Nutritional supplements that may be helpful: Because people
with HIV infection or AIDS often have multiple nutritional deficiencies, a broad-spectrum
nutritional supplement may be beneficial. In one trial, HIV-positive men who took a multivitamin-mineral supplement had slower onset of AIDS,
compared with men who did not take a supplement.8 Use of a multivitamin by pregnant and breast-feeding Tanzanian women with HIV did
not affect the risk of transmission of HIV from mother to child, either in utero, during
birth, or from breast-feeding.9
Selenium deficiency is an independent factor associated
with high mortality among HIV-positive people.10 HIV-positive people who took
selenium supplements experienced fewer infections,
better intestinal function, improved appetite, and improved heart function (which had been
impaired by the disease) than those who did not take the supplements.11 The usual
amount of selenium taken was 400 mcg per day.
Selenium deficiency has been found more often in people with HIV-related cardiomyopathy (heart abnormalities) than in those with
HIV and normal heart function.12 People with HIV-related cardiomyopathy may benefit
from selenium supplementation. In a small preliminary trial, people with AIDS and
cardiomyopathy, 80% of whom were found to be deficient in selenium, were given 800 mcg of
selenium per day for 15 days, followed by 400 mcg per day for eight days. Improvements in
heart function were noted after selenium supplementation.13 People wishing to
supplement with more than 200 mcg of selenium per day should be monitored by a doctor.
The amino acid, N-acetyl cysteine (NAC), has been shown to inhibit the
replication of HIV in test tube studies.14 In a double-blind trial, supplementing
with 800 mg per day of NAC slowed the rate of decline in immune function in people with HIV infection. NAC also
promotes the synthesis of glutathione, a
naturally-occurring antioxidant that is believed to be
protective in people with HIV infection and AIDS.15
The combination of glutamine, arginine, and the amino acid derivative,
hydroxymethylbutyrate (HMB), may prevent loss of lean body mass in people with
AIDS-associated wasting. In a double-blind trial, AIDS patients who had lost 5% of their body
weight in the previous three months received either placebo or a nutrient mixture containing
1.5 grams of HMB, 7 grams of L-glutamine, and 7 grams of L-arginine twice daily for eight
weeks.16 Those supplemented with placebo gained an average of 0.37 pounds, mostly
fat, but lost lean body mass. Those taking the nutrient mixture gained an average of 3 pounds,
85% of which was lean body weight.
In a double-blind trial, the non-disease-causing yeast Saccharomyces boulardii (1 gram three times per day) helped
stop diarrhea in HIV-positive people.17
However, people with severely compromised immune function have been reported to develop yeast infections in the bloodstream after consuming
some yeast organisms that are benign for healthy people.18 19 For that
reason, people with HIV infection who wish to take Saccharomyces boulardii, brewer’s yeast (Saccharomyces cerevisiae),
or other live organisms should first consult a doctor.
A deficient level of dehydroepiandrosterone sulfate (DHEAS) in the blood is associated with
poor outcomes in people with HIV.20 Large amounts of supplemental dehydroepiandrosterone (DHEA) may alleviate fatigue and depression in
HIV-positive men and women. In a preliminary trial, men and women with HIV infection took
200–500 mg of DHEA per day for eight weeks.21 All participants initially had
both low mood and low energy. After eight weeks of DHEA supplementation, 72% of the
participants reported their mood to be “much improved” or “very much
improved,” and 81% reported having significant improvements in energy level. DHEA
supplementation had no effect on CD4 cell (helper T-cell) counts or testosterone levels.
Vitamin A deficiency appears to be very common in
people with HIV infection. Low blood levels of vitamin A are associated with greater disease
severity22 and increased transmission of the virus from a pregnant mother to her
infant.23 However, in preliminary 24 and double-blind25
26 trials, supplementation with vitamin A failed to reduce the overall mother-to-child
transmission of HIV. HIV-positive women who took 5,000 IU per day of vitamin A (as retinyl
palmitate) and 50,000 IU per day of beta-carotene
during the third trimester (13 weeks) of pregnancy, plus an additional single amount of
200,000 IU of vitamin A at delivery, had the same rate of transmission of HIV to their infants
as those who did not take the supplement. However, lower rates of illness have been observed
in the children of HIV-positive mothers when the children were supplemented with
50,000–200,000 IU of vitamin A every two to three months.27
Little research has explored whether vitamin A supplements are helpful at halting disease
progression. HIV-positive children given two consecutive oral supplements of vitamin A
(200,000 IU in a gelcap) in the two days following
influenza vaccinations had a modest but significant decrease in viral load.28
In one trial, giving people an extremely high (300,000 IU) amount of vitamin A one time only
did not improve short-term measures of immunity in women with HIV.29
Beta-carotene levels have been found to be low in HIV-positive people, even in those
without symptoms.30 However, trials on the effect of beta-carotene supplements have
produced conflicting results. In one double-blind trial, supplementing with 300,000 IU per day
of beta-carotene significantly increased the number of CD4+ cells in people with HIV
infection.31 In another trial, the same amount of beta-carotene had no effect on
CD4+ cell counts or various other measures of immune function in HIV-infected
people.32
In HIV-positive people with B-vitamin deficiency, the use of B-complex vitamin supplements appears to delay progression
to and death from AIDS.33 Thiamine (vitamin
B1) deficiency has been identified in nearly one-quarter of people with AIDS.34
It has been suggested that a thiamine deficiency may contribute to some of the neurological
abnormalities that are associated with AIDS. Vitamin B6
deficiency was found in more than one-third of HIV-positive men; vitamin B6 deficiency was
associated with decreased immune function in this
group.35 In a population study of HIV-positive people, intake of vitamin B6 at more
than twice the recommended dietary allowance (RDA is 2 mg per day for men and 1.6 mg per day
for women) was associated with improved survival.36 Low blood levels of folic acid and vitamin B12
are also common in HIV-positive people.37
Preliminary observations suggest a possible role for
vitamin B3 in HIV prevention and treatment.38 A form of vitamin B3
(niacinamide) has been shown to inhibit HIV in test tube studies.39 However, no
published data have shown vitamin B3 to inhibit HIV in animals or in people. One study did
show that HIV-positive people who consume more than 64 mg of vitamin B3 per day have a
decreased risk of progression to AIDS or AIDS-related death.40 41
Clinical trials in humans are required to validate these preliminary observations.
Vitamin C has been shown to inhibit HIV replication in
test tubes.42 Intake of vitamin C by HIV-positive persons may be associated with a
reduced risk of progression to AIDS.43 Some doctors recommend large amounts of
vitamin C for people with AIDS. Reported benefits in preliminary research include greater
resistance against infection and an improvement in overall well-being.44 The amount
of vitamin C used in that study ranged from 40 to 185 grams per day. Supplementation with such
large amounts of vitamin C must be monitored by a doctor. This same researcher also reports
some success in using a topical vitamin C paste to treat herpes simplex outbreaks and
Kaposi’s sarcoma in people with AIDS.
In test-tube studies, vitamin E improved the
effectiveness of the anti-HIV drug zidovudine (AZT) while
reducing its toxicity.45 Similarly, animal research suggests that zinc and NAC
supplementation may protect against AZT toxicity.46 It is not known whether oral
supplementation with these nutrients would have similar effects in people taking AZT.
Blood levels of coenzyme Q10 (CoQ10) were also found
to be low in people with HIV infection or AIDS. In a small preliminary trial, people with HIV
infection took 200 mg per day of CoQ10. Eighty-three percent of these people experienced no
further infections for up to seven months, and the counts of infection-fighting white blood cells improved in three
cases.47
Blood levels of both zinc48 and selenium
49 are frequently low in people with HIV infection. Zinc supplements (45 mg per
day) have been shown to reduce the number of infections in people with AIDS.50
Iron deficiency is often present in HIV-positive
children.51 While iron is necessary for normal immune function, iron deficiency also appears to
protect against certain bacterial
infections.52 Iron supplementation could therefore increase the severity of
bacterial infections in people with AIDS. For that reason, people with HIV infection or AIDS
should consult a doctor before supplementing with iron.
The amino acid,
glutamine, is needed for the synthesis of
glutathione, an important antioxidant within cells
that is frequently depleted in people with HIV and AIDS.53 In well-nourished
people, the body usually manufactures enough glutamine to prevent a deficiency. However,
people with HIV or AIDS are often malnourished and may be deficient in glutamine.54
In such people, glutamine supplementation may be needed, along with NAC, to maintain adequate levels of glutathione. It is not
known how much glutamine is needed for that purpose; however, in other trials, 4–8 grams
of glutamine per day was used.55 In a double-blind trial, massive amounts of
glutamine (40 grams per day) in combination with several antioxidants (27,000 IU per day of
beta-carotene; 800 mg per day of vitamin C; 280 mcg per day of selenium; 500 IU per day of
vitamin E) were given for 12 weeks to AIDS patients experiencing problems maintaining normal
weight.56 Those who took the glutamine-antioxidant combination experienced
significant gains in body weight compared with those taking placebo. Larger trials are needed
to determine the possible benefits of this nutrient combination on reducing opportunistic
infections and long-term mortality.
People with AIDS have low levels of methionine. Some
researchers suggest that these low methionine levels may explain some aspects of the disease
process,57 58 59 especially the deterioration that occurs in
the nervous system and is responsible for symptoms such as dementia.60
61 A preliminary trial found that methionine (6 grams per day) may improve memory recall
in people with AIDS-related nervous system degeneration.62
In a preliminary trial, a thymus extract known as
Thymomodulin® improved several immune parameters among people with early HIV infection,
including an increase in the number of T-helper cells.63
Are there any side effects or interactions? Refer to the individual supplement for
information about any side effects or interactions.
Herbs that may be helpful: Many different herbs have been
shown in test tube studies to inhibit the function or replication of HIV. Few of these studies
have been followed up with any kind of investigation in HIV-positive humans. Some notable
exceptions to this rule are discussed below.
There are three categories of herbs used in people with HIV infection. The first are herbs
that are believed to directly kill HIV (antiretroviral herbs). The second are herbs that
strengthen the immune system to better withstand
HIV’s onslaught (immuno-modulating herbs). The third are herbs that combat opportunistic
infections (antimicrobial herbs). The following table
summarizes each category and herbs that belong in each. Note that some herbs fall into more
than one category.
| Category of Herb |
Supporting Evidence from Human Trials |
Supporting Evidence from Test Tube Studies |
| Antiretroviral |
Andrographis, boxwood, licorice, St. John’s
wort |
Garlic |
| Immuno-modulators |
Andrographis (possible antiretroviral), Asian ginseng, bupleurum,
echinacea, licorice, mistletoe, Sangre de Drago,
turmeric |
Herbs: ashwagandha,
eleuthero, schisandra
Mushrooms: coriolus, maitake, reishi, shiitake
|
| Antimicrobial |
Garlic, tea tree oil
|
|
One double-blind trial has found that 990 mg per day of an extract of the leaves and stems
of boxwood (Buxus sempervirens) could delay the progression of HIV infection (as
measured by a decline in CD4 cell counts).64 No adverse effects directly
attributable to the extract were reported. Taking twice the amount of boxwood extract did not
lead to further benefits and may have actually decreased its usefulness.
Licorice has shown the ability to inhibit reproduction
of HIV in test tubes.65 Clinical trials have shown that injections of glycyrrhizin
(isolated from licorice) may have a beneficial effect on AIDS.66 There is
preliminary evidence that orally administered licorice also may be safe and effective for
long-term treatment of HIV infection.67 Amounts of licorice or glycyrrhizin used
for treating HIV-positive people warrant monitoring by a physician, because long-term use of
these substances can cause high blood pressure, potassium depletion, or other problems. Approximately 2 grams
of licorice root should be taken per day in capsules or as tea. Deglycyrrhizinated licorice
(DGL) will not inhibit HIV.
An extract from stem bark latex of Sangre de Drago (Croton lechleri), an herb from
the Amazon basin of Peru, has demonstrated significant anti-diarrheal activity in
preliminary68 and double-blind trials. Additional double-blind research has
demonstrated the extract’s effectiveness for
diarrhea associated with HIV infection and AIDS.69 70 Very high
amounts of this extract (350–700 mg four times daily for seven or more days) were used
in the studies. Such levels of supplementation should always be supervised by a doctor. Most
of this research on Sangre de Drago is unpublished, and much of it is derived from
manufacturers of the formula. Further double-blind trials, published in peer-reviewed medical
journals, are needed to confirm the efficacy reported in these studies.
A constituent from St. John’s wort known as
hypericin has been extensively studied as a potential way to kill HIV. A preliminary trial
found that people infected with HIV who took 1 mg of hypericin per day by mouth had some
improvements in CD4+ cell counts, particularly if they had not previously used AZT.71 A small number of people developed signs of mild liver
damage in this study. Another much longer preliminary trial used injectable extracts of St.
John’s wort twice a week combined with three tablets of a standardized extract of St.
John’s wort taken three times per day by mouth. This study found not only improvements
in CD4+ counts but only 2 of 16 participants developed opportunistic infections.72
No liver damage or any other side effects were noted in this trial. In a later study, much
higher amounts of injectable or oral hypericin (0.25 mg/kg body weight or higher) led to
serious side effects, primarily extreme sensitivity
to sunlight.73 At this point, it is unlikely that isolated hypericin or
supplements of St. John’s wort extract supplying very high levels of hypericin can
safely be used by people with HIV infection, particularly given St. John’s wort’s
many drug interactions.
Garlic may assist in combating opportunistic infections.
In one trial, administration of an aged garlic extract reduced the number of infections and
relieved diarrhea in a group of patients with
AIDS.74 Garlic’s active constituents have also been shown to kill HIV in the
test tube, though these results have not been confirmed in human trials.75
A preliminary trial of isolated andrographolides, found in andrographis, determined that while they decreased viral load
and increased CD4 lymphocyte levels in people with HIV infection, they also caused potentially
serious liver problems and changes in taste in many of the participants.76 It is
unknown whether andrographis directly killed HIV or was having an immune-strengthening effect
in this trial.
Other immune-modulating plants that could theoretically be beneficial for people with HIV
infection include Asian ginseng, eleuthero, and the medicinal mushrooms shiitake and reishi. One
preliminary study found that steamed then dried Asian ginseng (also known as red ginseng) had
beneficial effects in people infected with HIV, and increased the effectiveness of the
anti-HIV drug, AZT.77 This supports the idea that immuno-modulating herbs could
benefit people with HIV infection, though more research is needed.
The Chinese herb bupleurum, as part of the herbal
formula sho-saiko-to, has been shown to have beneficial immune effects on white blood cells
taken from people infected with HIV.78 Sho-saiko-to has also been shown to improve
the efficacy of the anti-HIV drug lamivudine in the test
tube.79 One preliminary study found that 7 of 13 people with HIV given sho-saiko-to
had improvements in immune function.80 Double-blind trials are needed to determine
whether bupleurum or sho-saiko-to might benefit people with HIV infection or AIDS. Other herbs
in sho-saiko-to have also been shown to have anti-HIV activity in the test tube, most notably
Asian scullcap.81 Therefore studies on
sho-saiko-to cannot be taken to mean that bupleurum is the only active herb involved. The
other ingredients are peony root, pinellia root, cassia bark,
ginger root, jujube fruit, Asian ginseng root, Asian scullcap root, and licorice root.
Maitake mushrooms, which are currently being studied,
contain immuno-modulating polysaccharides (including
beta-D-glucan) that may be supportive for HIV infection.82 83
A controversy has surrounded the use of echinacea in
people infected with HIV. Test tube studies initially showed that echinacea’s
polysaccharides could increase levels of a substance that might stimulate HIV to
spread.84 However, these results have not been shown to occur when echinacea is
taken orally by humans.85 In fact, one double-blind trial found that Echinacea
angustifolia root (1 gram three times per day by mouth) greatly increased immune activity
against HIV, while placebo had no effect.86 Further studies are needed to determine
the safety of using echinacea in HIV-positive people.
The story of European mistletoe is similar to that of
echinacea. Though originally believed to be a problem based on test tube studies, preliminary
human clinical trials of mistletoe injections into the skin have shown only beneficial
effects.87 88 Oral mistletoe is very unlikely to have the same effects
as injected mistletoe. Injectable mistletoe should only be used under the supervision of a
qualified healthcare professional.
Turmeric may be another useful herb with immune effects
in people infected with HIV. One preliminary trial found that curcumin, the main active
compound in turmeric, helped improve CD4+ cell counts.89 The amount used in this
study was 1 gram three times per day by mouth. These results differed from those found in a
second preliminary trial using 4.8 or 2.7 grams of curcumin daily. In that study, there was no
apparent effect of curcumin on HIV replication rates.90
Cat’s claw is another immuno-modulating herb.
Standardized extracts of cat’s claw have been tested in small, preliminary trials in
people infected with HIV, showing some benefits in preventing CD4 cell counts from dropping
and in preventing opportunistic infections.91 92 Further study is needed
to determine whether cat’s claw is truly beneficial for people with HIV infection or
AIDS.
A 5% solution of tea tree oil has been shown to
eliminate oral thrush in people with AIDS, according to one preliminary trial.93
The volunteers in the study swished 15 ml of the solution in their mouths four times per day
and then spit it out. This may cause mild burning for a short period of time after use.
A trial of a combination naturopathic protocol (consisting of multiple nutrients, licorice, lomatium, a
combination Chinese herbal product, lecithin, calf thymus extract, lauric acid monoglycerol ester, and St. John’s wort) showed a possible slowing of the
progression of mild HIV infection and a reduction of some symptoms.94 Because there
was no placebo group in this trial, the findings must be considered preliminary; controlled
trials are needed to determine whether this protocol is effective.
Are there any side effects or interactions? Refer to the individual herb for
information about any side effects or interactions.
References:
1. The Group for the Scientific Reappraisal of the HIV/AIDS Hypothesis.
AIDS Proposal. Science 1995;267:945–6.
2. Duesberg PH. Inventing the AIDS Virus. Washington, DC:
Regnery Publishing, Inc., 1996.
3. Maggiore C, Mullis K. What if everything you thought you knew
about AIDS was wrong? Studio City, CA: American Foundation for AIDS Alternatives,
2000.
4. Gibert CL, Wheeler DA, Collins G, et al. Randomized, controlled trial
of caloric supplements in HIV infection. J Acquir Immune Defic Syndr
1999;22:253–9
5. Nellen H, Flores G, Wacher N. Treatment of human immunodeficiency
virus enteropathy with a gluten-free diet. Arch Intern Med 2000;160:244 [letter].
6. Roubenoff R, McDermott A, Weiss L, et al. Short-term progressive
resistance training increases strength and lean body mass in adults infected with human
immunodeficiency virus. AIDS 1999;13:231–9.
7. Mustafa T, Sy FS, Macera CA, et al. Association between exercise and
HIV disease progression in a cohort of homosexual men. Ann Epidemiol
1999;9:127–31.
8. Ince S. Vitamin supplements may help delay onset of AIDS. Med
Tribune 1993;9:18.
9. Fawzi WW, Msamanga G, Hunter D, et al. Randomized trial of vitamin
supplements in relation to vertical transmission of HIV-1 in Tanzania. J Acquir Immune
Defic Syndr 2000;23:246–54.
10. Baum MK, Shor-Posner G, Lai S, et al. High risk of HIV-related
mortality is associated with selenium deficiency. J Acquir Immune Defic Syndr Hum
Retrovirol 1997;15:370–4.
11. Olmsted L, Schrauzer GN, Flores-Arce M, Dowd J. Selenium
supplementation of symptomatic human immunodeficiency virus infected patients. Biol Trace
Elem Res 1989;25:89–96.
12. Chariot P, Perchet H, Monnet I. Dilated cardiomyopathy in
HIV-infected patients [letter; comment]. N Engl J Med 1999;340:732 (discussion
733–5).
13. Zazzo JF, Lafont A, Darwiche E, et al. Is non-obstructive
myocardiopathy (NOMC) in AIDS selenium-deficiency related? In: Neve J, Favier A, eds.
Selenium in biology and medicine. W. DeGruyter & Co.: Berlin New York, 1988,
281–2.
14. Roederer M, Staal FJ, Raju PA, et al. Cytokine-stimulated human
immunodeficiency virus replication is inhibited by N-acetyl-L-cysteine. Proc Natl Acad
Sci 1990;87:4884–8.
15. Herzenberg LA, De Rosa SC, Dubs JG, et al. Glutathione deficiency is
associated with impaired survival in HIV disease. Proc Natl Acad Sci
1997;94:1967–72.
16. Clark RH, Feleke G, Din M, et al. Nutritional treatment for acquired
immunodeficiency virus-associated wasting using beta-hydroxy beta-methylbutyrate, glutamine,
and arginine: a randomized, double-blind, placebo-controlled study. JPEN J Parenter
Enteral Nutr 2000;24:133–9.
17. Blehaut H, Saint-Marc T, Touraine J. Double blind trial of
Saccharomyces boulardii in AIDS-related diarrhea. International Conference on AIDS/Third
STD World Congress, 1992, Abstract #2120, July 19–24.
18. Eng RHK, Drehmel R, Smith SM, Goldstein EJC. Saccharomyces cerevisiae
infection in man. Sabouraudia: J Med Vet Mycol 1984;22:403–7.
19. Bassetti S, Frei R, Zimmerli W. Fungemia with Saccharomyces
cerevisiae after treatment with Saccharomyces boulardii. Am J Med
1998;105:71–2.
20. Ferrando SJ, Rabkin JG, Poretsky L. Dehydroepiandrosterone sulfate
(DHEAS) and testosterone: relation to HIV illness stage and progression over one year. J
Acquir Immune Defic Syndr 1999;22:146–54.
21. Rabkin JG, Ferrando SJ, Wagner GJ, Rabkin R. DHEA treatment for HIV +
patients: effects on mood, androgenic and anabolic parameters.
Psychoneuroendocrinology 2000;25:53–68.
22. Semba RD, Graham NMH, Caiaffa WT, et al. Increased mortality
associated with vitamin A deficiency during human immunodeficiency virus type 1 infection.
Arch Intern Med 1993;153:2149–54.
23. Semba RD, Miotti PG, Chiphangwi JD, et al. Maternal vitamin A
deficiency and mother-to-child transmission of HIV-1. Lancet
1994;343:1593–7.
24. Coutsoudis A, Pillay K, Spooner E, et al. Randomized trial testing
the effect of vitamin A supplementation on pregnancy outcomes and early mother-to-child HIV-1
transmission in Durban, South Africa. South African Vitamin A Study Group. AIDS
1999;13:1517–24.
25. Kennedy CM, Coutsoudis A, Kuhn L, et al. Randomized controlled trial
assessing the effect of vitamin A supplementation on maternal morbidity during pregnancy and
postpartum among HIV-infected women. J Acquir Immune Defic Syndr
2000;24:37–44.
26. Fawzi WW, Msamanga G, Hunter D, et al. Randomized trial of vitamin
supplements in relation to vertical transmission of HIV-1 in Tanzania. J Acquir Immune
Defic Syndr 2000;23:246–54.
27. Coutsoudis A, Bobat RA, Coovadia HM, et al. The effects of vitamin A
supplementation on the morbidity of children born to HIV-infected women. Am J Public
Health 1995;85:1076–81.
28. Hanekom WA, Yogev R, Heald LM, et al. Effect of vitamin A therapy on
serologic responses and viral load changes after influenza vaccination in children infected
with the human immunodeficiency virus. J Pediatr 2000;136:550–2.
29. Humphrey JH, Quinn T, Fine D, et al. Short-term effects of large-dose
vitamin A supplementation on viral load and immune response in HIV-infected women. J
Acquir Immune Defic Syndr Hum Retrovirol 1999;20:44–51.
30. Sappey C, Leclercq P, Coudray C, et al. Vitamin, trace element and
peroxide status in HIV seropositive patients: asymptomatic patients present a severe
beta-carotene deficiency. Clin Chim Acta 1994;230:35–42.
31. Coodley GO, Nelson HD, Loveless MO, Folk C. Beta-carotene in HIV
infection. J Acquir Immune Defic Syndr 1993;6:272–6.
32. Coodley GO, Coodley MK, Lusk R, et al. Beta-carotene in HIV
infection: an extended evaluation. AIDS 1996;10:967–73.
33. Kanter AS, Spencer DC, Steinberg MH, et al. Supplemental vitamin B
and progression to AIDS and death in black South African patients infected with HIV. J
Acquir Immune Defic Syndr 1999;21:252–3 [letter].
34. Butterworth RF, Gaudreau C, Vincelette J, et al. Thiamine deficiency
in AIDS. Lancet 1991;338:1086.
35. Baum MK, Mantero-Atienza E, Shor-Posner G, et al. Association of
vitamin B6 status with parameters of immune function in early HIV-1 infection. J Acquir
Immune Defic Syndr 1991;4:1122–32.
36. Tang AM, Graham NMH, Saah AJ. Effects of micronutrient intake on
survival in human immunodeficiency type 1 infection. Am J Epidemiol
1996;143:1244–56.
37. Boudes P, Zittoun J, Sobel A. Folate, vitamin B12, and HIV infection.
Lancet 1990;335:1401–2.
38. Murray MF. Niacin as a potential AIDS preventive factor. Med
Hypotheses 1999;53:375–9.
39. Murray MF, Srinivasan A. Nicotinamide inhibits HIV-1 in both acute
and chronic in vitro infection. Biochem Biophys Res Commun 1995;210:954–9.
40. Tang AM, Graham NMH, Saah AJ. Effects of micronutrient intake on
survival in human immunodeficiency type 1 infection. Am J Epidemiol
1996;143:1244–56.
41. Graham NMH, Saah AJ. Effects of micronutrient intake on survival in
human immunodeficiency type 1 infection. Am J Epidemiol 1996;143:1244–56.
42. Harakeh S, Jariwalla RJ, Pauling L. Suppression of human
immunodeficiency virus replication by ascorbate in chronically and acutely infected cells.
Proc Natl Acad Sci 1990;87:7245–9.
43. Tang AM, Graham NMH, Saah AJ. Effects of micronutrient intake on
survival in human immunodeficiency type 1 infection. Am J Epidemiol
1996;143:1244–56.
44. Cathcart RF III. Vitamin C in the treatment of acquired immune
deficiency syndrome (AIDS). Med Hypotheses 1984;14:423–33.
45. Gogu SR, Beckman BS, Rangan SR, Agrawal KC. Increased therapeutic
efficacy of zidovudine in combination with vitamin E. Biochem Biophys Res Commun
1989;165:401–7.
46. Gogu SR, Agrawal KC. The protective role of zinc and N-acetylcysteine
in modulating zidovudine induced hematopoietic toxicity. Life Sci
1996;59:1323–9.
47. Folkers K, Langsjoen P, Nara Y, et al. Biochemical deficiencies of
coenzyme Q10 in HIV-infection and exploratory treatment. Biochem Biophys Res Commun
1988;153:888–96.
48. Fabris N, Mocchegiani E, Galli M, et al. AIDS, zinc deficiency, and
thymic hormone failure. JAMA 1988;259:839–40.
49. Dworkin BM. Selenium deficiency in HIV infection and the acquired
immunodeficiency syndrome (AIDS). Chem Biol Interact 1994;91:181–6.
50. Mocchegiani E, Veccia S, Ancarani F, et al. Benefit of oral zinc
supplementation as an adjunct to zidovudine (AZT) therapy against opportunistic infections in
AIDS. Int J Immunopharmacol 1995;17:719–27.
51. Castaldo A, Tarallo L, Palomba E, et al. Iron deficiency and
intestinal malabsorption in HIV disease. J Pediatr Gastroenterol Nutr
1996;22:359–63.
52. Humbert JR, Moore LL. Iron deficiency and infection: a dilemma. J
Pediatr Gastroenterol Nutr 1983;2:403–6.
53. Robinson MK, Hong RW, Wilmore DW. Glutathione deficiency and HIV
infection. Lancet 1992;339:1603–4.
54. Shabert JK, Wilmore DW. Glutamine deficiency as a cause of human
immunodeficiency virus wasting. Med Hypotheses 1996;46:252–6.
55. Noyer CM, Simon D, Borczuk A, et al. A double-blind
placebo-controlled pilot study of glutamine therapy for abnormal intestinal permeability in
patients with AIDS. Am J Gastroenterol 1998;93:972–5 .
56. Shabert JK, Winslow C, Lacey JM, Wilmore DW. Glutamine-antioxidant
supplementation increases body cell mass in AIDS patients with weight loss: a randomized,
double-blind controlled trial. Nutrition 1999;15:860–4.
57. Muller F, Svardal AM, Aukrust P, et al. Elevated plasma concentration
of reduced homocysteine in patients with human immunodeficiency virus infection. Am J Clin
Nutr 1996;242–6.
58. Revillard JP. Lipid peroxidation in Human Immunodeficiency Virus
infection. J Acquired Immunodef Synd 1992;5:637–8.
59. Singer P, Katz DP, Dillon L, et al. Nutritional aspects of the
acquired immunodeficiency syndrome. Am J Gastroenterol 1992;87:265–73.
60. Tan SV, Guiloff RJ. Hypothesis on the pathogenesis of vacuolar
myelopathy, dementia, and peripheral neuropathy in AIDS. J Neurol Neurosurg
Psychiat 1998;65:23–8.
61. Keating JN, Trimble KC, Mulcahy F, et al. Evidence of brain
methyltransferase inhibition and early brain involvement in HIV-positive patients.
Lancet 1991;337:935–9.
62. Dorfman D, DiRocco A, Simpson D, et al. Oral methionine may improve
neuropsychological function in patients with AIDS myelopathy: results of an open-label trial.
AIDS 1997;11:1066–7.
63. Valesini G, Barnaba V, Benvenuto R, et al. A calf thymus lysate
improves clinical symptoms and T-cell defects in the early stages of HIV infection: Second
report. Eur J Cancer Clin Oncol 1987;23:1915–9.
64. Durant J, Chantre Ph, Gonzalez G, et al. Efficacy and safety of Buxus
sempervirens L. preparations (SPV30) in HIV-infected asymptomatic patients: a multicentre,
randomized, double-blind, placebo-controlled trial. Phytomedicine
1998;5(1):1–10.
65. Ito M, Sato A, Hirabayashi K, et al. Mechanism of inhibitory effect
of glycyrrhizin on replication of human immunodeficiency virus (HIV). Antivir Res
1988;10:289–98.
66. Hattori I, Ikematsu S, Koito A, et al. Preliminary evidence for
inhibitory effect of glycyrrhizin on HIV replication in patients with AIDS. Antivir
Res 1989;11:255–62.
67. Ikegami N, Akatani K, Imai M, et al. Prophylactic effect of long-term
oral administration of glycyrrhizin on AIDS development of asymptomatic patients. Int Conf
AIDS 1993;9:234 [abstract PO-A25–0596].
68. Koch J, Tuveson J, Carlson T, Schmidt J. SB-300: a new and effective
therapy for HIV-associated diarrhea. Poster presented at the Seventh European Conference on
Clinical Aspects and Treatment of HIV-Infection, Lisbon, Portugal, October 23–27,
1999.
69. Holodniy M, Koch J, Mistal M, et al. A double blind, randomized,
placebo-controlled phase II study to assess the safety and efficacy of orally administered
SP-303 for the symptomatic treatment of diarrhea in patients with AIDS. Am J
Gastroenterol 1999;94:3267–73.
70. Koch J. A phase III, double-blind, randomized, placebo-controlled
multi-center study of SP-303 (Provir™) in the symptomatic treatment of diarrhea in
patients with acquired immunodeficiency syndrome (AIDS). Posters presented at the 13th
international AIDS Conference in Durba, South Africa, July 14, 2000.
71. Cooper WC, James J. An observational study of the safety and efficacy
of hypericin in HIV+ subjects. Int Conf AIDS 1990;6:369 [abstract no. 2063].
72. Steinbeck-Klose A, Wernet P. Successful long term treatment over 40
months of HIV-patients with intravenous hypericin. Int Conf AIDS 1993;9:470 [abstract
no. PO-B26–2012].
73. Gulick RM, McAuliffe V, Holden-Wiltse J, et al. Phase I studies of
hypericin, the active compound in St. John’s wort, as an antiretroviral agent in
HIV-infected adults. AIDS clinical trial group protocols 150 and 258. Ann Intern Med
1999;130:510–4.
74. Abdullah TH, Kirkpatrick DV, Carter J. Enhancement of natural killer
cell activity in AIDS with garlic. Dtsch Zschr Onkol 1989;21:52–3.
75. Shoji S, Furuishi K, Yanase R, et al. Allyl compounds selectively
killed human immunodeficiency virus (type 1)-infected cells. Biochem Biophys Res
Commun 1993;194:610–21.
76. Miller S. Synopsis of PN355 Androvir study. Unpublished study.
Seattle: Bastyr University, 1997.
77. Cho YK, Kim Y, Choi M, et al. The effect of red ginseng and
zidovudine on HIV patients. Int Conf AIDS 1994;10:215 [abstract no. PB0289].
78. Inada Y, Watanabe K, Kamiyama M, et al. In vitro immunomodulatory
effects of traditional Kampo medicine (sho-saiko-to: SST) on peripheral mononuclear cells in
patients with AIDS. Biomed Pharmacother 1990;44:17–9.
79. Piras G, Makino M, Baba M. Sho-saiko-to, a traditional kampo
medicine, enhances the anti-HIV-1 activity of lamivudine (3TC) in vitro. Microbiol
Immunol 1997;41:435–9.
80. Fujimaki M, Hada M, Ikematsu S, et al. Clinical efficacy of two kinds
of kampo medicine on HIV infected patients. Int Conf AIDS 1989;5:400 [abstract no.
W.B.P.292].
81. Li BQ, Fu T, Yan YD, et al. Inhibition of HIV infection by
baicalin—a flavonoid compound purified from Chinese herbal medicine. Cell Mol Biol
Res 1993;39:119–24.
82. Yamada Y, Nanba H, Kuroda H. Antitumor effect of orally administered
extracts from fruit body of Grifola frondosa (maitake). Chemotherapy
1990;38:790–6.
83. Nanba H. Immunostimulant activity in-vivo and anti-HIV activity in
vitro of 3 branched b-1–6-glucans extracted from maitake mushrooms (Grifola frondosa).
VIII International Conference on AIDS, 1992 [abstract].
84. Luettig B, Steinmuller C, Gifford GE, et al. Macrocytic activation by
the polysaccharide arabinogalactan isolated from plant cell cultures of Echinacea
purpurea. J Natl Cancer Inst 1989;81:669–75.
85. Elsasser-Beile U, Willenbacher W, Bartsch HH, et al. Cytokine
production in leukocyte cultures during therapy with Echinacea extract. J Clin
Lab Anal 1996;10:441–5.
86. Berman S, See DM, See JR, et al. Dramatic increase in immune mediated
HIV killing activity induced by Echinacea angustifolia. Int Conf AIDS
1998;12:582 [abstract no. 32309].
87. Gorter R, Khwaja T, Linder M. Anti-HIV and immunomodulating
activities of Viscum album (mistletoe). Int Conf AIDS 1992;8:84 [abstract
no. PuB 7214].
88. Gorter R, Stoss M, el Arif N, et al. Immune modulating and anti-HIV
activities of Viscum album (Iscador). Int Conf AIDS 1993;9:496 [abstract no.
PO-B28–2167].
89. Copeland R, Baker D, Wilson H. Curcumin therapy in HIV-infected
patients. Int Conf AIDS 1994;10:216 [abstract no. PB0876].
90. Hellinger JA, Cohen CJ, Dugan ME, et al. Phase I/II randomized,
open-label study of oral curcumin safety, and antiviral effects on HIV-RT PCR in HIV+
individuals. 3rd Conf Retro and Opportun Infect 1996;Jan/Feb:78 [abstract].
91. Keplinger UM. Influence of Krallendorn extract on retroviral
infection. Zürcher AIDS Kongress Zurich, Switzerland, Oct 16–7, 1992
[abstract in German].
92. Keplinger UM. Therapy of HIV-infected individuals in the pathological
categories CDC A1 and CDC B2 with a preparation containing IMM-207. IV.
Österreichischer AIDS-Kongress, Vienna, Austria, Sept 17–8, 1993, 45
[abstract].
93. Jandourek A, Vaishampayan JK, Vazquez JA. Efficacy of melaleuca oral
solution for the treatment of fluconazole refractory oral candidiasis in AIDS patients.
AIDS 1998;12:1033–7.
94. Standish L, Guiltinan J, McMahon E, Lindstrom C. One year open trial
of naturopathic treatment of HIV infection class IV-A men. J Naturopathic Med
1992;3:42–64.