AIDS/HIV was once considered a death sentence, but thanks to advancements in medical research and treatment, people living with the virus can now lead long and healthy lives. According to hiv.org, a diagnosis of AIDS/HIV in the early 1990s was a grim prospect. At that time, there was limited understanding of the virus, and few effective treatments were available. Those diagnosed with the virus often had a life expectancy of just a few years. However, things have changed dramatically since then. The introduction of antiretroviral therapy (ART) in 1996 was a turning point in the treatment of AIDS/HIV. ART works by blocking the replication of the virus, slowing its progression and allowing the immune system to recover. With proper care and management, many people with AIDS can now expect to live a normal lifespan. In recent years, advances in medical research have led to the development of new and more effective antiretroviral drugs. These drugs are more potent and have fewer side effects, making them easier for people with AIDS to adhere to their treatment regimen. According to hiv.org, “many antiretroviral drugs can now be taken as a single pill once a day, improving the quality of life for people living with HIV.” In addition to ART, other advancements have been made in the fight against AIDS/HIV. For instance, pre-exposure prophylaxis (PrEP) is a daily pill that can be taken by people who are at high risk of contracting the virus. PrEP has been shown to be highly effective in preventing the transmission of the virus. Furthermore, ART has also been used as a form of prevention, known as treatment as prevention (TasP). ART can effectively suppress the virus in the body, reducing the likelihood of its transmission to others. As noted by hiv.org, “TasP has been shown to be a highly effective approach to reducing the spread of HIV.” In conclusion, the treatment of AIDS/HIV has come a long way since its early days. Today, with proper care and management, people with the virus can lead long and healthy lives. The introduction of ART, as well as advances such as PrEP and TasP, has greatly improved the quality of life for people with AIDS/HIV. Although there is still much work to be done, these developments give us hope for a brighter future. Sources: · hiv.org: “Treatment & Care for People Living with HIV” · hiv.org: “Pre-exposure Prophylaxis (PrEP)” · hiv.org: “Treatment as Prevention (TasP)” *This article was produced with the assistance of artificial intelligence. Please always check and confirm with your own sources, and always consult with your healthcare professional when seeking medical treatment.
An Increase in HIV diagnosis Brings Awareness to World AIDS Day
Acquired Immune Deficiency Syndrome (AIDS) is an illness caused by HIV. AIDS is the stage of infection that occurs when your immune system is badly damaged and you become vulnerable to opportunistic infections. Without treatment, people who are living with AIDS typically survive about 3 years. There are medications, such as Non-nucleoside reverse transcriptase inhibitors (NNRTIs), that are highly effective in fighting AIDS and its complications. They help reduce the HIV virus within the body and keep the immune system as healthy as possible with little complications. There are many more tools today to prevent HIV than ever before. To reduce your risk of HIV infection you should limit your number of sexual partners, practice safe sex by using condoms correctly and consistently including anal, oral, and vaginal, you should never share needles .It is also important to take advantage of newer biomedical options such as pre-exposure prophylaxis. Pre-exposure prophylaxis (PrEP) is a pill prevention option for those who are at high risk of getting HIV. PrEP does not mean it’s ok to have unprotected sex; one should always protect themselves by the use of condoms. At this time, there is no cure for HIV/AIDS, but there are effective medications that fight and help prevent HIV and its complications. Researchers and doctors have made tremendous strides in acquiring knowledge about both HIV and AIDS and remain optimistic. About Dr. Avni Mahiji Dr. Avni Mahiji, a Board Certified Pharmacist boasting both beauty and brains, resides in New York City. The summa cum laude graduate of Boston’s Massachusetts College of Pharmacy and Health Sciences has spent her entire career helping people maintain their health, and works to share her prescription and over the counter expertise worldwide. Dr. Mahiji focuses on counseling patients on over the counter items, assuring that patients’ medications are issued properly, checking for drug interactions, assisting patients with making cost effective decisions, and following up with patients on recovery and medication compliance. Dr. Mahiji aims to increase awareness of the connection between medications and overall wellness by educating patients about the benefits and potential risks of pharmaceuticals and homeopathic products. Please visit Dr. Avni Mahiji website.
Early HIV Drug Therapy Protects Sex Partners From Virus
By Steven Reinberg HealthDay Reporter THURSDAY, May 12 (HealthDay News) — People with HIV can reduce the risk of infecting their sex partners by more than 90 percent if they start treatment with antiretroviral drugs when their immune system is still relatively healthy, researchers announced Thursday. The study, which included 1,763 mostly heterosexual couples from nine countries, was supposed to last until 2015, but the results were released early because of the significance of the findings. The research confirmed a belief held by many scientists and physicians — that starting drug therapy early can help to limit rates of transmission of the virus that causes AIDS. “We set out to prove that if you took earlier therapy you could benefit your own health and you could prevent the transmission of HIV,” said lead researcher Dr. Myron Cohen, director of the Institute for Global Health and Infectious Diseases at the University of North Carolina at Chapel Hill. “Both of those hypotheses were realized,” he said. The study, which started in 2005, randomly assigned the couples to two treatment groups: In the first group the HIV-infected individual began taking a combination of three antiretroviral drugs immediately. In the second group, the HIV-positive person delayed drug therapy until their CD4 T-cell count — a blood test that measures immune system health — either dropped below 250 or an AIDS-related illness (such as pneumocystis pneumonia) set in. Both groups also received HIV care, which included counseling on safe sex, free condoms, treatment for sexually transmitted infections, regular HIV testing and evaluation, and treatment for any HIV-related complications. The trial was conducted at 13 sites in nine countries including the United States, Botswana, Brazil, India, Kenya, Malawi, South Africa, Thailand and Zimbabwe. In looking over the preliminary findings, the data and safety monitoring board shepherding the study identified 39 new cases of HIV among the previously uninfected partners. In 28 of these cases, genetic analysis confirmed that one partner had infected the other. Of these 28 infections, 27 — or 96 percent — occurred among couples in which the HIV-infected partner did not start antiretroviral therapy immediately. Cohen cautioned that the findings don’t apply to all HIV-positive people. “Our couples had big advantages,” he said. “We enrolled couples who probably have a low overall transmission [HIV] rate,” he said. The researchers also made sure that the patients were taking their antiretroviral medications. And, the medications were carefully selected. “The drugs are important,” Cohen said. “We didn’t use any combination possible — we used ones we thought would sterilize the genital tract,” he said. Commenting on the study, Dr. Alexis Powell, an assistant professor of infectious diseases at the University of Miami Miller School of Medicine, said that “it’s nice to finally have evidence-based information that clearly shows that earlier treatment with antiretrovirals can benefit the individual who is HIV-positive, but also protects sexual partners who are HIV-negative.” Most doctors would like to treat HIV patients sooner, Powell said. “We clearly understand that patients benefit with earlier treatment,” she said. “And this is another reason to start early.” Powell said she’d like to put HIV patients on antiretrovirals as soon as they are diagnosed, but there are barriers. They include criteria for treatment set by insurance companies and lack of funding to treat those without insurance, she said. “When you start talking about the dollars and cents of every day clinical practice, that’s when we are really going to see what we are going to be allowed to do,” Powell said. Another barrier is convincing some HIV-positive people to take the drugs. Some are reluctant to start taking medications that they will have to take for the rest of their lives, while others are wary of side effects. Some people think the drugs make you sicker than the virus. And still others distrust the medical system to act in their best interest, Powell said. She cautioned that the study findings do not mean that people can stop practicing safe sex. Men, especially, need to use a condom to protect themselves or their partners, Powell said. More information For more on HIV/AIDS, visit AIDS.gov. SOURCES: Myron Cohen, M.D., director, Institute for Global Health and Infectious Diseases, University of North Carolina at Chapel Hill; Alexis Powell, M.D., assistant professor, infectious diseases, University of Miami Miller School of Medicine; May 12, 2011, news release, U.S. National Institutes of Health Copyright © 2011 HealthDay. All rights reserved. This is a story from HealthDay, a service of ScoutNews, LLC.
Stroke Risk May Be Higher in HIV Patients
Stroke rates have increased among people with HIV in recent years while declining in the U.S. population at large, new research shows, raising the possibility that treatments for the AIDS-causing virus may put these patients at higher risk for cardiovascular trouble. There’s no direct proof linking the medications to the higher stroke rate, but previous research has suggested that HIV drugs can boost cholesterol and triglyceride levels, both of which contribute to stroke risk. “Until we have a better idea what’s happening, this is a call or reminder to clinicians to be cognizant of these risk factors for stroke in these HIV patients,” said study author Dr. Bruce Ovbiagele, a neuroscience professor at the University of California, San Diego. For their study, published online Jan. 19 in the journal Neurology, Ovbiagele and colleagues examined a database of hospitalizations for stroke from 1997, when a new generation of AIDS drugs was in its early days of use, through 2006. They found that while overall hospitalizations for stroke fell by 7 percent, the number of stroke hospitalizations in HIV-infected people rose by 60 percent in 2006. (The researchers adjusted their numbers to account for factors such as age and gender.) The researchers also looked at the two kinds of stroke — ischemic (when a blood vessel is blocked) and hemorrhagic (when a blood vessel bursts). There was no change in the percentage of hemorrhagic stroke patients who were HIV-positive, but the rate went up from 0.08 percent to .18 percent — more than doubling — among HIV patients who had ischemic strokes. The latter number suggests, but doesn’t prove, that more HIV patients are suffering from blockages in their blood vessels. Some previous research has suggested that HIV patients have higher levels of heart attacks, which also occur when vessels clog up. “We know that many of the drugs that are used for AIDS treatment have metabolic complications, which include the addition of belly fat and an increase in serum triglycerides,” Ovbiagele said. Both increase the risk of heart problems. It’s possible that HIV patients are living longer and simply getting to the age at which strokes are more common among all people, said Ovbiagele, who was at the University of California at Los Angeles, when the research was conducted. But the study also found that HIV patients had strokes earlier, on average, than other people. Overall, the risk that an HIV patient will have a stroke remains low. However, patients who are on AIDS drugs should be aware that stroke is “highly preventable,” Ovbiagele said, and they should work with their doctors to keep their weight and cholesterol levels under control. Dr. Alejandro A. Rabinstein, a professor of neurology at the Mayo Clinic in Rochester, Minn., said that even while the link between AIDS medications and stroke isn’t proven, HIV patients should go on low-fat, low-sodium diets and be monitored for high blood pressure and other risk factors. However, he said, strokes will remain rare among patients on HIV drugs. “The risk may be increased, but it is overall a small risk,” he said.
LYMPHOMA
WHAT IS LYMPHOMA? HOW IS NHL DIAGNOSED? WHAT CAUSES NHL? HOW IS NHL TREATED? THE BOTTOM LINE WHAT IS LYMPHOMA? Lymphoma is a cancer of white blood cells called B-lymphocytes, or B-cells. They multiply rapidly and form tumors. Lymphoma of the brain or spinal cord is called central nervous system (CNS) lymphoma. AIDS-related lymphoma is sometimes called Non-Hodgkin’s Lymphoma (NHL). In 1985, the Centers for Disease Control added NHL to the list of diseases that define AIDS. Hodgkin’s Disease, another type of lymphoma, is rare in people with HIV. The longer you live with a suppressed immune system, the higher the risk of NHL. It can occur even with a high CD4 count. It can be serious and often fatal, sometimes within a year. The use of combination antiretroviral therapy (ART) cut the rates of most opportunistic infections by about 80%. At first, this did not appear to be true for NHL. However, newer studies show a decrease of about 50% in NHL rates, especially CNS lymphoma. NHL still accounts for about 20% of the deaths of people with HIV. Approximately 10% of peole with HIV may eventually develop NHL. HOW IS NHL DIAGNOSED? NHL tumors can occur in the bone, abdomen, liver, brain or other parts of the body. The first signs of NHL are swollen lymph nodes, fever, night sweats, and weight loss of more than 10%. These symptoms occur with several AIDS-related illnesses. If health care providers cannot find another cause for these symptoms, they will test for NHL. NHL is usually diagnosed using imaging techniques or biopsies. The imaging techniques include various scans (CAT, PET, gallium and thallium.) A biopsy is an examination of cells from a suspected tumor. The cells are collected by a thin needle, or they are cut out surgically. WHAT CAUSES NHL? NHL is caused by long-term stimulation of the immune system. When B-cells multiply quickly for many years, more mutations occur. Some of these mutations cause cancer. About 4% of people with symptoms of HIV disease develop NHL each year. The rate of NHL in people with HIV is over 80 times higher than for the general population. The risk of NHL is increased by infection with Epstein-Barr virus and by genetic factors. The rate of NHL is twice as high in men as in women, and twice as high in Caucasians as in people of African or Caribbean ancestry. At the present time we don’t know how to prevent NHL. HOW IS NHL TREATED? Most cancers are treated by a combination of drugs (chemotherapy or chemo). Chemo is very toxic. It suppresses the immune system. It can cause nausea, vomiting, fatigue, diarrhea, swollen and sensitive gums, mouth sores, hair loss, and numbness or tingling in the feet or hands. Chemo also damages bone marrow. This can cause anemia (low red blood cells) and neutropenia (low white blood cells). Neutropenia increases the risk of bacterial infections. Additional drugs may be needed to fight these side effects. NHL in the central nervous system is very difficult to treat. Radiation therapy may be used instead of, or in addition to chemotherapy. ART makes it easier for HIV patients to tolerate strong chemotherapy for NHL. As a result, the death rate from NHL has dropped by over 80%. Seventy-four percent of patients recovered from NHL in a study using a newer combination of chemotherapy drugs known as EPOCH. Since people started using strong ART, the types of NHL seen in people with HIV are types that are easier to treat. As a result, people with HIV and NHL are living longer. Several types of chemo are used for NHL. Chemo clears up tumors in about 50% of patients. However, tumors return in many patients within a year. People diagnosed with NHL are at a higher risk of developing pneumocystis pneumonia (PCP) and should all take medications to prevent it. See Fact Sheet 515 for more information on PCP. ?Monoclonal antibodies? are being used against NHL, and researchers continue to study their use. These drugs are produced through genetic engineering. They attack the B-cells that are multiplying out of control. The names of monoclonal antibodies end in “-mab,” such as rituximab. They shrink tumors and increase the time before tumors return. THE BOTTOM LINE NHL, a cancer involving B-cells, affects people with advanced AIDS. It is serious and often fatal. The use of ART has reduced the number of new cases. This is especially true for NHL in the central nervous system. NHL is treated with chemotherapy drugs. In the CNS, radiation therapy is also used. Even if NHL tumors are cleared up, they tend to return in many people. Treatment of NHL is difficult. People who get it often have very weak immune systems. ART strengthens the immune system and permits the use of stronger chemotherapy. It also seems to make NHL easier to treat. Additional drugs are often needed to deal with the side effects of chemo. New genetically engineered drugs called monoclonal antibodies are now being used against NHL. Studies of the use of monoclonal antibodies and new combinations of chemo drugs are continuing source: The AIDS Infonet
MOLLUSCUM
WHAT IS MOLLUSCUM? HOW DOES MOLLUSCUM SPREAD? HOW DO I KNOW IF I HAVE MOLLUSCUM? HOW IS MOLLUSCUM TREATED? CAN MOLLUSCUM BE PREVENTED? DRUG INTERACTION PROBLEMS THE BOTTOM LINE WHAT IS MOLLUSCUM? Molluscum contagiosum is a skin infection. It is caused by a virus. Molluscum causes small bumps (lesions) to appear on the skin. Most of them are less than half an inch in diameter. They have a hard white core. Some lesions have a small dent or dimple in the center. The lesions are the same color as normal skin, but they look waxy. They usually don’t hurt or itch. The molluscum virus is very common, and almost everyone has it in his or her body. A healthy immune system will control molluscum so that if lesions appear, they do not last a long time. People with weakened immune systems can develop molluscum lesions that spread, last a long time, and are very difficult to treat. About 20% of people with AIDS will develop molluscum. Molluscum is not a serious health problem. However, many people find the molluscum lesions to be very unattractive. This can cause serious emotional or psychological problems. HOW DOES MOLLUSCUM SPREAD? Molluscum can be spread by direct skin contact. It often spreads through sexual activity. Molluscum can infect any part of the skin, but it is especially common on the face or in the groin and pubic areas. It can be spread from existing lesions to other parts of the body or to other people. It can also be spread by objects (or clothing) that came in contact with a lesion. Men with HIV often develop molluscum on their face. Shaving with a razor blade can spread it. HOW DO I KNOW IF I HAVE MOLLUSCUM? A health care provider can easily identify molluscum lesions. They are waxy, flesh-colored bumps that don’t hurt or itch. There are only one or two other infections that cause skin problems that look at all similar to molluscum. HOW IS MOLLUSCUM TREATED? Molluscum lesions are treated the same way as warts. Unfortunately, the lesions often return and need to be treated again. They can be frozen with liquid nitrogen. This is the most common method of treatment. They can be burned with an electric needle (electrocautery) or a laser. This treatment can be painful and sometimes leaves scars. They can be treated with chemicals used on warts such as trichloroacetic acid (TCA), podophyllin or podofilox. These chemicals can not be used on sensitive skin or near the eyes. They can be cut or "scooped" out surgically. This treatment can be painful and can leave scars. They can be treated with drugs used to treat acne such as tretinoin (Retin-A) or isotretinoin (Accutane). This is a newer approach. These drugs reduce the amount of oil in the skin. The top layer of skin dries out and peels off. These drugs can cause redness and soreness. Retin-A is a cream that is put onto the lesions. Accutane is taken in pill form. Another new approach is to use the antiviral medications cidofovir or imiquimod. These drugs are applied directly onto the lesions. They can cause local skin irritation. CAN MOLLUSCUM BE PREVENTED? Because the virus that causes molluscum is so common, it is not possible to avoid being exposed to it. However, if you have molluscum you should make sure that the lesions don’t touch anyone else. You should also be careful not to spread molluscum to different parts of your body. Be careful not to scratch the lesions or to cut them while shaving. Some health care providers think that using an electric shaver helps prevent the spread of molluscum. DRUG INTERACTION PROBLEMS The acne drugs tretinoin (Retin-A) and isotretinoin (Accutane) tend to dry out the skin. Dry skin is also a side effect of the protease inhibitor indinavir (Crixivan) and some other antiretroviral medications (ARVs). If you take use Retin-A or Accutane to treat molluscum along with ARVs that can cause dry skin, your skin problems could get worse. THE BOTTOM LINE Molluscum is a viral infection that can produce skin lesions. Although they are not medically dangerous, the lesions can cause serious emotional and psychological problems. Molluscum can be spread from person to person by direct skin contact. It can be spread during sexual activity. If you have molluscum, you can spread the lesions to new areas if you shave with a blade. Molluscum lesions are removed in the same ways as warts. Unfortunately, they often return and have to be treated again. source: The AIDS Infonet
1 in 4 HIV Patients Have Neurological Diseases: Study
MONDAY, Oct. 4 (HealthDay News) — One in four people infected with HIV suffer from neurological complications, new Canadian research reveals. And those that do have such problems harbor double the risk of dying compared with HIV patients who are not plagued with neurological diseases, the study authors reported in the Sept. 28 issue of Neurology. “The good news is that people with HIV are living much longer now that we have antiretroviral therapies,” Dr. Chris Power, a professor of neurology at the universities of Alberta and Calgary, said in a news release from Alberta Innovates–Health Solutions, a new agency funded by the government of Alberta, Canada. But the bad news is that “this study proves without a doubt that neurological disease is a major cause of disability for people with HIV,” added Power, who is also the Canada research chair in neurological infection and immunity. Power and his colleagues based their assessment on work they conducted with 1,651 HIV patients who were receiving treatment between 1998 and 2008. Of these, 404 had neurological problems, such as seizures, dementia, nerve pain in the limbs, memory loss, headaches/migraines, opportunistic infections of the central nervous system and movement disorders. The study authors also found that brain disorders appeared to be twice as common among patients with full-blown AIDS compared with those whose HIV infection had not advanced to that stage. “That motivates us to look closely at which drugs are working well, design optimal drug combinations to reduce brain diseases, and to explore in the lab new drugs that we can use to protect the brain,” Power said. More information For more on AIDS and neurological complications, visit the U.S. National Institute of Neurological Disorders and Stroke. SOURCE: Alberta Innovates–Health Solutions, news release, Sept. 28, 2010 Copyright © 2010 HealthDay. All rights reserved. This is a story from HealthDay, a service of ScoutNews, LLC.
HIV Travel/Immigration Ban: Background, Documentation
This background article addresses two different audiences. It is both an introduction for persons not familiar with AIDS and the HIV exclusion issue, and also a resource for activists; it includes information not generally available or not published before. Chronology * The U. S. Public Health Service (PHS) has long maintained a list of “dangerous and contagious diseases,” mostly sexually- transmitted diseases, for excluding persons for public-health reasons from the United States. This list is widely regarded as obsolete by health experts. * In June 1987 the PHS, under pressure from President Reagan, added AIDS to the list, but noted that the exclusion was not based on any new scientific knowledge and that “AIDS is not spread by casual contact which is the usual public concept of contagious.” * In July 1987 the “Helms amendment” by Senator Jesse Helms (Republican, North Carolina) added HIV infection to the exclusion list. Because AIDS was already on the list, Congress thought the change was not important, and through a political compromise the amendment was passed unanimously in the Senate. Later, however, it would be argued that since Congress had put HIV on the list, only Congress could take it off — although in regard to all other diseases, the list was maintained by the PHS. * In April 1989 Dutch AIDS educator Hans Paul Verhoef, on his way to an AIDS conference in San Francisco, was detained in Minneapolis by the U. S. Immigration and Naturalization Service (INS), an arm of the Department of Justice, when AZT was found in his luggage. Through legal action by the conference organizers, a waiver was obtained, but only when the conference was ending. The AIDS community then realized that the June 1990 Sixth International Conference on AIDS in San Francisco, the major scientific meeting on AIDS in the year, could be disrupted because persons with HIV would be unable to travel to San Francisco to attend. A year’s effort by the Conference organizers and the AIDS community failed to end the ban; various waiver rules were devised, but there were problems with them. Because of the travel ban, over 70 AIDS, medical, and government organizations, including the International Red Cross, the British Medical Association, and the European Parliament, boycotted the meeting. Although the Conference organizers sent waiver instructions to potential delegates and organized legal panels in case of problems at the border, it is likely that thousands of people stayed away; thousands of others demonstrated at the San Francisco meeting. As a result of this experience, Harvard University, which had been selected to organize the May 1992 Eighth International Conference on AIDS in Boston, announced that it would withdraw its sponsorship unless persons with HIV were able to travel freely to attend. * In March 1990 public-health experts at the U. S. Centers for Disease Control recommended that all diseases except active tuberculosis be removed from the list of excludable conditions; HIV was left on the proposed list because it had been put on by Congress. The Public Health Service never acted on this proposal. * In November 1990 the Immigration Reform Act of 1990 was signed. It directed the CDC to establish a new list of excludable conditions, based solely on “current epidemiological principles and medical standards,” by June 1, 1991. * On January 23, 1991, the CDC published in the Federal Register its proposal that only active tuberculosis remain on the list of excludable conditions. (Other provisions of the law allow exclusion of persons with a dangerous mental disorder, one who abuses drugs, or one likely to become a “public charge,” i.e., to require government assistance. These sections have not been involved in the HIV controversy, however.) * During a 30-day public comment period on this proposed rule, right-wing religious leaders generated 35,000 postcards and letters opposed to removing the HIV exclusion. And in Congress a letter from the Republican Study Committee, circulated by Representative William E. Dannemeyer (Republican, California) and signed by 67 members of the House of Representatives, opposed removing the ban. Opponents focused their arguments on immigration, not on travel, although for technical legal reasons it will be difficult to separate the two without new legislation, meaning that if the list proposed by the PHS (excluding only active tuberculosis) is not accepted, the travel ban will also continue. * About a week before the June 1 deadline, a major dispute surfaced between the U. S. Department of Health and Human Services (HHS) and the U. S. Department of Justice; the latter opposed removing HIV from the list. Until shortly before that time, no one in the AIDS community had known that the Department of Justice was involved in the issue; the law clearly gives sole authority to establish this list to HHS. But politically, although the two departments have theoretically equal Cabinet rank, Justice is closer to the White House, and therefore likely to win a dispute; in addition, the 35,000 letters opposed, and the letter from 67 members of Congress, gave it additional advantage. * Because of this conflict between Federal departments, an interim rule was put into effect last Saturday, June 1, and a new public comment period was extended for 60 days. The interim rule keeps the current exclusion list, including tuberculosis, HIV, and a number of other diseases, and keeps the waiver provisions negotiated in advance of the June 1990 International Conference on AIDS in San Francisco. However, this “interim” rule will not expire after the 60 days. It will remain indefinitely until replaced by another rule. Without an outpouring of public support for removing HIV from the list, the PHS will be reluctant to implement the decision — even one unanimously supported by medical and public-health experts. The current policy will continue — including the travel ban, which will affect the May 1992 International Conference on AIDS in Boston. Also continuing will be the deportation of HIV-positive applicants under the immigration Amnesty program, who have lived in the United States for at least nine years
HUMAN PAPILLOMAVIRUS (HPV)
WHAT IS HPV? HOW CAN HPV BE DETECTED? CAN HPV INFECTION BE PREVENTED? HOW ARE HPV INFECTIONS TREATED? THE BOTTOM LINE NOTE: In the US, counseling and referrals are available on a national human papillomavirus (HPV) hotline. Call toll-free at 877- HPV-5868 (877-478-5868.) WHAT IS HPV? There are over 100 viruses known as human papilloma virus (HPV.) They are common. One study found HPV in 77% of HIV-positive women. HPV is transmitted easily during sexual activity. It is estimated that 75% of all sexually active people between ages 15 and 49 get at least one type of HPV infection. Some types of HPV cause common warts of the hands or feet. Infections of the hands and feet are usually not transmitted through sexual activity. Several types of HPV cause genital warts on the penis, vagina, and rectum. Those with HIV can get worse sores in the rectum and cervical areas. HPV can also cause problems in the mouth or on the tongue or lips. Other types of HPV can cause abnormal cell growth known as dysplasia. Dysplasia can develop into anal cancer in men and women, or cervical cancer, or cancer of the penis. Dysplasia around the anus is called anal intraepithelial neoplasia (AIN). Anal intraepithelial neoplasia is the development of new abnormal cells in the lining of the anus. Dysplasia in the cervical region is called cervical intraepithelial neoplasia (CIN). AIN or CIN appear to be more common in people with HIV infection than those who are HIV negative. HOW CAN HPV BE DETECTED? To detect HPV, health care providers look first for the problems HPVs cause: dysplasia or genital warts. Dysplasia can be detected by Pap smears. They are usually used to check a woman’s cervix. They can also be used to check the anus in men and women. A swab is rubbed on the area being checked to pick up some cells. They are smeared on a glass slide and examined under a microscope. Reflex HPV testing is used to follow up on Pap smear results that are not clear. It can indicate who needs more careful examination or treatment. The reflex test identifies which types of HPV are present and can indicate if aggressive treatment is needed. Some researchers believe that anal and cervical smears should be checked each year for people with elevated risk: People who have had receptive anal intercourse Women who have had cervical intraepithelial neoplasia (CIN) Anyone with under 500 CD4 cells. However, other researchers think that careful physical examination can detect as many cases of anal cancer as anal Pap testing. Genital warts can appear anywhere from a few weeks to a few months after you are exposed to HPV. The warts might look like small bumps. Sometimes they are fleshy and look like small cauliflowers. They can get bigger over time. Your health care provider can usually tell if you have genital warts by looking at them. Sometimes a tool called an anoscope is used to look at the anal area. If necessary, a sample of the suspected wart will be cut off and examined under a microscope. This is called a biopsy. Genital warts are not caused by the same HPV that causes cancer. However, if you have warts, you may have also been exposed to other types of HPV that could cause cancer. CAN HPV INFECTION BE PREVENTED? There is no easy way to tell if someone is infected with an HPV. People who don’t have any signs or symptoms of HPV infection can transmit the infection. Condoms do not totally prevent transmission of HPVs. HPVs can be transmitted by direct contact with infected areas that aren?t covered by a condom. Men and women with HIV who are sexually active may want to have a regular Pap smear, anal and/or vaginal, to check for abnormal cells or early signs of warts. A positive result can be followed up to see if treatment is needed. A vaccine called Gardasil was approved in 2006. However, it has not been tested in or approved for people already infected with HPV. HOW ARE HPV INFECTIONS TREATED? There is no direct treatment for HPV infection. Some people “clear” an HPV infection (are “cured”). They can later be infected with HPV again. However, dysplasias and warts can be removed. There are several ways to do this: Burning them with an electric needle (electrocautery) or a laser Freezing them with liquid nitrogen Cutting them out Treating them with chemicals Other, less common treatments for warts include the drugs 5-FU (5-fluorouracil) and Interferon-alpha. A new drug, imiquimod (Aldara®), has been approved for treatment of genital warts. Cidofovir (Vistide®), originally developed to fight cytomegalovirus (CMV), might also help fight HPV. HPV infection can last for a long time, especially in people who are HIV-positive. Dysplasia and warts can return. They should be treated as soon as they are found to reduce the chances of the problem spreading or returning. THE BOTTOM LINE Human papilloma viruses (HPV) are fairly common. Different types of HPV cause warts or abnormal cell growth (dysplasia) in or near the anus or cervix. This abnormal cell growth can result in cervical or anal cancer. Genital HPV infections are transmitted through sexual activity. HPV infection can last a long time, especially in people with HIV. A Pap smear can detect abnormal cell growth in the cervix. It can also be used to check the anus of men and women. Although Pap smears may be the best way to detect early cervical cancer, careful physical examination may be the best way to detect anal cancers. The signs of HPV infection – warts or dysplasia – should be treated as soon as they show up. Otherwise, the problem could spread and be more likely to return after treatment. For more information, see the web site https://www.thehpvtest.com/ source: The AIDS Infonet
VITAMIN C: LABORATORY TESTS INDICATE ANTIVIRAL EFFECT
A series of laboratory tests at the Linus Pauling Institute of Science and Medicine in Palo Alto, California found that ascorbate (vitamin C) reduced the growth of HIV in cultured human lymphocytes, in concentrations not harmful to the cells. The experimental study, conducted by Steve Harakeh, Ph.D., and Raxit J. Jariwalla, Ph.D., appears in the September issue of the Proceedings of the National Academy of Sciences, USA; results were also presented September 11 at “Ascorbic Acid: Biological Functions and Relation to Cancer,” an international symposium sponsored by the U.S. National Cancer Institute, and National Institute of Diabetes and Digestive and Kidney Diseases, in Bethesda, Maryland. The study is extensive and hard to summarize, but it showed a substantial reduction in measures of viral activity (p24, reverse transcriptase, and syncytia formation) without toxicity to cells at concentrations of 25 to 150 mcg/ml, with the higher concentrations working better. How much vitamin C would be needed to reach these levels in blood serum? This study did not measure blood levels, but the published paper cited measurements by others. One researcher found an average blood level of 28.91 mcg/ml after oral use of 10 grams of vitamin C. Another found that intravenous infusion of 50 grams a day led to a peak plasma level of 796 mcg/ml. Comment This research appears to have been carefully done; many measurements were made and the results all point in the same direction. We raised several questions, however, and gave Dr. Jariwalla a chance to respond. One potential limitation is that this study used cultured cells and viruses, which have been bred in laboratories; recently scientists have learned that viruses and cells freshly obtained from patients can give different, and presumably more reliable, results in drug screening. In our interview, Dr. Jariwalla noted that at this time there is no evidence that strains differ in resistance to ascorbate — but that different strains have not yet been tested. One question about the usefulness of vitamin C concerns the relatively narrow range between effective and toxic doses found in this study. Effectiveness began to be seen at 25 mcg/ml, but toxicity was found at 400 and above; half or more of the cells were killed by exposure to 400 mcg/ml or greater for four days. The therapeutic range is therefore fairly narrow; for some drugs, the corresponding ratio between effective and toxic doses is a thousand or more, compared to 16 (400 divided by 25) in this laboratory test of vitamin C. Dr. Jariwalla said that “although this may be so, there is no evidence of ascorbate toxicity found in human beings when large doses have been taken. The only side effect of high doses of ascorbate is a mild laxative effect. There are no reliable reports of severe ascorbate toxicity, such as acidosis or kidney stones.” Several years ago there was much interest in high-dose vitamin C as an AIDS treatment. By the end of 1987 this interest had greatly diminished, although some people continue to use the treatment today. One reason we have been skeptical of vitamin C is that if the treatment had worked well, it seems unlikely that the community would have stopped using it. Dr. Jariwalla said that interest in vitamin C as a potential AIDS treatment had diminished for several reasons. fFirst, the emphasis shifted to AZT and other nucleoside analogs as antivirals. Second, no clinical trials of vitamin C and AIDS got off the ground. And third, no hard scientific evidence of the effect of ascorbate on the AIDS virus was available until now. At least two clinical trials were proposed years ago by leading AIDS researchers, but no funding was available. The Linus Pauling Institute, which has long been interested in vitamin C, has heard “a number of reports…from AIDS patients who had taken high doses of vitamin C and had experienced a marked improvement in their condition” (quote from a press release accompanying the recently published article). It is possible that results today could be better than those of several years ago, when treatment was only used late in the illness. Today, treatments are started earlier; and AZT and others antivirals make possible combination therapies, which were not available during the time of great interest in vitamin C. The article suggests a rationale for such combinations. We asked Dr. Jariwalla what the study suggested about an appropriate dose of vitamin C. He said other results indicate that at least 10 grams orally would be needed to obtain the minimum blood levels for antiviral effect. Higher doses can be obtained through intravenous infusion, to reach plasma levels in the range found most effective in the laboratory tests. He cautioned, however, that further clinical studies are required to establish the optimum method of administration for maintaining high levels of ascorbate in the blood. Note: large doses of vitamin C are usually taken as a powder, not as pills. We asked about the different forms of the vitamin which are available. The Linus Pauling Institute sent us an information sheet which said that “Vitamin C, from Bronson Pharmaceuticals, La Canada, California, is available in the form of ascorbic acid, sodium ascorbate, calcium ascorbate, or sodium ascorbate and ascorbic acid combination.” The sodium or calcium ascorbate salts are used to reduce slight acidity in the urine due to ascorbic acid. Dr. Jariwalla said that for oral use of high doses, the mixture of sodium ascorbate and ascorbic acid should be used — or calcium ascorbate for persons on a sodium-restricted diet. We suggest that patients discuss vitamin C, or any treatment they are considering, with their physician. A nutritionist told us that some patients have sought treatment for diarrhea, not realizing that it was caused by taking too much vitamin C; until they told their physician that they were using the vitamin, the actual cause of the diarrhea was not suspected. Persons should also realize that suddenly stopping high doses of vitamin C can cause deficiency symptoms, as the body is used