ehows that Ampligen, a mismatched dsRNA, significantly increases the activity of human LAK cells (obtained from blood of normal individuals) over that possible with IL-2 alone. Figure 3 compares the cytotoxicity at different doses of IL-2 with a constant dose of dsRNA. (At 1000 units per ml of IL-2, maximum cell killing has already occurred and it is not possible to boost it further with dsRNA.) Notice that the catalyst, dsRNA, in this system when used alone is completely inert. Therefore, the effect on tumor cell killing is not one of the simple arithmetic sum of 2 marginally active agents. Similar results are obtained in Figure 4, confirming the reproducibility of this remarkable phenomenon, which is equally applicable to a cell expressing neoantigens by virtue of either viral infection or a derangement in the self-immune (auto immune) regulation.

In separate experiments, it has also been shown that dsRNA (mismatched dsRNA) does not induce lymphocytes to produce IL-2. IL-2 concentration of in culture media was measured by the CTLL assay; the concentrations reported are expressed as the mean SEM. Rather, dsRNA may work in the IL-2 lymphokine system by various other means, including altering the density of certain antigens on target cells so that the efficiency of killing is increased. Also, dsRNA and IL-2 together may alter the late effects of killing, such as increasing S 15 effector-target cell binding or increasing the production of various cytotoxic factors or increasing the cycling of killer cells from one target tumor cell to the next target tumor cell.

Animal Studies show Increased Survival and 20 Reduced Tumor Spread. Increased survival and reduced tumor spread are shown by animal studies with the combination lymphokine/dsRNA over that with either the lymphokine or the dsRNA working alone.

The human melanoma tumor designated "BRD" was injected into the foot pad of groups of athymic mice. Athymic mice are unable to reject as foreign a human tumor. Eventually, in untreated mice, the tumor cells proliferate, spread to the lungs, and the animals die. In Figure 5, treated mice received dosages of 103-104 units/kilogram of IL-2 (about 2500 units per mouse) and dsRNA (500 micrograms) equivalent to about 100-300 mg for a 60 kilogram individual, both biologicals given twice weekly.

The objective was to simulate the safe human dose of each biologic and determine if a safe dose was indeed also efficacious.

The data presented in Figure 5 show a dramatic reduction in metastases to the lungs of animals treated with dsRNA plus IL-2 which was obviously unexpected over the results with the two agents given singly. This reduction in lung metastases was also correlated with an increase in survival; see the data of Figure 6. By increasing the dose of the non-toxic member of the therapeutic combination mismatched dsRNA it should now be possible to increase survival indefinitely. Similar results have been obtained with interferon (alpha) 20,000 IRU wherein mismatched dsRNA (500 micrograms twice weekly) in combination resulted in further enhancement of tumor inhibition Importantly, the lymphokine/dsRNA combinations did not produce detectable toxicity in the animals. They fed normally, gained the expected weight and showed normal blood chemistries.

Benefit of the Therapeutic Synergy at the Human Level. Figure 7 shows how the combination therapy of the present invention will reduce the toxicity of lymphokines in general and IL-2 in particular in clinical medicine. The toxicity data of IL-2 are well established by Litze and Rosenberg and present results indicate that IL-2 will now be 3 4 effective in the usually low range of 10 -10 units per kilogram only if combined with dsRNAs, whereas, if not combined with dsRNAs, it will be largely ineffective at this safe dosage.

In viral disorders, similar therapeutic benefits will be obtained, both for the reasons already cited and additional ones as well. For example, therapeutic interventions which attack only the immune deficits (IL-2 responsive) in HIV infections appear to be counterproductive. Consider that the so-called T4 helper cells with TAC receptors are responsive to the lymphokine IL-2 but, in AIDS victims, IL-2 causes expansion of cells which are directly vulnerable to the HIV and, as a result, there is a worsening of the disease Fauci and H.C. Lane, Annals Institute Pasteur/Virology- Immunology, in press, 1987). Thus, by judicious addition of dsRNA tc IL-2, the spectrum of IL-2, and potentially other lymphokines such as the interferon 15 and TNF, as useful antivirals should similarly enlarge and improve.

Mismatched double-stranded RNA is a known form of macromolecular RNA (see U.S. Patent No.

4,024,222 and U.S. Patent No. 4,130,641) in which destabilization of the double helix prevents base pairing. Mismatched dsRNA is well known for its interferon-induction properties which indicate a mechanism unrelated to interferon induction per se.

A typical therapeutic embodiment of mismatched double-stranded RNA is the synthetic dsRNA formed by complexes of polyriboinosinic and polyribocytidylic/uridylic acid, such as rIn r(Cx,U or G)n where x has a value from 4 to 29, rIn.r(C 12 U)n herein referred to as Ampligen®, a registered trademark of HEM Research, Inc., of Rockville, Maryland, USA. Many mismatched dsRNA polymers which behave similarly to Ampligen have been studied. The key therapeutic advantage of mismatched dsRNAs over other forms of natural and/or synthetic dsRNAs is their reduced toxicity in animals and man. For example, Lampson et al in U.S. Patent No. 3,666,646 described earlier complexes of dsRNA which are capable of triggering various interferon-related effects, but the toxicity of such compounds precluded any clinical utility in the treatment of cancer or related disorders.

By "mismatched dsRNA" are meant those in which hydrogen bonding (base stacking) between the counterpart strands is relatively intact, is interrupted on average less than one base pair in every 29 consecutive base residues. The term "mis-matched dsRNA" should be understood accordingly.

The dsRNA may be a complex of a polyinosinate and a polycytidylate containing a proportion of uracil bases or guanidine bases, 20 from 1 in 5 to 1 in 30 such bases (poly I- poly (C4-29 x U or The mismatched dsRNA may be poly I. poly C,U in which the ratio of .i C to U is about 13 to 1 and the sedimentation coefficients of poly I and poly C,U are both less than 9 and within 2 units of each other, that is preferably about 6.5 to The dsRNA may be of the general formula rI n(C12-13U)n. Other suitable examples of dsRNA are discussed below.

The mismatched dsRNAs preferred for use in the present invention are based on copolynucleotides selected from poly (Cn,U) and poly (C in which n is an integer having a value of from 4 to 29 and are mismatched analogs of complexes of polyriboinosinic and polyribocytidilic acids, formed by modifying rI .rC to incorporate n n unpaired bases (uracil or guanine) along the polyribocytidylate (rCn) strand. Alternatively, the dsRNA may be derived from poly poly(C) dsRNA by modifying the ribosyl backbone of polyriboinosinic acid (rI by including 2'-O-methyl ribosyl residues. These mismatched analogs of rl .rC preferred ones of which are of the general formula rI .r(C2',U)n, are described by Carter and Ts'o in U.S. Patents 4,130,641 and 4,024,222 the disclosures of which are hereby incorporated by reference. The dsRNA's 15 described therein generally are suitable for use according to the present invention.

Specific examples of mismatched dsRNA for use in the invention include: 20 poly poly (C 4

,U)

poly poly (C 7

U)

poly poly (C 13

U)

poly poly (C 2

U)

poly poly (C20, G) poly poly (C29, G) and poly poly (C 23 G>p Pharmaceutical compositions in accordance with this invention include the dsRNA, preferably mismatched, the lymphokine and, optionally a compound that inhibits cyclooxygenase activator, as the active components, together with a pharmaceutical carrier or diluent. Pharmaceutical compositions 13 contemplated by this invention include those adapted for parenteral administration in a suitable pharmaceutical vehicle.

.ee e e *e

Claims (9)

1. A method of treating tumour, virus-infected or immune-disregulated cells in a patient, said method comprising the step of administering to the patient, either together or separately, a mismatched dsRNA and interleukin 2 such that there is synergistic interplay between the dsRNA and interleukin 2 in the patient.

2. The method of claim 1, wherein the treatment comprises further administering to the patient an inhibitor of cyclooxygenase activator.

3. The method of claim 1 or claim 2, wherein the dsRNA is of the general formula rIn. (C 12 U)n.

4. The method of claim 2 or claim 3, wherein the inhibitor is indomethacin.

5. The method of any one of the preceding claims, wherein both NK and LAK cell levels in the patient are increased by the treatment without a paralleled increase in toxicity.

6. The method of any one of the preceding claims, wherein the dsRNA is administered in an amount sufficient to result in a level of 0.01 to 1000 micrograms per milliliter of the patient's body fluid and the interleukin 2 is administered in an amount sufficient to result in a level of from about 102 up to 106 interleukin 25 2 units per kilogram of the patient's weight.

7. A product containing mismatched dsRNA and interleukin 2 when used as a combined preparation for simultaneous, separate or sequential use in the treatment of tumour, virus-infected or immune-disregulated cells in 30 a patient, wherein there is synergistic interplay between S"the dsRNA and interleukin 2 in the patient.

8. The product of claim 7 further having an inhibitor of cyclooxygenase activator.

9. The product of claim 7 or claim 8, wherein the dsRNA is of the general formula rIn. (C1 2 U)n. The product of claim 8 or claim 9, wherein the inhibitor is indomethacin. S 11. The product of any one of claims 8-10, wherein the inhibitor increases the NK cell level in the patient without a paralleled increase in toxicity. Dated this 1 6 th day of November 2000 HEM RESEARCH INC. By Their Patent Attorneys CULLEN CO. e. *e