CA2118023A1 - Regulation of the immune system using androstene compounds - Google Patents

Abstract

2118023 9320696 PCTABS00027 The present invention provides an improved means for regulating the immune response, for ameliorating effects of stress, and for avoiding untoward effects of chemotherapy or exposure to irradiation by administration of androstenediol (AED) and androstenetriol (AET). The improved means of regulating immune response can be utilized in treating infectious diseases and immune diseases such as diabetes and chronic fatigue syndrome, both diseases now considered to be immune response related syndromes.

Description

2 3 W~93/20696 PCT/US92/03076 REGULATION OF THE IMMUNE SYSTEM

Field of the Invention:
The present invention provides an improved means for regulating the immune response, for ameliorating effects of stress, and for avoiding untoward effects of chemother-apy or exposure to irradiation by administration of andro-stenediol (AED) and androstenetriol (AET~. The improved means of regulating immune response can be utilized in treating infectious diseases and immune diseases such as diabetes and chronic fatigue syndrome, both diseases now considered to be immune response related syndrome~.

Backaround of the ~nvention:
In vertebrates the development of host protection against pathogens reguires a selective host immune re-sponse that involves the mobilization of the humoral and/or cellular mediated immune responses. Several fac-- tors adversely affect the body's protective response capability by causing prolonged immuno-suppression or "down-regulation" of the immune system~ It is, in reali-ty, more appropriate to speak of "mal-regulation" or "deregulation" of the immune system than of "down-regula-tion" since the result is a failure to protect the body from assault. Immuno-suppression provides an opportunity for pathogens to grow in the host. It does not matter what causes the primary insult to immunity. The resulting inability to muster the appropriate immune response has the same effect. Among the many different causes of immuno-suppression are viral, bacterial, fungal, yeast and parasitic infections, chemotherapy, irradiation, severe stress, chronic fatigue syndrome, diabetes mellitus and some forms of steroid therapy.
It has long been known that patients receiving ste-roid hormones of adrenocortical origin at pharmacological-W093/20~96 ~ 3 PCT/US~2/03076 ly appropriate doses show increased incidence of infec-tious disease. A.S. Fauci, immunolo.rev. 65, 133-155 ~1982); and J.E. Parillo and A.S. Fauci, Annual Review of Pharmacoloay and ~oxicoloqy 19, 179-201 (1979). Dehydro-epiandrosterone, also known as 3-B-hydroxyandrost-5-en-17-one or dehydroiso-androsterone (referred to hereinafter as DHEA), is a 17-ketosteroid which is quantitatively one of the major adrenocortical steroid hormones found in mam-mals. M.E. Windholz, The Merck Index, Ninth Edition (1976); K. Diem and C. Lentner, Geiay Scientific Tables (1975). (Although DHEA appears to serve as an intermedi-ary in gonadal steroid synthesis, the primary physiologi-cal function of DHEA has not been fully understood. It has ~ been known, however, that levels of this hormone begin to decline in the second decade of life, reaching 5~ of the original level in the elderly.) Clinically, DHEA has been used systemically and/or topically for treating patients suffering from psoriasis, gout, hyperlipemia, and in has been administered to post-coronary patients~ W. Regelson et al., New York Academy of Sciences 518, 260-273 (1988). In mammals DHEA has been shown to have weight optimizing and anticarcinogenic effects.
DHEA has been used clinically in Europe in conjunc-tion with estrogen as an agent to reverse menopausal symptoms and also has been used in the treatment of manic depression, schizophrenia, and Alzheimer's disease. DHEA
has also been used clinically at 40 mg/kg/day in the treatment of advanced cancer and multiple sclerosis.
(Regelson, supra) Mild androgenic effects, hirsutism, and increased libido were the side effects observed. These side effects can be overcome by monitoring the dose and/or by using analogues.
U.S. Patent 5,077,284 entitled "Use of Dehydroepian-drosterone to Improve Immune Response" describes the subcutaneous or oral administration of DHEA to improve the host's response to infections. U.S. Patent 4,978,~32 W093/20696 ~ 2 3 PCT/US92/03076 describes use of patch technology to deliver DHEA.
It is now disclosed that DHEA is a precursor in a metabolic pathway which ultimately leads to more powerful agents that increase immune response in mammals. That is, DHEA acts as a biphasic compound: it acts as an immuno-modulator when converted to androstenediol (5-androstene, 3B,17B diol hereinafter referred to as BAED) or andro~
stenetriol (5 androstene 3B,7B,17~ triol hereinafter referred to as BAET), but n vitro has a certain lympho-toxic and suppressive effect on cell proliferation prior to its conversion to BAED and/or BAET. It is, therefore, now understood that administration of DHEA shows superior immunity enhancing properties as a result of its partial ~ conversion to a more active metabolite.
An agent that would advance the protective regulation of the immune system without giving rise to undesirable side effects seen with DHEA administration would provide particularly advantageous improvement of host resistance against infection. Protective regulation of the immune system could then be effected using lower doses of the chemotherapeutic agent, and would provide more immediate `
response with a wider range of protection.

Description of the Invention:
The present invention provides compounds and composi-tions useful for enhancing the protective response of the immune system against infections. The medicinal composi-tions of the invention are also useful for treating other complications often accompanying immune suppression. The enhancement of the protective immune response may als~ be referred to herein as up-regulation or regulation of immune response.
The present invention provides means of synthesi2ing both ~ and ~ sterio isomers of AET. Both isomers are present in the body. However, since the activity of the isomers varies, it is important that means of making the separate isomers be provided. It is now known that the W093/206~6 ~ PCT/US92/03076 BAET is the active agent in regulation of immune response.
It is, however, probable that the ~AET, when in excess, is in equilibrium with BAET. However, because it is not known at this time what the response delay interval is, the BAET is the composition that is the isomer used thera-peutically.
Using BAED and BAET and protected analogues avoids certain side effects resulting from use of DHEA. The use of BAED and BAET avoids many of the androgenic side ef-fects that occur when the precursor DHEA is administered.
With BAED and BAET it is possible to obtain rapid, con-trolled enhancement of immune response. Furthermore, as shown b~ the information below in Table 1, the BAED is ~ unexpectedly superior to DHEA for purposes of protecting against viral assault since the protection offered differs both quantitatively and qualitatively from protection effected by DHEAo The structures of BAED and the ~ and B
isomers of AET are given below:
o~

~,ID~ ~/0~ ~
~ 4~ ~ ~ 4~ r ~ d~
In addition to the medicinal compositions, the inven-tion encompasses analogues and derivatives of BAED and ~AET. As indicated later in the exemplification of syn-thetic techniques, some of the substituted compounds are useful as starting materials or intermediates in making BAED and ~AET. BAED is available from commercial sources and has been used as a raw material for production of other steroids. (See U.S. Patent 2,521,586.) The product used in testing was obtained from Sigma. BAED and BAET
may also be substituted with protective groups which, on hydrolysis yield BAED or ~AET~ Hence, acylated and alky-lated derivatives are useful as precursors to the BAED and BAET~ Compounds such as those of the formula:

W093/20696 .~ ~ :'L ~ 1~ 2 ~ PCT/US92/03076 ~oiJ~

wherein Rl may be H, alkenyl of 2-8 carbons, alkyl of 1-8 carbons, phenylalkyl of 1-4 carbons, phenyl or CO~" where-in ~ is H: alkyl of 1-8 carbons , alkenyl of 2-8 c:arbons, phenylalkyl whereîn the alkyl has 1-4 carbons (including , benzyl) or phenyl~ Any phenyl moiety may have up to three substituents chosen from among hydroxy, car~oxy of 1-4 carbons, halo, alkoxy of 1-4 carbons, alkyl of 1-4 car-bons, or alkenyl of 2-4 carbons and wherein any alkyl may be a straight chain, branched chain, or the alkyl may be wholly or partially cyclized, The acute ~irus infection used as a model in the examples was chosen because of its widespread effects and the severity of the model to show protection. The Cox-sackievirus B4 is lethal to mice. In man, Coxsac~ie-virùses cause such varied pathologies as upper respiratory infection, pharyngitis, hemorrhagic conjunctivitis, menin-gitis, exanthem, encephalitis, hepatitis, infantile diar-rhea, paralysis, pericarditis, and myocarditis. It is now believed that ~iruses of this ~roup also have a role in the onset of ju~enile diabetes~
The use of BAED and ~AET and protected analogues as taught herein provides high levels of protection to verte-brates, including humans, against morbidity arising from infections or exposure to immune suppressive influences.
In clinical medicine, treatment with BAED and BAET can lower morbidity in patients exposed to pathogenic organ-isms. These agents can be effectively used prophylacti-c~lly in patients known to be particularly susceptible to W093/20696 ~ 2 3 PCT/US92/0307~

infection. Patients undergoing surgery or chemotherapy or patients suffering from burns, hypoplastic or aplastic anemias, or diabetes are such susceptible patients who would benefit from prophylactic administration of BAED
and/or BAET. Also among the causes of immuno-suppression are viral, bacterial, fungal, yeast and parasitic infec-tions, chemotherapy, irradiation, severe stress, chronic fatigue syndrome and some forms of steroid therapy. The compositions of the invention are particularly useful for lo treating patients suffering from infections caused by viruses that destroy the body's immune response, such as human immunodeficiency virus (HIV~ and hepatitis.
Both BAED and ~AET are most efficiently formulated ~ using lipophilic carriers such as DMSO. For subcutaneous administration to animals used in the examples, the active agents were dissolved 1:1 DMSO/ethanol, then diluted for subcutaneous administration to the animals. When the compositions were administered by mouth, they were added to chow to provide a composition containing .4~ AED. For application to the skin, the AED may, for example, be dissolved in carrier material containing DMSO and alcohol, then applied to a patch. In such instances, the AED in solution may be added to another carrier such as glycerol before application of the composition to the support material of the patch. For vaginal or rectal administra-tion, the AED may be administered by suppository, enema, or by application of creams, etc. Compositions of the invention may be administered by any method that will result in contact of the active agent with tissue of ectodermal origin. Such methods include subcutaneous or intradermal injection or topical application. One means of topical application is the use of skin patches impreg-nated with the active agent. This means of delivery is advantageous since it is non-invasive and easily adminis-tered by relatively unskilled care providers. Composi-tions of the invention can also be used in veterinary medicine to prevent morbidity that occurs during stress of WOg3/20696 ~ O~ ~ PC~/US92/~3076 shipping. Administration of BAED and BAET can be effec-tive as a means to prevent spread of infectious disease and introduction of infectious organisms into the foods for human consumption. BAED and BAET can be administered by subcutaneous injection, in food or drink, by patches applied to the skin, or by inhalation. A particular health concern is the spread of infection through eggs.
Eggs are frequently infected during development in the hen. Compositions containing active agents of the inven-tion may be added to the feed or water to prevent bacteri-al infection in the eggs.
When patches are used on animals or birds the skin should be exposed directly to the patch. When a patch is ~ used, it may be necessary to pluck or shave the bird or animal to expose the skin.
Othçr preferred methods of administration include buccal, sublingual, nasal or endotracheal routes. Sprays may be useful for this purpose. For nasal administration, the active agent may be delivered as a powder that is snorted. Inclusion complexes such as cyclodextrin inclu-sion complexes are appropriate compositions for adminis-tration to the oral-pharyngeal and nasal mucosa.
~AED and BAET may also be given with ~accines to en-hance immune response. These agents may be administered ?5 either in a composition containing the vaccine or may be given in a composition separate from the vaccine.
The compounds of the invention may also be admin-istered to the intestinal mucosa by oral or rectal routes.
Suppositories, solutions for use as retention enemas, and creams or jellies are appropriate carriers for use in rectal administration.
Compounds of the invention may be applied to the vaginal mucosa using creams, jellies, suppositories, or douching solutions. In order to enhance immune re-sponse at the site of exposure to infectious organisms, the compounds may be added to prophylactic vaginal prepa-rations or may be used as lubricants on condoms.

W093/20596 ~ O ~ 3 PCT/US92/03076 Administration of compositions of the invention has proven to be highly effective as a means of protecting against encephalitis and meningitis. The compositions of the invention may be administered intrathecally either at the spinal level or into the cisterna magna.
Active agents of the invention may be administered via ocular route using compositions in the form of drops, creams, or gel solutions or suspensions adapted for ocular application.
BAED and BAET inhibit the adherence properties of body cells. For purposes of effecting the anti-adherence properties of the active agents of the invention may be delivered directly to the epithelial tissue during sur-, gery. An example of such use would involve the applica-15 ' tion of compositions containing the active agents of the invention to the omentum in conditions such as infection, endometritis,and malignancies of the bowel and ovary wherein adherence of foreign cells or particles to normal cells of the peritoneal lining is a problem. Composi-tions of the invention could, for example, be administered as mists or sprays.
It has now been shown in,v~vo that DHEA is converted to the BAED and both isomers of AET. The BAED and BAET
then act as regulators of the immune response. In the skin, the conversion of DHEA to ~ED and subsequently to AET appears to be one of the me-abolic pathways of DHEA.
The human skin has the enzymatic machinery to form 7B-OH
DHEA and to cause 7B hydroxylation of AED to yield BAET, while the human adrenal cortex and liver can form only 7~-hydroxylation of DHEA, but not 7B-hydroxylation. The following table indicates the metabolic pathways of DHEA.

Trivial or common name systematic n~m~

(a) Dehydroepian~roSterone ~DHEA) 3B-Hydroxy-5-androsten-17-one (b) Dehydroepiandrosterone (DHEAS) 3B-Hydroxy 5 sulfate androsten-17-one-sulfate W093/20696 ~ 2 3 PCT/US92/03076 (c) 7 B-OH Dehydroepiandrosterone-- -------d) Androstenediol (AED) 5-androstene3~,17B,diol e) Androstenetriol (AET) 5-androstene-3~,7B,17~,triol tf) --- 7 keto-5- androstene-3B,17B, diol (g) ~ -androstene-3B,7~,17B,triol (h) --- 5-androstene-3B, 17~l diol-3-sulfate (i~ Testosterone 17B-Hydroxy-4-androstene-3One (j) Androstenedione 4-androstene-3,17 dione (k) Dihydrotestoserone 17B-Hydroxy-5 B androstane-3-one (1) Androsterone 3~-Hydroxy-5B androstan-17-one DHEA (a) is known to have immune enhancing activity.
However,~dehydroepiandrosterone sulphate, "(b)", has been found to have no enhancing effect on the immune system.
Both 5 androstene-3B, llB, 17B,-triol and 5 androstene~
16B, 17B,-triol have immunosuppressive effects. Testoster-one, "(i)", is known to have an effect on the host immune response, but this effect does not result in protection from ~ethal infections. The qualitative and ~uantitative effects of testosterone and the other sex hormones on the immune response are both of a different nature and scope.

xam~le 1:
Use of androstenediol (5 androstene-3B, 17B, diol, 3S BAED) results in marked and significant resistance against viral and bacterial infection. ~ose curve experiments were conducted in the following manner: BAED and DHEA were administered as a single depo dose of 8.3 mgs AED or 25 mgs. DHEA to SWR\J and C57BL\6J inbred mice. The mice were then challenged with varying amounts of Coxsackie-virus B4 (CB4) to determine protective value of the active agents. BAED provided 50~ protective dose against cox-sackievirus B4, which was as much as 100 times greater than protection provided by DHEA. In addition, to the W093/20~96 PCT/US92/03076 difference in ED50, the degree of protection against virus mortality achieved with androstenediol was also greater than the one obtained with DHEA injection. The increased protection effected by BAED against virus in-duced mortality was statistically significantly different that the protection obtained by DHEA (P < 0.05).

DHEA AND AED IN SWR/J MICE MORTALITY PER GROUP*

CB4 1 o5 VIRUS ALONE 1/ 6 DHEA o/ 6 AED O/ 6 CB4 1 o7 VIRUS ALONE 5/ 6 DHEA 1/6 AED 0/ 5 ~ *No deaths occurred in control groups.
AED versus control p-value = 0.0001.
DHEA versus control p-value = 0.0017.
DHEA versus AED p-value = 0~0588.
As seen from these results, BAED i~ markedly more effi-cient than the precursor DHEA in preventing mortality since an effective dose of BAED which is 1/3 or less the dose necessary to obtain an effect with DHEA is effective in achieving protection from mortality. A similar protection from virus mediated mortality was also observed in the inbred C57BL/6J(b) strain. The two inbred mouse strains, the SWR/J and the C57BL/6J, differ in their major hi~tocompati-bility haplotypes, which are q and b respectively. These results show that up-regulation of the immune response achieved with BAED in str~ins of different histocompatibili-ty may be independent of the major histocompatibility genes on chromosome 17.
Recent reports show that the skin may have unique immune functions. J.W. Streilein and R.E. Tigelar, Photo-immunolooY, Parrish et al. eds. (Plenum Publishing, New York, 1983) pp. 95-130. Indeed the skin is known to contain a population of cutaneous immune cells, which include the epidermal Langerhans cells and keratinocytes that produce an epidermal thymocyte-activating factor, similar to IL-l, in wo 93,206g6 ~ U ~ 3 Pcr/usg2/o3076 the murine system's Thy-l+ dendritic epidermal cell.

Exam~le 2:
A composition containing 8 mg BAED was administered S subcutaneously to outbred ICR mice who were then challenged with a lethal dose of Streptococcus faecalis strain XlS15.OGlRF. Animals given BAED showed marked resistance to morbidity as evident from reduction in mortality from 57% in animals challenged with bacteria only, to 0% mortality in animals infec~ed and treated with a single subcutaneous (SC) dose of BAED. Moreover, BAED above a certain threshold dose mediates a considerable proliferation of lymphocyte cells in the spleen and thymus, but only in infected animals.
~ Administration of 8 mg/animal BAED without exposure to the lS virus did not cause proliferation. Histopathological examination of the organs of in~red SWR/J mice infected with virus only and animals treated with BAED only, or BAED
treated and virus infected revealed that ~AED is effective in protecting from virus-induced myocardiopathy, a~d pancreopathy. Data presented in Table 2 below, shows that ~AED protec~s the host ICR inbred strain (Inst. of Cancer Research strain now supplied by Holland Sprague Dowley Company) from S. faecalis, but at a dose which is 1/3 the dose of DHEA required for the same effect.

DOSE
B~CTE~UM AGENT mg/ANIM~ 24 hr. MD~n~TY

S. faecalis . none O 4/7 57%
S. faecalis DHEA 25 o/7 o S. faecalis AED 8.3 o/~ o Protection was accomplished in an extremely acute infection where deaths occurred within 24 hours (4/7 deaths in non-treated groups ~ersus 0/7 in the treated). Mice were challenged with a lethal dose of plasmids containing bacterium S. faecalis isolate X1515.OGlRF.

W093/20696 ~ ~ 3 - PCT/US92/03076 Example 3:
Wells containing monolayered urinary bladder tumor cells were covered with a 5~ ~molar solution of either BAED
or DHEA overnight before being used in the assay. The resu~ts are shown in Ta~le 3 below.

X1515.OGlRF
WEL~ D08E NO. ADHERED% ADHERED
Media 1.78 x 106 1.77 x 106 99.4 DMSO 1.78 x 106 1.98 x Io6111.2 DHEA 1.78 x 106 1.01 x 10~ 56.7 AED 1. 78 X 106 1 . 05 X 10659 . O
As can be seen from Table 3, both DHEA and BAED inhibit the adherence of the bacteria to human urinary bladder tumor cells. It is believed that BAED and AET have an effect on either membrane fluidity, or on a component which influences adhesion and/or penetration into the ceil. Urinary Bladder Tumor cells (EJ6) were analyzed by flow cytometry using the fluorescent probe 1-4, trimethylammonio-phenyl-6 1,3,5 hexa-triene tTMA DPH) as a membrane probe to determine the effects of AED on membrane fluidity.
Result A. Samples 1 and 2 represent CONTROL cells grown in standard tissue cultùre media.
B. Samples 3 and 4 represent cells grown in the above control media with 50 ~M AED added.
Sample A 1. 0.121256 Sample A 2. 0.120548 CONTROL AVERAGE 0.120902 AED 50 ~M 3. 0.135151 AED 50 ~M 4. 0.142453 TEST AVERAGE 0.138802 The difference of 0.017899 between the control and BAED-treated cells is significant and demonstrates that BAED
caused a significant change in cell membrane adhesion. It may be that an increase in cell membrane rigidity (decrease fluidity) influences adherence.

~llf~23 WO93/206g6 PCT/US92/03076 ExamDl~ 4:
Cell culture media was inoculated with 4 x 107 Hela cells. DHEA was added to a concentration 50 ~M and BAED
was added to a concentration of 50 ~M. The cell culture exposed to DHEA showed a two-fold decrease in cell number.
The cell culture ~xposed to the ~AED, the control, and the culture exposed to the carrier alone showed a two fold increase or no change in the number of viable cells. These observations indicate BAED lacks deleterious effects of DHEA
lo during the initial phase of cell response. Neither DHEA
nor BAED had an effect on the nu~ber of virus infectious particles in vitro.

, Ex~mplo 5:
Mice were injected with 8 mg BAED or 25mg DHEA subcuta-neously.~ The mice were then infected with Coxsackievirus B4, 105 particles. The mice were sacrificed after 7 days.
The spleen lymphocytes were removed and stimulated with Concavalin A, 5 ~g/ml in vitro. Stimulation was measured by 3H-thymidine incorporation method. The BAED had a profound effect on the proliferation of spleen lymphocytes with as much as 6.6 fold greater proliferation evidenced. The data also indicates that, during the initial phase following administration of the steroid DHEA results in some suppres-sion of the i D une system.
The results described above indicate clearly the advantage of using BAED or BAET rather than DHEA to increase immune response to infections, since the initial immune suppression or toxicity that precedes the immune up-regula-tion that is seen in treatment with DHEA is avoided. Hence, therapy with BAED and BAET, rather than DHEA is preferred to improve immune response to infectious organisms.
The only change in structure between DHEA and AED is a reduction of the keto group at the 17 position to a B
hydroxyl group. The AET which has the hydrogen at the 7 position replaced with a B hydroxyl group is produced by a metabolic pathway in the skin. In other words, ~AET is a o 2 3 down-stream product of metabolic pathway from DHEA in the skin. The ~AET appears to be the most effective compound for effecting immune up-regulation and protection from untoward effects of stress, chemotherapy, and irradiation.

Preparatory methcd #l An important aspect of the invention is the prepar~tion of sterio-specific BAET for use as a medicinal. The synthesis was accomplished using the 7-oxo-3~, 17~ acetoxy-androst-5-ene as a starting material.

SYNTHESIS OF 3B,7~, 17B-TRIHYDROXYANDROST-5-ENE(I) and 3B, 7~, 17~-TRIHYDROXYANDROST-5-ENE(II3:
~ Chromic oxide oxidation of 3B,17~-diacetoxyandrost-5-lS ene in glacial acetic acid gave 3B,17~-diacetoxyandrost-5en-7-one, (III), the intermediate to (I) or (II).
Aluminum isopropoxide reduction of (III) in isopropanol gave ~I). li~hium tri ~sec-butyl) borohydride reduction of (III) in tetrahydrofuran yielded (II~.
PREPARATION OF 3B,17B-DIACETOXYANDROST-5-EN-7-ONE(III) 37.4 g(.l mol) 3B,17B-diacetoxyandrost-5-ene (Steral-oids A7850) in 400 ml glacial acetic acid was reacted with 30.06 g ( .3 mol) chromium(VI) oxide ~Aldrich 23,265-3) dissolved in 20 ml H20 and 20 ml glacial acetic acid. The CrO3 501ution was added drop-wise to the 3B,17B-diacetoxy-androst-5-ene solution while maintaining the temperature at 55C for 4 hours. In order to decompose any unreacted CrO3, methanol was added to the reaction mixture followed by aqueous salt solution and ether. Evaporation of the ether yielded 7.8 g(20% yield) of crude III,(details are given in lab book #1, pp. 10-16). Crystallization from 95%`EtOH
yielded (III) m.p. 214-215-C, DSC peak 191-224 C, max at 220C Lit.,l m.p. 218-219-C, Lit. ,2 m.p. 224-225C (from methanol).
Normal phase tlc: EtOAC-cyclohexane-EtOH (45:45:10), Rf=0.86. IR bands (cm -1: 1737,1666 (Lit. ,2 1728,1668).

W093/20696 ~ U 2 3 PCT/US92/03076 H NMR (CDC13),(d), ppm: 0.81(s,3H), 1.25 (s,3H), 2.02(s,6H), 2.25(m,H at C-4), 2.5(m,H at C-8),4.6(t,H at C-17),4.7(m,H
at C-3), 5.72(s,1H); (Lit. ,2 0.80(s,3H), 1.20(s,3H), 2.03 (s,6H), 4.62(m,lH), 5.71(g,lH).) Reverse phase lc/ms(fast atom bombardment detection) detected m/z 389(M+HJ' ion in the major lc peak,(Lit.,2 m/z 388(M ). Tentative C-13 nmr, (d), ppm assignments (CDC13) are:
Carbon 1 2 3 4 5 6 7 8 9 ppm 38.35 3S.74 72.04 43.03 164.22 126.44 201.18 65.82 49.69 Carbon 10 11 12 13 14 15 16 17 18 ppm 37.76 27.26 35.95 44.72 44.95 25.83 27.55 81.90 12.05 Carbon 19 20 21 22 23 ppm 20.67 171.14 21.24 170.23 21.17 PREPARATION OF 3B,7B,17B-TRIHYDROXYANDROST-5-ENE~I)

3~,~17B-diacetoxyandrost-5-en-7-one was subjected to reduction by aluminum isopropoxide in isopropanol to give 3B,7~,7B-trihydroxyandrost-5-ene.

PREPARATION OF 3~,7~,17B-TRIHYDROXYANDROST-5-ENE~II) 5.1 ml(5.1 ~mol) lithium tri(sec-butyl)borohydride (Aldrich L-Selectride) in tetrahydrofuran was rapidly added to 499 mg(l.28 mmol) of 3B,17~-diacetoxyandrost-5-en-7-one in 15 ml of freshly distilled tetrahydrofuran under nitrogen while stirring for 1.5 hours at ice-bath temperature. 0~9 g KOH in 15 ml methanol was added, reaction mixture refluxed for 0.5 hours, and then added 37.5 ml of 10~ NaCl solution.
After cooling in freezer(-20~, crystals formed which were filtered to yield 123.6 mg (19%) (II), m.p. 239-45C.
Crystallization from methanol yielded (II), m~p. 249.5-253-C. 1 H nmr (CD(OD)3), (d),ppm: 0.75(s,3H),1.01(s,3H), 3.1(m,1H), 3.6(t,1H),3.7(d,1H),5.50(d,1H).
Tentative C-13 nmr, (d),ppm assignments (CD(OD)3) are:
Carbon 1 2 3 4 5 6 7 8 ppm 37.49 32.12 72.01 42.91 146.75 124.88 65.46 39.09 Carbon 9 10 11 12 13 14 15 ppm 43.58 38.55 21.49 30.65 93.65 45.35 38.13 W093/20696 PCT/US92/03~76 hl~ ~02:~

Carbon 16 17 18 19 ppm 42.57 82.30 11.5719.53 DISCUSSION
Stereochemistry was assigned to 3~,7B,17B-trihydroxy-androst-5ene(I) and 3B,7~,17B-trihydroxyandrost-5-ene(II) by comparison with cholest 5-ene-3B,7B-diol and cholest-5-ene-3B,7~-diol proton nmr(Lit.3). L-Selectride reduction of (III) to produce (II) was carried out using the same reaction conditions given by Morisaki for the preparation of 7~-hydroxycholesterol4. Carbon-13 resonances for stere~-isomers (I) and (II) are shown. (Multiplicities (ppm)) , ISOMER(II) ISOMER(I) 1 37.19 T37.77 2 ~ 32.12 T32.30 3 72.01 D72.12

4 42.91 T41.24 14~.75 *144.10 6 121.88 ~127.43 7 65.46 D74~00 8 39.09 D38.29 9 43.58 D50.08 38.55 *37.73 11 21.49 T21.90 12 30.65 T30.86 13 43.65 *44.27 14 45O35 D52.31 38.31 T2~.60 16 42.57 T42.57 17 82.30 D82.30 18 11.57 Q11.57 19 19.53 Q19.53 Q=quartet, T=triplet, D=doublet and *= quaternary C
(ISOMER II, 7-OH axial)(ISOMER I 7-OH equatorial) W O 93/20696 PC~r/US92/03076 FE ~ NCES
1. Adolf Butenandt et al. Ber. 71B, 1316-22(1938).
2. Anthony J. Pearson et al., J. Chem. Soc. Perkin Trans.
I, 267-273(1985).
3. Leland L. Smith et al., J.Org.Chem.,Vol.38, No.l, 119-123 (1973).
4. Masuo Morisaki et al., Chem. Pharm. Bull. 35(5)1847-i852, (1987) 1o PreP~ratory method #2 A second method of preparing the ~ and B isomers of AET has been developed. The process uses, as a starting material, 3B, 17B diacetoxyandrost-5-ene, a commercially , available reagent (Stereloids A7850). This compound is - 15 oxidized with chromium hexacarbonyl (Cr(Co) 6) to form 3B.
17B-dîacçtoxyandrost-5-en-7-one as described by Pearson (Pearson, et al., J. Chem Soc. Perkin. Trans. 1, 1985, 267.) The enone formed was then reduced with triisobutyl-aluminum (TIBA) to give the acetylated 7~-hydroxy (3a) or 7B-hydroxy (3b) product depending on the solvent used.
.

PREPARATION OF 3B, 7~. 17~-TRIHYDROXYAN~OST-5-ENE.
A solution of 3~,17~-diacetoxyandrost-5-en-7-one (0.499~ g., 1.285 mmol) and tetrahydrofuran (20 mL, dried over MgSO4) were mixed under a nitrogen atmosphere. TIBA~
(2 mL, 2mmol, in lM toluene) was added dropwise by syringe The solution was stirred at room temperature for about 7 hours. The reaction was terminated by the addition of ethyl acetate (1.4mL), the methanol ~lOmL), and finally, by addition of 10 mL of 50% acetic acid. This solution was added to 100 mL water and extracted with ethyl ace-tate (3 times with 50 mL.) The organic layers were com-bined and then washed with saturated sodium bicarbonate solution tSO mL), saturated sodium chloride solution (2 times with 50 mL) and water ~50 mL). The organic layer was then dried over magnesium sulfate and the solvent removed ~y rotary evaporation to yield >~6% crude product.

W093/20696 ~ 2 3 PCT/US92/03076 ~H NMR indicated that the crude product contained 3B,17~-diacetoxyandrost-5-en-7-one (starting material), 65% and 3B,17B-diacetoxy-7~-hydroxyandrost-5-ene, 35%.

PREPARATION OF 3B,7B,17B-TRIHYDROXYANDROST-5-ENE
A solution of 3B,17~ diacetoxyandrost-5-en-7-one (0.9581 g, 2.466 mmol) and pentane (30 mL), dried over MgSO4) were mixed under a nitrogen atmosphere. TIBA (9.5 mL, 9.5 mmol, lM in toluene) was then added dropwise by syringe. The solution was stirred at room temperature for about 1 hour. The reaction was terminated by the addition of diluted hydrochloric acid (approximately 5mL). This solution was added to water ~lOO mL) and extracted with , ethyl acetate (3 times with 50 mL). The organic layers were combined and then washed several times with saturat-ed sodium bicarbonate solution (50 ml), saturated sodium chloride solution (two times with 50 mL,) and water ~SO
mL). The organic layer was dried over magne-ium sulfate and the solv~nt removed by rotary evaporation to yield 86%
crude product. tH NMR indicated that the crude product contained 3B,17B,-diacetoxy-7-B-hydroxyandrost-5-en-7-one (~6%) and 3B,17B diacetoxy-7-~-hydroxyandrost-5-ene.
In both of the above instances, the final products were reduced in accord with preparatory method #1~
The compositions of the invention containing BAED
and BAET, are useful in treatment any condition wherein a condition related to immune response is present including diabetes mellitus, chronic fatigue syndrome, stre~s, chemotherapy, and exposure to irradiation. One of the more depressing results of many of these conditions that involve aberrations of the immune response includes alope-cia. The compounds of the învention are effective for treating the alopecia resulting from such aberrations of immune response, including effec~s of chemotherapy and irradiation. In alopecia, the ~AET should be of consider-able benefit for use in treàtment. The compositions of both BAED and BAET are useful in overcoming other untoward `~

W O 93/20696 ~ PC~r/US92/03076 effects of immune suppression arising in these conditions.

Example 6-.
SWR/J inbred mice were injected with single depo doses of 0.5, 2.0, 4.0 and 8.0 mg/animal of BAED, then challenged with 107 PFU Coxsackievirus B4. The results are shown below:
AED dose, mg/animal ~ cumulative sur~ival ~.5 83 Based on these results, the theoretical dose (extrap-olated) Qf ~AED necessary to achieve 50~ protection from infection wi~h 107 PFU of CB4 is 0.25 mg/animal.
The example demonstrates that ~AED is 50 to 100 times more potent than DHEA for protection from Coxsackievirus B4.

Example 7:
In an attempt to evaluate effect of BAED on patholo-gies of the heart and pancreas in infected mammals, three groups of inbred SWR/J mice were compared. The groups studied included animals infected with virus only, animals treated with BAED only, and animals infected with virus and protected with BAED. The comparison revealed the following:
Heart Pancreas AED unremarkable unremarkable VIRUS focal areas of multiple severe necrosis necrosis with substantial (Pancreopathy) myocardial calcification.
AED PLUS no evidence of no evidence of `
virus induced myocardiopathy virus induced pancreopathy W093/20696 ~ 0 2 3 - PCT/US92/03076 These results demonstrate that BAED given as a single depo dose at 8.0 mg/mouse protected the heart tissue from virus induced myocardiopathy, and also protected the pancreas from virus induced necrosis of this organ. These results show that BAED can be used effectively in the protection from virus-induced cardiovascular and pancre-atic disease, in particular myocardiopathies and pancreo-pathies. Previously there were no effective drugs to protect these organs from ~irus induced damage.
Exam~le 8:
Effectiveness of BAED, ~AET, and BAET were compared by challenging mice with Coxsackievirus B4, 5.0 x 107 ~ pfu/animal. The foliowing data represents total umulative - 15 mortality (n/6) at indicated days post infection with virus.

Cumulative mortality Treatment Group (DaYs Post Infection) 2 4 6 8 _ 10 12 14 16 Virus alone 0 1 6 * * * * *
BAED .5 mg/virus 0 0 1 1 6 * * *
~AET .5 mg/virus o 1 4 4 4 4 4 4 ~AET .5 mg/virus 0 0 1 1 2 2 4 4 While the ~AET appeared to protect two animals from the virus, the înitial mortality would indicate that at least in early stages, there is little or no protection from the ~AET. Other studies indicate that there is far less protection with ~AET than with either ~AE~ or BAET.
Clearly, the BAET is the most effective agent for both early and longer term protection. It appears that there is a limited protection attributable to ~AET. Therefore, this isomer would not be as beneficial as ~AET for effect-ing enhancement of immune response.
The use of ~AED or BAET as active agents to provide regulation of the immune system makes it possible to ef-wo 93/206g6 ~ Dr~3 PCT/US92/03076 fectively regulate the host immune response against viral, bacterial and other infections~ In the case of virus-induced heart or pancreatic infection where no other anti-viral chemotherapeutic modality exists BAED and BAET have value as prophylactic prote tive agents. The protective value of ~AED and BAET is particularly important to pa-tients undergoing surgical procedures or suffering inju-ries where resistant strains of organisms such as pseudo-monas present a serious threat. Examples of such patients are those undergoing bowel surgery or suffering from gun-shot wounds of the abdomen. Patients with history of con-ditions such as rheumatic fever would also benefit from prophylactic use of BAED and ~ET. The mode of adminis-, tration in a particular case will depend on the infectious agent against which protection is sought and the target tissue o~f the organism. While the administration subcuta-neously as a depo is effective against systemic infections as shown by the data presented above, when the composi-tions are given to assist the body in meeting an infection in a particular tissue, it may be advantageous to admin-ister the active agents to the tissues most affected.
The carrier used in a given instance will depend on the mode of administration. Both AED and AET are lipo-philic compounds. They are more soluble than DHEA in water. Solvents for lipophilic steroids are known in the art and would be used as carriers for these compounds.
Examples of such carriers are ~lycols such as polypropyl-ene glycol, polyethyl ne glycol. and cyclodextrins, espe-cially the intrinsically amorphous cyclodextrins. Other vehicles that should be considered include fatty acid esters of polyoxyethylene sorbatan (Tweens) or sorbitan (Spans) to prepare oil-in-water emulsions.

ExamPle 9:
Capsules of a formulation of AED for oral adminis- -tration is prepared by containing 15 mg. BAED, 150 mg.
starch, and 5 mg. magnesium stearate. The capsules are W093/20696 ~ 0 2 3 PCT/US92/03076 administered daily or twice a day to achieve a daily dos-age of 15 mg. per day.
In the laboratory, BAED was added to the chow of the animals at a rate of .4% of the diet. When the animals who had been fed the diet containing BAED were exposed to Coxsackievirus B4 by injection in accord with the teach-ings of Example 1, the animals who had been fed the BAED
survived, while ~ontrol animals all died.

Exam~le 10:
A preparation for application to the skin or mucosa may be prepared in the following manner:
Ingredient %w/w , AED 0.5~
glyceryl monostearate 3.0%
propylene glycol 13.0~
Petrolatum 83.5%

When BAED or BAET or their analogues are administered orally, the active agents may be utilized more efficiently îf t}.e active agents are protected from destruction and absorption in the upper gastro-intestinal tract. The ac-tive agents are most effective when the period of exposure to the mucosa of the intestinal tract is increased. Hence use of capsules containin~ the active agents in formula-tions that effect slow release in the intestine are ap~ro-priate for treatment of intestinal disorders such as Crohn's disease and colitis. Use of retention enemas for treatment of inflammation of the large bowel is also appropriate.
A formulation for administration as a retention enema may be formulated in the following manner:

Exam~le 11:
Ingredient w/w BAET 4%
Propylene glycol 96%

WO93/206g6 ~ PCT/US92/03~76 When the active agent is administered to the mucosa of the oral cavity, it may be administered as a ~uccal tablet or spray for use in the oral-pharyngeal cavity and the nasal cavities.
The compositions could also be administered to the bronchial tree via inhalation. This means of administra-tion would be particularly useful in treating patients with lung infections or in treating other lung conditions such as black lung disease or emphysema that often are complicated by opportunistic infections. The compositions could be given by aerosol into the trachea or administered in mist along with other agents used in respiration thera-PY- .
~ The administration of the BAED and BAET to the skin can be accomplished using patches wherein a support is impregna~ed with the active agent or using implants that provide slow release of the active agents.
A patch for the administration of AET or AED can be formulated as adhesive patches containing the drug. For example, the patch may be a discoid in which a pressure-sensitive silicone adhesive matrix containing the active agent may be covered with a non-permeable backing. The discoid may either contain the active agent in the adhe-sive or may have attached thereto a suppor~ made of mate-rial such as polyurethane foam or gauze that will hold the active agent. Before use, the material containing the active agent would be covered to protect the patch.

Example 12:
.
A patch composed of trilaminate of an adhesive matrix sandwiched between a non-permeable backing and a protec-tive covering layer is prepared in the following manner:
To a pressure-sensitive silicone adhesive composition BIOPSATM Q7-292Q (Dow Corning Corp., Midland, Michigan, U.S.A.) in cyclohexane (50% w/v) is added sufficient BAED
to provide a .5% BAED composition. The adhesive is ap-plied to a polyester film to provide in successive layers -W~93/20696 PCT/US92/03076 ~1~o~23 to provide about 2 mg of active agent per cm2. The film containing the adhesive is then made into patches of 10 cm2. For patches would be covered with a protective layer to be removed before application of the patch. Patches may be prepared containing permeation enhancers such as cyclodextrin, butylated hydroxyanisole, or butylated hydroxytoluene. However, it should be remembered that the active agants of this invention are effective on applica-tion to the epidermal tissue. When the patches are to be applied to thin or abraded skin, there is little need to add a permeation enhancer.
Compositions of the invention can be administered as a prophylactic during radiation therapy or chemotherapy or , after exposure to irradiation whether the exposure occurs as a result of environmental accident or therapy. Other instances when use of these immune up-regulators would be appropriate is in treatment of ~urns, hypoplastic and ap-lastic anemias, diabetes, and in the elderly during epi-demics. Their use is also beneficial in preventing or mitigating ef~ects of exposure to dangerous infectious organisms, as was demonstrated by the data related to car-diopathies and pancreopathies. Such use is particularly indicated in populations exposed to organisms that target the immune system, such as HIV infections. In certain instances the compositions ta~ght herein can also be used as immune modulators in the production of blocking anti-bodies to counteract hypersensitivity reactions.
As indicated previously, patients scheduled to under-go bowel surgery or other "dirty" surgical procedures could receive a dose of BAED or BAET prophylactically.
Use of the compositions as taught herein before invasive dental procedures or oral surgery should be considered.
As indicated in the tables and previous discussion, the compositions of the invention can be usad to prevent adhesion of bacteria to the tissues. The prevention of cell to cell adhesion resulting from administration of the compositions also has applications for prevention of - W093/20696 h ~ i ~ O ~ 3 PCT/US92/03076 thrombosis. Compositions of the invention can be adminis-tered as a slow drip into blood vessels when prevention of formation of a thrombus is necessary. An example of such use would be a drip into an artery following thrombo-lectomy or for prevention of cerebral throbosis. Instil-lation into the bladder could also be beneficial for prevention or treatment of urinary infection. The admin-istration of the BAED or BAET can be employed as a means of preventing formation of infectious foci.
BAED and ~AET are both effective in overcoming ef-fects of ultraviolet depravation. Hence, administration of the compositions to overcome the effects of depression related to light deprivation (usually called seasonal ~ adaptive disorder) is appropriate.
~AED and ~AET may be used as adjuncts in vaccination to incr~ase response to an immunogen. Not only will these agents increase response to the vaccine, they will also incrase ability to protect against disease befor2 the body has responded with increase in specific antibodies. Such use is particularly appropriate in instances where inhi-bition of immune response can be a complicating factor as is the case in patients suffering from, for example, malignancies, AIDS, or environmental factors such as ex- -posure to pesticides. It is, of course, understood that use as adjunct to vaccination would be appropriate in vertebrates other than man, including vaccination of pets, dairy animals, meat-producing animals, fish, and chickens.
Chickens are particularly prone to develop infectious diseases when living in confined conditions. CoccidiosisJ
Salmonella infections, viral infections, including those giving rise to malignancies such as leukemia and sarcoma (caused by a retrovirus) are particularly common among ~-chickens grown under modern commercial conditions. The active agents of the invention may be given by any means that results in contact of the agent with tissue of ecto~
dermal origin. `
The effect of Coxsackie~irus on humans has been noted ~`-W093/2069~ PCT/US92/03076 previously. The value of avoiding such effects, espe-cially in children, is clear. Effects of other viruses such as chickenpox-herpes zoster is considered an impor-tant cause of debilitating illness in the elderly. Fur-thermor,e, chickenpox in susceptible adults often causes severe illness. In children, chicken pox can cause death when the child is subjected to immuno suppressive therapy or is genetically i~mune deficient. BAED and BAET a use-ful for prophylatic treatment of susceptible persons who have been exposed to infection. Finally, the protection of the fetus and newborn from HSV infection is a very im-portant application of the invention. BAED and ~AET can be administered during the third trimester to HSV-infected , women as a means of protecting the newborn.
In vitro, these compounds can be used in commercial setting ~o induce lymphocyte proliferation. The use of BAED and BAET would increase yield of products of such proliferation in tissue culture. In the clinical setting, BAED and BAET can be given to e~fectively enhance pa-tients' ability to combat infections. Patient lymphocytes may be withdrawn, reproduced in vitro in media containing BAED or BAET to increase proliferation of lymphocytes, and the lymphocy~es so primed for response could then be rein-troduced i`nt`o the patient~ In cases such as malignancy or other cellular disease, the malfunctioning cells can be inactivated by known means before proliferation in growth media.
The compositions of the invention may also be used prophylactically to protect animals from the consequences of infection by pathogenic organi5ms. It is known that under the stress of shipment to market animals often become susceptible to infections that are not ordinarily serious, but that can cause the animals to loss much weight en route to the packing house. Such loss may be avoided by administration BAED and BAET and analogues disclosed herein. The active agents can be given by patch, injection, or in feed. Because the active agents W093/2069~ 2 3 PCT/US92/03076 are most effective when the period of exposure to the tis-sue of ectodermal origin is extended, when the active agents are administered through the GI tract, compositions should be modified to extend the period of exposure of the active agent to the intestinal mucosa and to protect the agents from destruction in the upper GI tract. Hence, use of capsules that effect slow release in the intestine is appropriate. The capsules may be placed in baits for administration to animals. To treat infections of the large bowel, the active agents may be given by retention enema.
~AED and BAET may be administered to the mucosa of oral, pharyngeal, and nasal cavity by tablet, a lozenge, , by administration as a spray for use in the oral-pharyn-geal cavity, or as a nasal spray.
Administration to the skin may be accomplished using patches wherein a support to be applied to the skin is impregnated with the active agent. If the host is a mammal or bird, it may be necessary to shave or pluck the region to which the patch is applied. -A preferred method of administration is by subcutane-ous injection as a depo. The method is particularly appropriate for administration of the active agents to mammals, since subcutaneous injection is easily performed and the effect is relatively long lasting.
BAED and BAET are already present in the body as natural components. They do not pose a serious toxic problem at levels known to be safe; they appear to be are chemically quite stable.
The dosages used will depend on the size and condi-tion of the host. Test data indicated in this application was obtained in small animals. In larger adult mammals daily dosage of .2 to 30 mg/da. of AED a preferred dosage.
For AET the preferred dosage is usually in the range of .001 to 20 mg/da, with .001 to 1 mg/da. being the more preferred dosage. However, the dosage will vary depend-ing on the route of administration. Subcutaneous, inha-W093/206~6 ~ O~ ~ PCT/US92/03076 lation and intrathecal administration are to be methods that would require lower dosages of the active agents.
It is, of course, understood that analogues of ~AED
and BAET having protective groups can be administered to the host as a means of delivering BAED or BAET to target tissues. Acylation is a preferred method af protecting the compounds. Acylated compounds wherein R1 is COR2 are also appropriate compounds for use as starting material from which to make BAED and BAET.
The active agents, ~AED and ~AET, can be given in conjunction with other active agents which may be given simultaneously or may be incorporated in compositions containing BAED or BAET. BAED and BAET can be given with , anti-infective agents such as antibiotics, antiviral agents, antifungals, antiparasitic agent to potentiate the activity~ of these drugs by up-regulating protective immune response. Antiviral agents include, for example, Di-deoxyinosine, AZT, acyclovir, etc. Other a~tive agents that may be combined with the AED and AET include antial- -lergic medications such as epinephrine.
Finally, medicinal compositions containing BAED and BAET are particularly valuable for use in combating viral infections in patients who have suffered from infections exacerbated by immuno-suppressive therapy. One of the major complications in patients with tissue transplants is the opportunistic infection with viruses that ordinarily do not cause serious disease symptoms. Use of the compo-sitions of the invention, which result in rapid protective regulation of the immune response, allows the medical team to place the patient on ~Isee-saw~ therapy to avoid trans-plant rejection while regulating the immune response to avoid overwhelming infection.

Claims (27)

29

1. A composition of matter comprising as an active agent 5-androstene 3.beta.,17.beta. diol (.beta.AED), 5-androstene 3.beta.,7.beta.,17.beta. triol (.beta.AET) or 5-androstene 3.beta.,7.alpha.,17.beta.
triol (.beta.AET) or at least one compound of the formula wherein R1 may be H, alkenyl of 2-8 carbons, alkyl of 1-8 carbons, phenylalkyl of 1-4 carbons, phenyl or COR2, wherein R2 is H; alkyl of 1-8 carbons , alkenyl of 2-8 carbons, phenylalkyl wherein the alkyl has 1-4 carbons (including benzyl) or phenyl. Any phenyl moiety may have up to three substituents chosen from among hydroxy, carboxy of 1-4 carbons, halo, alkoxy of 7-4 carbons, alkyl of 1-4 carbons, or alkenyl of 2-4 carbons and wherein any alkyl may be a straight chain, branched chain, or the alkyl may be wholly or partially cyclized in a pharmaceutically acceptable carrier.

2. A composition of claim 1 wherein the active agent is .beta.AED or .beta.AET.

3. A composition of claim 1 containing a glycol.

4. A composition of claim 1 wherein the active agent is attached to a support.

5. A composition of claim 4 wherein the composition is a patch.

6. A composition of claim 1 in a closed container.

7. A composition of for oral administration in capsule form.

8. A composition of claim 1 adapted for implantation.

9. A method of preventing or ameliorating untoward ef-fects of chemotherapy or irradiation therapy in a mammal by administration of an effective amount of a composition of claim 1.

10. A method of claim 9 wherein the active agent used is .beta.AET.

11. A method of claim 9 wherein the active agent is .beta.AED.

12. A method of claim 9 wherein the active agent is ad-ministered through a patch or an implant.

13. A method of enhancing immune response in a vertebrate by administration of an immune up-regulating amount of a composition of claim 1.

14. A method of claim 13 wherein the composition is ad-ministered subcutaneously, intradermally, or by topi-cal application.

15. A method of claim 13 wherein the composition is ad-ministered intrathecally.

16. A method of claim 13 wherein the composition is ad-ministered as a patch.

17. A method of claim 13 wherein the composition is ad-ministered intranasally.

18. A method of claim 13 wherein the composition is ad-ministered in a manner that will result in the compo-sition contacting the vaginal wall.

lg. A method of claim 13 wherein the composition is ad-ministered by mouth.

20. A method of claim 18 wherein the composition is ad-ministered as a lubricant for condoms.

21. A composition of claim 1 that contains petrolatum.

22. A method of preventing cells from adhering to one another by exposing said cells to a adhering-inhibit-ing amount of AED or AET.

23. A method of increasing lymphocyte proliferation in vitro by adding to a growth media a lymphocyte pro-liferation enhancing amount of AED or AET.

24. A method of increasing lymphocytes of autogenous origin in a patient by the steps of:
1. Removing and separating lymphocytes from a pa-tient;
2. Growing the lymphocytes obtained in step (1) in a media containing AED or AED: and 3. Separating the lymphocytes from the growth media and administering the lymphocytes to the patient from whom they were removed in step 1.

25. A method of enhancing immune response in a vertebrate by administration of .beta.AED, .alpha.AET, .beta.AET, or a compound of the formula:
wherein R1 may be H, alkenyl of 2-8 carbons, alkyl of 1-8 carbons, phenylalkyl of 1-4 carbons, phenyl or COR2, wherein R2 is H; alkyl of 1-8 carbons , alkenyl of 2-8 carbons, phenylalkyl wherein the alkyl has 1-4 carbons (including benzyl) or phenyl. Any phenyl moiety may have Up to three substituents chosen from among hydroxy, carbQxy of 1-4 carbons, halo, alkoxy of 1-4 carbons, alkyl of 1-4 carbons, or alkenyl of 2-4 carbons and wherein any alkyl may be a straight chain, branched chain, or the alkyl may be wholly or partially cyclized in the food or water of the verte-brate.

26. A method of claim 13 wherein the vertebrate is a human suffering from chronic fatigue syndrome.

27. A method of claim 13 wherein the vertebrate is a human suffering from chronic yeast infection.